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Document Type and Number:
WIPO Patent Application WO/1991/001133
Kind Code:
Peptides and pharmaceutical compositions comprising immunogenic peptides of a marker T cell receptor (TCR) characteristic of an immune-related disease, capable of preventing, suppressing, or treating the disease, are disclosed. In a preferred embodiment, the amino acid sequence of the peptide corresponds to at least part of a complementary determining region (CDR) or a hypervariable region of the TCR. Antibodies and/or T cells immunologically reactive to the TCR peptide capable of preventing, suppressing, or treating an immune-related disease by passive transfer are also disclosed.

Application Number:
Publication Date:
February 07, 1991
Filing Date:
July 19, 1990
Export Citation:
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International Classes:
A61K38/00; A61K39/395; A61P3/08; A61P25/00; A61P29/00; A61P37/06; A61P43/00; C07K7/08; C07K14/00; C07K14/705; C07K14/725; C07K16/00; A01N37/18; C07K16/28; C12N5/02; C12P21/02; C12P21/04; C12P21/08; G01N33/68; C12R1/91; A61K; (IPC1-7): A01N37/18; A61K31/00; A61K35/14; A61K37/00; A61K37/02; A61K39/00; C07K3/00; C07K5/00; C07K7/00; C07K13/00; C07K15/00; C07K17/00; C12P21/04
Other References:
Journal of Immunology, Vol. 144, No. 12, issued June 1990, G.A. HASHIM et al., "Antibodies Specific for VB8 Receptor Peptide Suppress Experimental Autoimmune Encephalitis", pages 4621-4627, see entire article.
Biological Abstracts, issued 1990, D.N. BOURDETTE et al., "Characterization of Basic Protein-Specific T-Cell Lines Selected from Lewis Rats with Relapsing Experimental Autoimmune Encephalomyelitis", pages 81-85, see Abstract 89059282.
Biological Abstracts, issued 1989, A.A. VANDENBARK et al., "Immunization with a Synthetic T-Cell Receptor V-Region Peptide Protects Against Experimental Autoimmune Encephalomyelitis", pages 541-544, see Abstract 38033335.
Biological Abstracts, issued 1989, G.A. HASHIM et al., "Defective T Helper Cell Epitope Responsible for the Failure of Region 69-84 of the Human Myelin Basic protein to Induce Experimental Allergic Encephalomyelitis in the Lewis Rat", pages 222-230, see Abstract 89016844.
Journal of Immunology, Vol. 141, No. 11, issued December 1988, H. OFFNER et al., "Encephalitogenic T Cell Clones with Variant Receptor Specificity", pages 3828-3832, see entire article.
Attorney, Agent or Firm:
Goldstein, Jorge A. (Kessler Goldstein & Fox, 1225 Connecticut Avenue, N.W., Suite 30, Washington DC, US)
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1. A peptide having about 1530 amino acids comprising an amino acid sequence of a T cell receptor, or a functional derivative of said peptide, wherein said T cell receptor is a marker T cell receptor characteristic of an immunerelated disease, said peptide being capable of inducing protection from said disease.
2. The peptide of claim 1 wherein said amino acid sequence is encoded by a T cell receptor V gene.
3. The peptide of claim 2 wherein said amino acid sequence is encoded by a VDJ region of said V gene.
4. The peptide of claim 2 wherein said amino acid sequence is encoded by a VJ region of said V gene.
5. The peptide of claim 2 wherein said amino acid sequence comprises at least part of a complementarity determining region.
6. The peptide of claim 5 wherein said complementarity determining region is the second complementarity determining region, CDR2.
7. The peptide of claim 2 wherein said amino acid sequence comprises at least part of a hypervariable region.
8. The peptide of claim 1 wherein said amino acid sequence is AspMetGlyHisGlyLeuArgLeuIleHisTyrSerTyr AspValAsnSerThrGluLysGly.
9. The peptide of claim 1 conjugated to a carrier.
10. The peptide of claim 1 conjugated to an antibody.
11. The peptide of claim 10 wherein said antibody is a monoclonal antibody.
12. A pharmaceutical composition comprising the peptide of any of claims 111 in admixture with a pharmaceutically acceptable exc pient.
13. The peptide of claim 1 wherein said disease is an autoimmune disease.
14. The peptide of claim 13, wherein said autoimmune disease is selected from the group consisting of rheumatoid arthritis, adjuvant arthritis, myasthenia gravis, encephalo¬ myelitis, multiple sclerosis, thyroiditis, diabetes, inflammatory bowel disease, and systemic lupus erythematosus.
15. The peptide of claim 1 wherein said disease is a malignant disease.
16. The peptide of claim 15 wherein said malignant disease is T cell lymphoma.
17. A method for preventing an immunerelated disease comprising administering to a subject an effective amount of the peptide of claim 1.
18. t.
19. A method for preventing an immunerelated disease comprising administering to a subject an effective amount of the . pharmaceutical composition of claim 12.
20. A method for suppressing an immunerelated disease 5 comprising administering to a subject an effective amount of the peptide of claim 1.
21. A method for suppressing an immunerelated disease comprising administering to a subject an effective amount of the pharmaceutical composition of claim 12.
22. 10 21.
23. A method for treating an immunerelated disease comprising administering to a subject an effective amount of the peptide of claim 1.
24. A method for treating an immunerelated disease comprising administering to a subject an effective amount of the 15 pharmaceutical composition of claim 12.
25. The method of any of claims 1722 wherein said disease is an autoimmune disease.
26. A method for selecting a peptide having an amino acid sequence of a T cell receptor, wherein said T cell receptor is a 20 marker T cell receptor characteristic of an immunerelated disease, said peptide being capable of inducing protection from * said disease, comprising the steps of: (a) removing T cells from a subject susceptible to said A disease; .
27. (b) expanding said T cells of step (a) in culture in the presence of an autoantigen preparation; (c) identifying the T cell receptor expressed by said expanded T cells of step (b); and (d) selecting said peptide from the amino acid sequence of said T cell receptor.
28. 25 The method of claim 24 wherein said identifying step (c) comprises determining the nucleotide sequence of at least part of the V gene encoding said said T cell receptor.
29. The method of claim 24 wherein said identifying step (c) comprises determining the amino acid sequence of at least part of said T cell receptor.
30. A method for preparing a peptide having an amino acid sequence of a T cell receptor, wherein said T cell receptor is a marker T cell receptor characteristic of an immunerelated disease, said peptide being capable of inducing protection from said disease, comprising the steps of: (a) selecting a peptide according to the method of any of claims 2426; and (b) synthesizing said peptide.
31. The method of claim 27 wherein said synthesis is by chemical synthesis.
32. The method of claim 27 wherein said synthesis is by expression of a nucleotide sequence encoding said peptide.
33. A method for preparing a polyclonal antibody capable of protecting a subject from an immunerelated disease comprising: (a) administering to an animal the peptide of claim 1 or 9; and „ (b) preparing said antibody from a body fluid of said animal . 5 31. A method for preparing a monoclonal antibody capable of protecting a subject from an immunerelated disease comprising: (a) administering to an animal the peptide of claim 1 or 9; 10 (b) removing spleen cells or B cells from said animal; (c) fusing said spleen or B cells with a fusion partner cell line resulting in production of a hybridoma which secretes said monoclonal antibody; and (d) preparing said secreted monoclonal antibody. 15 32. The method of claim 30 or 31 wherein said animal is a subject susceptible to said immunerelated disease.
34. 33 An antibody specific for the peptide of claim 1.
35. 34 The antibody of claim 33 which is a polyclonal antibody.
36. 20 35. The antibody of claim 33 which is a monoclonal antibody.
37. 36 The antibody of claim 33 which is chimeric. i 37. The antibody of any of claims 3336 conjugated to a cytotoxic agent.
38. 38 The antibody of claim 37 wherein said cytotoxic agent is a riboso al inhibitory protein.
39. 39. The antibody of claim 38 wherein said ribosomal inhibitory protein is a ricin A chain.
40. 40 A method for preventing an autoimmune disease comprising administering to a subject an effective amount of the antibody of any of claims 3339.
41. 41 A method for suppressing autoimmune disease comprising administering to a subject an effective amount of the antibody of any of claims 3339.
42. 42 A method for treating an autoimmune disease comprising administering to a subject an effective amount of the antibody of any of claims 3339.
43. 43 A method for preparing a protective T cell capable of protecting a subject from an autoimmune disease comprising: (a) removing T cells from said subject; (b) expanding the T cells of step (a) in culture in the presence of the peptide of claim 1 to produce a protective T cell; (c) preparing said protective T cell from said expanded T cells of step (b).
44. 44 The method of claim 44 additionally comprising, before step (a), the step of administering to said subject the peptide of claim 1.
45. 45 A method for preventing an autoimmune disease comprising administering to a subject an effective amount of protective T cells prepared according to the method of claim 43 or 44.
46. 46 A method for suppressing an autoimmune disease comprising administering to a subject an effective amount of protective T cells prepared according to the method of claim 43 or 44.
47. 47 A method for treating an autoimmune disease comprising administering to a subject an effective amount of protective T cells prepared according to the method of claim 43 or 44.
48. 48 A method for preventing an autoimmune disease comprising administering to a subject a combination of an effective amount of protective T cells prepared according to the method of claim 43 and an effective amount of the antibody of claim 33.
49. 49 A method for suppressing an autoimmune disease comprising administering to a subject a combination of an effective amount of protective T cells prepared according to the method of claim 43 and an effective amount of the antibody of claim 33.
50. 50 A method for treating an autoimmune disease comprising administering to a subject a combination of an effective amount of protective T cells prepared according to the method of claim 43 and an effective amount of the antibody of claim 33.

Cross-Reference to Related Application

This is a continuation-in-part of U.S. Patent Application Serial No. 07/467,577, filed January 19, 1990, which is a continuation-in-part of U.S. Patent Application Serial No. 07/382,804, filed July 19, 1989.


Field of the Invention The invention in the field of immunology and immunotherapy is directed to peptides and their pharmaceutical compositions which are capable of preventing, suppressing or treating immune- related diseases such as autoimmune and malignant diseases.

Description of the Background Art Autoimmune diseases are characterized by an unwanted and unwarranted attack by the immune system on the tissues of the host. While the mechanism for progress of these diseases is not well-understood, at least some of the details with respect to antigen presentation in this (and other) contexts is being elucidated. It is now thought that antigens, including autoantigens, are processed by antigen-presenting cells (APC), and the resulting fragments are then associated with one of the cell surface proteins encoded by the major histocompatibility complex (MHC). As a result, recognition of a peptide antigen is said to be MHC "restricted." When the MHC/antigen fragment complex binds to a complementary T cell receptor (TCR) on the surface of a T lymphocyte, it leads to activation and proliferation of the clone or subpopulation of T cells that bear that particular TCR. Once activated, T cells have the capacity


to regulate other cells of the immune system which display the processed antigen and to destroy cells or tissues which carry epitopes of the recognized antigen.

A review of the role of TCRs in autoimmune diseases by Acha-Orbea, H., et al. fAnn. Rev. Immunol. 7:371-405 (1989)) discussed the tremendous variation in TCRs available in the immune system of an individual and the generation of this diversity by germ line gene organization and rearrangement of the DNA encoding TCR a and β chains. The a chains are encoded by various combinations of variable (V), junction (J) and constant

(C) region gene segments. TCR β chains are additionally encoded by a diversity (D) region gene segment, and, thus comprise a rearranged VDJC sequence. Due to allelic exclusion, a clone of T cells expresses only one type of TCR O-B heterodimer. A growing number of human diseases have been classified as autoimmune in nature (see, Theofilopoulos, A., In: D.P. Stites, et al .. eds., Basic and Clinical Immunoloqv« Lange Medical Publications, Los Altos, CA, 1988) of which several examples are rheumatoid arthritis (RA), myasthenia gravis (MG), multiple sclerosis (MS), systemic lupus erythematosus (SLE), autoimmune thyroiditis (Hashimoto's thyroiditis), Graves' disease, inflammatory bowel disease, autoimmune uveoretinitis, polymyositis and certain types of diabetes. Animal models have been developed for a number of these human autoimmune diseases. Among the best studied model is experimental allergic encephalo yelitis (EAE, also called experimental autoimmune encephalomyelitis), a model for MS.

Because it is now known that these and other autoimmune diseases involve the action of T helper cells stimulated by the binding of their TCR to an MHC/autoantigen (or non-autoantigen) complex, prevention and/or treatment strategies have been proposed which are based on the disruption of interactions

■» between the MHC/antigen complex and the TCR. Wraith, D.C., et al. (Cell 57:709-715 (1989)), proposed approaches based on this i principle, including vaccination with whole T cells (as initially described by I.R. Cohen's laboratory, discussed below), passive 5 blockade using antibodies which bind to the TCR, passive blockade using antibodies that bind to the MHC portion of the complex, administration of antibodies reactive with the T helper cell marker, CD4, and the use of peptides which mimic the antigen of interest and compete for binding to the MHC or the TCR molecule.

10 Myelin basic protein, MBP, is the major autoantigen involved in EAE and is the leading candidate as an encephalitogen involved in MS.

Heber-Katz's group (Heber-Katz, E., et al.. Ann. N.Y. Acad. Sci. 540:576-577 (1988); Owhashi, M., et al.. J. EXP. Med.

15 168:2153-2164 (Dec. 1988)) has analyzed the fine specificity of recognition of MBP epitopes by rat T cells. When T cells from rats immunized with MBP were hybridized to a mouse T lymphoma line and cloned, the pattern of fine specificity and Southern blot analysis of the TCR Vβ gene rearrangement indicated a

20 polyclonal response, even though 75% of the clones reacted to the

68-88 encephalitogenic determinant. Amonoclonal antibody (mAb), designated 10.18, directed at one encephalitogenic T cell hybridoma proved to be an anti-idiotype or anti-clonotype which reacted only with T cell clones specific for the MBP 68-88

25 epitope. The mAb could block or reverse EAE when injected with, or 5 days after, the encephalitogenic MBP peptide. Soluble mAb 10.18 blocked the specific T cell clones, and immobilized mAb

' 10.18 stimulated their proliferation. Following induction of EAE with MBP, the proportion of mAb 10.18-binding cells increased

30 from initially very low frequencies. The authors concluded that the 10.18 * T cells probably represent the dominant pathogenic T cell repertoire of EAE in Lewis rats. However, it was not known

whether mAb 10.18 recognized a V region or an idiotypic determinant.

T cells expressing the TCR OB heterodi er can induce idiotypic and V gene family-specific antibodies that can regulate T cell function (Owhashi, M., et al., supra; Gascoigne, N.R.J., et al., Proc. Natl. Acad. Sci.. USA 84:2936 (1987); Kappler, J.W., et al.. Nature 332:35 (1988); Kappler, J.W., et al.. Cell 49:263 (1987); MacDonald, H.R., et al.. Nature 332:40 (1988)). For example, antibodies that recognize the TCR VB8 sequence have been effective in the prevention and treatment of autoimmunity in mice and rats (Owhashi, M., et al .. supra; Acha-Orbea, H., et al.. Cell 54:263-273 (1988); Urban, J., et al.. Cell 54:577-592 (1988)). Obtaining such antibodies selective for V region gene products has been dependent upon the availability of T cell clones that express TCR encoded by the relevant V gene family, and requires a laborious screening procedure using whole cells to establish specificity.

While antibody therapies in which antibodies are directed to MHC molecules and CD4 molecules have been generally successful in several animal models of autoimmunity, these approaches may be too nonspecific and potentially overly suppressive, since 70% of T cells bear the CD4 marker, and since all T cell-mediated responses and most antibody responses require MHC-associated antigen presentation. I.R. Cohen's laboratory has developed an approach to the immunospecific treatment of autoimmunity which utilizes whole live or attenuated T lymphocytes as vaccines to treat or prevent EAE, experimental autoimmune thyroiditis (EAT), and experimental arthritis. This approach is reviewed in Cohen, I.R., Immunol . Rev. 94:5-21 (1986), which discusses several animal models of autoimmune disease wherein vaccination with disease-specific T lymphocytes has been used to generate prophylactic or therapeutic

effects. The fine specificity of vaccination was dictated by the fine specificity of the T cell recognition, possibly implicating the TCR. For example, two different ant -MBP T cell lines, each reactive to a different epitope of MBP, were found to vaccinate against EAE specifically induced by the particular epitope, indicating some form of anti-idiotypic immunity. However, when attempts were made to isolate clones of MBP-specific or thyroglobulin-specific T cells (in a thyroiditis model) from the non-clonal cell lines, only clones producing disease, but not resistance, were obtained. This led to the finding that appropriate aggregation or rigidification of cell membranes, by either hydrostatic pressure or chemical cross-linking, yielded cells which could induce protection more consistently. Similarly, low doses (sub-encephalitogenic) of MBP-specific cells could also induce resistance to lethal EAE. The protective state was termed "counter-autoimmunity." This state involves T cell clones which can specifically proliferate in response to the vaccinating T cells, can suppress effector clones in vitro (non- specifically, presumably through release of a suppressive lymphokine), and can adoptively transfer counter-autoimmunity in vivo. Such counter-autoimmunity is accompanied by suppressed delayed hypersensitivity (DH) responses to the specific epitope and prevention or remission of clinical disease.

A major difficulty with the foregoing approaches is that they require the use of complex biological preparations which do not comprise well-defined therapeutic agents. Such preparations suffer from complex production and maintenance requirements (e.g., the need for sterility and large quantities of medium for producing large number of "vaccine" T cells), and lack reproducibility from batch to batch. The T cell "vaccine" preparations, to be useful in humans, must be both autologous and individually specific, that is, uniquely tailored for each

patient. Furthermore, the presence of additional antigens on the surface of such T cells may result in a broader, possibly detrimental, immune response not limited to the desired T cell clones (Offner, H. et al.. J. Neuroimmunol. 21:13-22 (1989). There is a great need, therefore, for agents and pharmaceutical compositions which have the properties of specificity for the targeted autoimmune response, predictability in their selection, convenience and reproducibility of preparation, and sufficient definition to permit precise control of dosage.


This invention was made in response to a clear need for therapeutic agents and compositions capable of preventing, suppressing or treating immune-related diseases in a clone- specific manner, without causing generalized suppression of immunity, as is the case with most current immunotherapeutic and immunopharmacologic approaches. The invention was developed from the knowledge that lines or clones of T cells specific for autoantigens, which actually mediated autoimmune disease, could be converted into therapeutics by complex attenuation protocols, and injected directly into animals to prevent or treat the disease.

The inventor's attempts to achieve such cellular im unotherapy resulted in less than optimal results. When using attenuation methods disclosed in the prior art, the inventor achieved varying, unpredictable levels of protection, and the resultant immunity was not clonally limited, presumably because whole cell "vaccines" introduce a variety of antigens.

In an attempt to simplify and standardize this general approach and achieve highly specific immunity wherein only those clones of T cells that recognized the disease-associated antigen were affected, the inventor conceived of the present invention. It was recognized for the first time by the present inventor that an immunogenic peptide can be synthesized which mimics a portion of a disease-associated immunological "marker," such as the TCR of T cells involved in the disease process. Unexpectedly, immunization of a subject with the peptide directs the host immune response against the "marker" and thereby prevents or suppresses the development of the disease or treats the ongoing disease.

One hallmark of the invention is a method for selecting which peptide to use for preventing, suppressing or treating an immune-related disease, based on identifying the amino acid sequence of a marker TCR associated with the disease, predicting which segment of the TCR sequence is immunogenic based on several known algorithms, and determining which site or sites in the TCR structure is an appropriate target for an immune response which will result in protection from the disease.

One embodiment of the invention is a peptide having about 15-30 amino acids comprising an amino acid sequence of a TCR which is a marker TCR associated with an immune-related disease.

The peptide, or its functional derivative is capable of inducing protection from the disease.

Other embodiments of the invention are directed to the above peptide, the sequence of which is encoded by a TCR V gene or specific portions of the V gene, such as the VDJ region, at least a part of a complementarity determining region (CDR) of the TCR such as CDR2, or at least part of a hypervariable region. The invention also encompasses the peptide conjugated to a carrier, such as an additional heterologous amino acid sequence, in order to enhance the peptide's immunogenicity.

The invention is also directed to a pharmaceutical composition comprising the peptide or its functional derivative, in admixture with a pharmaceutically acceptable excipient. Thus, the invention provides chemically defined peptides and therapeutics which can be specifically applied to designated immune-related diseases to disrupt the specific immunological responses responsible for induction or promotion of the disease process. The diseases for which the invention is particularly useful include autoimmune diseases, such as rheumatoid arthritis, adjuvant arthritis, myasthenia gravis, encephalomyelitis,

multiple sclerosis, thyroiditis, diabetes, inflammatory bowel disease and systemic lupus erythematosus. The invention is also directed to malignant disease, such as T cell leukemias and lymphomas wherein the TCR serves as a tumor marker. The invention provides methods for preventing, suppressing, or treating an immune-related disease comprising administering one of the above TCR peptides, their functional derivatives, or a pharmaceutical compositions comprising the peptide.

One embodiment of the invention is a method for selecting a peptide having an amino acid sequence of a T cell receptor which is a immune-related disease marker, comprising:

(a) removing T cells from a subject susceptible to the disease; (b) expanding the T cells in culture in the presence of an an autoantigen preparation;

(c) identifying the TCR V genes expressed by the expanded T cells; and

(d) selecting the peptide from the amino acid sequence of the TCR. The TCR V genes are identified through the use of TCR-specific antibodies or by determining the TCR amino acid sequence.

The invention further provides a method for preparing a peptide having an amino acid sequence of a TCR associated with an immune-related disease, comprising; (a) selecting a peptide, as described above; and

(b) synthesizing the peptide by chemical or recombinant means.

Other embodiments of the invention are directed to polyclonal, monoclonal, or chimeric antibodies specific for the TCR peptide which are capable of protecting a subject from an immune-related disease, and to methods for preparing such antibodies. Also encompassed by this invention are the

antibodies conjugated to cytotoxic agents, including ribosomal inhibiting proteins such as the ricin A chain.

The invention also includes methods for preventing, suppressing or treating autoimmune disease by passive immunization with one of the above antibody preparations.

An additional embodiment provides protective T cells capable of preventing, suppressing, or treating autoimmune disease, and methods for preparing such T cells which comprise:

(a) removing T cells from a subject susceptible to the disease;

(b) expanding the T cells of step (a) in culture in the presence of TCR-bearing material such as a TCR peptide; and

(c) preparing protective T cell from the expanded cultured T cells.


Figure 1. Peptide-specific inhibition of antibody reactivity. Antisera from 4 rats immunized with either the TCR Vβ8(39-59) peptide alone or a combination of the TCR peptide and the GP-S49S MBP-derived autoantigen were pooled and diluted 40- 360 fold. The antisera were tested for reactivity in direct ELISA with 25 ng peptide bound to m crop!ate wells. This amount of peptide is equivalent to 10 pM TCR VB8(39-59) (MW = 2390 daltons) or 15 pM GP-S49S (MW = 1630 daltons). Varying concentrations of inhibitor peptides were added in a range of 0.005 - 50 *g/well. The Absorbance measurements were determined in triplicate wells, and the reactivity calculated as the % of uninhibited control wells. Figure 2. Antibodies to the TCR VB8(39-59) peptide stain

VB8 + encephalitogenic T cells. Normal thymocytes (A and C) or

GP-S49S-specific T line cells (B and D) were incubated with rabbit antibodies to TCR Vβ8(39-59), followed by a mouse anti-

; rabbit IgG facilitating antibody and fluorescein-labeled goat anti-mouse IgG antibody. Flow cytometric analysis of staining

5 was performed using a Coulter Epics C Cytofluorograph. A and C represent dot-plots of 10,000 cells showing cell size versus fluorescence intensity; B and D represent the corresponding histograms. The fluorescence intensity of T line cells stained with anti-TCR VB8(39-59) antibody (>90% stained) is increased

10 compared to the 5% of normal thymocytes which stained with this antibody. Both thymocytes and T line cells incubated with normal rabbit IgG as a control for anti-TCR Vβ8(39-59) IgG showed background levels of staining (dotted line in box D).

Figure 3. Prevention, suppression and treatment of EAE

15 with 50 *g TCR VB8-39-59 peptide/CFA. Rats were injected s.q. with the TCR peptide 40 days prior to, at the same time, or at disease onset 12 days after the induction of EAE with 50 *g GP-


Figure 4. Suppression of EAE with 50 *g TCR VB8-39-59 20 peptide given i.d. in the ear at the same time, or on days 7 or

11 after induction of EAE with 50 ,g GP-MBP/CFA.

Figure 5. Treatment of EAE with 10 or 50 *g TCR VB8-39-59 peptide given i.d. in the ear at onset of clinical signs (day 12) after induction of EAE with 50 *g GP-MBP/CFA. 25 Fi ure 6. Peptide specificity of human MPB-specific T cell lines from MS pateints and normals.

Figure 7. Percentage of total proliferation response of T t cell lines directed at each peptide compared to percentage of total clones responding to each peptide. 30 Fi ure 8. Cellular responses to TCR VB8- and VB14 peptides from EAE-recovered and TCR peptide-i munized rats. DTH is given

in mm/100 and proliferation in CPM/1000, both background subtracted.

Figure 9. Treatment of relapsing EAE with TCR VB17 peptide.


In the following description, reference will be made to various methodologies known to those of skill in the art of immunology, cell biology, and molecular biology. Publications and other materials setting forth such known methodologies to which reference is made are incorporated herein by reference in their entireties as though set forth in full.

The compositions, methods, and products of this invention are applicable to human and veterinary uses. The peptides of the present invention comprise sequences of about 15-30 amino acids which are immunogenic, that is, capable of inducing an immune response when injected into a subject.

By "functional derivative" is meant a "fragment," "variant," "analog," or "chemical derivative" of the peptide, which terms are defined below.

It is understood that the amino acid sequence comprising the peptide of this invention can be used alone or bound to, or contained within the sequence of, a longer peptide. The longer peptide may carry additional sequence derived from the TCR of interest or may include sequences of an unrelated peptide, such as a carrier protein used to enhance the immunogenicity of the TCR oligopeptide. Such carriers are well known in the art and include heterologous proteins such as, for example, keyhole limpet hemocyanin (KLH), bovine serum albumin, tetanus toxoid and the like. Also included within the scope of this invention is the peptide conjugated to an antibody, and the peptide conjugated to a toxin. The toxins of this invention include the ribosomal inhibitory protein, such as, for example, the ricin A chain or Pseudo onas toxin. As used herein, "marker TCR" refers to a TCR which is characteristic of a specified immune-rel ted disease, such as autoimmune disease or malignant disease (i.e. cancer).

The term "immune-related disease" as used herein refers to a disease in which the immune system is involved in the pathogenesis of the disease, or in which appropriate stimulation of the immune system can result in protection from the disease. A preferred example of an immune-related disease to which this invention is directed is an autoimmune disease. Non-limiting examples of the autoimmune diseases contemplated by this invention are rheumatoid arthritis (RA), myasthenia gravis (MG), multiple sclerosis (MS), systemic lupus erythematosus (SLE), autoimmune thyroiditis (Hashimoto's thyroiditis), Graves' disease, inflammatory bowel disease, autoimmune uveoretinitis, polymyositis and certain types of diabetes.

Thus, a marker TCR for MS is a TCR which is capable of binding the complex between self MHC and the MBP fragment (or the MBP fragment alone), the MBP comprising the major autoantigen characteristic of this disease. In other autoimmune diseases, other TCRs serve as markers, as they are specific for the complex between MHC molecules and the autoantigens involved in these diseases. For example, in myasthenia gravis (MG), the autoantigen is thought to be the nicotinic acetylcholine receptor

(AChR). Therefore, an identifiable TCR which binds AChR in the context of self MHC (or directly) and is expressed by AChR- reactive T cells which mediated the disease is a "marker TCR" for MG. Those of skill will recognize that determination of a marker TCR and of i munogenic peptides may be accomplished with the exercise of routine skill, using screening methods as are well- known in the art, when the teachings of the present invention are fully appreciated.

Also intended as immune-related diseases as used herein are malignancies wherein the tumor cell carries a tumor marker, such as a tumor antigen, capable of being recognized and responded to

by the immune system. The TCR can serve as a tumor marker on T cell leukemia or T cell lymphoma cells.

In a subjected afflicted with, or susceptible to, an immune-related disease, introduction of the peptide carrying the amino acid seqeuence of a portion of the marker TCR results in generation of an immune response directed to the TCR and protection from the immune-related disease.

By the term "protection" from the disease as used herein is intended "prevention," "suppression" or "treatment" of the disease. "Prevention" involves administration of the protective composition prior to the induction of the disease. Thus, for example, in the animal model, EAE, successful administration of a protective composition prior to injection of the encephalitogen that induces the disease results in "prevention" of the disease.

"Suppression" involves administration of the composition after the inductive event but prior to the clinical appearance of the disease. Again, using the EAE example, successful administration of a protective composition after injection of the encephalitogen, but prior to the appearance of neurological symptoms comprises "suppression" of the disease.

"Treatment" involves administration of the protective composition after the appearance of the disease. In the EAE example, successful administration of a protective composition after injection of the encephalitogen and after clinical signs have developed comprises "treatment" of the disease.

It will be understood that in human medicine, it is not always possible to distinguish between "preventing" and "suppressing" since the ultimate inductive event or events may be unknown, latent, or the patient is not ascertained until well after the occurrence of the event or events. Therefore, it is common to use the term "prophylaxis" as distinct from "treatment"

to encompass both "preventing" and "suppressing" as defined herein. The term "protection," as used herein, is meant to include "prophylaxis."

For the embodiment of the invention directed to autoimmune disease, the subject's immune response is directed to the particular TCRs which mark those T cells mediating the autoimmune process, and the peptides according to the invention thus are able to interfere with the binding of the MHC/antigen complex (or the antigen alone) needed for initiation or propagation of the autoimmune response.

In general, the peptide sequence represents a portion of the TCR itself and preferably corresponds to a portion of the TCR which is extracellular, exposed to antibody or other T cells, and is of biological importance in the activity of the T cell bearing the TCR. For the purposes of this invention, the peptide must be immunogenic, as defined below.

Peptides of the invention include those corresponding to a portion of the V region of the TCR. More preferbly, the peptide corresponds to a segment of the VDJ region of the TCR β chain or the VJ region of the TCR α chain. In a preferred embodiment, the peptide corresponds to at least part of one of the three complementarity determining regions (CDRs) of the TCR heterodimer, such as second CDR (CDR2). Also intended within the scope of this invention are peptides corresponding to at least part of the TCR γ and TCR s chains, their V regions, and CDR structures or their ho ologs in the γ* heterodimer (see Strominger, J.L., Cell 57:895-898 (1989); and Clevers, H. et al .. Ann Rev. Immunol. 6:629-662 (1988)).

The CDRs of the TCR are defined by analogy to the structure of the immunoglobulin molecule wherein the CDRs comprised the amino acid sequences of the heavy or light chain variable regions which contacted antigen and constituted crucial portions of the

# antigen-binding site. All three TCR CDRs are believed to participate in binding to antigen and MHC (Davis, M.M., et al .. Nature 334:395-402 (1988); Claverie, J.M., et al.. Immun. Today 10 . :10-14 (1989)). By directing the immune response of the 5 subject, the protective antibodies or the protective T cells of this invention against one of the CDRs of the "marker TCR," the likelihood of disrupting necessary binding or recognition events between the autoimmunity-associated T cell the and autoantigen and/or MHC is increased.

10 A "fragment" of the peptide of the present invention, refers to any subset of the molecule, that is, a shorter peptide.

A "variant" of the peptide refers to a molecule substantially similar to either the entire peptide or a fragment thereof. Variant peptides may be conveniently prepared by direct

15 chemical synthesis of the variant peptide, using methods well- known in the art.

Alternatively, amino acid sequence variants of the peptide can be prepared by mutations in the DNA which encodes the synthesized peptide. Such variants include, for example,

20 deletions from, or insertions or substitutions of, residues within the amino acid sequence. Any combination of deletion, insertion, and substitution may also be made to arrive at the final construct, provided that the final construct possesses the desired activity. Obviously, the mutations that will be made in

25 the DNA encoding the variant peptide must not alter the reading frame and preferably will not create complementary regions that could produce secondary mRNA structure (see European Patent Publication No. EP 75,444).

At the genetic level, these variants ordinarily are

30 prepared by site-directed mutagenesis of nucleotides in the DNA encoding the peptide molecule, thereby producing DNA encoding the variant, and thereafter expressing the DNA in recombinant cell

culture. The variants typically exhibit the same qualitative biological activity as the nonvariant peptide.

Preparation of a peptide variant in accordance herewith is preferably achieved by site-specific mutagenesis of DNA that encodes an earlier prepared variant or a nonvariant version of the TCR protein or peptide. Site-specific mutagenesis allows the production of peptide variants through the use of specific oligonucleotide sequences that encode the DNA sequence of the desired mutation, as well as a sufficient number of adjacent nucleotides, to provide a primer sequence of sufficient size and sequence complexity to form a stable duplex on both sides of the deletion junction being traversed. The technique of site- specific mutagenesis is well known in the art, as exemplified by Adelman et al.. DNA 2:183 (1983). Typical vectors useful in site-directed mutagenesis include vectors such as the M13 phage, for example, as disclosed by Messing et al .. Third Cleveland Symposium on Macromolecules and Recombinant DNA. Walton, A., ed., Elsevier, Amsterdam (1981). These phage are readily commercially available and their use is generally well known to those skilled in the art. Alternatively, plasmid vectors that contain a single-stranded phage origin of replication (Veira et al ., Meth. Enzymol . 153:3 (1987)) may be employed to obtain single-stranded DNA.

In general, site-directed mutagenesis in accordance herewith is performed by first obtaining a single-stranded vector that includes within its sequence a DNA sequence that encodes the relevant peptide. An oligonucleotide primer bearing the desired mutated sequence is prepared, generally synthetically, for example, by the method of Crea et al ., Proc. Natl. Acad. Sci. (USA) 75:5765 (1978). This primer is then annealed with the single-stranded protein-sequence-containing vector, and subjected to DNA-polymer zing enzymes such as E. coli polymerase I Klenow

fragment, to complete the synthesis of the mutation-bearing strand. Thus, a mutated sequence and the second strand bears the desired mutation. This heteroduplex vector is then used to transform appropriate cells and clones are selected that include recombinant vectors bearing the mutated sequence arrangement.

The mutated protein region may be removed and placed in an appropriate vector for protein production, generally an expression vector of the type that may be employed for transformation of an appropriate host. An example of a terminal insertion includes a fusion of a signal sequence, whether heterologous or homologous to the host cell, to the N-terminus of the peptide molecule to facilitate the secretion of mature peptide molecule from recombinant hosts.

Another group of variants are those in which at least one amino acid residue in the peptide molecule, and preferably, only one, has been removed and a different residue inserted in its place. Such substitutions preferably are made in accordance with the following list when it is desired to modulate finely the characteristics of a peptide molecule.

Substantial changes in functional or immunological properties are made by selecting substitutions that are less

conservative than those in the above list, that is, by selecting residues that differ more significantly in their effect on maintaining (a) the structure of the peptide backbone in the area of the substitution, for example, as a sheet or helical conformation, (b) the charge or hydrophobicity of the molecule at the target site, or (c) the bulk of the side chain. The substitutions that in general are expected to those in which (a) glycine and/or proline is substituted by another amino acid or is deleted or inserted; (b) a hydrophilic residue, e.g., seryl or threonyl, is substituted for (or by) a hydrophobic residue, e.g., leucyl, isoleucyl, phenylalany!, valyl, or alanyl; (c) a cysteine residue is substituted for (or by) any other residue; (d) a residue having an electropositive side chain, e.g., lysyl, arginyl, or histidyl, is substituted for (or by) a residue having an electronegative charge, e.g., glutamyl or aspartyl; or (e) a residue having a bulky side chain, e.g., phenylalanine, is substituted for (or by) one not having such a side chain, e.g., glycine.

Most deletions and insertions, and substitutions in particular, are not expected to produce radical changes in the characteristics of the peptide molecule. However, when it is difficult to predict the exact effect of the substitution, deletion, or insertion in advance of doing so, one skilled in the art will appreciate that the effect will be evaluated by routine screening assays. For example, a variant typically is made by site-specific mutagenesis of the peptide molecule-encoding nucleic acid, expression of the variant nucleic acid in recombinant cell culture, and, optionally, purification from the cell culture, for example, by im unoaffinity adsorption on an anti-peptide antibody column (to absorb the variant by binding it to at least one epitope).

The activity of the cell lysate or purified peptide variant is then screened in a suitable screening assay for the desired characteristic. For example, a change in the immunological character of the peptide nolecule, such as binding to a given antibody, is measured by a competitive type im unoassay. Changes in T cel recognition of the variant peptide is measured by a DH assay in vivo or a T cell proliferation assay in vitro. Modifications of such peptide properties as redox or thermal stability, hydrophobicity, susceptibility to proteolytic degradation or the tendency to aggregate with carriers or into multimers are assayed by methods well known to the ordinarily skilled artisan.

An "analog" of a peptide refers to a non-natural molecule substantially similar to either the entire molecule or a fragment thereof.

A "chemical derivative" of a peptide of this invention contains additional chemical moieties not normally a part of the peptide. Covalent modifications of the peptides are included within the scope of this invention. Such modifications may be introduced into the molecule by reacting targeted amino acid residues of the peptide with an organic derivatizing agent that is capable of reacting with selected side chains or terminal residues.

Cysteinyl residues most commonly are reacted with o- haloacetates (and corresponding amines), such as chloroacetic acid or chloroacetamide, to give carboxymethyl or carboxyamido ethyl derivatives. Cysteinyl residues also are derivatized by reaction with bromotrifluoroacetone, o-bromo-β-(5- imidozoyl)propionic acid, chloroacetyl phosphate, N- alkylmaleimides, 3-nitro-2-pyridyl disulfide, methyl 2-pyridyl disulfide, p-chloromercuribenzoate, 2-chloromercuri-4- nitrophenol, or chloro-7-nitrobenzo-2-oxa-l,3-diazole.

Histidyl residues are derivatized by reaction with diethylprocarbonate at pH 5.5-7.0 because this agent is relatively specific for the histidyl side chain. Para- bromophenacyl bromide also is useful; the reaction is preferably performed in 0.1 M sodium cacodylate at pH 6.0.

Lys nyl and amino terminal residues are reacted with succinic or other carboxylic acid anhydrides. Derivatization with these agents has the effect of reversing the charge of the lysinyl residues. Other suitable reagents for derivatizing β- amino-containing residues include i idoesters such as methyl picol inimidate; pyridoxal phosphate; pyridoxal; chloroborohydride; trinitrobenzenesulfonic acid; O-methylissurea; 2,4 pentanedione; and transaminase-catalyzed reaction with glyoxylate. Arginyl residues are modified by reaction with one or several conventional reagents, among them phenylglyoxal, 2,3- butanedione, 1,2-cyclohexanedione, and ninhydrin. Derivatization of arginine residues requires that the reaction be performed in alkaline conditions because of the high pK a of the guanidine functional group. Furthermore, these reagents may react with the groups of lysine as well as the arginine epsilon-amino group.

The specific modification of tyrosyl residues per se has been studied extensively, with particular interest in introducing spectral labels into tyrosyl residues by reaction with aromatic diazonium compounds or tetranitromethane. Most commonly, N- acetylim dizol and tetranitromethane are used to form 0-acetyl tyrosyl species and 3-nitro derivatives, respectively. Tyrosyl residues are iodinated using 15 I or 131 I to prepare labeled proteins for use in radioimmunoassay, the chloramine T method being suitable.

Carboxyl side groups (aspartyl or glutamyl) are selectively modified by reaction with carbodiimides (R'-N-C-N-R') such as 1-

cyclohexyl-3-(2-morpholinyl-(4- ethyl) carbodiimide or l-ethyl-3 (4 azonia 4,4-dimethylpentyl) carbodiimide. Furthermore, aspartyl and glutamyl residues are converted to asparaginyl and glutaminyl residues by reaction with ammonium ions. Glutaminyl and asparaginyl residues are frequently deamidated to the corresponding glutamyl and aspartyl residues. Alternatively, these residues are deamidated under mildly acidic conditions. Either form of these residues falls within the scope of this invention. Derivatization with bifunctional agents is useful for cross-linking the peptide to a water-insoluble support matrix or to other macromolecular carriers. Commonly used cross-linking agents include, e.g., l,l-bis(diazoacetyl)-2-phenylethane, glutaraldehyde, N-hydroxysuccinimide esters, for example, esters with 4-azidosalicylic acid, homobi functional imidoesters, including disuccinimidyl esters such as 3,3'- dithiobis(succinimidylpropionate), and bifunctional malei ides such as bis-N-maleimido-l,8-octane. Derivatizing agents such as methyl -3- [(p-azidophanyl)dithio]propioimid ate yield photoactivatable intermediates that are capable of forming crosslinks in the presence of light. Alternatively, reactive water- insoluble matrices such as cyanogen bromide- activated carbohydrates and the reactive substrates described in U.S. Patent Nos. 3,969,287; 3,691,016; 4,195,128; 4,247,642; 4,229,537; and 4,330,440 are employed for protein immobilization.

Other modifications include hydroxyl ation of proline and lysine, phosphorylation of hydroxyl groups of seryl or theonyl residues, methyl ation of the β-amino groups of lysine, arginine, and histidine side chains (T.E. Creighton, Proteins: Structure and Molecule Properties. W.H. Freeman & Co., San Francisco, pp.

79-86 (1983)), acetylation of the N-terminal amine, and, in some instances, amidation of the C-terminal carboxyl groups.

Such derivatized moieties may improve the peptide's solubi¬ lity, absorption, biological half life, and the like. The moieties may alternatively eliminate or attenuate any undesirable side effect of the peptide and the like. Moieties capable of mediating such effects are disclosed, for example, in Remin g ton's

Pharmaceutical Sciences. 16th ed., Mack Publishing Co., Easton, PA (1980) Malignant Disease

Also susceptible to methods of the invention are lymphomas and leukemias. Lymphomas and many leukemias are tumors made up of lymphocytes that undergo uncontrolled proliferation (e.g., are malignant). Since several classes of leukemia and lymphoma are composed of T cells derived from a single malignant T cell precursor, all of the tumor cells bear the same TCR, which thus serves as a "tumor marker" which can be the target of protective compositions of this invention. Similarly, surface immunoglobulins can serve as tumor markers for B cell leukemias or lymphomas.

One embodiment of the invention is directed to the enhancement of an ant -tumor response by targeting the TCR of those T cells reacting against the "tumor marker" rather than the tumor marker itself. Thus, an immune response directed to the TCR on a tumor-specific T cell can be used to upregulate the antitumor response for the benefit of the host. In fact, it will be appreciated that any disease involving a cell having a surface molecule that distinguishes that cell from other cells of the same histological type and from cells of a different histological type, contains a characteristic

"marker," and will be susceptible to treatment by compositions which induce an immune response to the "marker," thereby altering activity of the cell bearing the "marker."

According to the present invention, the marker molecule itself may be relatively nonimmunogenic; it requires, at minimum, a characteristic antigenic epitope. This epitope itself may be inherently immunogenic, or it can be rendered immunogenic by treatments well known in the art, such as conjugation to an immunogenic carrier molecule. Thus, an epitope of a marker protein, either as a free peptide or in a form rendering it immunogenic, is capable of eliciting an antibody response, a cell-mediated immune response, or both, as conceived in the invention. Therefore, a composition which incorporates not the entire marker protein, but rather, a specific peptide region which is immunogenic or antigenic, will comprise a useful preparation for treating an immune-related disease characterized by this marker.

Identification of Marker TCR-Bearinq T Cells

The present invention utilizes a synthetic peptide that represents a region of the TCR having biological importance in ligand/MHC binding, such as CDR2, and that is characteristic of a TCR V gene family. The invention therefore provides a much simpler approach for obtaining TCR V region-specific antibodies or T cells. Using other sequences from the same B chain to induce a spectrum of TCR V region-specific antibodies or T cells, those of skill will be able to map exposed epitopes of the TCR, and to establish the importance of these regions in ligand/MHC binding, with the exercise of routine skill.

Marker TCRs associated with a given disease are identified using known techniques. A genetic approach using patients known to have MG or MS was described by Oksenberg, J.R., et al .. Proc. Natl. Acad. Sci. USA 86:988-992 (1989). Sequences of the appropriate TCR β chain have been obtained by genomic analysis using restriction fragment length polymorphisms found in families

having a prevalence of the particular autoimmune disease, as described by Seboun, E., et al.. Cell 87:1095-1100 (1989); Burns, F.R., et al.. J. Exo. Med. 169:27-39 (1989)).

It thus will be appreciated that, for the purposes of the present invention, determination of the marker TCR associated with an autoimmune disease and identification of peptides comprising an immunogenic sequence do not require that the autoantigen be characterized. It is sufficient that (a) the autoimmune disease involves a T cell-mediated immune response as a necessary part of the pathogenetic process, and (b) the disease has an organ-, tissue- or cell-specific target. In fact, as is known in the art (see, for example, Theofilopoulos, A., supra), the autoimmune disease may not involve an autoantigen at all at the inductive stage, but rather, may represent a response to an exogenous antigen, such as a bacterial or viral antigen, which is cross-reactive with self antigens, or results in an immunopathologic response directed to the exogenous antigen present in the host.

T cells recognizing an autoantigen or autoimmune disease- associated antigen (such as certain viral or bacterial antigens) are cloned, and may be fused to an immortalizing cell, such as a long term T cell line, a T cell lymphoma line or a T cell hybridoma, and are grown in culture. The cultured cells serve as the source of cDNA encoding the appropriate TCR. Such cDNA is cloned and expressed by methods well known in the art. (See, for example, Maniatis, T., et al .. Molecular Cloning: A Laboratory Manual. (1982)).

In addition to the foregoing approaches, it will be appreciated that advantage may be taken of animal models to identify the TCR variable region loci which are associated with the autoimmune disease. Animals which are susceptible to any of a number of autoimmune diseases, non-limiting examples of which

include EAE, experimental MG, experimental autoimmune thyroiditis, adjuvant arthritis, collagen-induced arthritis, and the like, have a particular TCR variable locus associated with the disease which can be identified in vitro. By the term "susceptible to a disease" is intended a state in which the animal possesses a gene or genes known to be associated with the disease, thereby increasing the risk that the individual with that gene or genes will develop that disease compared to the general population. Genes known to be associated with autoimmune diseases, for example, include MHC genes

(especially class II), immunoglobulin V genes, TCR V genes, and the like. The term "susceptible" is also intended to encompass those individuals who actually have the disease. While a complete correlation between an autoimmune disease and the usage of a particular TCR is neither expected nor necessary to successfully practice the present invention, high correlations of about 60-70% have been found for presence or expression of a particular variable region gene and susceptibility to autoimmune disease in animals. In an alternate embodiment of this invention, T cells isolated from humans who are susceptible to an autoimmune disease, and in particular susceptible individuals who have the autoimmune disease, are expanded in culture. Techniques for T cell expansion are described by Zamvil et al .. Nature 317:355-358 (1985), and Nature 324:258-260 (1986).

In one embodiment employing this method, patient peripheral blood lymphocytes are removed and stimulated with the autoantigen or a specific peptide derived therefrom or related thereto, which is capable of stimulation comparable to that of the autoantigen. The autoantigen (or related peptide) is added to the lymphocyte cultures for several days. In one embodiment, cells are simulated with autoantigen for 5-6 days. In other embodiments,

cells are stimulated for longer periods of time. The time required for stimulation is a function of the proportion of reactive cells in the blood sample, the activation state of these cells, and the potency of the stimulating preparation, and is readily determinable by one of skill in the art. After culture under such selective conditions, about 5 x 10 5 viable cells are isolated and restimulated with about 3 x 10 7 autologous antigen- presenting cells (irradiated to prevent their prol feration, such as with about 2500-4500 rad) and about 20 *g/ml of the autoantigen (or related peptide). About 7 days later, viable cells are collected and cloned by limiting dilution in the presence of about 10 3 - 10 6 antigen presenting cells, for example about 5 x 10 5 antigen-presenting cells, and human IL-2 or crude or pure combinations of lymphocyte growth factors (such as, for example, IL-4). The cells of such a T cell line are expanded and grown in tissue culture flasks for about one to two weeks. Such lines can be multiply restimulated with antigen-presenting cells, autoantigen preparations, and IL-2. Restimulation can typically be carried out once a week. If desired, such T cells can be cloned by any of a number of methods known in the art, such as, for example, limiting dilution or by picking cells from colonies growing in soft agar, generally about 2 days after restimulation.

In another embodiment, lymphocytes from an organ or body fluid are first cultured in the presence of IL-2. Under these conditions, selection will occur for cells already activated and only such cells grow. Subsequently, such T cells are stimulated with antigen-presenting cells and an autoantigen preparation. Using this approach, MBP-specific T cells from the spinal cord of rats with EAE can be selectively expanded in vitro. As used in the present invention, the term "autoantigen" is not intended to be limiting to a defined or known macromolecule. For example, in the case of type I diabetes, the particular

antigen associated with pancreatic islet (or beta) cells that is the trigger or target antigen of the T cell-mediated autoimmune response is unJnown. For the present invention, the autoantigen used to stimulate cells in vitro, as described above, can comprise whole pancreatic islet cells, crude membrane preparations derived from such cells, partially purified purified membrane components, or when identified, the diabetogenic autoantigen. The same is true for other autoimmune diseases for which a unique autoantigen has not yet been identified, including Hashimoto's thyroiditis, arthritis in which the autoantigen is not collagen, Sjogren's disease, poly yositis, arteriosclerosis, and the like. One of skill will appreciate that as long as the immunogenic moiety to which the T cells respond is present in the stimulatory preparation, the methods of the invention can be carried out as described.

The presence of autoantigen-specific reactive T cells in the cloned, expanded T cell population can be readily determined by testing the ability of the cells to be activated in the presence of the autoantigen. Many assays are available, and well known in the art, to measure early or late events in the T cell activation process. Example of such methods include, but are not limited to, T cell proliferation (which can be measured as the uptake of radiolabeled thymidine), the secretion of interleukin- 2, intracellular calcium mobilization, translocation of particular membrane enzymes involved in inositol phosphate metabolism, and changes in expression of cell surface molecules (which can be determined by flow cytometry).

The TCR expressed by a T cell clone responding to a particular autoantigen can be identified using TCR-specific antibodies, either polyclonal, monoclonal or chimeric (see below) which are specific for a TCR variable segment, to detect surface expression, employing techniques of fluorescence microscopy, flow

cytometry, immunocytochemistry, or other techniques known in the art. Such antibodies have been described for a number of TCR a - chain V regions (see, for example, Owhashi, M., et al .. supra; Gascoigne, N.R.J., et al .. supra: Kappler, J.W., et al ., 1987, 1988 fsupra); and MacDonald, H.R., supra).

Alternatively, the DNA or mRNA of the T cell clone can be probed directly, or after amplification by the polymerase chain reaction (Synha et al.. Science 239:1026 (1988); Saiki et al.. Nature 324:163 (1986), by specific hybridization with nucleic acid probes for the various TCR gene families, using hybridization methods well known in the art. The TCR sequence, or a part thereof, can then be obtained directly from the amplified, rearranged DNA or mRNA.

Expression of a particular TCR can also be identified by determining the nucleic acid sequence encoding at least part of the TCR, for example, after cloning the TCR V gene, or by determining the amino acid sequence of at least part of a TCR protein. It will be apparent that any of the abovementioned approaches, or additional approaches known to one of skill in the art, will result in the identifying of the TCR expressed on a T cell or clone or line of T cells. This information is needed for the selection of an amino acid sequence which comprises the peptide or pharmaceutical preparations of this invention.

Where no specific autoantigen has been identified, the oligoclonality of T cells in the anatomic region associated with the disease can be used as a basis for enrichment of reactive T cells. For instance, cells uniquely associated with rheumatoid arthritis are found in the synovia! fluid of the joint; cells uniquely associated with MS are found in the cerebrospinal fluid (CSF); and disease-associated T cells infiltrate the thyroid tissue in Hashimoto's thyroiditis and in Graves' disease. In these instances, T cells are isolated from the relevant

anatomical location, and the cells expanded in culture as described above. (See also, Londei, M. et al .. Science 228:85-89 (1985); Londei, M. et al. Acta Endocrinol. 115(SUDP1.281):86-89 (1987); Stamenkovic, I. et al. Proc. Natl. Acad. Sci. USA 5 85:1179-1183 (1988); Lipoldova, M. et al. J. Autoimmun. 2:1-13

(1989); Oksenberg, J.R., et al.. supra). The DNA or mRNA of such cells is isolated, cDNA prepared, and the differences in sequences of cDNA encoding the variable TCR loci are established by comparison of afflicted with unafflicted subjects. As an

10 alternative to expanding the cells in culture, cellular DNA or, preferably, cDNA made from mRNA, can be obtained directly from T cells isolated from the subject, and the nucleic acid expanded by the PCR reaction, as above.

The antigens associated with a number of human and animal

15 model autoimmune disease are presently known. Type II collagen and Mvcobacterium tuberculosis 65 kD heat shock protein are antigens associated with rheumatoid arthritis; AChR is associated with MG, and with experimental allergic myasthenia gravis (EAMG) which can be induced in mice. Thyroglobulin is

20 known to be the antigen associated with experimental allergic thyroiditis (EAT) in mouse. A similar disease, Hashimoto's thyroiditis involves an immune response to an antigen on thyroid follicular cells. In Graves' disease, the immune response is directed to the thyrotropin receptor on thyroid cells. Myelin

25 basic protein (MBP) and proteolipid protein (PLP) are known to be associated with experimental allergic encephalomyelitis (EAE) in mouse and rat. EAE is a recognized model for multiple sclerosis in humans.


Therefore, those of skill will appreciate that the present 30 invention is directed in one aspect to identification of peptides

+ useful for prevention or therapy of human and animal diseases, including but not limited to those mentioned above.

Selection of Antigenic Peptides

An important embodiment of this invention comprises the combined method of identifying a TCR associated with an autoimmune disease, determining which oligopeptide sequence of the TCR is both immunogenic and important for T cell action in the disease process, synthesizing that peptide, and using it as a therapeutic agent.

Regions of relevant TCR sequences are identified for synthesis on the basis of their predicted antigenic or immunogenic properties. By the term "immunogenic" is intended the capacity of a peptide to induce an immune response, either T cell-mediated, antibody, or both. By the term "antigenic" is intended the capability of a peptide to be recognized, in free form by antibodies and in the context of MHC molecules in the case of antigen-specific T cells. Regions of a protein or peptide that are likely to be immunogenic or antigenic for T cells are identified, for examle, using the approaches and algorithms described by Margalit, H. et al. (J. Immunol. 138:2213-2229 (1987) and Rothbard, J.B. et al . EMBO J. 7:93-100 (1988)). The Margalit et al . approach is based on analysis of immunodo inant helper T cell antigenic sites leading to development of an algorithm based on an amphipathic helix model, in which antigenic sites are postulated to be helices with one predominantly polar and one predominantly apolar face. The approach of Rothbard et al ., recognizes motifs similar to epitopes recognized preferentially by T helper or T cytotoxic cell clones, which can predict accurately areas within protein sequences that are capable of being recognized by MHC class I and II molecules, such recognition being assumed as necessary for T cell immunogenicity and antigenicity.

In one approach for selecting TCR peptides, the regions of the TCR which are of immunoregulatory importance for the purposes

of this invention (based on current models of the structure of the TCR and analogy to antibody structure) fall within CDR1, CDR2, or CDR3, or in TCR hypervariable regions not strictly part of a CDR, such as residues 39-49 of the Vβ segment (see Davis, M.M. et al.. Nature 334:395-402 (1988)).

The use of the above approach to select peptide sequences for use in treating EAE in rats exemplifies the success of this approach. For example, a peptide comprising 16 amino acids corresponding to CDR1 of the the marker TCR for EAE in Lewis rats, VB8 (25-41) was predicted by the above algorithms not to be immunogenic for T cells. In fact, this peptide does not induce T cell immunity and does not protect Lewis rats from EAE. A peptide corresponding to the CDR1 of a different TCR β chain which is not associated with EAE, VB14(25-41), was predicted to be immunogenic for T cells, and indeed was found to induce T cell immunity in Lewis rats, but, as expected, did not protect from EAE. Similarly the CDR2 peptide, Vβl4(39-59), corresponding to an TCR not associated with EAE, was predicted to be immunogenic, and did induce immunity, but, again, did not protection from EAE. According to the invention, the CDR2-related peptide of the relevant TCR, Vβ8(39-59), was predicted to be both immunogenic and protective in EAE, and indeed, was shown to be so (see Examples, below).

The size of the peptide selected for use in this invention is largely determined by the requirement for immunogenicity, while maintaining the minimal epitope structure such that a T cell or antibody specific for the peptide will recognize and react with the TCR on an intact T cell. For example, peptides of this invention, in order to be sufficiently immunogenic and to have a high probability of including the relevant epitope of the

TCR which can lead to modulation of T cell activity, are of the range of about 15-30 amino acids, although peptides of differing

length are also contemplated. The successful use of a 21 amino acid TCR peptide present on the TCR _ chain associated with EAE in rats to treat EAE according to the methods of this invention is amply demonstrated in the Examples below. Immunogenicity of peptides useful in the present invention can be screened by well-known methods, such as use of a DH response in an animal. In such a response, an animal is "sensitized" by injection of an appropriate dose of an antigen, typically subcutaneously (SC), frequently with an adjuvant, such as complete Freund's adjuvant (CFA). Generally about 5-15 days later, the response is "elicited" by challenging the animal, typically intradermally (ID), with an appropriate dose of the antigen, typically in saline or other buffer. The response is assessed 24-48 hours later. Non-limiting examples of assay methods which measure DH include size of erythema (redness) and induration (swelling) at the site of antigen injection, ear swelling, footpad swelling, tail swelling, accumulation of systemically injected 125 I-labeled iododeoxyuridine in the challenge site, accumulation of intravenously (IV) injected radio!abeled serum protein, such as albumin, in the challenge site, and accumulation of IV-injected labeled inflammatory cells, such as lymphocytes or neutrophils, in the challenge, site. For example, an ear swelling response upon appropriate ID challenge in the ear pinna of about 0.15-0.25 mm, and preferably about 0.20 mm (in a Lewis rat) represents a positive DH response. One skilled in the art will understand that variations in peptide size, dose, route of sensitization or elicitation of DH, carriers used, adjuvants used, etc., will affect the timing and extent of the DH response. For a peptide to be considered immunogenic, as intended here, a dose of about 10-200 *g per animal, and preferably about 25-100 *g of the peptide per animal should be able to sensitize

an animal for a DH response. Furthermore, in a sensitized animal, a dose of about 1-100 *g, and preferably about 5-50 *g, of the peptide is able to elicit a DH response upon ID challenge.

Synthesis of Peptides and Assay

The desired peptides, with sequences determined as described above, are prepared using standard synthesis techniques including solution and solid phase sequential amino acid conjugation and recombinant production in prokaryotic or eukaryotic hosts. Verification that the peptide prepared is immunogenic can easily be determined using a DH reaction in an animal (e.g., mouse or rat), as described above. The peptide is administered subcutaneously, and the animal is challenged about 9-14 days later ID in the ear pinna. The ear swelling response, measured 24 or 48 hours after challenge, serves as a simple and reliable measure of the presence of T cell-mediated immunity to the peptide.

Verification of the ability of the immunogenic peptide to actually modulate autoimmunity may be attained using an appropriate animal model, taking into account the species differences in the TCR-related peptides. For example, although it is preferred to use a sequence representing the CDR2 of a human marker TCR in treating humans, the corresponding region of the marker TCR for the animal disease model is used in the animal disease.

Animal model systems which can be used to screen the effectiveness of the peptides in protecting against or treating the disease are available, as discussed above. Of course, the identical peptides may not be effective in humans since they may not correspond to an appropriate site of the disease-associated human TCR, or may not be sufficiently immunogenic in humans. It is to be understood that modifications of the peptide sequence

delineated in a particular animal model may be required in order to treat subjects belonging to other species, including humans. Thus, verification that, for example, a particular CDR2- associated peptide sequence is effective in protecting against a particular disease can be obtained in these models, leading to predictions that the corresponding human sequence would be a preferred candidate as an effective peptide therapeutic for humans. Determination of the corresponding TCR sequence in the human (or in different non-human animal species), using approaches described above, thus permits modification of the peptide for use in the human (or other species).

The following is a non-exclusive list of animal disease models of human autoimmune diseases with which a TCR peptide can be assessed for its ability to modify disease, and to induce antibodies and T cells which are capable, upon transfer, of modifying disease. Systemic lupus erythematosus (SLE) is tested in susceptible mice as disclosed by Knight et al .. J. EXP. Med.

147:1653 (1978) and Reinertsen et al.. N. Enq. J. Med. 299:515

(1978). MG is tested in SJL/J female mice by inducing the disease with soluble AChR protein from another species as described in Lindstrom, J., et al .. Adv. Immunol. 42:233-284

(1988). Arthritis is induced in a susceptible strain of mice by injection of Type II collagen as described by Stuart, J.M., et al.. Ann. Rev. Immunol. 2:199-218 (1984). Adjuvant arthritis is induced in susceptible rats by injection of Mycobacterial heat shock protein as described by Van Eden, W., et al .. Nature

331:171-173 (1988). Thyroiditis is induced in mice by administration of thyroglobulin as described by Maron, R., et al.. J. EXP. Med. 112:1115-1120 (1980). Insulin-dependent diabetes mellitus (IDDM) occurs naturally or can be induced in certain strains of mice such as those described by Kanasawa et al.. Diabetologia 27:113 (1984). Other mouse strains can be

caused to exhibit this disease by transferring lymphocytes from this strain.

EAE in mouse and rat serves as a model for MS in humans. In this model, the de yelinating disease is induced by administration of yelin basic protein (MBP) or proteolipid protein (PLP), or Theiler's virus, as described by Paterson, P.Y., Textbook of Immunopathology (Mischer et al .. eds.), Grune and Stratton, New York, pp. 179-213 (1986); McFarlin, D.E., et al.. Science 171:478-480 (1973); and Satoh, J., et al.. j Immunol. 138:179-184 (1987).

For measuring preventative, suppressive, or therapeutic benefit of the compositions of this invention in humans, certain clinical outcome measures are used. In MS, for example, quantitative parameters include: (a) clinical disability, (b) on- study exacerbation rate, and (c) magnetic resonance imaging (MRI) brain plaque load (which is an important recent parameter used to evaluate MS patients). These measures involve separate blinded examination or unblinded examination by a treating physician. Neuropsychological measures of cognitive impairment are used as an independent deteminant of disability. Clinical disability is typically measured by the McAlpine Scale, the Kurtzke Score, a modification Kurtzke Score termed the Expanded Disability Status Score (EDSS). An improvement of k unit on the EDSS (Range of 1- 9) is considered significant. One clinical measure, the patients ability to walk, is rated by the A bulation Index, wherein an improvement of 1 or more units is considered significant. These clinical measures are well known in the art and are described in detail in McAlpine, D., et al ., Multiple Sclerosis, Livingston Press, Edinburgh (1955); Binken, P.J. et al .. Handbook of Clinical Neurology. Volume 9, Amsterdam-North Holland Publishers,

Amsterdam (1970); and Field, E.J. et al .. Multiple Sclerosis: A

Critical Review, M.M.T.P Press, Ltd., Lancaster, England, (1977).

Measurement of improvement in RA, for example, is based on a number of primary clinical endpoints, including resolution or reduction of swelling, reduction in duration of morning stiffness, decreased erythrocyte sedimentation rate and/or C- reactive protein, resolution of rheumatoid-associated conditions as rheumatoid nodules, and reduction in lymphocyte counts. Secondary endpoints include reduction in fatigue and improvement in overall condition as assessed by the patient and the physician. Clinical outcomes are divided into the following: (a) Complete Response - greater than 90% decrease in joint swelling, tenderness, and morning stiffness; (b) Marked Response - 50-90% decrease in joint swelling, tenderness, and morning stiffness; (c) Moderate Response - 30-50% decrease in joint swelling, tenderness, and morning stiffness; and (d) No Response - <30% decrease in joint swelling, tenderness, and morning stiffness.

Similar measurements which allow evaluation of the preventive, suppressive, or treatment effects of the peptides, antibodies, T cells and other compositions of the present invention in additional immune-related disease are known to those of skill in the art.

Passive Immunity

In addition to the use of a TCR peptide for active immunization, further embodiments of the present invention involve T cells which have been activated by the TCR peptide, and antibodies specific for the TCR peptide, for passive transfer of anti-TCR immunity. Passive antibody-mediated immunity may involve any of a number of effector mechanisms, such as, for example, antibody-dependent cellular cytotoxicity, or complement- dependent cytotoxicity. Alternatively, the antibody is used to

deliver a toxic agent in a specific manner, such as ricin A chain, for example.

For passive vaccination, a subject animal is injected with the appropriate peptide, as described below, and the peripheral blood lymphocytes or lymphocytes from another organ, such as a draining lymph node, are harvested. The T cells may be used directly to transfer immunity. Alternatively, the T cells may be grown in culture in the presence of the TCR peptide as a selective stimulus, expanded with the aid of IL-2 or other T cell growth factors which are known in the art, maintained as a T cell line or clone, and then used to transfer immunity. B cells may be recovered from the initial cell population taken from the TCR peptide-immunized animal, and immortalized by fusion to cell line fusion partners using standard techniques to produce hybridomas for production of monoclonal antibodies specific for the TCR peptide. Hybridomas producing appropriate antibodies are screened by conventional immunoassays, such as direct ELISA assays, for reactivity with the TCR peptide antigen or with the relevant T cells. Monoclonal antibodies (mAbs) to specific antigens, such as the TCR peptides of this invention, may be obtained by methods known to those skilled in the art. See, for example, Kohler and Milstein, Nature 256:495-497 (1975) and U.S. Patent No. 4,376,110. Such antibodies may be of any immunoglobulin class, including IgG, IgM, IgE, IgA, IgD, and any subclass thereof.

Alternatively, antibodies can be prepared from polyclonal antisera taken from animals immunized with the TCR peptide, subjected to various purification schemes known in the art, and used directly for passive transfer of anti-TCR immunity. Monoclonal antibodies of rodent origin are "humanized" by linking a cDNA molecule encoding the V region of the mAb to DNA encoding the human constant region, using any of several

approaches described in Cabilly et al.. U.S. Patent 4,816,567 (3/28/89) and Eur. Patent Pub. EP125023 (11/14/84); Taniguchi et al.. Eur. Patent Pub. EP171496 (2/19/86); Morrison et al.. Eur. Patent Pub. EP173494 (3/5/86); Neuberger et al.. PCT Pub. W08601533 (3/13/86); Kudo et al.. Eur. Patent Pub. EP184187

(6/11/86); Robinson et al.. PCT Pub. WO 8702671 (5/7/87); Cabilly et al.. Proc. Natl. Acad. Sci. USA 81:3273-3277 (1984); Morrison et al.. Proc. Natl. Acad. Sci. USA 81:6851-6855 (1984); Boulianne et al.. Nature 312:643-646 (1984); Morrison, Science. 229:1202- 1207 (1985); Neuberger et_£L, Nature 314:268-270 (1985); Takeda et al.. Nature 314:452-454 (1985); Tan et al .. J. Immunol. 135:3564-3567 (1985); Jones et al.. Nature 321:522-525 (1986); Oi et al .. BioTechniques 4:214 (1986); Sahagan et al ., J. Immunol . 137:1066-1074 (1986); Sun et al.. Hvbridoma 5 (SUPP. 1 :S17-S19 (1986); Sun et al .. Proc. Natl. Acad. Sci. USA 84:214-218 (1987);

Liu et al.. Proc. Natl. Acad. Sci. USA 84:3439-3443 (1987); Liu et al.. J. Immunol. 139:3521-3526 (1987); Better, M., et al.. Science 240:1041-1043 (May 20, 1988); and Horwitz, A. H., et al .. Proc. Natl. Acad. Sci. USA 85:8676-8682 (1988)). The preferred method of chimeric antibody production combines five elements: (1) Isolation of messenger RNA (mRNA) from a mouse B cell hybridoma line producing the monoclonal antibody, cloning and cDNA production therefrom; (2) Preparation of a full length cDNA library from purified mRNA, from which the appropriate variable (V) region gene segments of the light (L) and heavy (H) chain genes can be (i) identified with appropriate probes, (ii) sequenced, and (iii) made compatible with a constant (C) region gene segment; (3) Preparation of C region gene segment modules by cDNA preparation and cloning; (4) Construction of complete H or L chain coding sequences by linkage of the cloned specific immunoglobulin V region gene segments described in (2), above, to cloned human C region gene segment modules described in

(3); and (5) Expression and production of chimeric L and H chains in selected hosts, including prokaryotic and eukaryotic cells.

_. Many vector systems are available for the expression of cloned H and L chain genes in mammalian cells (see Glover, D.M., 5 ed., DNA Cloning. Vol. II. ppl43-238, IRL Press, 1985).

Different approaches can be followed to obtain complete H 2 L 2 antibodies. It is possible to co-express H and L chains in the same cells to achieve intracellular association and linkage of H and L chains into complete tetrameric H 2 L 2 antibodies. The

10 co-expression can occur by using either the same or different pl smids in the same host. Genes for both H and L chains can be placed into the same plasmid, which is then transfected into cells, thereby selecting directly for cells that express both chains. Alternatively, cells may be transfected first with a

15 plasmid encoding one chain, for example the L chain, followed by transfection of the resulting cell line with an H chain plasmid containing a second selectable marker. Cell lines producing H 2 L 2 molecules via either route can be transfected with plasmids encoding additional copies of H, L, or H plus L chains, in

20 conjunction with additional selectable markers, to generate cell lines with enhanced properties, such as higher production of assembled H 2 L 2 antibody molecules or enhanced stability of the transfected cell lines.

The chimeric antibodies of this invention have both the

25 TCR-recognizing specificity of the mouse mAb and the biological properties of human antibodies, which include resistance to clearance in the human and much less immunogenicity (allowing Ϊ multiple treatments).

The anti-TCR peptide antibodies (polyclonal, monoclonal and t 30 chimeric) of this invention can be used therapeutically as immunoconjugates (see for review: Dillman, R.O., Ann. Int. Med.

111:592-603 (1989)). They can be coupled to cytotoxic proteins,

including ribosomal inhibitory proteins such as Ricin-A, Pseudomonas toxin, and Diphtheria toxin, as well as other proteins such as tumor necrosis factor. Toxins conjugated to antibodies or other ligands, are known in the art (see, for example, Olsnes, S. et al.. Immunol. Today 10:291-295 (1989)).

An additional example of such a conjugated antibody is XomaZyme- CD5 Plus, which is an anti-CD5 mAb conjugated to ricin A chain. This preparation is effective in prophylaxis and therapy of graft-versus-host disease, and of refractory rheumatoid arthritis in humans. This particular toxin-conjugated antibody is specific for most T lymphocytes and a subset of B lymphocytes. Cells having the CD5 marker drop rapidly in response to treatment. Since antibody to a TCR peptide will react with a much smaller proportion of total lymphocytes, higher doses of an anti-TCR antibody conjugated to ricin A will be tolerated by patients, or conversely, lower doses will be effective. Effective doses of a ricin A conjugated monoclonal antibody to a TCR peptide are in the range of about 0.005 to 0.5 mg/kg/day, with the preferred dose in the range of about 0.05 to 0.2 mg/kg/day. The anti-TCR peptide antibodies of this invention can be conjugated to additional types of therapeutic moieties including, but not limited to, radionuclides and cytotoxic drugs, to treat individuals with autoimmunity or with malignant or lymphoproliferative disease. Non-limiting examples of radionuclides which can be coupled to antibodies and delivered in vivo to sites of antigen include 2ϊ2 Bi, 131 I, 186 Re, and 90 Y. Such radionuclides exert their cytotoxic effect by locally irradiating the cells, leading to various intracellular lesions, as is well- known in the art of radiotherapy. Cytotoxic drugs which can be conjugated to antibodies and subsequently used for in vivo therapy include, but are not limited to, daunorubicin, doxorubicin, methotrexate, and

mitomycin C. Cytotoxic drugs interfere with critical cellular processes including DNA, RNA, and protein synthesis. For a fuller exposition of these classes of drugs which are known in the art, and their mechanisms of action, see Goodman, A.G., et a ., Goodman and Gilman's The Pharmacological Basis of

Therapeutics. 7th Ed., Macmillan Publishing Co., (1985).

Treatment of an individual using the antibodies, fragments or derivatives of this invention comprises parenterally admininstering a single or multiple doses of the antibody, fragment or derivative thereof. The effective dose is a function of the individual antibody, the presence and nature of a conjugated therapeutic agent, the subject and his clinical status, and can vary from about 10 ng/kg body weight to about 100 mg/kg body weight. The route of administration may include IV, SC, intramuscular, intrapulmonary, intraperitoneal (IP), intranasal, intrathecal, intradermal, transdermal or other known routes. Formulation of Peptides

The preclinical and clinical therapeutic use of the present invention in the treatment of disease or disorders will be best accomplished by those of skill, employing accepted principles of diagnosis and treatment. Such principles are known in the art, and are set forth, for example, in Braunwald, E. et al .. eds., Harrison's Principles of Internal Medicine. 11th Ed., McGraw- Hill, publisher, New York, N.Y. (1987).

The peptides and compositions of the present invention, or their functional derivatives, are well suited for the preparation of pharmaceutical compositions. The pharmaceutical compositions of the invention may be administered to any animal which may experience the beneficial effects of the compositions of the invention. Foremost among such animals are humans, although the invention is not intended to be so limited.

The pharmaceutical compositions of the present invention may be administered by any means that achieve their intended purpose. For example, administration may be by parenteral, subcutaneous, intravenous, intradermal, intramuscular, intraperi- toneal, transdermal, or buccal routes. Alternatively, or concur¬ rently, administration may be by the oral route. The peptides and pharmaceutical compositions can be administered parenterally by bolus injection or by gradual perfusion over time.

The dosage administered will be dependent upon the age, sex, health, and weight of the recipient, kind of concurrent treatment, if any, frequency of treatment, and the nature of the effect desired.

The dose ranges for the administration of the compositions of the present invention are those large enough to produce the desired effect, whereby, for example, an immune response to the peptide, as measured by DH or antibody production, is achieved, and the immune-related disease is significantly! prevented, suppressed, or treated. The doses should not be so large as to cause adverse side effects, such as unwanted cross reactions, generalized im unosuppression, anaphylactic reactions and the like.

Preferred doses for humans range between about 0.001 - 25 mg/kg body weight.

In addition to peptides of the invention which themselves are pharmacologically active, pharmaceutical compositions may contain suitable pharmaceutically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically. Preferred compositions include the inclusion of an adjuvant, such as alum, or other adjuvants known in the art. (See, for example, Warren, H.S. et al .. Ann. Rev. Immunol.

4:369-388 (1986); Chedid, L., Feder. Proc. 45:2531-2560 (1986)).

To enhance delivery or bioactivity, the peptides can be incorporated into liposomes using methods and compounds known in the art.

Preparations which can be administered orally in the form

5 of tablets and capsules, preparations which can be administered rectally, such as suppositories, and preparations in the form of solutions for injection or oral introduction, contain from about

0.001 to about 99 percent, preferably from about 0.01 to about 95 percent of active compound(s), together with the excipient.

10 Suitable excipients are, in particular, fillers such as saccharides, for example lactose or sucrose, mannitol or sorbitol, cellulose preparations and/or calcium phosphates, for example tricalcium phosphate or calcium hydrogen phosphate, as well as binders such as starch paste, using, for example, maize

15 starch, wheat starch, rice starch, potato starch, gelatin, tragacanth, methyl cellulose, hydroxypropylmethylcellulose, sodium carboxymethylcellulose, and/or polyvinyl pyrrolidone.

Other pharmaceutical preparations which can be used orally include push-fit capsules made of gelatin, as well as soft,

20 sealed capsules made of gelatin and a plasticizer such as glycerol or sorbitol. The push-fit capsules can contain the active compounds in the form of granules which may be mixed with fillers such as lactose, binders such as starches, and/or lubricants such as talc or magnesium stearate and, optionally,

25 stabilizers. In soft capsules, the active compounds are preferably dissolved or suspended in suitable liquids, such as fatty oils, or liquid paraffin. In addition, stabilizers may be

_ added.

Possible pharmaceutical preparations which can be used

,, 30 rectally include, for example, suppositories, which consist of a combination of one or more of the active compounds with a suppository base. Suitable suppository bases are, for example,

natural or synthetic triglycerides, or paraffin hydrocarbons. In addition, it is also possible to use gelatin rectal capsules which consist of a combination of the active compounds with a base. Possible base materials include, for example, liquid triglycerides, polyethylene glycols, or paraffin hydrocarbons.

Suitable formulations for parenteral administration include aqueous solutions of the peptides in water-soluble form, for example, water-soluble salts. In addition, suspensions of the peptides as appropriate oily injection suspensions may be administered. Suitable lipophilic solvents or vehicles include fatty oils, for example, sesame oil, or synthetic fatty acid esters, for example, ethyl oleate or triglycerides. Aqueous injection suspensions may contain substances which increase the viscosity of the suspension include, for example, sodium carboxy- methyl cellulose, sorbitol, and/or dextran. Optionally, the suspension may also contain stabilizers.

The peptides are formulated using conventional pharma¬ ceutically acceptable parenteral vehicles for administration by injection. These vehicles are nontoxic and therapeutic, and a number of formulations are set forth in Remington's

Pharmaceutical Sciences, (supra). Nonli iting examples of excipients are water, saline, Ringer's solution, dextrose solution and Hank's balanced salt solution. Formulations according to the invention may also contain minor amounts of additives such as substances that maintain isotonicity, physiological pH, and stability.

The peptides of the invention are preferably formulated in purified form substantially free of aggregates and other protein materials, preferably at concentrations of about 1.0 ng/ml to 100 mg/ml .

Effective doses of the peptides of this invention for use in preventing, suppressing, or treating an immune-related disease

are in the range of about 1 ng to 100 mg/kg body weight. A preferred dose range is between about 10 ng and 10 mg/kg. A more preferred dose range is between about 100 ng and 1 mg/kg.

The immunogenicity of the peptide may be enhanced by including it in a longer peptide or chain or by conjugating it to

"immunological" carriers, such as KLH, serum albumin, tetanus toxoid, and the like, using standard linking techniques. A variety of such methods is known in the art, e.g., use of condensing agents such as dicyclohexylcarbodiimide or use of linkers, such as those commercially available from Pierce

Chemical Co., Rockford, IL.

For the passive immunization with the TCR peptide-specific T cell preparations of this invention, the harvested T cells are suspended in a suitable vehicle, such as physiologically buffered saline, and injected into the subject in an amount of approximately 10 5 -10 9 cells per injection. Doses of TCR peptide- specific antibodies vary as a function of antibody species origin, isotype, affinity, nature (polyclonal, monoclonal, chimeric) and other characteristics which are known to one of skill. For example, a monoclonal antibody to a TCR peptide will be administered at a dose of between 0.01 - 50 mg/kg.

Also contemplated within the scope of this invention is passive immunization with a combination of protective T cells and TCR peptide-specific antibodies (polyclonal, monoclonal, or chimeric) in free or conjugated form.

The following examples are intended to be illustrative, but not to limit, the invention.



Introduction EAE is a well-recognized rat model of the human autoimmune disease, multiple sclerosis. Accordingly, the utility of the present invention was demonstrated by showing that the administration of the peptide representing the appropriate CDR2 peptide of the TCR which, in rats, is a marker TCR for EAE, prevents EAE in these animals. In this model, the disease is induced by injecting the subject rat with an encephalitogenic form of myelin basic protein, such as, for example, guinea pig basic protein (GPBP) or a synthetic peptide that corresponds to residues 72-89 of GPBP (GPBP(72-89)). Injection of either of these peptides in complete Freund's adjuvant (CFA) induces encephalitogenic T cell clones that utilize preferentially the rat homologs of mouse TCR Vo2 and VB8 genes (Chou, Y.K., et al ., J. Neurosci. Res. 22:181-187 (1989); Burns, F.R., et al .. J. EXP. Med^ 169:27-39 (1989)). The inventors reported the complete nucleotide and deduced amino-acid sequence for the rearranged rat TCR and B chain genes (with sequence homology to the mouse Vo2 and VB8 families respectively) used in response to the major encephalitogenic epitope of basic protein, GPBP(72-89)( Burns, F.R., et al.. supra). Within the TCR VB8 region, a 21-amino acid sequence was identified and synthesized that included the second complementarity determining region (CDR2) and was predicted to be immunogenic for T cells (based on the algorithms of Margalit et al. and Rothbard et al . (supra). This peptide has the sequence: Asp-Met-Gly-His-Gly-Leu-

Arg-Leu-Ile-His-Tyr-Ser-Tyr-Asp-Val-Asn-Ser-Thr-Glu-Lys-G ly and is termed "TCR V B 8(39-59)."

A control peptide was synthesized from the corresponding region for a different TCR VB sequence that was homologous to the mouse VB14 family (Williams et al .. supra). Specific Immunitv to TCR Peptide Four rats were immunized by subcutaneous (SC) injection of

400 ng TCR peptide in CFA (100 *g Mycobacterium/rat) and peptide- specific immune responses were measured after 30 days.

To measure antibodies specific for TCR VB8(39-59) peptide, serum from the immunized rats was tested by direct ELISA. THe TCR peptide was coated onto plastic microplates (25 ng of TCR peptide/well). Serum dilutions were added and the plates incubated for 2 hours. The reaction was developed by addition of peroxidase-conjugated antibodies specific for Ig H and L chains. A chromogenic substrate for peroxidase was added and the colored reaction product was measured as the absorbance at 405 nm

(A 405 ) using a colorimetric plate reader.

A 1:200 dilution of immune serum gave an absorbance of 0.63 ± 0.12 units. Control sera from rats immunized with the control peptide (derived from the corresponding CDR2 region of an unrelated TCR chain, Vβl4) gave a reaction of only 0.02 ± 0.01 units. Thus, a specific antibody response was obtained to the TCR peptide.

In addition, the rats showed a specific T cell response in vivo, measured as a delayed hypersensitivity (DH) reaction to intradermal (ID) challenge with the VB8(39-59) TCR peptide, but not with the Vβl4 peptide.

Table 1

Immunization with TCR VΛ8 Peptide Prevents Induction of EAE

I tπ o

I comp e e reun s a uvan ays a er pep e or sa ne


2 Rats were Injected SC with either: (1) 100 μg of the TCR peptide [DMGHGLRLIHYSDVNSTEKG (single-letter code)) representing residues 39-59 of the rat cDNA clone VΛ510, homologous to the mouse VΛ8 family (Burns et a1, f J. Exp. Med. i£9_:27-39 (1989)); (2) 100 μg of TCR peptide [APGGTLQQLFYSFNVGQSELF] representing residues 39-59 of the rat cDNA clone CRTB188 homologous to the mouse VΛ14 family (Williams, CB. et al.. J. Immunol. 142:1037-1035 (1989)); or (3) saline. The peptides or saline were mixed with CFA containing 100 μg Mvcobacterla prior to Injection.

3 Values represent the mean of the maximum severity of EAE. 0, no signs; 0.5, lethargy, weight loss; 1, limp tall; 2, h1nd-leg weakness; 3, hind-quarter paralysis, incontinence; 4, moribund.

TCR Peotide-Specific Immunity Protects Against Clinical EAE

In addition to showing specific immunity toward the TCR + peptide, the peptide-immunized rats were found to be protected against clinical EAE. 5 Immunization of Lewis rats with the TCR VB8(39-59) peptide, but not with the TCR Vβl4 peptide or saline, prevented completely the induction of EAE (Table 1). The VB8(39-59)- immunized rats developed both specific antibodies to the Vβ8(39- 59) peptide and a delayed hypersensitivity (DH) response of 0.17 10 mm ear swelling to 50 *g TCR Vβ8(39-59) peptide. The control

Vβl4 peptide also induced specific immunity to itself but did not confer protection against EAE. TCR Peotide-Specific Immunity Generates Specific T Cells

In addition to demonstration of antibody production, DH, 15 and protection against EAE, the TCR peptide elicited demonstrable antigen-specific (i.e., TCR peptide-specific) T cells.

Rats were immunized SC with 400 *g TCR Vβ8(39-59) peptide in CFA (containing 1 mg M. tuberculosis) and were challenged SC with either 50 *g GPBP in CFA at the same time or with 100 *g of 20 GPBP 30 days later. Twenty days after the simultaneous challenge, draining lymph nodes (LN) were removed and lymphocyte suspensions prepared.

A fraction of the cells were tested for proliferative response to antigens or mitogens in vitro (5 x 10 s cells/well).

25 The remainder of the cells were restimulated in bulk culture (in 6 cm. diameter petri dishes) with the appropriate TCR

- peptide (50 *g/ml) for 3 days followed by transfer to IL-2 rich medium for an additional 4 days. These cells were subsequently

* tested for proliferative responses to antigens or and mitogens by

30 restimulation in the presence of irradiated thymic accessory cells ((2 x 10 A cells/well). In some cases, stimulation by TCR

peptide was carried out in the presence of 2 *g/well monoclonal antibodies. Results are shown in Table 2 (underlined values show statistically significant responses).

Lymph node (LN) cells isolated from the protected rats responded to the TCR VB8(39-59) peptide as well as to GPBP and

PPD (purified protein derivative of M. tuberculosis). This was further evidence for the concurrent presence of TCR-specific as well as autoantigen-specific T cell reactivity.

T-cell lines were selected from the LN of the protected rats that responded specifically to the VB8(39-59) but not to the

Vβl4 peptide (Table 2). The TCR VB8(39-59)-specific T cells were strongly positive by immunofluorescence for the CD4 marker and weakly positive for the CD8 marker. The proliferative response to the Vβ8(39-59) peptide was restricted only by MHC class I molecules.

A GPBP-specific T-cell line was also selected from protected rats immunized with both the TCR VB8(39-59) peptide and GPBP. This line had an uncharacteristically low response to the encephalitogenic 72-89 peptide in comparison to its responsiveness to GPBP. Once selected and activated, GPBP- specific T cell line cells from TCR peptide-protected rats were encephalitogenic (administration of 10 7 cells caused hind-leg paralysis in 3 rats), indicating that TCR VB8(39-59) peptide immunization did not result in the deletion of precursors of encephalitogenic T cells.

Mixing of the TCR VB8(39-59)-specific and BP-specific T cells did not impair the response to GPBP, even in the presence of the TCR peptide (Table 2). The presence of TCR

Table 2

Specificity of T Cell Lines Derived from Rats Protected from EAE by the TCR V^8 Peptide

Underlined values indicate significant stimulation. --, not done.

VB8(39-59)-specific T cells, however, caused an increased response to all of the peptides of GPBP except the encephal togenic 72-89 sequence. The TCR peptide-specific T cells therefore altered the peptide recognition pattern of GPBP- reactive T cells, which provides evidence of the existence of cell-cell interactions.

Direct Interactions Between TCR Peotide-Specific and BP-Specific T Cells

T cells from the LN of the immunized rats were tested for responsiveness in vitro to attenuated VB8 + or Vβ8 " T cells. The stimulator T cells were irradiated (2500R), and 2 x 10 cells were cultured (in the absence of additional accessory cells) with 2 x 10 5 isolated TCR-specific T cells for 3 days, pulsed for the last 18 hours with 3 H-thymidine, and isotope uptake was measured by liquid scintillation spectroscopy.

In the absence of a stimulator T cell line, "background" responses were on the order of 7000 cpm (Table 3). When the stimulator line was specific for the GPBP S72-89 epitope, and therefore expressed the VB8 TCR, the response was 31,000 cpm. However, the when the stimulator line was specific for the GPBP

55-74 peptide, and therefore did not express the VB8 TCR, there was no significant response above background (8000 cpm). Thus, only V B 8 + cells could be recognized by T cells specific for the TCR peptide, indicating the presence of direct recognition of the VB8 peptide on the target T cell by a regulatory Vβδ-specific T cell. The results indicate the direct recognition of the TCR sequence on the surface of the stimulator T cell. The TCR peptide-specific T cells, however, were not cytotoxic for the BP- reactive target cells.

Passive Transfer of EAE Protection bv TCR Peotide-Specific T Cells The protective ability of Vβ8(39-59) peptide-specific T cells was established by adoptive transfer. Rats injected with as few as 10 7 VB8(39-59)-specific T cells did not develop EAE

(Table 4). The transferred protection appeared to be T-cell mediated; Vβ8(39-59)-specific antibodies were not detectable in the serum of protected rats. DT results (Table 4) indicated that the adoptively transferred T cells could prevent the induction of EAE without compromising T cell recognition of other antigens.

Table 3

Response of TCR VΛ8 Peptlde-spedflc T Cell Line to Attenuated V^8 + or Vø8" T Cells

Proliferation of Specificity of V/J8 Expression Responder T Cell Line Stimulator Line of Stimulator Line (cpm x 10 *3 )

None added 712 tn GPBP (S72-89) 31 13 I GPBP (55-74) 811

T cell line cells were Irradiated (2,500 R) and 2 x 10* cells (as stimulators) were mixed with 2 x 10 5 TCR-spec1f1c responder T cells for 3 days. Cultures were pulsed with 3 H-thym1d1ne for the final 18h, the cells were harvested, and proliferation assessed as 3 H-thym1d1ne uptake. Background proliferation of irradiated T cells specific for GPBP (S72-89) and GPBP (55-74) was 0.1 and 0.2 cpm (x 10 *3 ) . respectively.

Table 4 TCR V08 Peptide-specific T-cells Protect against EAE

Induction of EAE (GPBP/CFA) DH

(mm x 10"

Transffeerr Day of -• dose 1 Incidence Onset Duration Severity 2 GPBP PPD 3

None , 5/5 12 6.5 3.1 32 21 ^

3 x 10' 0/5 -- -- 0 24 21 7*

1 x 10 7 0/4 -- -- 0 ND ND

1 T cell line cells were stimulated with TCR VΛ8 peptide plus thymlc accessory cells for 3 days prior to intraperltoneaf transfer into naive recipient rats. The recipient rats were challenged on the same day with GPBP/CFA.

2 Values represent the mean of the maximum severity of EAE. See legend to Table 1.

3 Ear swelling 1n response to ID challenge with GPBP or PPD was measured 24 h. after challenge and represents a DH response to the antigen.

Specificitv of T Cell Lines Derived From Protected Rats

The ability of Vβ8(39-59)-specific T cells to (a) alter the response patterns of GPBP-specific T cell lines in vitro, (b) protect naive rats from EAE, and (c) reduce DH reactions in vivo. indicated that the pattern of response to BP epitopes might be altered in rats protected by TCR peptide-specific T cells. As shown in Table 5, LN cells from the EAE-protected animals responded well to the TCR peptide of GPBP as compared to LN cells from the control group. In contrast, LN cells from the protected group showed a significant response to the 87-99 peptide of BP, whereas LN cells from the control group did not respond to this peptide. The selection of a TCR Ve8(39-59)-specific T cell line from the LN of adoptively protected rats (Table 5) indicated that TCR peptide-specific T cells had migrated to and persisted in the LN that drained the site of GPBP injection.


These results demonstrate for the first time the use of a synthetic peptide from the CDR2 region of the TCR to induce VB8- specific regulatory T cells that prevent the induction of EAE. Computer modeling of ternary interactions among TCR chains, antigenic peptides, and MHC restriction molecules is consistent with CDR involvement in peptide/MHC binding when the TCR is folded in an energetically favorable conformation (Davis et al. and Claverie et al ., supra). The regulatory effects of T cells specific for CDR2 support the notion that this region has biological importance. Although the inventors do not intend to be bound by any particular theory, it seems unlikely that the responder T cell interacts directly with the functional TCR Vβ8 molecule on the target T cell surface. Indeed, it is conceivable that endogenous TCR peptide could be 'processed" and expressed preferentially on the T-cell surface in association with class I molecules (Long, E.O., Immunol. Today 10:232-234 (1989)). If a

natural form of the TCR peptide is associated with the MHC molecule on the T cell surface, the interacting TCR-specific T cell could interfere with normal T cell activation by a BP epitope.

Table 5

Antigen Specificity of T Cell Lines Oerived from the Lymph Nodes of Rats Protected from EAE by the Transfer of TCR V38 Peptide-specific T cells

* Lymph node (LN) cells were collected 20 days after simultaneous injection of (A) 3 x 10' TCR V«8 peptide-specific T line cells, or (B) saline, along with GPBP/CFA. H LN cells were tested directly (LN column).

3 T cell lines were selected from these LN cells by culture with TCR V«8 peptide (second column) or GPBP (third column) followed by IL2 as described in Underlined values indicate significant stimulation.

Vaccination with attenuated T cells indicates that protective immunity is induced against target structures shared by different T cell clones specific for the same disease-inducing 5 epitope, but do not implicate the TCR directly. The immunogenicity and im unoregulatory activity demonstrated here of a defined region of the TCR Vβ8 chain expressed by encephalitogenic T cells is an important step forward in understanding anti-idiotypic regulation, and provides a clear

10 explanation for the protective effects of the peptide immunization approach. The approach of the present invention, using a synthetic peptide to induce TCR peptide-specific antibodies, is of value in producing a variety of highly specific antibodies for assessing sequences important in TCR function.

15 The potential regulatory properties of antibodies raised to the

VB8(39-59) peptide are illustrated in Example II.

TCR peptide vaccination has application in human autoimmune or malignant conditions that are characterized by common TCR V- gene usage.



This Example provides an evaluation of the effects of immunization with the TCR V B 8(39-59) peptide on EAE induced with the encephalitogenic guinea pig basic protein (GPBP) peptide,

25 S87-99. and on antibody responses to GPBP peptides S49S or S87-

99. Antibody responses against the TCR V B 8(39-59) peptide are

* described and the ability of these antibodies to react with V B 8 + T cells and to suppress clinical signs of EAE are evaluated.

* The results demonstrate that the TCR V B 8(39-59) peptide can 30 induce both protection against EAE and elevated titers of antibody specific for either of the GPBP epitopes which are

encephalitogenic in Lewis rats. Furthermore, anti-TCR V B 8(39-59) antibodies are shown to suppress EAE independent of regulatory T cells. Thus, both humoral and cellular regulatory mechanisms are generated after immunization of the Lewis rats with the TCR V B 8(39-59) peptide.


1. Peptide synthesis and purification. All peptides used in this study were synthesized by a minor modification (Hashim, G.A., et al.. J. Neurosci. Res. 16:467 (1986)) of the solid phase method (Merrifield, R.B., J. Amer.

Chem. Soc. 85:2149 (1963)) using Boc-amino acid-resin-ester (Peninsula Laboratories, San Carlos, CA). The peptides (Table 6) were synthesized with t-Boc-L-amino acid derivatives, starting with t-Boc-L-Glycine-O-resin ester (0.65 mmole/g: 0.78 mmole). Coupling and deblocking reactions were routinely monitored by the

Kaiser test (Kaiser, E., et al.. Anal. Biochem. 34:595 (1970)) for free amino groups. Single deblocking and occasional double coupling reaction steps were sufficient for the synthesis of all peptides used in this study. Peptide Gp-S49S defines region 69- 84 of GPBP and has a C-terminal glycine. Residue numbers of GPBP peptides used in this study correspond to those reported for bovine myelin basic protein (Eylar, E.H., et al .. J. Biol. Chem. 246:5770 (1971)).

Peptides containing tryptophan were first treated with 10% piperidine for 30 minutes to remove the formyl blocking groups and then, like all other peptides, were cleaved from the resin, together with other side chain deprotection, by treatment with HF at 0 β C in the presence of anisole. After removal of the HF, the resin-peptide mixture was washed 4 times with ether and dried. The peptide was extracted with water, lyophilized and filtered through a Sephadex G10 column (2.5 X 100 cm) that was equilibrated with and eluted by 5% acetic acid. Acid insoluble

* peptides were extracted from the resin-peptide mixture with 0.03 M ammonium carbonate, filtered on a Sephadex G10 column that was

* equilibrated with and eluted by 0.03 M ammonium bicarbonate, and lyophilized. Further purification of the peptide was achieved

5 using HPLC with a Bondapak C18 column equilibrated with 0.1% trifluoroacetic acid (TFA) in water and eluted with a linear gradient up to 40% acetonitrile containing 0.1% TFA over a period of 60 minutes. The purity of the peptides was documented by HPLC and by amino acid composition analysis.

10 2. Test and control oeotides. The TCR V B 8(39-59) peptide was synthesized according to the sequence identified by Burns, F.R., et al . (J. EXP. Med. 169:27 (1989)). As controls for TCR V B gene family specificity and for the CDR2 hypervariable region, additional peptides were synthesized, including TCR

15 V B 14(39-59), which comprises the corresponding CDR2 of the V B 14 gene family (Williams, C.B., et al .. J. Immunol. 142:1027 (1989)), and TCR V B 8(25-41), corresponding to a sequence in the CDR1 region adjacent to peptide TCR V B 8(39-59) (Burns, F.R., et al .. op. cit.). Other control peptides included a series that

20 defines specific regions of GPBP. Peptides Gp-S49S and Gp-S87-99 define respectively the major and minor encephalitogenic sequences for Lewis rats. Peptides Gp-S67 (residues 69-81) and Gp-S53 (residues 75-84) define respectively T cell and B cell epitopes within the major encephalitogenic epitope encompassed in

25 peptide Gp-S49S (residues 69-84). Peptide Gp-S55-74 defines a non-encephalitogenic T cell determinant in Lewis rats (Offner, H., et al.. J. EXP. Med. 170:355 (1989)), and Gp-NAc-1-16 encompasses the encephalitogenic sequence for the PL/J strain of mouse (Zamvil, S.S., et al.. Nature 324:258 (1986)). * 30 3. Peptide coupling to KLH.

Keyhole limpet he ocyanin (KLH) (Calbiochem Corp., La Jolla, CA) was dissolved in phosphate buffered saline (PBS),

dialyzed against PBS at 4*C overnight and lyophilized. A known weight of KLH (8 mg or 1-2 *moles) together with the peptide to be coupled (10 *mo1es) were dissolved in 1 ml deionized water. After the pH was adjusted to 4.5 with 0.01 N HCl, 375 mg of l- ethyl-3 (3-dimethylaminopropyl)-carbodiimide (Pierce Chemical

Co., Rockford, IL) in 0.5 ml water were added and the reaction mixture was stirred for 1 hour at room temperature. The mixture was then placed in dialysis bags and dialyzed against 3 changes of PBS at 4'C and lyophilized. The amount of peptide coupled to KLH was calculated from the increase in mass of the non- dialyzable portion of the KLH.

Table 6

Amino Acid Sequence of Peptides Derived from the TCR and Related Peptides from Hyel in Basic Protein

TCR Vø8(39-59) :

39 40 45 50 55 59

AspMetGlyHisGlyLeuArgLeuIleHisTyrSerTyrAspValAsnSerThrGlu LysGly

TCR V^8(25-41) :

25 30 35 4041


TCR VβU(39-59):

3940 45 50 55 59

AlaProGl Gl ThrLeuGlnGlnLeuPheTyrSerPheAsnValGlyGlnSerGluLeuVal

TCR V^14(24-41):

24 30 35 40 41

ThrVal LysGlyThrSerAsnProAsnLeuTyrTrpTyrTrpGlyAl aProGly

69 70 71 72 73 74 75 76 79 80 81 82 83 84

Gp-S49S GlySerLeuProGlnLysSerGln ArgSerGlnAspGl uAsn

Gp-S53 SerGln ArgSerGlnAspGluAsn

Gρ-S67 GlySerLeuProGlnLysSerGln ArgSerGln

55 60 63 65 70 74

Gp-(S55-74) : SerGlyLysAspSerHisHisAlaThrArgThrThrHisTyrGlySerLeuProGlnLys

87 90 95 99

Gp-(S87-99) : ValHisPhePheLysAsnlleValThrProArgThrPro

1 5 10 16

Gp-NAc(l-16) : N-Ac-Al aSerGlnLysArgProSerGlnArgHisGlySerLysTyrLeuAl a

All peptides were synthesized by the sol id phase method, purified by gel filtration and high pressure l iquid chromatography as described in the methods section. Peptides from the TCR are numbered according to Burns et al ■ (supra) and Wil l iams et al . (supra) and guinea pig myel in basic protein (GPBP) peptides are numbered according to Eylar et al . (J . Biol . Chem. 246:5770 (1971 ) ) . Peptide Gp- (S55-74) has an unnatural threonine for al anine substitution at position 63.

4. Preparation of anti-peptide antibodies. Male Lewis rats weighing 200-250 g were immunized with a single dose of 100 *g of the free peptide. The peptide was emulsified in complete Freund's adjuvant (CFA) and injected SC. Each rat received 100 *1 of the emulsion containing 100 *g peptide and 100 *g M. butyricum. Likewise, Lewis rats were immunized with 100 *g of a particular peptide and challenged either simultaneously or at a later date with another peptide. Immunized rats were pre-bled from the tail vein before and at intervals after immunization.

New Zealand white rabbits, weighing 6-7 lbs., were pre-bled and immunized with 0.5 ml CFA emulsion containing 4 mg peptide and 2 mg M. butyricum. The emulsion was injected SC in multiple sites in the dorsal area of the neck and the tail. Rabbits were immunized either with the free peptide or with peptide conjugated to KLH. Immunized rabbits were boosted on days 7, 14 and 21 with 1 mg peptide emulsified in incomplete Freund's adjuvant and injected SC on the flank. All rabbits were bled via the ear vein after they were placed in restraining cages and tranquilized with acepromozine. To prevent hypovolemia, the amount of blood removed was replaced with sterile saline. Sera from individual rats or rabbits were prepared from clotted blood by centrifugation. All sera were decomplemented for 30 minutes at 56*C and frozen in small aliquots to which sodium azide was added.

5. Preparation of im unoqlobulin. IgG was prepared from serum by published methods (Steinbuch, M., et al.. Arch. Biochem. Biophvs. 134:279 (1969)) and purified by ion exchange chromatography with DEAE-sephadex. The serum was diluted with one volume of 0.06 M acetate buffer and the pH adjusted to 4.8 at room temperature. Caprylic acid, 6.8 g/100 ml serum, was added dropwise under vigorous stirring

t for 30 minutes. The mixture was then centrifuged, the supernatant was adjusted to pH 5.7, dialyzed against deionized water and lyophilized.

6. Antibody assays. 5 Antibody reactivity was determined by an adaptation for peptides (Hashim, G.A., et al.. J. Neurosci. Res. 24:222 (1989)) of the direct enzyme-linked immunosorbent assay (ELISA) and by the inhibition ELISA as described by Cleveland, W.L., et al . (Methods in Enzv ol . 121:95 (1986)). Peroxidase-labeled rabbit

10 anti-rat or goat anti-rabbit i munoglobulin (affinity-purified H and L chains, Cooper Biomedical, Malvern, PA) was used together with O-phenylenediamine for enzyme substrate, and the optical density was measured at 450-650nm in a colorimetric plate reader (Model Vmax, Molecular Devices, Mento, CA).

15 7. EAE Induction.

EAE was induced in male Lewis rats (225-250 g) as described (Hashim, G.A., et al.. J. Neurosci. Res. 24:222 (1989)). Each rat received a single SC injection of a CFA emulsion containing 100 *g peptide and 100 ng M. butyricum. Immunized rats were

20 inspected daily for clinical signs of EAE and were terminated between days 25 and 30 following challenge. At this time, sera from individual rats were collected, and the brain and spinal cord tissues were processed for histology.

8. Prevention and suppression of EAE in Lewis rat.

25 Male Lewis rats were immunized with 100 *g TCR V B 8(39-59) peptide emulsified in CFA and injected SC. The immunized rats were bled from the tail for antibody determination and were challenged with 100 ng of an encephalitogenic peptide (Gp-S49S or

Gp-S87-99). Groups of rats were challenged either on the same

30 day or on day 40-41 after they were immunized, , based on the observed time course of anti-TCR V B 8(39-59) antibody production.

To study EAE suppression by anti-TCR V B 8(39-59) antibodies, Lewis rats were challenged with the encepha itogenic peptide Gp- S49S and injected intraperitoneally with either saline (control) or either Lewis rat or rabbit anti-TCR V B 8(39-59) IgG, given every other day for 14 days. Each rat received a total of either

49 or 70 mg rat or rabbit IgG, respectively, and was terminated on day 24 after the challenge. When injected in sterile saline over a period of 14 days, rabbit IgG remained at high levels in the circulation of recipient rats on days 12 and 24 after transfer and did not interfere with the development of anti-Gp-

S49S antibodies.

9. Antibody staining of V c 8* and V c 8 * T cells. Rat or rabbit IgG (10 *g) from normal or TCR V B 8(39-59) immunized animals was incubated at various concentrations for 30 minutes with 10 6 normal rat thymocytes (known to be mostly V B 8° or a Gp-S49S-reactive, GPBP-specific T cell line (known to be V B 8 + ). After several washes, the cells were incubated with 10 *g mouse anti-rat or anti-rabbit IgG for an additional 30 minutes as an amplification step. After further washing, the cells were stained with fluoresceinated goat anti-mouse IgG (H + L chain specific), washed, fixed in 2% formalin, and evaluated for fluorescence intensity at 488 nm using a Coulter Epics C Cytofluorograph. The cells were gated electronically on the basis of forward angle versus right angle scatter patterns to include the major lymphocyte populations, which were then evaluated for FITC fluorescence.


1. Prevention of EAE bv TCR V c 8(39-59) peptide immunization.

To evaluate prophylactic effects of anti-TCR V B 8(39-59) immunity on EAE induced by various encephalitogenic epitopes,

Lewis rats were first immunized with the TCR V B 8(39-59) peptide, and 44 days later, .EAE was induced with either Gp-S49S or Gp-S87- 99. As is shown in Table 7, immunization with the TCR V B 8(39-59) peptide reduced markedly the severity of Gp-S49S-induced EAE, and prevented completely S87-99-induced EAE. Although histological scores in both protected groups were reduced, inflammation in the CNS was generally less affected by TCR V B 8(39-59) peptide immunization than were clinical parameters.

2. Suppression of EAE with the TCR V c 8(39-59) oeotide. To evaluate suppression of EAE, the TCR V B 8(39-59) peptide was given simultaneously with the encephalitogenic dose of GPBP or Gp-S49S. As is shown in Table 7, the TCR V B 8(39-59) peptide prevented GPBP-induced EAE in most rats, and markedly reduced the clinical severity in the remaining animals. A similar result was obtained in with Gp-S49S-induced EAE. In contrast, the TCR

V B 14(39-59) control peptide had no suppressive effects on EAE (Table 7). Again, histological signs of EAE were relatively less affected by TCR V B 8(39-59) immunization than clinical signs.

3. Antibody responses against the TCR V D 8(39-59) peptide. TCR V B 8-specific antibodies raised against intact T cell clones (Owhashi, M., et al.. J. EXP. Med. 168:2153 (1988); Gascoigne, N.R.O., et al ., Proc. Natl. Acad. Sci.. USA ,34:2936 (1987); Kappler, J.W., et al.. Nature 332:35 (1988); Kappler, J.W., et al .. Cell 49:263 (1987); MacDonald, H.R., et al . , Nature 332:40 (1988)) have proven efficacious in


Table 7

Prevention and Suppression of EAE by Immunization with the TCR Vβ8(39-59) Peptide

Groups of Lewis rats were immunized with the listed antigens on the indicated treatment days ("Imra"). Each rat received 2 SC injections in the base of the tail of 0.1 ml containing 100 μg free peptide emulsified in CFA. Immunized rats were challenged on indicated days ("Chall") with either the encephalitogenic GPBP (50 μg) , Gp-S49S (100 μg) or Gp-(S87-99) (100 μg) , injected in the foot pad as an emulsion (0.1 ml) in CFA. Rats were inspected daily for clinical signs of disease. Tissues were taken for histology 23 to 26 days after challenge. The clinical scores represent the mean of all rats per group and are scored as described in Table 1. Ranges of clinical scores appear in brackets. The histological scores of brain (Br) and spinal cord (Sc) of individual rats are based on the number of lesions: 1-1-2 lesions; 2-3-5; 3-6-8; 4-9 or more lesions in a hematoxy n-stained sagittal section of the brain or the entire length of the spinal cord.

the prevention and treatment of EAE in both Lewis rats (Owhashi,

M., et al.. J. EXP. Med. 168:2153 (1988)) and PL/J mice (Acha- Orbea, H., et al.. Cell 54:263 (1988); Urban, J., et al.. Cell 54:577 (1988)). It thus was very important to determine whether antibodies could be raised against the synthetic TCR V B 8(39-59) peptide, and if so, whether they had clinical utility.

Such antibodies could indeed be raised and were found to be clinically effective. Antibodies against TCR V B 8(39-59) were detected in the sera of Lewis rats as early as 7 days after a single injection of 100 ng of the free peptide in CFA (Table 8).

Although a high degree of variability in the antibody response was observed, the antibody titers increased gradually over time. None of the TCR peptide-immunized rats developed any signs of EAE, and all remained healthy throughout the 41 day observation period.

Rabbits immunized with either the free or KLH-conjugated TCR V B 8(39-59) peptide produced much higher titers of antibodies than did rats (Table 8). Antibody titers remained high for over 6 months, showing detectable reactivity at dilutions of up to 1/320,000.

Table 8


Day After Serum Reactivity Against Clinical Signs Challenge Dilution N TCR V^8(39-59) of EAE








Hale Lewis rats (225-250g) were challenged SC with 100 μg TCR V08(39-59) + 100 μg H. butyricum in CFA. Each rat was bled from the tail vein on indicated days after challenge. Rabbits (6 lbs) received a course of wmunization that is detailed in the Materials and Methods. Antibody reactivity of individual sera against TCR Vø8(39-59) was documented by direct ELISA and the average reactivity of individual sera per group is presented as Absorbance Units (xlO 3 ). In brackets are shown the ranges of antibody reactivity of all antisera per group. All sera were heat inactivated and diluted before assay against 25 ng of plated peptide. The term "None" designates the complete absence of clinical signs of EAE.

4. Antibody responses against the encephalitogenic peptide S49S. Immunization of Lewis rats with GPBP or GP-S49S (residues 69-84) peptide induces antibodies that recognize several different epitopes, one of which is comprised of residues 82-84 (Asp-Glu-Asn) and is evidenced by antibody binding to Gp-S53 (residues 75-84) (Day, E.D., et al.. J. Neurosci. Res. 18:214 (1987); Hashim, G.A., et al .. J. Neurosci. Res. 17:375 (1987)). These antibody responses depend on T cell help, which can be provided by encephalitogenic T cells specific for the GP-S49S peptide. Although immunization with the TCR V B 8(39-59) peptide prevents and suppresses EAE mediated by Gp-S49S-specific T cells of the helper phenotype, it is important to determine the effect of such immunization on anti-S49S antibody formation. The antibody response to Gp-S49S was detected as early as

7 days after immunization with the Gp-S49S in CFA (Table 9). Periodic bleeding of the immunized rats showed marked increases in antibody titers to both Gp-S49S and Gp-S53 during the next 48 days, the anti-Gp-S53 response appearing only after the development and eventual recovery from EAE.

After preimmunization and protection against EAE with TCR V B 8(39-59), the 26 day antibody responses to Gp-S49S and Gp-S53 were elevated two to four fold relative to the that in rats not treated with the TCR peptide (Table 9). Similarly, anti-S87-99 responses were increased >4 fold in rats preimmunized and protected with the TCR V B 8(39-59) peptide (Table 9). Thus, an immune response directed against V B 8 + T cells actually enhanced antibody responses to several distinct B cell epitopes of GPBP.

Table 9



TCR V fl 8-39-59 on day 0 Gp-S(87-99) on d. 44 None Bleed on d. 65

1:320 621 38 46 348 0/4 rats (4968) (784)

Rats were either immunized with 100 μg TCR V58(39-59) peptide or injected with saline and were challenged on indicated days with either Gp-S49S or Gp(S87- 99), SC in emulsion containing 100 μg M. butyricum in CFA. Rats were bled on the indicated days. Groups immunized with TCR V58(39-59) and challenged with either Gp-S49S or Gp-(S87-99) were terminated on days 26 and 21 after challenge, respectively. Antibody reactivity (binding to 25 ng/well of peptide ) of individual sera was measured in direct ELISA. Results are presented as average Absorbance (x 10 3 ) at 450-650 nm (automatically corrected for background). Theoretical Absorbances (shown in parentheses) were normalized to a 1:40 dilution. Hind leg paralysis (HLP) was accompanied by incontinence. Because of the severity of the disease, 2 of the Gp-S49S-challenged rats died on days 14 and 18, respectively. Variation within groups of 2-3 samples was less than 5%.

5. Specificity of anti-peptide antibodies.

* To evaluate the specificity of several antisera, binding to a panel of synthetic TCR and GPBP peptides was assessed. The results (Table 10), show that anti-Gp-S49 antiserum which

5 recognized GP-S49S and its C-terminal fragment, Gp-S53, did not react with the N-terminal fragment of Gp-S49 (i.e., Gp-S67), with any other regions of GPBP, or with any of the TCR V region peptides. Similarly, rat or rabbit antisera to the TCR V B 8(39- 59) peptide, recognized only the immunogen, and not other TCR

10 sequences (including the 3 overlapping residues - AspMetGly - present on TCR V B 8(25-41), or GPBP peptides. Antisera from rats immunized simultaneously with TCR V B 8(39-59) peptide plus Gp-S49S or Gp-S87-99 demonstrated the same specificity for each of the immunogens as antisera from singly-immunized rats (Table 5). The

15 specificity of antibody reactivity to TCR V B 8(39-59) and to Gp-

S49S was confirmed by peptide-specific, dose dependent inhibition of binding in ELISA (Figure 1).

6. Antibodies to TCR V c 8(39-59) recognize V.8 * T cells.

To interpret potential regulatory effects of antibodies to 20 TCR V B 8(39-59), it was crucial to establish whether or not the peptide-specific antibodies interacted directly with V B 8 + T cells. To evaluate such reactivity, V B 8 * encephalitogenic T cells or normal thymocytes which are predominantly V B 8 " were incubated with rat or rabbit anti-TCR V B 8(39-59) IgG antibody, followed by mouse 25 anti-rat or anti-rabbit facilitating antibody, and fluorescein-

* labeled goat anti-mouse IgG antibody. As is shown in Figure 2, the rabbit IgG raised to the KLH-conjugated TCR V B 8(39-59)

* peptide caused an increased fluorescence intensity in the entire V B 8 + encephalitogenic T cell population (>90% positive versus a

30 control antiseru ), as opposed to approximately 5% of the normal

thymocyte population. Rat IgG and rabbit IgG raised against unconjugated TCR peptide also stained selectively the V B 8 + T cells, although with less intensity. These results indicate that antibody to the TCR V B 8(39-59) peptide can bind specifically to V B 8 + T cells. None of the antisera were cytotoxic

Table 10


VA8 VΛ14 V.14

9-59 25-41 39-59 24-41

14 20 21 18 2211 1535 16 17 7 14

Rat anti-TCR Vfl8(39-591: (1:160 dilution)

222 11 21 9 12 8 12 14 5 10

Rat anti-TCR Vff8(39-S9) and GD-S49S: (1:640 dilution)

421 16 20 11 2190 1639 8 14 5 12 (1684) (8760) (6556)

Rat anti-TCR Vo8f39-59) and GD-(S87-99): (1:320 dilun)

621 13 - 18 38 6 8 14 348 12 (1242) (696)

Rabbit anti-TCR Vg8f39-59)-KLH: (1:40,000 dilution)

408 0 25 3 2 4 0 0 5 1 (102000)

Lewis rats were immunized with 100 μg of Gp-S49S, TcR Vø8(39-59) or both, SC in Freund's adjuvant (100 μg H. butyricum/rat). Antisera were prepared between days 54 and 62 after immunization and pools of high titer antisera were made from 2 to 4 immunized rats. Rabbit antisera was isolated on day 43 after immunization with the TCR peptide conjugated to KLH. All antisera were heat-1nactivated for 30 min at 57'C. Antibody reactivity, at the Indicated dilutions, against the various peptide antigens was measured by-direct ELISA using rabbit anti-rat or goat anti- rabbit IgG (L+H)-peroxidase labeled. The values shown are the Absorbance measurements at 450-650 nm (x 10 3 ). All figures were automatically corrected for background reactivity in the absence of plated peptides. Numbers in brackets represent theoretical Absorbance values calculated for a 1:160 dilution.

for V B 8 + T cells in the presence of complement, as measured by both chromium release or dye exclusion, suggesting that antibody binding altered T cell function without killing the cells.

7. Suppression of EAEwith anti-TCR V c 8f39-59) antibody.

Lewis rats immunized with TCR V B 8(39-59) were not only protected against EAE, but developed circulating antibodies specific for the immunizing peptide. To evaluate the role of these antibodies in down-regulating EAE, Lewis rats were challenged with Gp-S49S in CFA and were then treated with TCR V B 8(39-59)-specific IgG (rat or rabbit). Rats receiving Lewis rat IgG every other day for 12 days developed mild clinical signs of EAE with reduced histology in the brain, but more extensive lesions in the spinal cord compared to controls (Table 11). Rats receiving rabbit IgG developed minimal clinical signs with little change in histological scores (Table 6). Thus, passive administration of anti-TCR V B 8(39-59) antibodies over a 12 day period suppressed clinical but not histological signs of EAE.


The results presented herein constitute the first demonstration of the ability of a synthetic TCR V-region peptide to induce specific antibodies that can suppress the induction of EAE. These TCR V B 8(39-59) peptide-specific antibodies are able to bind T cells bearing the entire, intact TCR, and thereby alter the function of these cells without lysing them. Coupled with results presented in Example I, these results indicate that both antibody and cell-mediated immune responses can provide independent immunoregulatory actions on encephalitogenic T lymphocytes that utilize common V region genes in response to epitopes of MBP. Both regulatory mechanisms have potent

preventative and suppressive effects on the induction of clinical signs of autoimmune disease.

Table 11


100 of n uc on an every o er ay or ays, exper men a groups rece ve e er 7 mg Lewis rat IgG (which contained 17 Absorbance Units/mg IgG) or 10 mg rabbit IgG (which contained 6570 Absorbance Units/mg IgG) from animals that had been immunized with TcR Vβ8(39-59). The IgG was dissolved in sterile saline and injected intraperitoneally. Treatment with non-immune rat or rabbit IgG did not influence the course of EAE. All animals were inspected daily for clinical signs of EAE, bled from the tail vein nn indicated days. Sera were tested for antibody to TCR or GPBP peptide in direct ELISA (results are Absorbance x 10 3 ). All animals were sacrificed on day 24 after EAE induction and brains (Br) and spinal cords taken for histological evaluation as described in the legend to Table 7.

The TCR V B 8(39-59) peptide, which was predicted to be a good T cell immunogen based on the algorithms of Margalit et al . and Rothbard et al. (supra), proved to be a potent B cell immunogen, especially in rabbits. THe antibodies were highly specific for the immunizing peptide (by both direct reaction and inhibition assays), stained only V B 8 + T cells, and suppressed EAE mediated by V B 8 + T cells.

In conclusion, the synthetic peptide TCR V B 8(39-59) induced both T cell immunity and antibody production in Lewis rats. Both T cells and antibodies, alone or together, are capable of regulating the immune response to an encephalitogenic challenge. The ability of this TCR peptide to activate regulatory T cells and protective antibodies demonstrates the utility of this approach for the control of human autoimmune diseases.



The ability of the TCR VB8(39-59) given either SC (in adjuvant) or ID (in saline) to disrupt the disease process when given at various times after induction of EAE with GPBP was tested (Table 12). In Experiment 1, the TCR peptide was administered either on day 10 (line 2) or when the first rat in a group showed clinical signs of EAE (lines 3 and 4) at the time of onset. In both cases, with both routes of injection of the peptide, there was a significant reduction in the duration of the disease, though not in the severity or time of onset. The efficacy of the peptide given in saline via the ID route is of particular importance to human therapy, as it is preferred to SC injection in adjuvant.

Table 12


TCR refers to the peptide TCR V^8(39-59).

In Experiment 2, the time of ID administration of the TCR

, peptide was varied, as was the dose. As shown in Table 12, 50 *g of the peptide administered on either days 0 (day of WE induction), 7, or 14 resulted in a significant reduction in the

5 duration of disease. A delay in onset of the disease was also observed. Furthermore, the percentage of animals showing signs of the disease decreased. A larger dose of the peptide (200 *g) appeared less efficacious than the lower dose, possibly due to a short-term overload of the peptide which could have comprised the

10 immune response generated against the TCR. Treatment with a similarly sized peptide corresponding to an irrelevant TCR had no effect on onset, severity or incidence of EAE, but may have reduced the duration somewhat (last line of Table 12).





The proliferative responses and specificity of T cells in the draining LN (popliteal) of rats treated with TCR Vβ8(39-59)

20 peptide for EAE on day 13 after disease induction were examined (Table 13). On day 0, Lewis rats received an EAE-inducing regimen of GP-BP + CFA SC into their hind footpads. On day 13, they were divided into three groups and received either saline (column 1),

25 100 *g TCR VB8(39-59) peptide (+ CFA) SC in the hind footpads

(column 2) or 50 *g of TCR VB8(39-59) in saline ID in the ear pinna. On day 20, about 7 days after onset of EAE, popliteal LNs were removed and T cell proliferative activity in response to the indicated antigens or mitogens were tested directly.

30 LN cells from control rats responded best to Con A, PPD,

GPBP and GPBP (72-89), and GPBP (45-89) (which includes the 72-89

sequence and another immunogenic but non-encephalitogenic peptide). In contrast, LN cells from rats given the TCR peptide SC in CFA, did not show significant proliferative responses to GPBP or to any of the BP fragments. LN cells from rats treated ID with the TCR peptide

Table 13


Results are shown as net ^H-thymidine incorporation of 5 x 10^ cells stimulated in microwells.

responded similarly to the control cells, with the exception of a reduced response to GPBP(72-89). In addition, the latter group showed an increased response to GPBP(90-170), which is not known to be encephalitogenic. This indicates that epitope switching had occurred. An aliquot of each of the above 3 groups of LN cells was stimulated in culture with either GPBP or with the TCR peptide for 3 days, and the cells expanded in IL-2 for 5 more days. The proliferative responses to the various antigens and mitogens of these selected T cells were examined, as above. The results are shown in Table 14.

Control T cells (Table 14, column 1) responded well to

GPBP, GPBP(72-89), Pl and rat BP (indicating homologous recognition in the CNS). THe last line of the Table indicates that when T cells of this group were injected into naive rats, they were encephalitogenic.

T cells from the group of animals treated with the TCR peptide in CFA, SC, and selected in culture with GPBP (column 2) responded poorly to GPBP, GPBP(72-89) and rat BP. The response to GPBP Pl was apparently due to the second (non- encephalitogenic) epitope, since the response to the GPBP(72-89) epitope was weak. The potent response to the TCR peptide indicated that a 7 day exposure (with no further selection with this peptide) was sufficient for anti-TCR peptide immunity. Of great significance is the observation that these cells were unable to transfer EAE, indicating that the encephalitogenic clones could not be selected during culture in the presence of the GPBP antigen.

The cells from the above TCR-immunized animals, when selected in vitro with the TCR peptide rather than with GPBP (column 3), appeared to respond only to the TCR peptide (and, of course, the T cell mitogen, Con A).

* Finally, cells from rats treated with the TCR peptide ID and selected in culture with GPBP (column 4) behaved essentially

• like the control cells. That is, they recognized the GPBP(72-89) encephalitogenic epitope and were able to transfer EAE. This

5 indicates that encephalitogenic T cell precursors were still present in the rats treated in this manner and could be selected in culture. This suggests the possibility that the reduced duration of EAE seen in rats treated with TCR peptide ID (see Example III and Table 12) does not involve regulation of the 10 draining LN cells. However, it is important to note that the LNs draining the site of ID injection (i.e., the cervical LN when ID injection is in the ear pinna) may show different regulatory properties.

Table 14


TCR V^8(39-59) + CFA TCR Vø8(39-59) ID GPBP Vø8(39-59) GPBP

10 25

122 10

122 52 28 12 11 9 26




In the present example, a mAb is produced by immunizing mice with the TCR Vβ8(39-59) peptide and carrying out the methods for making a hybridoma as described above. The mAb is then conjugated to the ricin A chain, to yield an im unotoxin. The toxin conjugated antibody is injected into rats along at the same time as an encephalitogenic dose of GPBP (prophylaxis), and into other rats after onset of EAE (therapy).

Prophylactic treatment with the ricin A chain-conjugated anti-TCR peptide antibody (1-4 injections at doses of 0.05 to 0.2 mg/kg) results in a significantly reduced incidence and severity of EAE. Therapeutic treatment with similar doses of the conjugate results in a significant shortening of the duration and a lessening in the severity of the disease.


The present example describes how human rheumatoid arthritis is treated by the composition and methods of the invention. It is modeled by two animal models: (1) Arthritis induced in susceptible mice by injection of Type II collagen

(Stuart, J.M., et al.. Ann. Rev. Immunol. 2:199-218 (1984) and

(2) arthritis induced in susceptible rats by injection of Mycobacterial heat shock protein (HSP) (Van Eden, W., et al ..

Nature 331:171-173 (1988)). Arthritogenic T cells responsive to collagen or HSP and capable of transferring the disease are selected in vitro in the presence of collagen or HSP using methods described above. The TCR associated with disease- mediating T cells is identified, and the presumptive amino acid

sequence is determined by nucleic acid sequencing, as above.

Using the algorithms of Margalit et al. and Rothbard et al.

(suora). an immunogenic portion of the TCR that involves a CDR or hypervariable region is synthesized and used to immunize mice (for collagen arthritis) or rats (for adjuvant arthritis).

Animals treated with the TCR peptide in conjunction with disease induction are significantly protected from development of arthritis, as measured by joint swelling and by T cell reactivity to the arthritogen. Animals treated with the TCR peptide after onset of the disease show a significant shortening of the duration and a lessening in the severity of the symptoms of arthritis.

Passive immunization with antibodies induced against the

TCR peptide associated with arthritis also show similar prophylactic and therapeutic effects on arthritis induction.

Successful treatment is achieved by polyclonal antibodies, mAbs, chimeric antibodies, and immunotoxin-conjugated antibodies.

Passive immunization with T cells specific for the arthritis-associated TCR peptide induce protective immunity, both prophylactic and therapeutic, against development and progression of arthritis.


Human thyroiditis, including Hashimoto's thyroiditis and Graves' disease, is treated by the composition and methods of the invention as described in the present example. Although the precise nature of the target autoantigen is uncertain, immune reactivity to thyroglobul n and to thyrotrophin receptor, respectively, is associated with these diseases. Thyroiditis is modeled in mice by administration of thyroglobulin (Maron, R., et

al.. J. EXP. Med. 152:1115-1120 (1980)). T cells responsive to thyroglobul n and to thyroid follicular cell antigens, and capable of transferring the disease, are selected in vitro in the presence of either thyroglobulin, thyroid cells, or thyroid cell membrane preparations using methods described above. The TCR associated with disease-mediating T cells is identified, and the presumptive amino acid sequence is determined by nucleic acid sequencing, as above. Using the algorithms of Margalit et al . and Rothbard et al . (supra), an immunogenic portion of the TCR that involves a CDR or hypervariable region is synthesized and used to immunize mice.

Animals treated with the TCR peptide in conjunction with disease induction are significantly protected from development of thyroiditis and and of T cell reactivity to the thyroid antigens. Animals treated with the TCR peptide after onset of the disease show a significant shortening of the duration and a lessening in the severity of the symptoms of thyroiditis.

Passive immunization with antibodies induced against the TCR peptide associated with thyroiditis also shows similar prophylactic and therapeutic effects on disease induction.

Successful treatment is achieved by polyclonal antibodies, mAbs, chimeric antibodies, and immunotoxin-conjugated antibodies.

Passive immunization with T cells specific for the thyroiditis-associated TCR peptide induces protective immunity, both prophylactic and therapeutic, against development and progression of thyroiditis.


Insulin-dependent diabetes ellitus (IDDM), or type I diabetes, is an autoimmune disease characterized by immune

reactivity directed to pancreatic islet (or beta) cells, resulting in the cells' destruction and shutdown of insulin production. The target antigens for this immune attack have not been characterized with certainty. The present example describes how IDDM is treated by the compositions and methods of this invention.

The disease is modeled in animals in which it occurs naturally, or can be induced in certain strains of mice ( anasawa et al .. Diabetoloqia 27:113 (1984). Other mouse strains can be caused to exhibit this disease by transferring lymphocytes from the susceptible strains.

T cells responsive to pancreatic islet cell antigens and capable of transferring the disease are selected in vitro in the presence of either islet cells, or islet cell membrane preparations using methods described above. The TCR associated with disease-mediating T cells is identified, and the presumptive amino acid sequence is determined by nucleic acid sequencing, as above. Using the algorithms of Margalit et al . and Rothbard et al. (supra), an immunogenic portion of the TCR that involves a CDR or hypervariable region is synthesized and used to immunize mice.

Animals treated with the TCR peptide in conjunction with disease induction are significantly protected from development of diabetes and and of T cell reactivity to the islet cell antigens. Animals treated with the TCR peptide after onset of the disease show a significant shortening of the duration and a lessening in the severity of the symptoms of diabetes.

Passive immunization with antibodies induced against the TCR peptide associated with diabetes also show similar prophylactic and therapeutic effects on disease induction.

Successful treatment is achieved by polyclonal antibodies, mAbs, chimeric antibodies, and i munotoxin-conjugated antibodies.

Passive immunization with T cells specific for the

* diabetes-associated TCR peptide induces protective immunity, both prophylactic and therapeutic, against development and progression of diabetes.




Immunization of rats and mice with myelin basic protein

10 (MBP) induces encephalitogenic T cells that express a limited repertoire of T cell receptor V region genes. Preceding examples demonstrate that a synthetic peptide from the VB8 sequence shared by most encephalitogenic rat T cell clones induces protection against EAE by stimulating specific regulatory T cells and

15 antibodies. In the present example, the same TCR peptide, which corresponds to the 39-59 residues of the VB8 sequence and includes the second complementarity determining region, is demonstrated to be highly effective as therapy for EAE.

The TCR VB8-39-59 peptide, when given s.q. in complete

20 Freund's adjuvant to rats with moderate EAE, halted disease progression and significantly shortened disease course. When the TCR peptide was given i.d. in the ear, the effects were delayed for 1 day, but again led to a faster resolution of clinical signs. MBP-selected T cell lines from the treated rats responded

25 poorly to MBP, but retained reactivity to the TCR peptide and failed to transfer to normal recipients. The rapid clinical

* effect of the TCR peptide suggested triggering of a pre-existing regulatory network evoked in response to EAE development. In

* support of this concept, direct evidence is presented in the 30 present example of T cell recognition of the TCR peptide in untreated rats undergoing EAE.


Animals: Female Lewis rats, 6-8 weeks old, were obtained from Harlan Sprague Dawley (Indianapolis, IN). Rats were housed and maintained at the Portland VAMC Animal Resource Facility in accordance with Federal and Institutional guidelines.

Antigens: GP- or Rt-MBP was extracted and purified according to the method of Eylar (Eylar, E.H., et al .. J. Biol. Chem. 246:5770 (1971)). Enzymatic cleavage fragments of GP-MBP encompassing residues 1-37, 43-89, and 90-169, a synthetic peptide of GP-MBP corresponding to residues 72-89, and the synthetic peptides corresponding to the 39-59 residues of TCR VB8 and TCR VB14 were synthesized and purified as described previously (Vandenbark, A. A., et al .. Nature 341:541 (1989); Eylar, E. H., et al.. J. Biol. Chem. 246:5770 (1971)). These peptides were >90% pure by high pressure liquid chromatography analysis.

Clinical Protocols: EAE was induced in all experiments by a single subcutaneous (s.q.) injection in one hind footpad of 50 ng GP-MBP in complete Freund's adjuvant containing 100 heat killed M. tuberculosis H37RA (DIFCO, Detroit, MI). In the prevention protocol, rats were injected s.q. on one hind footpad 40 days prior to EAE induction with 100 *g TCR Vβ8-39-59 or TCR VB14-39-59 in CFA containing 100 μg M. tuberculosis. In suppression protocols, the TCR peptides were injected at the same time (100 μg s.q. in CFA, or 50 g i.d. in 0.1 ml saline in the ear), 7 days (i.d.), or 11 days (i.d.) after challenge with GP- MBP. In the treatment protocols, the TCR peptides were given either s.q. in CFA or i.d. in the ear on the first day that clinical signs of EAE were noted (usually day 12 after challenge with GP-MBP). Animals were scored daily for clinical signs of

EAE, using a rating scale of 0-4, in which 0 = no signs; 1 = limp tail; 2 = hind leg weakness, ataxia; 3 = hind quarter paralysis;

4 = front and hind quarter paralysis, moribund condition. Treatment groups were compared with control groups for

Λ differences in maximum disease severity and duration of clinical signs by Student's unpaired t test. Delayed type 5 hypersensitivity reactions were measured by the ear swelling assay (Offner, H., et al.. J. Exper. Med. 170:355 (1989)) 24 and 48 hours after injection i.d. of 50 μg antigen. GP-MBP-specific T cell lines were selected from TCR peptide treated and untreated rats as described previously (Vandenbark, A. A., et al., _L.

10 Immunol. 135:223 (1985)). Ten million GP-MBP activated line cells were transferred i.p. into naive rats to test for encephalitogenic activity, scored as described above for actively induced EAE.

Lymphocyte Proliferation: Activation of T cells was

15 measured by 3 H-Tdy uptake. 500,000 lymph node cells or 20,000 line cells in the presence of 1 million irradiated thymic accessory cells were incubated with culture medium and antigens in microtiter wells for 18 hours prior to the addition of 0.5 μBq labeled thymidine. The cell cultures were harvested onto glass

20 fiber filters and counted by liquid scintillation techniques.

Mean CPM were calculated from triplicate cultures. Standard deviations (SD) from repl cate cultures varied <10% from the mean value. B. RESULTS

25 To evaluate the regulatory effect of the TCR peptides on

EAE, the VB8-39-59 peptide, a control peptide VB14-39-59, or saline were injected prior to, simultaneously with, or after the injection of the encephalitogenic emulsion, GP-MBP/CFA. The average daily clinical scores of the most effective prevention, 30 suppression, and treatment protocols are presented in Figures 3-

5, and all groups tested are summarized in Table 15.

Clinical effects of TCR/CFA. Injection of the VB8-39-59 peptide in CFA 40 days prior to challenge with GP-MBP induced complete protection against clinical EAE (Figure 3). Furthermore, simultaneous injection of the peptide in CFA with the encephalitogenic emulsion suppressed EAE, reducing the incidence (8/13 in the treated group versus 26/26 in controls), severity (score of 1.3 versus 3.4), and duration (2.0 versus 6.6 days) of clinical disease (Figure 3, Table 15). Rats injected 40 days prior to or at the same time as EAE induction with the Vβl4- 39-59 peptide in CFA, or with CFA alone, developed EAE that was indistinguishable from the controls (Table 15).

TABLE 15 Prevention, Suppression and Treatment of EAE with TCR V.38-39-59


* p < 0.05; ** p < 0.01

To evaluate its therapeutic effects, the TCR VB8-39-59 peptide in CFA was injected s.q. into rats on the first day or onset of clinical signs. Rats at the time of this treatment exhibited hind leg weakness, ataxia, and incontinence (an average grade of 1.8). As is shown in Figure 3, treatment with the TCR peptide/CFA prevented further progression of clinical signs and shortened the duration of EAE from 6.6 days (controls) to 3.5 days. Treatment with TCR VB14-39-59/CFA or CFA alone had no effect on clinical EAE (Table 15). Clinical Effects of TCR Peptide Given i.d. To avoid the use of CFA, an evaluation was made of the effects on EAE of administering a saline solution of the TCR peptide intradermally in the ear. As is shown in Figure 4, i.d. administration of 50 g of the TCR peptide at the same time as the encephalitogenic challenge (day 0), or on days 7 or 11 after challenge, all had similar suppressive effects on EAE, reducing the maximum clinical severity from 3.4 to 1.7-1.8, and shortening the duration of EAE from 6.6 days to 3-4 days (Table 17).

When the TCR peptide was injected on the day clinical signs were first noted (average clinical score of 1.9), no clinical effect on EAE was observed during the first day; however, during subsequent days, the severity of EAE was reduced markedly versus controls (Fig. 5). The 50 μg/rat dose of TCR peptide caused a faster resolution of EAE (3.1 days) than the lower 10 μg/rat dose of peptide (4.0 days), compared to 6.6 days for the controls.

The rapid effect of the TCR VB8-39-59 peptide in resolving clinical EAE suggested that treatment with the peptide may have triggered a recall response to the TCR, induced initially in response to EAE. To document this possibility vn vivo, rats undergoing or recovered from EAE induced with GP-

MBP/CFA (without prior exposure to the TCR peptide) had

, significant DTH response to the VB8 peptide (p < 0.01 compared to naive or CFA immunized rats), but not to the Vβl4 peptide (Table j, 16). The magnitude of the response to Vβ8 peptide in rats undergoing EAE was understandably less than the response in rats 5 immunized previously with a protective regime of TCR peptide in

CFA (Table 16).

T cell responses in protected rats. To evaluate the effects of TCR VB8 peptide therapy on T cell responses, lymph node cells (LNC) draining the site of GP-MBP/CFA injection were

10 tested for antigen-induced proliferation, and then expanded into

T cell lines. As is shown in Table 17, LNC from rats treated with TCR VB8-39-59 had a high level of background proliferation (47,000 CPM), and similar responses to GP-MBP and other test antigens. T cell lines selected with GP-MBP (MBP/lst) responded

15 weakly to the selecting antigen and not at all to Rt-MBP and GP-

S72-89. The highest response of this line was to the TCR-VB8-39- 59 peptide. With weak GP-MBP recognition and strong TCR response, it was not surprising that the T cell line failed to transfer clinical signs of EAE to naive rats (Table 17). A

20 similar pattern of high TCR response and low reactivity to GP-MBP and other antigens was also observed in the T cell line (Vββ/lst) selected with TCR VB8-39-59 (Table 17).

In contrast, LNC from untreated EAE-recovered rats responded predictably to GP-MBP, Rt-MBP, and GP-S72-89 (Table

25 17). Unexpectedly, however, these LNC also responded to the TCR

VB8-39-59 peptide and to a lesser degree to the TCR VB14-39-59 peptide. When selected with GP-MBP, the resulting T cell line i responded strongly to MBP

TABLE 16 Delayed Hypersensitivity Responses to TCR Peptides.

48 hour DTH Response

c ro co

H H c rπ ω

I EAE onset. rπ

** p < 0.01 versus naive or saline/CFA immunized controls.

The DTH response was evaluated in naive Lewis rats or rats immunized with either GP¬ BP/CFA or saline/CFA without prior exposure to TCR peptides. Similarly, rats immunized with either TCR Vi88-39-59/CFA or TCR V/314-39-59/CFA were tested with either peptide. The ear swelling response (DTH) was measured 48 hours after the i.d. injection. In parentheses are shown the number of animals tested.

(0 c

03 CO H


C rπ co

I m m

a Treated rats were injected s.q. with 50 ig TCR v/?8-39-59 peptide/CFA on the first day of clinical EAE induced 12 days ealier with GP-BP/CFA. Untreated rats received only GP-BP/CFA (see Fig. 1). b LN cells collected after the untreated group recovered from EAE (day 21) were stimulated with GP-BP, TCR V/?8-39-59 peptide, or TCR V/J14-39-59 peptide, and were expanded in IL-2 prior to restimulation w,ith the indicated antigens (indicated as BP/lst, Vj88/lst, or V/?14/lst). For EAE transfer studies, 10' GP-BP activated T cells from treated (protected) and untreated groups were injected i.p. into naive rats. Underlined values indicate significant difference versus control cultures.

epitopes, and transferred severe clinical EAE to naive recipients in spite of low-level residual activity to the TCR VB8 peptide (Table 17). Upon further selection with the TCR VB8 peptide, the specific response to this TCR peptide was amplified, although a low level response to GP-MBP and S72-89 persisted. Further selection with the TCR VB14 peptide amplified only VB14 reactive T cells. Thus, in both TCR-selected lines, the response pattern verified the presence of TCR reactive T cells from the LN of EAE- recovered rats. As shown in Figure 8, strong DTH and proliferative responses were observed in animals preimmunized with the respective TCR peptides/CFA. Rats preimmunized with TCR VB8- but not with VB14 peptides were protected from subsequent challenge with GP-MBP/CFA. Significant DTH and strong proliferative responses to the TCR Vβδ-peptide were also observed in rats recovering from EAE that had never been immunized with the synthetic peptide, indicating that a natural regulatory response to the TCR Ve8-peptide was induced as a consequence of the EAE disease process.

An additional well known MS model is EAE in mice, which, in contrast to rats, is characterized by a relapsing clinical progression. Groups of 6 SJL/0 mice were injected with the 139- 151 peptide of proteolipid apoprotein (PLP) in CFA. On the first day of the onset of clinical signs (day 14), the mice received 50 μg of a synthetic peptide corresponding to residues 1-17 of the TCR VB17 sequence by i.v., i.d., or s.q. administration. As shown in Figure 9, both s.q. and i.d. injection of the TCR peptide reduced the severity and shortened the duration of disease in the initial episode and in relapsing EAE.

C. DISCUSSION This example demonstrates clearly the therapeutic administration of the TCR Vβ8-39-59 peptide in EAE, which is

t consistent with previous examples demonstrating the effectiveness of the TCR peptide in preventing and suppressing EAE. The rapid j, clinical effect, as well as DTH and lymphocyte proliferation responses to the TCR peptide, indicate that T cell responses to 5 the TCR VB8 peptide were already present in rats undergoing EAE that had never been immunized purposefully with the synthetic peptide.

Preimmunization with the Vβ8 peptide in CFA for 40 days prior to GP-MBP challenge was the most effective protocol tested

10 (Figure 3 and Table 15). It is apparent that this period of immunization is optimal for the induction of both protective T cells and antibodies to the TCR Vs8 peptide. Injection of the

TCR VB8 peptide at the same time as GP-MBP challenge was less protective than preimmunization, but this protocol still

15 suppressed completely all clinical signs of EAE in more than 30%

(6/19) of the rats (Table 15). In the remainder, the clinical course of EAE was shorter and milder. Injection of the TCR VB8 peptide after GP-MBP challenge but before onset of clinical EAE was also effective, completely preventing onset of EAE in 4/19

20 rats, and generally reducing disease severity and duration in the rest (Table 15).

A surprising aspect of the present example is the almost immediate clinical effect of the TCR VB8 peptide injected into sick animals. All rats receiving TCR peptide therapy recovered

25 from EAE faster than controls. Those injected with TCR peptide in CFA did not progress clinically before recovery. Those injected with TCR peptide intradermally did progress the first

* day, but then recovered as fast as the TCR/CFA injected rats.

B th the 10 μg and 50 g doses of peptide speeded recovery, but i 30 the higher dose resolved EAE one day sooner than the lower dose.

The TCR peptide therapy appeared to be effective by down- regulating T cell responses to encephalitogenic determinants of

GP-MBP. Lymph node cells from the GP-MBP-challenged, TCR peptide-treated rats had high levels of proliferating cells, but no specific BP responses (Table 17). However, T cell lines selected with GP-MBP proliferated in the presence of GP-MBP and TCR VB8 peptide, but not TCR VB14 peptide, indicating the presence of both effector and regulatory T cell specificities. That this cell mixture could not transfer EAE may be attributable to the apparent dominance of TCR VB8 reactive cells (net 49,000 CPM) over GP-MBP reactive cells (net 12,000 CPM) or S72-89 reactive cells (net 3,000 CPM). In contrast, LNC from EAE- recovered rats that were challenged initially with GP-MBP but not treated with TCR VB8 peptide recognized GP-MBP, Rt-MBP, and S72- 89, and to a lesser degree the TCR VB8 and VB14 peptides (Table 17). T cell lines selected with GP-MBP were highly encephalitogenic, due most likely to the dominance of GP-MBP- reactive T cells (net 84,000 CPM) over TCR Vβ8-reactive T cells (net 9,000 CPM). The persistence of TCR Vε8-ρeptide-reactive T cells in lines selected with GP-MBP is somewhat unusual in that T cell lines selected with one antigen typically lose responses to all other antigens. No cross-reactivity has been detected between GP-MBP and the TCR-VB8 peptide.

Lewis rats do not relapse spontaneously when EAE is induced with MBP/CFA. Although this monophasic course of EAE does not allow testing of TCR VB8-39-59 peptide therapy on relapsing disease, it does provide the opportunity to determine if the strong recovery mechanisms in this strain include immune respon¬ ses to the TCR VB8 peptide. Lewis rat T cells that respond to either encephalitogenic determinant (72-84 or 87-99 sequence) of MBP utilize preferentially the VO2/VB8 gene combination in their TCR. Injection of live or attenuated encephalitogenic T cells can induce protection against EAE, as well as idiotypic and "ergotypic" responses. The increased frequency of encephalito-

, genie T cells induced during EAE may have the same effect of perturbing the regulatory network, and it is conceivable that at least a part of this network is directed naturally at the TCR VB8-39-59 sequence. 5 The present data support this contention. Sick or recovered rats given the TCR VB8 peptide i.d. had small but significant DTH responses to this peptide, but no DTH to the corresponding Vβl4 peptide (Table 16). Furthermore, lymph node cells from recovered rats responded better to the VB8 TCR

10 peptide, and T cells specific for either peptide could be enriched by in vitro selection techniques (Table 17). Together, those findings provide direct evidence for the natural induction of immunity to the TCR VB8-39-59 sequence expressed by encephali¬ togenic T cells. However, this may not be the only important

15 determinant on the TCR, since other sequences within the TCR α or

B chains also induce regulatory T cells and antibodies. The protective, suppressive and therapeutic effects of the TCR VB8- 39-59 region clearly demonstrate its importance as a determinant for the idiotypic regulation of EAE.

20 Further, data presented for SJL/J mice, which experience a biphasic clinical course of EAE, demonstrate that adminsistration of a TCR VB17 peptide at the onset of clinical signs reduces the severity and duration of symptoms during both the initial episode and relapse. This provides additional support for the importance

25 of TCR V region peptides as tools in the treatment of autoimmune diseases modeled by EAE.




Myelin basic protein (MBP) is highly antigenic, and causes experimental autoimmune encephalomyelitis (EAE) in a variety of animal species when injected with adjuvants (Alvord, E.C., Jr., In Experimental Allergic Encephalomyelitis: A useful model for multiple sclerosis. Alvord, E ., Jr., et al. (eds.), Alan R.

Liss, Inc., New York, pp. 523-537 (1984)).

The encephalitogenic property of MBP is encompassed within a discrete number of immunodominant epitopes (about 10). Within each strain, one or more of these epitopes, in association with the available Class II MHC molecules, induces CD4+ T effector lymphocytes that home to the central nervous system (CNS), causing perivascular inflammatory lesions and nerve dysfunction (Zamvil, S.S., et al.. J. Immunol. 139:1075 (1987); Offner, H., et al.. J. Exp. Med. 170:355 (1989)). The genetic background, including both MHC and non-MHC genes, influences which MBP epitopes are encephalitogenic (Beraud, E., et al.. J. Immunol.136:511 (1986); Zamvil, S.S., et al.. J. EXP. Med. 162:2107 (1985)), the clinical course and severity of the disease (Fritz, R.B., et al ., J. Immunol . 134:2328 (1985); Hinrich, D.J., et al.. J. EXP. Med. 166:1906

(1987); Linthicu , D.S., et al.. J. EXP. Med. 155:31 (1982); Dietsch, G.E., et al.. J. Immunol. 142:1476 (1989); Mokhtarian, F., et al .. Nature (London ) 309:356 (1984)), demyelination (Mokhtarian, F., et al.. Nature (London) 309:356 (1984)), and resistance mechanisms (Bernard, CC, Clin. EXP. Immunol. 29:100

(1977); Welch, A.M., et al .. J. Immunol. 125:186 (1980); Varriale, S., et al .. J. Immunol. 125:186 (1989); Whitham, R.H., et al.. Cell. Immunol. 126:290 (1990)).

The spectrum of clinical and histologic signs induced by MBP-specific T cells resembles in many ways the human diseases multiple sclerosis (MS) and acute disseminated encephalomyelitis (ADE) (Paterson, P.Y., Adv. Immunol.5:131 (1966); Waksman. B.H..

t et al.. Proc. Soc. EXP. Biol. Med 175:282 (198411. Consequently, human T cell recognition of MBP has been of considerable inter- i est.

There are several lines of evidence that suggest the 5 involvement of T cells, including those specific for human MBP, in the pathogenesis of MS. Genetic studies indicate linkage disequilibrium between T cell receptor V and C region genes within families with MS (Hauser, S.L., et al .. Neurology 39:275 (1989); Beall, S.S., et al .. J. Cell. Biochem. 11D:223 (1987)) or

10 among patients generally (Oksenberg, J.R., et al .. Proc. Natl.

Acad. Sci. USA 86:988 (1989)). However, the actual involvement of MBP-reactive T cells in the pathogenesis of MS can only be demonstrated if selective regulation or removal of MBP-reactive T cells can affect the disease process. Such selective

15 regulation is now possible in EAE.

In the present example, a synthetic TCR peptide was used to induce regulatory T cells and antibodies directed against the TCR on the pernicious T cells. This approach prevented the induction of EAE. Moreover, as demonstrated in the previous example,

20 administration of the TCR peptide to clinically sick rats arrested disease progression and speeded recovery. The application of this approach for regulating potentially encephalitogenic T cells in MS patients depends on whether or not MBP-reactive T cells preferentially utilize a limited number of

25 TCR V region genes in response to immunodominant epitopes of human MBP.

To this end, T cell lines from MS patients and controls were selected in a manner that allowed emergence of T cells that recognize immunodominant MBP epitopes. From these lines, 109

30 MBP-specific T cell clones were isolated and characterized for phenotype, epitope specificity, MHC restriction, and TCR V gene expression. The data demonstrate at the clonal level that T

cells from MS patients recognize more and different MBP epitopes than do T cells from normal donors. Furthermore, in one MS donor with the disease-associated HLA-DR2/DQwl haplotype, 4 of 8 T cell clones tested expressed the VB5.2 phenotype, indicating preferen- tial TCR V gene use in response to MBP.


Human Subjects: The MS patients evaluated in this study included 11 patients with clinically or laboratory-supported definite MS who were attending the Oregon Health Sciences University MS clinic. There were 7 females and 4 males (mean age of 46, range 34-67 years), who had MS for 6-35 years. The patients had an average ambulation index (Al) of 3.4+1.6 (range 1-6) and an average Kurtzke disability status score (KDSS) of 4.3±2.0 (range 2-4) (Kurtzke, J.F., Neurology 15:654 (1965)). The normal individuals included 6 female and 3 male employees (mean age of 36, range 25-55 years) from the Veterans Affairs Medical Center and Oregon Health Sciences University. These normal individuals were selected on the basis of positive PBL proliferation responses to human MBP as described previously (Vandenbark, A.A., et al.. J. Neurosci. Res. 23:21 (1989)).

All subjects were HLA-typed retrospective to T cell line selection by a standard serological method utilized by the Oregon Health Sciences University Transplantation Laboratory. The frequency of HLA Class II alleles (DR,DQ) showed an uneven distribution for DR2 (7 of 11 patients-63%-were DR2 positive; 3 of 9 normals-33%-were DR2 positive), that in general represented the expected occurrence for these two groups (Theofilopoulos, A.N., in Basic and Clinical Immunology. Stites, D.P., et al . (eds.), Appleton and Lange Publishers, Los Altos, CA, pp. 151-154 (1987)).

Antigens: Human (Hu-) MBP was extracted and purified from snap frozen human brain (Eylar, E.H., et al .. Arch. Biochem. Biophvs. 132:34 (1969)). Peptides of Hu-MBP, including Pl (residues 45-89), P2 (residues 1-38) and P4 (residues 90-170), 5 were obtained by peptic cleavage and purified by Sephadex, ion exchange chromatography, and high pressure liquid chromatography (Chou, C.H.-J., et al.. J. Neurochem. 28:115 (1977)). A series of synthetic peptides corresponding to the Hu-MBP sequences 13- 28, 39-54, 55-74, 72-84, 87-99, 90-109, 110-129, 130-149, and

10 149-170 was synthesized by the Merrifield solid-phase method and purified by HPLC according to methods described previously (Hashim, G.A., et al.. J. Neurosci. Res. 16:467 (1986)).

T Cell Lines: Human MBP-reactive T cell lines were selected from the blood of 11 MS patients and 9 normal

15 individuals who were responsive to Hu-MBP in previous screening tests (Vandenbark, A.A., et al .. J. Neurosci. Res. 23:21 (1989)). Blood mononuclear cells (MNC) were separated by Ficoll density gradient centrifugation and cultured with 50 ug/ml Hu-MBP in complete medium (RPMI 1640 with 10% human AB serum, L-glutamine,

20 sodium pyruvate and antibiotics) at a cell density 5xl0 5 per well of a flat-bottomed 96-well plate for 5 days at 37 β C in a 5% CO2 atmosphere. The stimulated cells were transferred into IL-2 rich medium (containing 50 u/ml recombinant IL-2, AMGEN Biologicals, Thousand Oaks, CA) for expanding activated T cells. When growth

25 in IL-2 slowed, the T cells were re-stimulated with 25 ug/ml Hu-

MBP presented by autologous monocytes contained in irradiated peripheral blood MNC (4,500 rad) at the ratio of 1:10 (T:MNC). , The T cell lines were re-stimulated 4-5 times until the cell number was sufficient for assessing MBP epitope specificity, MHC ι30 restriction, and phenotype.

T Cell Cloning: T cell clones were obtained by limiting dilution of MBP-specific T cell lines that had been re-stimulated

twice with Hu-MBP. After 4 days in IL-2-enriched medium, T lymphoblasts were diluted to 1, 10 and 30 cells/20 ul of culture medium containing Hu-MBP (50 ug/ml), IL-2 (50 u/ml) and irradiat¬ ed MNC (1.5 x 10 6 ), and the cell mixture was placed into each well of a 60-well Tarasaki microtest tray (NUNC Inc., Naperville,

IL) (Lamb, J.R., et al.. J. Immunol. 128:233 (1982)). Recovery of human MBP-specific clones was most efficient when at least 10 Hu-MBP reactive line cells were seeded per well, producing a 20% rate of recovery. When only one line cell was seeded per well, the rate of recovery was 2%. Hu-MBP reactive T cells were recloned by seeding at 1 cell/well. The Tarasaki trays were incubated at 37 β C and 5% CO2 for 7 days. For re-stimulation, the cells from each positive well were transferred to a single well of a round-bottomed 96-well plate, into which were added 200 ul of complete medium with 25 ug/ml Hu-MBP and 2xl0 5 irradiated MNC.

50 μ/ml of IL-2 were added to the cells on the third day after stimulation and the cells maintained in IL-2 for another four days. When the cell number reached 2-4xl0 5 , the cultures were transferred into a 24 well plate in 1 ml, and re-stimulated with Hu-MBP in the presence of 3xl0 6 autologous irradiated MNC, and later expanded in 2 ml of IL-2 rich medium.

Proliferation Assay: The specificity of the cell response was evaluated by incubating 2xl0 4 T cells with lxlO 5 irradiated (4,500 rad) autologous blood MNC in 0.2 ml triplicate cultures in a 96 well, round bottomed microtiter plate in the absence of antigens and in the presence of 2 ug/ml Con A, 50 ug/ml Hu-MBP, 50 ug/ml Hu-MBP fragments (Pl, P2 and P4), 50 ug/ml of synthetic peptides of Hu-MBP, and 1/200 diluted Herpes simplex virus (HSV) antigen (Whittaker M.A. Bioproducts, Walkersville, MD). Micro- titer cultures were incubated for 3 days at 37 β C at 5% CO2, and were pulsed with 0.5 uBq 3 H-TdR for the l st 18 hr. The cells were harvested on glass fiber filters and incorporated 3 H-TdR was

counted using a β-scintillation counter. Proliferation was expressed as CPM of stimulated culture ± SD (background subtract-

, ed). Backgrounds ranged from 200 to 2,000 CPM. MHC restriction was evaluated by incubating the T cells plus Hu-MBP, Hu-MBP 5 fragments or synthetic peptides of Hu-MBP in the presence of antibodies specific for framework determinants of molecules from the HLA-DP, -DQ or -DR locus (antibodies were purchased from Becton Dickinson Pharmaceuticals, Mountain View, CA).

Phenotvping T Cells: T cell lines and clones were

10 phenotyped using Leu 3a (anti-CD4+ T helper) and Leu 2a (anti-

CD8+ T cytotoxic/suppressor) monoclonal antibodies (Becton Dickinson), as described previously (Vandenbark, A.A., et al .. OL. Neuroim unol . 8:103 (1985)). T cell clones were phenotyped for the expression of TCR VB chain gene products using mouse

15 monoclonal antibodies specific for human TCR VS5.2/5.3 (5A),

VB5.3 (5B), VB6.7, VB8.1, and VB12 (DIVERSI-r as TcR Screening Panel IA, T Cell Sciences Inc., Cambridge, MA). Two x 10 5 T cells were incubated with 5 ul of each antibody for 1 hr at 4 * C, followed by 3 washes with medium containing 5% human AB serum and

20 further incubation with FITC-conjugated goat anti-mouse IgG for

30 min. After 2 washes and fixation in 2% formaldehyde, the stained cells were evaluated for i munofluorescence using a FACScan flow cytometer.


25 Characterization of Hu-MBP Specific T Cell Lines from MS

Patients and Normals. Hu-MBP specific T cell lines were selected from the blood of 11 patients with MS and 9 normal donors with previously demonstrated proliferation responses to Hu-MBP. Each

* line was selected from 30-50 million blood cells by repeated

30 stimulation with whole Hu-MBP and expansion with IL-2. From previous experience in selecting rodent T cell lines, these

conditions should allow expansion and focusing of representative T cell responses towards immunodominant Hu-MBP epitopes.

The T cell lines from MS patients and normal donors responded equally well to both Hu-MBP and Con A, with negligible responses to HSV antigens (Figure 6). T cell lines were evaluated for response to highly purified enzymatic cleavage fragments spanning the entire sequence of Hu-MBP, including Pl (residues 45-89), P2 (residues 1-38) and P4 (residues 90-170). Eight of 11 MS lines responded to all 3 Hu-MBP fragments, two responded to 2 of 3 fragments, and only 1 line responded to a single fragment. In contrast, 5 of 9 normal lines responded to a single fragment, 3 lines responded to all fragments and 1 line did not respond to any fragment. The rate of responders to the 45-89 fragment was significantly greater in the MS group versus controls, and on average, the MS T cell lines were significantly more reactive to both the 45-89 (Pl) and 1-38 (P2) fragments of Hu-MBP (Figure 6). However, there was no difference in frequency or magnitude of response to the 90-170 (P4) fragment. All of the human T cell lines had a mixed phenotype of CD4+ and CD8+ T cells. However, the T cell lines from MS patients had a rela¬ tively higher rate of CD4+ and lower rate of CD8+ subpopulations compared to normal donors (78 ± 13% versus 58 ± 8% for CD4+ cells; 15 + 6% versus 30 ± 12% for CD8+ cells, Table 18).

Selection and Characterization of Hu-MBP Specific T Cell Clones. Although the general range of immunodominant T cell epitopes on Hu-MBP can be inferred from the pattern of reactivity of T cell lines to Hu-MBP peptides, proof of T cell recognition must be derived from analysis of clones. To this end, a total of 109 human MBP-specific T cell clones from 7 MS T cell lines (50 clones) and 6 normal T cell lines (59 clones) were evaluated for response to Hu-MBP and Hu-MBP fragments and synthetic peptides. The T cell line donors were comparable except for HLA-DR2

distribution (86% of MS patients versus 33% of normals were DR2 positive; see Table 19).

All of the T cell clones responded to Hu-MBP, but not to Herpes simplex virus (HSV) antigen, with a similar response level in both groups. In total, 48 T cell clones (distributed equally between the two groups) were phenotyped for CD4 and CDB markers. Of these, 45 clones were CD4+ and 3 (from one normal donor) were CD8+ (Table 18). This predominance of CD4+ clones was expected from previous experience in rats and mice, but did not reflect the relative proportion of these subsets in the T cell lines from which the clones were derived (Table 18). Clonal Specificities Reflect the Pattern of T Cell Line

Responses. In order to establish the validity of the clonal analysis, it is important to evaluate how well the T cell clonal specificities represent the T cell line responses. In the lines which yielded sufficient clones for comparison, the number of clones responding specifically to a distinct fragment of MBP showed a significant correlation with the Hu-MBP fragment- directed response of the parent T cell line (paired Chi Square test, p < 0.05).


Table 18

Phenotype Distribution of M8P-Specific 7 Cell Lines and Clones from MS Patients and Normal Individuals

Total 59.3+8 30.0+12 21 24

Table 19

Peptide Specificities of T Cell Clones from MS Patients and Normal Individuals

Donor Clone number responding to



Table 19 (continued)

Donor Clone number responding to

* Antigens in linkage disequilibrium with DR antigens are present, but expected antigens did not type clearly. ** ( )=% of total clones; compared to normals, p<0.01.

* Representative comparisons from 3 MS and 2 normal donors are shown in Figure 7. Based on the pattern of T cell line

1 responses, it was expected that more clones reactive to Pl and to

P2 would be selected from the MS T cell lines than from control 5 lines, but that the frequency of P4 reactive clones would be relatively equal. This indeed was the case, as is shown in Table 19. Unexpectedly, 46 of the 109 MBP-reactive T cell clones did not respond to any single fragment of Hu-MBP, even though the response to Hu-MBP was vigorous, ranging from 10,000 to 27,000

10 cpm with only 1,000-2,000 cpm background. This finding was more frequent in the normal group than in the MS group, largely on the basis of a single normal donor (Table 19).

Biased Clonal Specificities within P4. Although the P4 region of Hu-MBP represents the C terminal half of the molecule,

15 approximately 2/3 (41 of 63) of the clones reactive to Hu-MBP peptides responded to this fragment. To identify epitope specificities, 23 of these clones from 4 normal and 4 MS donors were tested in a proliferation assay against a series of synthet¬ ic peptides corresponding to different portions of the P4 region.

20 As is shown in Table 20, the clonal distribution was biased in normal donors towards the 110-129 sequence, and in MS donors towards the 130-149 sequence. Responses to the 149-171 sequence were similar in both groups, and only one MS clone responded to the 87-99 sequence (Table 20).

25 HLA-DR2 Is Capable of Restricting Multiple Hu-MBP Epitopes.

The association of the HLA-DR2/DQwl haplotype with MS suggests that these Class II molecules, especially DR2, could play a

* critical role in restricting CD4+ T cell responses to CNS autoantigens. To this end, the Hu-MBP epitopes recognized by 17

* 30 T cell clones from 3 HLA-DR2/DQwl donors are summarized in Table

21. In total, this set of T cell clones recognized P2 (3 clones), Pl (1 clone), P4 (8 clones), or no peptide (5 clones).

ithin P4, 1 MS clone recognized the 87-99 epitope, 1 normal clone recognized the 110-129 epitope, 1 MS clone recognized the 130-149 epitope, and 4 clones (3 MS and 1 normal) recognized the 149-171 epitope. Responses in 7 of 7 P4-reactive clones tested were inhibited with anti-HLA-DR antibody, clearly implicating DR2 as the restriction element (Table 21). Since the DR locus is used predominantly in restricting human T cell responses to MBP, it is likely that the majority of the 10 untested clones were also DR2 restricted. In any case, it is clear that DR2 can restrict a wide variety of Hu-MBP epitopes in humans.

TCR VB Gene Usage bv Hu-MBP Reactive T Cell Clones. The preferential use of TCR Vα and Vβ gene families by encephalito¬ genic MBP-specific T cells from rats and mice has led to success¬ ful vaccination and therapeutic strategies directed against common TCR sequences on the pernicious T cells. It is unknown, however, if a similar mechanism in humans leads to the restricted use of TCR V genes in response to MBP or other antigens. To begin the analysis of TCR V gene use, 38 T cell clones (19 from each group) were phenotyped for expression of VB gene products, using a panel of 5 monoclonal antibodies specific for VB5.2,

VB5.3, VB6.7, VB8.1, and VB12 (Table 22). TCR V gene expression could be positively identified in six of the clones, all from MS donors: Two of these clones expressed VB6.7, whereas the other 4 clones expressed VB5.2. Of the VB5.2+ clones, 1 was from a DR2,4 donor, and 3 were from a DR2 homozygous donor. One additional clone from the DR2 homozygous donor expressed rear¬ ranged mRNA for VB5.2 , indicating that in this

Table 20

Epitope Specificities of P4-Reactive T Cell Clones from MS Patients and Normal Individual s

Number of clones responding to

Donor Number Total(DR2+) 87-99 91-109 110-129 130-149 149-171 Total to

MS 4(4) 1 0 1** 3**(2)* 4(3)* 9 I Normal 4(2) 0 0 9(3)* 0 5(2) 14

*( ) Number of donors responded. ** Compared to normals, p < 0.01.

Table 21

Human MBP Epitope Specificities in DR2/Dqwl Homozygous Donors

Proliferation (cpm/1000 minus background)

ro o


Table 22 T Cell Receptor VB Chain Expression of MBP-Reactive T Cell Clones

*DIVERST-Tm aβ TcR screening panel IA (T Cell Sciences, Inc., Cambridge, MA) included Vβ5a (Vβ5.2 and 5.3), Vs5b (VB5.3), VB6 (VB6.7), VB8 (VB8.1) and VB12 (VB12) mAbs against TcR VB chain. **Responded to whole Human MBP, but not to any peptides. ***Three CD8+ clones were included.

individual, 4/8 clones analyzed use the same TCR VB gene in response to Hu-MBP, even though each has a distinct epitope specificity (Table 22).

C. DISCUSSION The present example clearly demonstrates at the clonal level that MS patients have a more complex and altered pattern of T cell recognition of immunodominant Hu-MBP epitopes than do normal Hu-MBP responders. These data suggest an increased exposure to immunogenic forms of Hu-MBP in MS patients, thereby increasing the likelihood of inducing or perpetuating encephalitogenic T cells. The potential relevance of T cell recognition of Hu-MBP in human paralytic conditions such as MS must be viewed in light of the potent encephalitogenic function of MBP-reactive T cells in animals, and the increased frequency of activated MBP-reactive T cells in the blood and CSF of MS patients (Allegretta, M., et al.. Science 247:718 (1990); Link, H., et al.. Neurology 40-fSuppl. 1):283 (1990)).

The T cell clones evaluated in this study were isolated from Hu-MBP specific T cell lines selected in vitro to allow the emergence of specificities directed at immunodominant Hu-MBP epitopes. Encephalitogenic determinants display imunodominance during the selection of rat and mouse T cell lines with whole MBP (Bourdette, D., et al.. Cell. Immunol. 112:351 (1988); Vanden- bark, A.A., et al .. J. Immunol. 135:229 (1985)), and it is likely that T cells to immunodominant Hu-MBP determinants could also be encephalitogenic under permissive conditions. In this study, the immunodominant epitopes inferred from T cell line responses showed a significant correlation with the specificities identi¬ fied through clonal analysis (Figure 7). These results validate conclusions drawn from the line data regarding specificity, and document that the clones which

ϊ survived the selection procedure were representative of the Hu-

MBP responsive T cell population within the lines.

* However, the phenotype of the clones was uniformly CD4+ (with the exception of 3 clones from a single normal donor), even

5 though the T cell lines all contained substantial levels of CD8+

T cells. It is not clear if the CD8+ T cells within the lines were Hu-MBP specific, or if they were simply carried in the lines by the relatively high levels of IL-2 added to the cultures. It was apparent, however, that the normal T cell lines consistently

10 contained a higher percentage of CD8+ cells than the MS lines.

It is interesting and potentially relevant to the regulation of T cell function that one of the CD8+ clones could inhibit MBP- induced proliferation of a CD4+ clone from the same normal donor. Such regulatory CD8+ T cells, if present in increased numbers in

15 vivo, could account for the lack of clinical disease in normal individuals with Hu-MBP reactive T cells. A critical level of these CD8+ T cells in conjunction with increased levels of adherent suppressor cells (similar to those observed in mice (Whitham, R.H., et al.. Cell. Immunol. 126:290 (1990))) could

20 account for the inability to select Hu-MBP specific T cell lines from more than 60% of normal donors (Vandenbark, A.A., et al., «_____ Neurosci. Res. 23:21 (1989)).

In contrast, T cell lines can be selected from more than 80% of MS patients. These regulatory cell types would not be

25 expected to influence the efficiency of recovering MBP-specific

T cell clones by limiting dilution directly from blood, without prior line selection, as reported by others (Hafler, D.A., et

* ____ > J. Immunol. 139:68 (1987); Richert, J.R., et al., jL Neuroimmunol. 23:55 (1989); Richert, J.R., et al., Ann. Neurol.

* 30 26:342 (1989)).

T cell responses to Hu-MBP in MS patients included a broader range of specificities than the responses in normal

individuals (Figure 6). In addition to common epitopes, T cells from MS patients showed a biased response to the N terminal half of MBP and towards at least one epitope in the C terminal half of the molecule. The most consistent difference in response between MS and normal donors was to Pl (residues 45-89). Previous studies have shown that in MS, immunoreactive fragments of Hu- MBP-like material are present in the cerebrospinal fluid (CSF), with the dominant antigenic form spanning residues 45-89 (Whitaker, J.N., J. Immunol. 129:2729 (1982)). The detectable concentration of this fragment increases in CSF after central nervous system injury, providing a feasible explanation for the increased occurrence of Pl-reactive T cells in MS patients. The bias of MS responses to P2 and to the 130-149 epitope within P4 could also be explained by the release of immunoreactive frag- ments of Hu-MBP during demyelination, although MHC restriction effects cannot be ruled out as yet. From animal studies, it is clear that long-term immunization with MBP induces an expanding repertoire of T cells to less and less dominant combinations of MHC and MBP epitopes (Offner, H., et al., J. EXP. Med. 170:355 (1989)). These additional T cell specificities may or may not be encephalitogenic, depending on their ability to recognize homologous MBP. The increased complexity of Hu-MBP responsive T cell specificities in MS patients is consistent with increased exposure to immunogenic fragments of MBP released during demye- lination, and it is conceivable that the long-term, chronic nature of MS involves the continuous induction or re-stimulation of encephalitogenic T cell specificities.

Approximately 40% of the Hu-MBP reactive T cell clones, especially the clones from normal T cell lines, did not respond to any Hu-MBP fragment. Such a response could involve junctional epitopes spanning the cleavage sites of Hu-MBP (eg. residues 30- 55 or 80-100), conformational epitopes destroyed by cleavage, or

i isoforms or post-translational variants of Hu-MBP lost during purification of cleavage fragments. Although the function of

• these cells in humans is unclear, similar cells occur at high frequency (50%) in EAE-recovered Lewis rats. Such T cells

5 transfer delayed hypersensitivity responses to MBP, but do not transfer EAE or protection against EAE.

Responses in both MS and normal T cell clones were predomi¬ nantly restricted by HLA-DR, although no strong association was found between any specific epitope and a given DR alleie. HLA-

10 DR2, which is over-represented in MS patients, was capable of restricting multiple epitopes of Hu-MBP, and some epitopes (e.g., 149-171) could be restricted by several HLA-DR alleles. In a previous T cell line study (Chou, Y.K., et al., J. Neurosci. Res. 23:207 (1989)), HLA-DR alleles were reported to be restricted to

15 26/33 Hu-MBP epitope-specific T cell responses, whereas HLA-Dq restricted 6/33 responses only in patients, and HLA-DP restricted a single normal donor response to P2.

The present data from T cell clones confirm the overwhelming restriction function of HLA-DR molecules on Hu-MBP

20 recognition, as well as the ability of an undefined HLA-DP allele

(from a different normal donor, DR7,?/Dqw2,3) to restrict epitopes within the Hu-MBP 1-38 region recognized by three individual clones. However, no HLA-Dq restricted clones were found.

25 A major question regarding the use of TCR VB peptides to regulate T cell responses in humans is whether or not MBP- specific T cells utilize a limited set of V genes. The present

* data, using antibodies specific for only about 1/lOth of the TCR VB repertoire, positively identified 6/38 clones, all from MS 30 donors. In one HLA-DR2/Dqwl homozygous donor with chronic progressive MS, 4 of 8 T cell clones specific for different Mu- MBP epitopes expressed the same VB5.2 gene in the T cell receptor

(all phenotypically VB5.2 positive clones were confirmed by PcR), suggesting for the first time a bias in TCR V gene use by humans in response to Hu-MBP. The use of the same TCR V region gene in response to different Hu-MBP epitopes is similar to MBP responses in rats and mice, and indicates that the choice of the TCR is not epitope driven.

One important practical implication of this observation is that biases in TCR repertoire can be ascertained without defining the epitope specificities of MBP-reactive clones. Table 23 presents PcR data which demonstrate that MBP-specific T cell clones from human MS patients are skewed in their TCR VB gene use. Total mRNA was extracted from individual T cell clones specific for human MBP from MS patients and normal donors, and rearranged TCR VB message was amplified by PcR and identified by specific probes. Preferential use of VB5.2 in MS donors MS-1 and

MS-2, and preferential use of VB14 by normal donor N-l by MBP- specific T cell clones was demonstrated. This provides additional support for the conclusion that humans also respond preferentially with V region genes to autoantigens such as MBP.


BP-Specific TCR Vβ Gene Use

Donor HLA Type # Clones Vβ Gene

Conclusion: BP-specific T cell clones are skewed in their TCR Vβ gene use, with vβ5.2 expressed by 18/24 MS clones.

Having now fully described this invention, it will be appreciated by those skilled in the art that the same can be performed within a wide range of equivalent parameters, concentrations, and conditions without departing from the spirit and scope of the invention and without undue experimentation.

While this invention has been described in connection with specific embodiments thereof, it will be understood that it is capable of further modifications. This application is intended to cover any variations, uses, or adaptations of the inventions following, in general, the principles of the invention and including such departures from the present disclosure as come within known or customary practice within the art to which the invention pertains and as may be applied to the essential features hereinbefore set forth as follows in the scope of the appended claims.