BACKGROUND OF THE INVENTION Drug discovery in the post-genomics era provides enormous opportunities as well as new challenges. The targets of the drug discovery process have changed greatly over the last 50 years. The development of advanced purification technologies and the tools of molecular biology have brought molecular targets into the current discovery process. In the last ten years, there has been a trend towards selecting molecular targets for the screening process, and the human and other genome projects have made available many thousands of additional targets for drug discovery.

In addition to these novel targets with unknown potential, there are a significant number of well-validated targets associated with major human diseases.

Most of these are either nuclear receptors or G protein-coupled receptors. It was found, that in some cases, one compound which has an effect through one receptor, can also act through another receptor, and that several compounds can work through the same receptor. Unfortunately, even when the mechanism of a disease process is understood, for example by identifying the receptor (s) responsible for such a process, this information has not always resulted in the development of new treatments. For

example, subjects who suffer from inflammation associated diseases and disorders have a great and desperate demand for novel drugs as therapeutic agents. Current therapies are merely palliative and have not been significantly improved in recent years.

Recent scientific advances provide some hope that new treatments will soon be available for these diseases. Sequencing of the human genome, which contains nearly 30,000 genes, has been recently completed. This significant achievement in the frontiers of human medicine will allow the identification of genes involved in the onset and progression of human diseases and pathological states. Many of these genes will serve as valid targets in the discovery process of drugs which will be more effective in the treatment of inflammatory diseases. Along with a massive flow of novel genes with potential therapeutic properties, there is a growing need for more rapid and efficient ways to discover lead compounds with enhanced (agonistic) or inhibitory (antagonistic) properties.

Chemokines are among the biological factors which are, amongst other functions, involved in the inflammatory disease process. Chemokines belong to a group of small,-8-14 kDa, mostly basic, heparin binding proteins that are related both in their primary structure and the presence of 4 conserved cysteine residues. The chemokines are chemotactic cytokines that have been shown to be selective chemoattractants for leukocyte sub-populations in vitro, and to elicit the accumulation of inflammatory cells in vivo. In addition to chemotaxis, chemokines mediate leukocyte de-granulation (Baggiolini and Dahinden, 1994) and the up-regulation of adhesion receptors (Vaddi and Newton, 1994), and have recently been implicated in the suppression of human immunodeficiency virus replication (Cocchi et al. , 1995).

Chemokines can be divided into 4 groups (CXC, CX3C, CC, and C) according to the positioning of the first 2 closely paired and highly conserved cysteines of the amino acid sequence. The specific effects of chemokines on their target cells are mediated by members of a family of 7-transmembrane-spanning G-protein-coupled receptors. These chemokine receptors are part of a much bigger super family of G- protein-coupled receptors that include receptors for hormones, neurotransmitters, paracrine substances, inflammatory mediators, certain proteinases, taste and odorant molecules and even photons and calcium ions.

The chemokine receptors have received increasing attention due to their critical role in the progression of immune disease states such as asthma, atherosclerosis, graft rejection, AIDS, multiple sclerosis and others. It would be useful to have therapeutic agents capable of inhibiting the binding of ligands of some chemokine receptors in order to lessen the intensity of or cure these diseases.

Chemokines themselves play an essential role in the recruitment and activation of cells from the immune system. They also have a wide range of effects in many different cell types beyond the immune system, including for example, in various cells of the central nervous system (Ma et al. , 1998) or endothelial cells, where they result in either angiogenic or angiostatic effects (Strieter et al. , 1995). Recent work has shown that particular chemokines may have multiple effects on tumors, including promoting growth, angiogenesis, metastasis, and suppression of the immune response to cancer, while other chemokines inhibit tumor mediated angiogenesis and promote anti-tumor immune responses. Recently, it was shown that the SDF-la/CXCR4 chemokine/chemokine receptor pathway is involved in dissemination of metastatic breast carcinomas (Muller A, 2001). This example illustrates that both chemokines and their receptors are potentially valuable targets for therapeutic intervention in a wide range of diseases.

SUMMARY OF THE INVENTION The background art does not teach or suggest sequences or compositions containing peptidic modulators capable of binding to chemokines and inhibiting or activating their biological functions. The background art also does not teach or suggest sequences or compositions containing the basic consensus sequences which characterize families of such peptidic chemokine-binding modulators In addition, the background art does not teach or suggest the nucleic acid molecules encoding for such peptidic chemokine-binding modulators. Finally, the background art does not teach or suggest methods of treatment employing such peptidic chemokine-binding modulators.

The present invention overcomes these deficiencies of the background art by providing peptidic chemokine-binding modulators, with defined amino acid sequences, which have been found to bind to specific chemokines, including but not limited to human SDF-la, MIG, IL-8, MCP-1 and Eotaxin, and which modulate the binding of these chemokines to their respective receptors and/or which otherwise have an inhibitory or stimulatory effect on the biological activity of chemokines.

It should be noted that the term"peptidic"as used herein, also includes peptidomimetics and hybrid structures comprised of at least one amino acid and at least one molecule that is not an amino acid, or at least not a naturally occurring amino acid. The term amino acid may optionally also include non-naturally occurring amino acids as well as naturally occurring amino acids, and derivatives and analogs

thereof. It also includes every small molecule, regardless of whether that molecule is a peptide, that binds to one or more of the chemokines.

Preferably, the present invention features basic consensus sequences which characterize families of such peptidic chemokine-binding modulators.

More specifically, if the biological activity caused by the target protein, i. e. chemokine receptor, when activated through binding the target ligand, i. e. chemokine, involves activation of some biological function, then the inhibitory peptide preferably inhibits such activation. On the other hand, if the biological activity caused by the receptor involves inhibition of some biological function, then the inhibitory peptide preferably blocks inhibition of the biological function.

The peptidic chemokine-binding modulators are then preferably used to develop one or more lead compounds for new therapies. Alternatively or additionally, the peptidic chemokine-binding modulators themselves may have therapeutic value, and as such, may optionally be used for treatment of a subject.

Also additionally or alternatively, binding of the peptidic chemokine-binding modulators may optionally be used to identify lead proteins, which are reference proteins whose reactivity descriptors are substantially similar to those of the protein of interest such as novel chemokines.

Also additionally or alternatively, the peptidic chemokine-binding modulators may optionally be used as antigens to produce antibodies to these peptides, which can also bind chemokine-binding receptors, or optionally may be used to stimulate the production of auto-antibodies against these peptides that can also bind chemokine receptors. The latter use would involve using these peptides (or other modulators) as a vaccine, optionally with any suitable vaccine carrier that could easily be selected by one of ordinary skill in the art, including but not limited to, adjuvants, carriers and the

like. More preferably, the modulators which are used to produce the antibodies are selected from one of the peptides described herein. It should be noted that the vaccine may also optionally comprise the antibody itself.

According to another preferred embodiment of the present invention, there is provided a composition for treating inflammatory and cancer metastasis conditions in a subject, comprising a pharmaceutically effective amount of a therapeutic agent for administering to the subject, the therapeutic agent being composed of the peptidic chemokine-binding modulators as the active ingredient as well as a suitable pharmaceutical carrier if necessary.

According to a preferred embodiment of the present invention, the therapeutic agent may be administered topically, intranasally and by inhalation. Alternately, the therapeutic agent may be administered by systemic administration.

According to the present invention, there is provided a peptidic chemokine modulator for modulating a biological effect of a chemokine, comprising a molecule composed of the amino acids H, S, A, L, I, K, R, T and P, and featuring at least 2 Histidines spread along the molecule, wherein the molecule features an overall positive charge (family 1). Preferably, the molecule comprises a peptide having an amino acid sequence selected from the group consisting of SIFAHQTPTHKN, SIPSHSIHSAKA, SAISDHRAHRSH, SAGHIHEAHRPL, CHASLKHRC, AHSLKSITNHGL, ESDLTHALHWLG, HSACHASLKHRC, WSAHIVPYSHKP YATQHNWRLKHE, CAHLSPHKC, GVHKHFYSRWLG, HPTTPIHMPNF, SVQTRPLFHSHF, and VHTSLLQKHPLP. More preferably, the peptide has an amino acid sequence SIFAHQTPTHKN. The peptidic chemokine modulator may optionally be used for binding to a chemokine selected from the group comprising MIG, MCP-1, IL-8, SDF-1 alpha and Eotaxin.

According to another embodiment of the present invention, there is provided a peptidic chemokine modulator for modulating a biological effect of a chemokine, comprising a molecule composed of the amino acids H, P, T, L, R, W, F, and featuring at least two neighboring histidines, wherein the molecule features an overall positive charge (family 2). Preferably, the molecule comprises a peptide having an amino acid sequence selected from the group consisting of GDFNSGHHTTTR, HHFHLPKLRPPV, HHTWDTRIWQAF, LDYPIPQTVLHH, LLADTTHHRPWP, TRLVPSRYYHHP, CHHNLSWEC and SFWHHHSPRSPL. More preferably, the peptide has an amino acid sequence LLADTTHHRPWP.

According to another embodiment of the present invention, there is provided a composition for treating a condition involving abnormal cell migration in a subject, the composition comprising a pharmaceutically effective amount of a therapeutic agent for administering to the subject, the therapeutic agent comprising a chemokine modulator as described above. Preferably, the condition comprises an inflammatory condition. Alternatively, the condition comprises cancer metastasis. Optionally, the therapeutic agent is administered by topical administration, such that the composition further comprises a pharmaceutically acceptable carrier for topical administration.

Preferably, the topical administration is to the skin of the subject. Optionally, the therapeutic agent is administered by inhalation, such that the composition further comprises a pharmaceutically acceptable carrier for inhalation. Alternatively, the therapeutic agent is administered intranasally, such that the composition further comprises a pharmaceutically acceptable carrier for intranasal administration.

Optionally, the therapeutic agent is characterized by an ability to inhibit binding of the chemokine to a chemokine receptor.

Optionally, the therapeutic agent is characterized by an ability to enhance binding of the chemokine to a chemokine receptor.

According to another embodiment of the present invention, there is provided a method for treating a disease modulated through and/or caused by binding of a chemokine to a chemokine receptor in a subject, comprising administering a pharmaceutically effective amount of a therapeutic agent to the subject, the therapeutic agent comprising a peptidic chemokine modulator as described above.

Preferably, the therapeutic agent binds to at least one of the chemokines and wherein the therapeutic agent directly modulates the activity of the chemokine by modulation of binding to the chemokine receptor.

Optionally and preferably, the disease is selected from the group consisting of : inflammation (primary or secondary), allergy, a non-optimal immune response, an autoimmune reaction (including rheumatoid arthritis, systemic lupus erythematosis, multiple sclerosis and others), allograft rejection, diabetes, sepsis, cancer and any type of malignant cell growth, acute and chronic bacterial and viral infections, arthritis, colitis, psoriasis, atherosclerosis, hypertension and reperfusion ischemia.

According to still another embodiment of the present invention, there is provided an antibody for binding to a chemokine-binding receptor, comprising: an antibody being capable of recognizing at least a portion of a chemokine-binding receptor, wherein the antibody also recognizes a peptide having a sequence as described above.

Optionally, there is also provided a vaccine formed with the above antibody.

According to still another embodiment of the present invention, there is provided a method for producing an antibody, comprising: inducing formation of antibody against a peptide having a sequence according to the above description,

wherein the antibody is also capable of recognizing a chemokine-binding receptor.

Preferably, the antibody comprises a monoclonal antibody. Alternatively, the antibody comprises a polyclonal antibody. Preferably, the antibody forms a vaccine.

Hereinafter, the term"biologically active"refers to molecules, or complexes thereof, which are capable of exerting an effect in a biological system. Hereinafter, the term"fragment"refers to a portion of a molecule or a complex thereof, in which the portion includes substantially less than the entirety of the molecule or the complex thereof.

Hereinafter, the term"amino acid"refers to both natural and synthetic molecules which are capable of forming a peptide bond with another such molecule.

Hereinafter, the term"natural amino acid"refers to all naturally occurring amino acids, including both regular and non-regular natural amino acids. Hereinafter, the term"regular natural amino acid"refers to those alpha amino acids which are normally used as components of a protein. Hereinafter, the term"non-regular natural amino acid"refers to naturally occurring amino acids, produced by mammalian or non-mammalian eukaryotes, or by prokaryotes, which are not usually used as a component of a protein by eukaryotes or prokaryotes. Hereinafter, the term"synthetic amino acid"refers to all molecules which are artificially produced and which do not occur naturally in eukaryotes or prokaryotes, but which fulfill the required characteristics of an amino acid as defined above. Hereinafter, the term"peptide" includes both a chain and a sequence of amino acids, whether natural, synthetic or recombinant. Hereinafter, the term"peptidomimetic"includes both peptide analogues and mimetics having substantially similar or identical functionality thereof, including analogues having synthetic and natural amino acids, wherein the peptide bonds may be replaced by other covalent linkages.

BRIEF DESCRIPTION OF THE DRAWINGS AND TABLES The invention is herein described, by way of example only, with reference to the accompanying drawings and tables, wherein: FIG. 1 shows the results of binding of chemokines to BKT-P1, BKT-P3, BKT- P22, and BKT-P37 peptides, which bind, respectively, to at least one of the following chemokines, SDF-la, MCP-1, Eotaxin and IL-8; FIG. 2 shows the binding of synthetic peptides from Table 1 which can either bind to various chemokines (such as BKT-P1, shown in Fig. 2B), or can alternatively bind specifically to a single chemokine (such as BKT-P9 alone, as shown in Fig 2A); FIG. 3 shows the results of binding of one of the synthetic peptides from family 1, BKT P3, to various chemokines. BKT-P18, which does not belong to the family, is shown as a control; FIG. 4 shows a graphical representation of the biological activity results for BKT-P3, from family 1 in a biovalidation assay system in which the chemokine MIG and the adhesion receptor VCAM-1 are used to activate the binding of T cells (see "Material and Methods") (FIG. 4A); BKT-P10, which does not belong to the family, is shown as a control (FIG. 4B).

Fig. 5 shows a graphical representation, of the level of immunity (O. D. ) of antibody raised against BKT-P3 and BKT-P2, belongs to family 1, to the relevant peptides, BKT-P3 and BKT-P2. The preimmune serum of the same mice used as a control. "Blank"is the O. D. level of antibody binding to the plastic (of the Elisa experiment), with no addition of peptides.

Table 1 shows the sequences of peptides that bind to the chemokines MCP-1, SDF-1 cc, MIG, Eotaxin and IL-8;

Table 2 shows a family of peptides (family no. 1) that bind to MIG, MCP-1, IL- 8, SDF-la and Eotaxin and are predominantly composed of the amino acids H, S, A, L, I, K, R, T and P, featuring at least 2 Histidines spread along the molecule. The abundance of positively charged amino acids such as H, K and R, resulted in peptides having an overall positive charge. The remaining amino acids, mentioned above, might participate in the determination of the three dimensional structure of the peptides; Table 3 shows a family of peptides (family no. 2) that bind mostly to MCP-1 and in individual cases to IL-8, SDF-l-a and Eotaxin; the binding motif for peptides in this family is predominantly composed of the amino acids H, P, T, L, R, W, F, featuring at least 2 Histidines next to each other. The abundance of positively charged amino acids, such as H and R, resulted in peptides having an overall positive charge.

The remaining amino acids, mentioned above, might participate in the determination of the three dimensional structure of the peptides; Table 4 shows a summary of the results of the biological activity of four representatives from family 1, in a biovalidation assay system, in which various chemokines and the adhesion receptor VCAM-1 are used to activate the binding of T cells (as described in"Materials and Methods").

DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention is composed of peptidic modulatory molecules with defined amino acid sequences which have been found to bind to specific chemokines, including, but not limited to, human SDF-loe, MIG, IL-8, MCP-1 and Eotaxin, and which inhibit or stimulate the binding of these chemokines to their respective receptor/s and/or which otherwise have an inhibitory or stimulatory effect on the biological activity of chemokines. Preferably, the present invention specifies basic

consensus sequences, with overall positive electrostatic charge, which characterize families of such modulatory chemokine-binding peptide molecules.

The chemokine binding peptides mimic chemokine receptor structures or motifs. It is therefore predicted that the chemokine-binding peptides, when injected or otherwise introduced into mice or humans, may produce antibodies against chemokine receptors that can be either used for the production of monoclonal antibodies or used for development of a vaccine against a particular chemokine receptor. Whether antibodies are produced, or alternatively, binding to a particular chemokine receptor is blocked and/or enhanced, may depend upon the method of introduction to the subject. For example, antibody production may be potentiated if the peptides (and/or other peptidic modulatory molecule according to the present invention) are introduced with an adjuvant. Concentration of the peptide or other molecule may also be important. In any case, one of ordinary skill in the art could easily determine conditions for antibody production, as opposed to having the effect potentiated or mediated directly through the peptides and/or other peptidic modulatory molecules according to the present invention.

The modulatory chemokine-binding peptide molecules of the present invention could therefore be useful for treating a disease selected from the group consisting of inflammation (primary or secondary e. g. uveitis, bowel inflammation), allergy, non- optimal immune response, autoimmune reaction (including rheumatoid arthritis, systemic lupus erythematosis, multiple sclerosis and others), delayed-type hypersensitivity, allograft rejection, diabetes, sepsis, cancer and any type of malignant cell growth, (including, but not limited to breast cancers such as infiltrating duct carcinoma of the breast or other metastatic breast cancers, lung cancers such as small cell lung carcinoma, bone cancers, bladder cancers such as bladder carcinoma,

rhabdomyosarcoma, angiosarcoma, adenocarcinoma of the colon, prostate or pancreas, or other metastatic prostate or colon cancers, squamous cell carcinoma of the cervix, ovarian cancer, malignant fibrous histiocytoma, skin cancers such as malignant melanoma, lymphomas and leukemia, leiomyosarcoma, astrocytoma, glioma and heptocellular carcinoma), acute and chronic bacterial and viral infections, vasculitis, arthritis, colitis, psoriasis, atherosclerosis, Graves disease, anorexia nervosa; hemorrhagic shock caused by septicemia, HIV infection in AIDS, pemphigus, asthma, renal diseases, liver diseases, bone marrow failure, vitiligo, alopecia, and myositis, hypertension and reperfusion ischemia.

The examples provided below, describe certain experiments performed with the peptidic modulatory of the present invention, demonstrating the binding efficacy of these molecules to the various chemokines. It also demonstrates the efficacy of the peptidic chemokine-binding modulator in a biological system. In addition, the examples also describe formulations for administering the compounds of the present invention, and methods of treatment thereof.

EXAMPLE 1 EFFICACY OF THE PEPTIDES OF THE PRESENT INVENTION This Example demonstrates the efficacy of the peptidic chemokine-binding modulators of the present invention, in a number of different assays, including binding assays and assays for measuring a functional biological effect.

Materials and methods Chemokines

Recombinant chemokines were ordered from PeproTech, Inc. (Rocky Hill, NJ, USA). Human SDF-la (Cat. No. 300-28A), human MIG (Cat. No. 300-26) and human IL-8, (72 amino acids) (Cat. No. 200-08M), belong to the a-chemokines (C-X-C) family. Human MCP-1 (MCAF) (Cat. No. 300-04) and human Eotaxin (Cat No. 300- 21) belong to the beta-chemokines (C-C family). All chemokines were prepared according to the company recommendations.

Peptide synthesis Peptides were synthesized in the Weizmann Institute of Science, Rehovot, Israel, in order to perform tests for characterization of their influence on the biological activity of the chemokines. The format of the various synthesized peptides was as follows: The cyclic peptides, ACX7CGGGSK-biotin-G and the linear peptides, XI2GGGSK-biotin-G. The peptides were biotinylated on their C-termini ; the biotin will serve as a detector during the following experiments. Each synthetic peptide was dissolved to concentration of lmg/ml (-0. 6 mM) in 4% DMSO (Dimethyl Sulphoxide, Sigma, Cat. # D-2650).

ELISA analysis of the synthetic chemokine-binding peptide NUNC-Immuno maxisorp plates (Cat. No. 4-42404) were coated with the appropriate chemokine (0.1 ml/well, 0.1-1. 0 pg/ml in 0.1 M NaHCO3, pH 8.6), overnight at 4°C. The plates were then blocked with 0.2 ml/well of blocking buffer (5mg/ml BSA in 0.1 NaHCO3).. Control wells were treated with blocking buffer alone, with no addition of target protein (chemokine). The plates were washed 6 times with PBST (0.1% Tween 20 in PBS), followed by incubation for 45 minutes at room temperature with 10-fold serial dilutions of individual synthetic peptides (lOpg-1011g)

with 1% BSA (PBST-BSA) /well. After the plates were washed 6 times with PBST, the bound peptides were probed by HRP-SA Conjugate, diluted 1: 10,000 to 1: 20,000 in PBST-BSA, 0.1 ml/well for 45 minutes at room temperature. The target-bound synthetic peptides probed with HRP-SA were quantified by DAKO TMB one-step substrate system, followed by the addition of stop solution, HCl-H2SO4 mixture (0.1 ml/well) (IN HC1, 3N H2S04). The results were analyzed by ELISA reader at OD450.

Biovalidation Laminar flow assays were performed as follows. Polystyrene plates (B. D) were coated with soluble VCAM-1 at 10 pg/ml in the presence of 2 ag/ml HSA carrier. The plates were washed three times with PBS and blocked with HSA (20 , ug/ml in PBS) for 2 hrs at room temperature. Alternatively, washed plates were coated with 10 ug/ml MIG chemokine in PBS for 30 min at room temperature, before being blocked with HSA. The plates were assembled as the lower wall of a parallel wall flow chamber and mounted on the stage of an inverted microscope. The peptide, as described previously, (10, ug/ml) was allowed to settle on the substrate coated chamber wall for 10 min, at 37°C and then washed. T cells (5xl06/ml, purity >98%) were suspended in binding buffer, perfused into the chamber and allowed to settle on the substrate coated chamber wall for 1 min, at 37°C. Flow was initiated and increased in 2 to 2.5 fold increments every 5 sec. generating controlled shear stresses on the wall. Cells were visualized in a 20x objective of an inverted phase-contrast Diaphot Microscope (Nikon, Japan) and photographed with a long integration LIS- 700 CCD video camera (Applitech ; Holon, Israel), connected to a video recorder (AG-6730 S-VHS, Panasonic, Japan). The number of adherent cells resisting detachment by the elevated shear forces was determined after each interval by

analysis of videotaped cell images, and was expressed as the percent of originally settled cells. All adhesion experiments were performed at least three times on multiple test fields.

Results Identification of chemokine binding peptides with antagonistic effect The present invention identifies chemokine-binding peptides with biological activity. The binding specificities of the various peptides to the chemokines were determined by screening against BSA, Actin and Fibronectin-coated wells as negative controls in parallel experiments. The binding level of the peptides to the various chemokines, which reached at least two fold of the binding level to the control proteins, was considered a specific binding. The different peptides that were found to bind to chemokines, are listed in Table 1.

Graphical representations of four examples of such peptide-containing carriers, from the list in Table 1, are shown in Figure 1. As can be seen, each of those peptides was found to bind to at least one different chemokine, which was chosen to be presented in this graph: peptide BKT-P1 was found to bind SDF-la ; peptide BKT-P3 was found to bind, in this representation, to MCP-1; peptide BKT-P22, was found to bind Eotaxin and peptide BKT-P37, was found to bind IL-8. The specificity of the binding was calculated by comparing the binding level of the proteins to chemokines to that of binding level to control proteins, as explained above. It should also be noted that the binding of each of the peptides shown in Figure 1 is not necessarily the only binding capability shown by those peptides.

Peptides that showed affinity/binding to one or more chemokines were then analyzed in several individual experiments, and were chosen for further analysis. The

specific binding of the peptides was detected by screening methodology, using ELISA, as described in"Materials and Methods", employing microplates coated with the various chemokines to be checked. The binding specificities of the various peptides to the various chemokines were determined by screening against BSA, Actin and Fibronectin-coated wells as negative controls in parallel experiments.

As can be seen in Figure 2, peptides which can specifically bind to one specific chemokine, such as BKT-P9, were identified (Fig. 2A). In addition, peptides which can bind to more than one chemokine, such as BKT-P1, were also identified (Fig. 2B). Again, the specificity of the binding, either to one chemokine or more, was established by comparing binding level with the control binding level to non-related proteins, (shown in the Figure as a broken line). Control binding showed a level of one fold increase. As such, each of the peptides which showed a level of binding to a particular chemokine of less than, or close to, such a one-fold increase, was considered to be non-specifically bound to that chemokine. Specific binding was considered as that which showed at least a two fold increase over the control binding level. Peptides that specifically bound to one or more chemokines were chosen for further examination and for analysis with a biovalidation assay, to prove their ability to not only bind the various chemokines but also to modulate the biological activity of those chemokines.

According to the present invention, two families of chemokine-binding peptides were identified. These families contain peptides with similar amino acid compositions, a high percentage of histidines, and are also characterized by overall positive electrostatic charge.

A detailed list of the potential consensus sequences of the two families is presented in Tables 2 and 3. The peptides of family no. 1 (Table 2) bind to MIG,

MCP-1, IL-8, SDF-la and Eotaxin, as illustrated in Table 2, and are predominantly composed of the amino acids H, S, A, L, I, K, R, T and P. Each peptide in this family contains at least 2 histidines distributed along the molecule. The abundance of positively charged amino acids such as H, K and R, results in peptides having an overall positive charge. The remaining amino acids, mentioned above, might participate in the determination of the three dimensional structure of the peptides.

Table 3 shows a family of peptides (family no. 2) that bind mostly to MCP-1 and in individual cases to IL-8, SDF-la and Eotaxin (illustrated in the Table). The binding motif for peptides in this family is predominantly composed of the amino acids H, P, T, L, R, W, F, while each peptide also features at least two histidines, one next to the other. The abundance of positively charged amino acids such as H and R, resulted in peptides having an overall positive charge. The remaining amino acids, mentioned above, may participate in the determination of the three dimensional structure of the peptides.

As defined here, a consensus sequence is composed of an amino acid sequence that is found repeatedly in a group of peptides which bind various chemokines and probably have certain biological functions in common. The group or family of such peptides is characterized by the consensus sequence, high abundance of the amino acid histidine and overall positive electrostatic charge. These peptides may be described as potential agonists or antagonists of chemokines.

The binding of one synthetic peptide, BKT-P3 (family 1), to various chemokines is shown in Figure 3. As can be seen, this peptide binds to all five chemokines tested, in contrast to the control peptide, BKT-P18, which does not belong to the family, and also shows no binding to the chemokines. As discussed above, the level of binding was calculated by comparing binding of the peptides to the

chemokines with peptide binding to controls. Level of control binding was defined as level 1 (up to a one-fold increase in binding). This control binding level is illustrated in the Figure as a dashed line. It can be seen that although BKT-P3 binds several different chemokines, the level of the binding is different in each case, which suggests different affinities and maybe different influences on the activity of each of the chemokines.

Further examination of BKT-P3 for efficacy in biovalidation was performed to check the ability of BKT-P3 to bind and modulate the activity of MIG chemokine, to which BKT-P3 showed the highest binding level (Fig. 3). The result of the experiment is graphically illustrated in Figure 4.

As can be seen in Figure 4B, when a control peptide which does not belong to the family was added to the flow chamber in order to test for its ability to bind to and modulate the activity of MIG, no influence on the activity of MIG was seen. MIG activity continued to show the same level of activity (about 25% of arrested cells) as was seen in the absence of peptide. Hence, as can be seen in FIG. 4B the same percentage of arrested cells could be detected in the presence of the chemokine, with our without the addition of BKT-P10 (the control peptide) (Fig 4B, Mig+plO and Mig, respectively). On the other hand, when BKT-P3 was added to the flow chamber, the percentage of arrested cells that reached about 30% in the presence of Mig (Fig.

4A, Mig), was dramatically reduced (Fig. 4A, Mig + p3) to the control level achieved in the presence of VCAM-1 alone, with no addition of chemokine (Fig. 4A, control).

These results revealed an obvious antagonistic effect of BKT-P3 against human MIG, the chemokine to which it was able to bind (Figure 4A), in contrast to the non-binding control peptide, BKT-P10 (Figure 4B).

Table 4 shows a summary of the biological activity results for four representative synthetic peptides belonging to family 1. Various different chemokines were used in the biovalidation assay together with the adhesion receptor VCAM-1, in order to activate the adhesion of T cells in the system (as described in"Materials and Methods") As can be seen in Table 4, all the peptides that were checked clearly showed antagonistic effect on the various chemokines that were introduced into the flow chamber. On the other hand, although all the peptides showed antagonistic effects, the efficiency of the effect varied between the different peptides and between the same peptides tested against different chemokines. Thus, BKT-P3 caused complete arrest of the biological activity of both chemokines that were checked, MIG and IL-8. BKT-P2, which shows high sequence similarity to BKT-P3, caused only about 50% reduction in the activity of MIG. BKT-P45, which caused 100% abolishment of the activity of IL-8, as did BKT-P3, only reduced the activity of MIG by about 20%. BKT-P39, on the other hand, which had no effect on IL-8, caused 100% blocking of the activity of Eotaxin. It therefore seems that although the sequence similarity between the members of the family is quite high, the amino acid composition (the percentage of each amino acid in the final peptide sequence) and their particular order within the peptide sequence are important.

Further examination of BKT-P3 and BKT-P2 (both belonging to family 1) for the immunity of these peptides, was performed by injecting those peptides to mice.

The result of the experiment is graphically illustrated in Figure 5. The control, preimmune serum of the same mice to which the peptides were injected, showed no binding to the two peptides (the O. D. results of both preimmune sera were the same as the O. D. achieved by binding of all sera to the plastic with no peptide addition). On the other hand, the immune sera showed high O. D. levels, in the presence of the two

peptides. These results showed that the sera collected from the mice after injection of the peptides probably contain antibodies against the two peptides.

The results summarized above are very important, since it is known that one chemokine can bind to more than one receptor and as such, can be involved in more than one pathological disorder. On the other hand, more then one chemokine can bind to one receptor, which means that several chemokines might be involved in one pathological disorder. So, in some cases, in order to block one pathological disorder, one may need to block the activity induced by more than one chemokine.

Alternatively, in some cases, the activity of only one specific chemokine may need to be blocked in order to interfere with the progression of one specific pathological disorder.

The results, shown in FIGS. 2 and 3, and Table 4, demonstrate that there is a possibility of modulating either the activity of one specific chemokine, or the activity of several different chemokines which lead to the development of one pathological disorder, and thereby interfering with the progression of the various diseases.

The results shown in Figure 5 demonstrate the immunogenicity of the peptides. The ability to raise antibodies against the peptides, which would therefore mimic the chemokine receptors, provides support to other applications of the present invention, including but not limited to, the development of vaccines against the chemokine receptors. These receptors are known to be involved in various pathological disorders. Such vaccines would thus enable treatment and/or prevention of such disorders.

EXAMPLE 2

METHODS AND COMPOSITIONS FOR ADMINISTRATION The peptides of the present invention, and their homologues, derivatives or related compounds, hereinafter referred to as the"therapeutic agents of the present invention", can be administered to a subject by various ways, which are well known in the art. Hereinafter, the term"therapeutic agent"includes a peptidic chemokine-binding modulator, as previously defined, including but not limited to, any of the above biologically useful peptides and their homologs, analogs, peptidomimetics and derivatives thereof.

Hereinafter, the term"subject"refers to the human or lower animal to which the therapeutic agent is administered. For example, administration may be done topically (including ophthalmically, vaginally, rectally, intranasally and by inhalation), orally, or parenterally, for example by intravenous drip or intraperitoneal, subcutaneous, or intramuscular injection.

Formulations for topical administration may be included but are not limited to lotions, ointments, gels, creams, suppositories, drops, liquids, sprays and powders.

Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable.

Compositions for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, sachets, capsules or tablets. Thickeners, diluents, flavorings, dispersing aids, emulsifiers or binders may be desirable.

Formulations for parenteral administration may include but are not limited to sterile aqueous solutions, which may also contain buffers, diluents and other suitable additives.

Dosing is dependent on the severity of the symptoms and on the responsiveness of the subject to the therapeutic agent. Persons of ordinary skill in the art can easily determine optimum dosages, dosing methodologies and repetition rates.

EXAMPLE 3 METHODS OF TREATMENT WITH THE COMPOUNDS As noted above, the therapeutic agents of the present invention have been shown to be effective modulators of cell adhesion and cell migration which characterize inflammatory reaction, cancer metastasis and any other suitable conditions in which a particular target ligand binds to its target receptor. The following example is an illustration only of a method of treating an inflammatory condition, cancer metastasis and any other suitable condition involving cell migration, with the therapeutic agent of the present invention, and is not intended to be limiting.

The method includes the step of administering a therapeutic agent, in a pharmaceutically acceptable carrier, to a subject to be treated. The therapeutic agent is administered according to an effective dosing methodology, preferably until a predefined endpoint is reached, such as the absence of a symptom of the inflammatory condition, blockage of tumor metastasis and any other suitable condition in the subject, or the prevention of the appearance of such a condition or symptom in the subject.

The modulatory chemokine-binding peptide molecules of the present invention could therefore be useful for treating a disease selected from the group consisting of inflammation (primary or secondary e. g. uveitis, bowel inflammation), allergy, non- optimal immune response, autoimmune reaction (including rheumatoid arthritis, systemic lupus erythematosis, multiple sclerosis and others), delayed-type

hypersensitivity, allograft rejection, diabetes, sepsis, cancer and any type of malignant cell growth, (including, but not limited to breast cancers such as infiltrating duct carcinoma of the breast or other metastatic breast cancers, lung cancers such as small cell lung carcinoma, bone cancers, bladder cancers such as bladder carcinoma, rhabdomyosarcoma, angiosarcoma, adenocarcinoma of the colon, prostate or pancreas, or other metastatic prostate or colon cancers, squamous cell carcinoma of the cervix, ovarian cancer, malignant fibrous histiocytoma, skin cancers such as malignant melanoma, lymphomas and leukemia, leiomyosarcoma, astrocytoma, glioma and heptocellular carcinoma), acute and chronic bacterial and viral infections, vasculitis, arthritis, colitis, psoriasis, atherosclerosis, Graves disease, anorexia nervosa; hemorrhagic shock caused by septicemia, HIV infection, pemphigus, asthma, renal diseases, liver diseases, bone marrow failure, vitiligo, alopecia, and myositis, hypertension and reperfusion ischemia.

Table 1. Peptide Name Sequence of peptide BKT-P50 AHLSPHK BKT-P10 DIPWRNE BKT-P17 DPLRQHS BKT-P58 DSLGHWL BKT-P15 DYTTRHS BKT-P59 HGTLNPE BKT-P56 HHNLSWE BKT-P60 HIWTLAS BKT-P61 HNTFSPR BKT-P62 IPLHASL BKT-P63 ITTTSLS BKT-P64 KITTCKD BKT-P65 KNHTTFW BKT-P66 LKLLSRS BKT-P67 LLKAHPS BKT-P68 LNQLKQA BKT-P69 MINFPSPH BKT-70 PQSPTYT BKT-P57 PSSAIHT BKT-P71 PTSTARI BKT-P72 QASSFPS BKT-P73 QPYFWYR BKT-P14 QTLTPSI BKT-P74 SKLGHLW BKT-P75 SKTPERI BKT-P76 SNNNRMT BKT-P77 SPILSLS BKT-P16 SPTNFTR BKT-P78 SRPAMNV BKT-P79 STKAYPN Peptide Name Sequence of peptide BKT-P80 STSSCGS BKT-P81 SYWGHRD BKT-P13 TAHDANA BKT-P82 TANSEKT BKT-P83 THPKASM BKT-P84 TKTINGK BKT-P85 TNMQSPL BKT-P86 TPFTKLP BKT-P87 TPTTDSI BKT-P88 TQQNGHP BKT-Pll TTPSKHQ BKT-P12 ACTTPSKHQC BKT-P89 TYNVAKP BKT-P90 ACAPLMFSQC BKT-P48 ACHASLKHRC BKT-P91 AHFSPNLLLGG BKT-P44 AHSLKSITNHGL BKT-P92 AKTLMPSPFPRT BKT-P93 ASAVGSLSIRWQ/L/G BKT-P94 ASWVDSRQPSAA BKT-P95 CPQLTVGQHRT BKT-P8 DLPPTLHTTGSP BKT-P96 DSSNPIFWRPSS BKT-P97 EFLGVPASLVNP BKT-P51 ESDLTHALHWLG BKT-P98 EVHSTDRYRSIP BKT-P99 FGLQPTGDIARR BKT-P9 FSMDDPERVRSP BKT-P100 FSPLHTSTYRPS BKT-P27 GDFNSGHHTTTR BKT-P28 GPSNNLPWSNTP Peptide Name Sequence of peptide BKT-P33 GVHKHFYSRWLG BKT-P101 HAPLTRSPAPNL BKT-P102 HGSLTTLF/LRYEP BKT-P45 HHFHLPKLRPPV BKT-P55 HHTWDTRIWQAF BKT-P54 HPTTPFIHMPNF BKT-P103 HRDPXS (P) PSAA/GRP BKT-P104 HNVTTRTQRLMP BKT-P49 HSACHASLKHRC BKT-P105 HSACKLTTCKDG BKT-P6 HSACLSTKTNIC CLSTKTNIC ACLSTKTNIC ACLSTKTNIC ACLSTKTNIC BKT-P106 IAHVPETRLAQM BKT-P107 IFSMGTALARPL BKT-P108 INKHPQQVSTLL BKT-P7 ISPSHSQAQADL BKT-P46 LDYPIPQTVLHH BKT-21 LFAAVPSTQFFR BKT-P22/38 LGFDPTSTRFYT BKT-P37 LLADTTHHRPWT BKT-P109 LPWAPNLPDSTA BKT-P110 LQPSQPQRFAPT BKT-Plll LSPPMQLQPTYS BKT-P112 MHNVSDSNDSAI BKT-P113 NSSMLGMLPSSF BKT-P114 NTSSSQGTQRLG BKT-P42 PGQWPSSLTLYK BKT-P23 QIPQMRILHPYG BKT-P24 QIQKPPRTPPSL BKT-P115 QLTQTMWKDTTL BKT-P116 QNLPPERYSEAT Peptide Name Sequence of peptide BKT-P117 QSLSFAGPPAWQ BKT-P118 QTTMTPLWPSFS BKT-P119 RCMSEVISFNCP BKT-P120 RSPYYNKWSSKF BKT-P39 SAGHIHEAHRPL BKT-P40 SAISDHRAHRSH BKT-P121 SEPTYWRPNMSG BKT-P32 SFAPDIKYPVPS BKT-P31 SFWHHHSPRSPL BKT-P3 SIFAHQTPTHKN BKT-P2 SIPSHSIHSAKA BKT-P122 SIRTSMNPPNLL BKT-P123 SLPHYIDNPFRQ BKT-P29 SLSKANILHLYG BKT-P124 SLVTADASFTPS BKT-P125 SMVYGNRLPSAL BKT-P126 SPSLMARSSPYW BKT-P127 SPNLPWSKLSAY BKT-P1 SQTLPYSNAPSP BKT-P128 SSTQAHPFAPQL BKT-P129 STPNSYSLPQAR BKT-P4 STVVMQPPPRPA BKT-P34 SVQTRPLFHSHF BKT-P130 SVSVGMKPSPRP BKT-P131 SYIDSMVPSTQT BKT-P132. SYKTTDSDTSPL BKT-P133 TAAASNLRAVPP BKT-P5 TAPLSHPPRPGA BKT-P134 TGLLPNSSGAGI BKT-P135 TGPPSRQPAPLH BKT-P30 TLSNGHRYLELL BKT-P25 TPSPKLLQVFQA BKT-P136 TPSTGLGMSPAV BKT-P137 TPVYSLKLGPWP Peptide Name Sequence of peptide BKT-P47 TRLVPSRYYHHP BKT-P138 TSPIPQMRTVPP BKT-P139 TTNSSMTMQLQR BKT-P140 TTTLPVQPTLRN BKT-P141 TTTWTTTARWPL BKT-P142 TVAQMPPHWQLT BKT-P143 TWNSNSTQYGNR BKT-P144 TWTLPAMHPRPA BKT-P26 VHTSLLQKHPLP BKT-P35 VLPNIYMTLSA BKT-P145 VMDFASPAHVLP BKT-P146 VNQEYWFFPRRP BKT-P147 VYSSPLSQLPR BKT-P148 VPPIS (R) TFLF (L) ST (K) S BKT-P149 VPPLHPALSRON BKT-P43 VSPFLSPTPLLF BKT-P150 VSRLGTPSMHPS BKT-P151 WPFNHFPWWNVP BKT-P52 WSAHIVPYSHKP BKT-P152 WWPNSLNWVPRP BKT-P53 YATQHNWRLKHE BKT-P153 YCPMRLCTDC BKT-P154 YGKGFSPYFHVT BKT-P155 YPHYSLPGSSTL BKT-P156 YPSLLKMQPQFS BKT-P157 YQPRPFVTTSPM BKT-P158 YSAPLARSNVVM BKT-P36 YTRLSHNPYTLS BKT-P41 YTTHVLPFAPSS BKT-P159 YTWQTIREQYEM Table 2:

Peptide Peptide sequence Bound name chemokines at least BKT-P3 SIFAHQTPTHKN MIG, IL-8, MCP-1 BKT-P2 SIPSHSIHSAKA MCP-1, Eotaxin, IL-8 BKT-P40 SAISDHRAHRSH IL-8 BKT-P39 SAGHIHEAHRPL Eotaxin, SDF-la, IL-8 BKT-P48 ACHASLKHRC MCP-1 BKT-P44 AHSLKSITNHGL MCP-1 BKT-P51 ESDLTHALHWL MCP-1 BKT-P49 HSACHASLKHR MCP-1 BKT-P52 WSAHIVPYSHKP MCP-1 BKT-P53 YATOHNWRLKHE MCP-1 BKT-P50 CAHLSPHKC MIG BKT-P33 GVHKHFYSRWLG Eotaxin BKT-P54 HPTTPFIHMPNF MIG BKT-P34 SVQTRPLFHSHF Eotaxin BKT-P26 VHTSLLQKHPLP MCP-1 Amino Acid Composition H=33 S=22 A=16 L=15 <BR> <BR> <BR> 1=7<BR> <BR> <BR> <BR> <BR> <BR> K=10 R=8 T=9 P=12 N=3 G=3 W=4 Y=3 V=3 E=1 Q=3 0=1 D=2 Table 3 : Peptide name Peptide sequence Bound chemokines (at least) BKT-P27 GDFNSGHHTTTR MCP-1 BKT-P45 HHFHLPKLRPPV IL-8, MCP-1, MIG BKT-P55 HHTWDTRIWQAF MCP-1 BKT-P46 LDYPIPQTVLHH MCP-1 BKT-P37 LLADTTHHRPWP IL-8 BKT-P47 TRLVPSRYYHHP MCP-1 BKT-P56 CHHNLSWEC SDF-la BKT-P31 SFWHHHSPRSSPL Eotaxin

Amino Acid Composition H=18 P=11 T=9 L=9 R=6 W=5 F=4 D=4 G=2 N=1 S=7 K=1 V=2 <BR> <BR> <BR> 1=2<BR> <BR> <BR> <BR> <BR> Q=1<BR> <BR> <BR> <BR> <BR> Y=2 A=2 Table 4 Biovalidation Results

Peptide Peptide Sequence Chemokine Level of name checked Antagonistic Effect BKT-P3 SIFAHQTPTHKN MIG +++ IL-8 +++ BKT-P2 SIPSHSIHSAKA MIG ++ BKT-P45 HHFHLPKLRPPV IL-8 +++ MIG + BKT-P39 SAGHIHEAHRPL Eotaxin +++ IL-8

Legend: The percentage of antagonistic effect is as follows: + 20% ++ 50% +++ 100% - No effect

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