CONTINUING APPLICATION DATA

This application claims the benefit of U.S. Provisional Application Serial No. 62/473,878, filed March 20, 2017, and U.S. Provisional Application Serial No. 62/589,760, filed November 22, 2017, each of which is incorporated by reference herein.

SEQUENCE LISTING

This application contains a Sequence Listing electronically submitted to the United States Patent and Trademark Office via EFS-Web as an ASCII text file entitled "541-00020201_ST25.txt" having a size of 26 kilobytes and created on March 19, 2018. Due to the electronic filing of the Sequence Listing, the electronically submitted Sequence Listing serves as both the paper copy required by 37 CFR §1.821(c) and the computer readable form (CRF) required by §1.821(e). The information contained in the Sequence Listing is incorporated by reference herein.

BACKGROUND

Interleukin 37 (IL-37) is a member of the IL-1 family. IL-37 can bind to interleukin 18 receptor (IL-18R) and to interleukin 18 binding protein (IL18BP), an inhibitory binding protein of interleukin 18 (IL-18). Five alternatively spliced transcript variants encoding distinct isoforms of IL-37 have been reported, and IL-37 has been reported to reduce innate inflammation as well as acquired immunity.

SUMMARY OF THE INVENTION

This disclosure describes IL-37 fusion proteins; methods of making IL-37 fusion proteins, including constructs used to express IL-37 fusion proteins; and methods of using IL-37 fusion proteins. In some embodiments, the IL-37 fusion protein includes amino acids 46-206 of isoform B of IL-37 and a heavy chain portion of an antibody.

In one aspect, this disclosure describes a fusion protein including a fragment of IL-37 and a heavy chain portion of an antibody. The fragment of IL-37 includes amino acids 46-206 of isoform B of IL-37. In some embodiments, the fragment of IL-37 consists of amino acids 46-206 of isoform B of IL-37.

In some embodiments, the fusion protein and/or the fragment of IL-37 includes SEQ ID NO:2. In some embodiments, the fragment of IL-37 consists of SEQ ID NO:2.

In some embodiments, the heavy chain portion of an antibody includes an IgG-Fc sequence.

In some embodiments, the heavy chain portion of an antibody includes an IgGl-Fc sequence. In some embodiments, the fusion protein and/or the heavy chain portion of an antibody include SEQ ID NO:4.

In some embodiments, the fusion protein and/or the heavy chain portion of an antibody include mutations to a complement (Clq) binding site and/or to an Fc gamma receptor (FcyR) binding site. In some embodiments, the fusion protein and/or the heavy chain portion of an antibody include L234A and L235A (LALA) substitutions. In some embodiments, the fusion protein and/or the heavy chain portion of an antibody includes SEQ ID NO: 5.

In some embodiments, the fusion protein includes a peptide linker. In some embodiments, the peptide linker includes the amino acid sequence GGGS. In some embodiments, the peptide linker connects the fragment of IL-37 and the heavy chain portion of an antibody.

In some embodiments, the fusion protein includes a signal peptide. A signal peptide can include, for example, a CD33 signal peptide. In some embodiments, the fusion protein and/or the signal peptide include SEQ ID NO:6.

In another aspect, this disclosure describes a method of using a fusion protein, as described herein. In some embodiments, the method includes administering an effective amount of an IL-37 fusion protein to a subject.

In a further aspect, this disclosure describes a method of making a fusion protein, as described herein.

In this disclosure, "operably linked" refers to a juxtaposition of components such that they are in a relationship permitting them to function in their intended manner. For example, in the context of a gene, "operably linked" means that expression of a gene is under the control of a promoter with which it is spatially connected. A promoter may be positioned 5' (upstream) or 3' (downstream) of a gene under its control. The distance between the promoter and a gene may be approximately the same as the distance between that promoter and the gene it controls in the gene from which the promoter is derived. As is known in the art, variation in this distance may be accommodated without loss of promoter function. In some embodiments, "operably linked" refers to the association of nucleic acid fragments in a single fragment so that the function of one is regulated by the other. For example, a promoter is operably linked with a nucleic acid fragment when it is capable of regulating the transcription of that nucleic acid fragment.

The words "preferred" and "preferably" refer to embodiments of the invention that may afford certain benefits, under certain circumstances. Other embodiments may also be preferred, however, under the same or other circumstances. Furthermore, the recitation of one or more preferred embodiments does not imply that other embodiments are not useful and is not intended to exclude other embodiments from the scope of the invention.

The terms "comprises" and variations thereof do not have a limiting meaning where these terms appear in the description and claims.

Unless otherwise specified, "a," "an," "the," and "at least one" are used interchangeably and mean one or more than one.

Also herein, the recitations of numerical ranges by endpoints include all numbers subsumed within that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, 5, etc.).

For any method disclosed herein that includes discrete steps, the steps may be conducted in any feasible order. And, as appropriate, any combination of two or more steps may be conducted simultaneously.

Unless otherwise indicated, all numbers expressing quantities of components, molecular weights, and so forth used in the specification and claims are to be understood as being modified in all instances by the term "about." Accordingly, unless otherwise indicated to the contrary, the numerical parameters set forth in the specification and claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.

Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. All numerical values, however, inherently contain a range necessarily resulting from the standard deviation found in their respective testing measurements.

All headings are for the convenience of the reader and should not be used to limit the meaning of the text that follows the heading, unless so specified. The above summary of the present invention is not intended to describe each disclosed embodiment or every implementation of the present invention. The description that follows more particularly exemplifies illustrative embodiments. In several places throughout the application, guidance is provided through lists of examples, which examples can be used in various

combinations. In each instance, the recited list serves only as a representative group and should not be interpreted as an exclusive list.

BRIEF DESCRIPTION OF THE FIGURES

Figure 1 A shows a diagram of exon-intron structure of the human IL-37 gene. Exon usage in the five splice isoforms is depicted. The size of exons is indicated just below the exon boxes. The size of the intervening introns is shown at the top. Figure IB shows an alignment of the predicted amino acids sequences of the five IL-37 isoforms. The exon position is shown according to the arrangement in the gene. Positions of predicted β-strands are underlined. Propeptide cleavage sites are marked by black arrows. The predicted caspase-1 cleavage site is located between D20 and E21 (present in isoforms b-e). Another experimentally-detected cleavage site is located between F45 and V46 (present in isoforms b and c), and a predicted, elastase cleavage site in exon 3 of IL-lF7a is positioned between L21 and R22 (arrow with question mark). Exon 3 also contains a putative, bipartite nuclear localisation signal (NLS), spanning residues R5 to R22 (highlighted in gray). Figure 1C shows a diagram of exemplary fusion protein constructs. Figure ID shows a diagram of vector constructs that can be used to produce the fusion proteins of Figure 1C. Figure IE shows the expressed sequence of amino acids 46-206 of isoform B of human IL-37 fused to an Fc domain (human IL-37 Fc aa46-206) (SEQ ID NO:7). The amino acid sequence of IL-37 aa 46-206 is in bold. The sequence of human IgG/Fc is doubly underlined, and the linker peptide, GGGS, is singly underlined. Figure IF shows the expressed sequence of amino acids 53-206 of isoform B of human IL-37 fused to an Fc domain (human IL-37 Fc aa53-206) (SEQ ID NO:8). The amino acid sequence of IL-37 aa 53-206 is in bold. The sequence of human IgG/Fc is doubly underlined, and the linker peptide, GGGS, is singly underlined. Figure 1G shows the expressed sequence of amino acids 46- 206 of isoform B of human IL-37 fused to an Fc domain and a CD33 signal sequence (SEQ ID NO: 14). The sequence of CD33 signal sequence is highlighted in gray. The amino acid sequence of IL-37 aa 46-206 is in bold. The sequence of human IgG/Fc is doubly underlined, and the linker peptide, GGGS, is singly underlined. Figure 2 shows that a construct including amino acids 53-206 of isoform B of human IL-37 ("IL-37 aa53-206" or "rIL-37 (53-206)") and a construct including amino acids 46-206 of isoform B of human IL-37 ("IL-37 aa46-206" or "rIL-37 (46-206)") exhibit near similar activities. Neither construct includes an Fc domain.

Figure 3 shows a schematic of a treatment protocol.

Figure 4(A-B) shows airway resistance (Figure 4A) and dynamic compliance (Figure 4B), both indicators of lung function, measured in mice treated according to the treatment protocol of Figure 3. IL-37 (R&D) includes amino acids 46-218 of IL-37 and is not fused to an Fc domain.

Figure 5(A-B) shows infiltration of eosinophils in mice treated according to the treatment protocol of Figure 3. These results show that a construct including a sequence encoding amino acids 53-206 of isoform B of human IL-37 operably linked to a sequence encoding an Fc protein ("IL-37 Fc aa53-206") provided significantly less eosinophil infiltration than a construct including a sequence encoding amino acids 46-206 of isoform B of human IL-37 operably linked to a sequence encoding an Fc protein ("IL-37 Fc aa46-206").

Figure 6 shows a schematic of a treatment protocol. 1 microgram ^g) of IL-37 Fc aa46-206 or Isotype-Control was injected intraperitoneally (i.p.) into mice every 3 days.

Figure 7 shows IL-37 Fc aa46-206 treatment, according to the protocol of Figure 6, did not alter the tumor growth of 4T1 tumor cells.

Figure 8 shows IL-37 Fc aa46-206 treatment, according to the protocol of Figure 6, did not change the weight of the lungs, and no significant decrease in tumor weight was observed.

Figure 9 shows IL-37 Fc aa46-206 treated mice, treated according to the protocol of Figure 6, did not lose as much weight as to isotype-treated mice.

Figure 10 shows IL-37 Fc aa46-206 treated mice, treated according to the protocol of Figure 6, demonstrated a significantly lower percentage of CD1 lb ⁺ cells in the blood.

Figure 11 shows IL-37 Fc aa46-206 treated mice, treated according to the protocol of Figure

6, demonstrated significantly increased percentages of cDCs and NK cells in the blood, as measured by flow cytrometry.

Figure 12 shows a change in the percentage of CD3 ⁺ T cells in the blood of IL-37 Fc aa46- 206 treated mice, treated according to the protocol of Figure 6,when compared to isotype-treated mice, as measured by flow cytrometry. Figure 13 shows a significant increase in macrophages in a tumor in IL-37 Fc aa46-206 treated mice, treated according to the protocol of Figure 6, when compared to isotype-treated mice, as measured by flow cytrometry.

Figure 14 shows no differences in the percentages of CD3 ⁺ T cells in the tumor were observed tumor in IL-37 Fc aa46-206 treated mice, treated according to the protocol of Figure 6, when compared to isotype-treated mice.

Figure 15 shows differences in the effects of different IL-37Fc constructs on LPS-induced IL-6 in human blood monocyte-derived Ml differentiated macrophages (donor 34). Cells in each group were treated with 10 ng/mL LPS.

Figure 16 shows differences in the effects of different IL-37Fc constructs on IL-Ιβ in

J774A.1 cells stimulated with LPS/nigericin.

Figure 17 shows a treatment protocol in which IL-37Fc is administered intraperitoneally to mice as a model of systemic treatment for lung disease, and LPS was used to simulate acute lung injury.

Figure 18(A-B) shows the results of administering IL-37Fc (human IL-37 Fc aa46-206) intraperitoneally, as shown in Figure 17, on the number of inflammatory cells per milliliter of bronchoalveolar lavage (BAL) after challenge with LPS.

Figure 19 shows the results of administering IL-37Fc (human IL-37 Fc aa46-206) intraperitoneally, as shown in Figure 17, on the number of inflammatory cells per milliliter of bronchoalveolar lavage (BAL) after challenge with LPS.

Figure 20 shows a treatment protocol in which IL-37Fc (human IL-37 Fc aa46-206) is administered intraperitoneally to mice as a model of systemic treatment for lung disease, and Poly I:C was used to simulate of acute lung injury.

Figure 21(A-H) shows exemplary results of administering IL-37Fc (human IL-37 Fc aa46- 206) intraperitoneally, as shown in Figure 20, on IL-Ιβ in bronchoalveolar lavage (BAL) cells (Figure 21A, Figure 21B), KC (the mouse homologue of the human neutrophil chemokine IL-8) levels in BAL cells (Figure 21C), IL-Ιβ levels in whole lung homogenates (Figure 21D), IL-la levels in whole lung homogenates (Figure 2 IE), IL-6 levels in whole lung homogenates (Figure 2 IF), KC levels in whole lung homogenates (Figure 21G), and TNFa levels in whole lung homogenates (Figure 21H) after challenge with Poly I:C. DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS This disclosure describes IL-37 fusion proteins; methods of making IL-37 fusion proteins, including constructs used to express IL-37 fusion proteins; and methods of using IL-37 fusion proteins. In some embodiments, these fusion proteins provide increased half-life in vivo compared to IL-37. In some embodiments, the fusion proteins described herein provide unexpectedly potent effects.

IL-37 Fusion Proteins

In some embodiments, an IL-37 fusion protein includes an IL-37 protein. An IL-37 protein can include a full-length IL-37 protein, a fragment of an IL-37 protein, an IL-37 protein isoform, or a fragment of an IL-37 protein isoform. In some embodiments, the IL-37 protein is preferably a human IL-37 protein.

Five alternatively spliced transcript variants encoding five distinct isoforms of IL-37 have been reported. (See Figures 1 A and IB; Boraschi et al., Eur. Cytokine Netw. 2011, 22(3): 127-147.) The expression pattern and processing of the isoforms are incompletely characterized.

Among the five isoforms of IL-37, isoform B (218 amino acids) and isoform A (192 amino acids) have domains expected to give them more potent functions.

Members of the IL-1 family tend to be processed nine amino acids prior to a three amino acid sequence characterized by an aliphatic amino acid (A), any amino acid (X), and an aspartic acid (D), known as an AXD sequence or AXD domain. The last three amino acids of IL-37 contain an AXD sequence in all isoforms. Thus, isoforms of IL-37 may be processed (cleaved) in vivo nine amino acids before the terminal AXD motif (VSD). Upon such cleaving, the C-terminus of expressed IL-37 isoform B would be Val206 and of isoform A Vall55. Notably, the sequence of amino acids 53-206 of isoform B of IL-37 is identical to the sequence of amino acids 27-181 of isoform A of IL-37.

Isoform B of IL-37 also contains an AXD motif 9 amino acids after position 53, suggesting a putative N-terminus of Lys53. (See Dinarello et al. 2016, Eur. J. Immunol. 46: 1067-1081.) However, at least some IL-37 expressed in mammalian cells has been sequenced and found to start at Val46 (Pan et al. 2001, Cytokine 13 : 1-7). The un-cleaved (unprocessed) sequence has also been detected.

In some embodiments, an IL-37 fusion protein includes a fragment of IL-37 (that is, a fragment of an IL-37 protein or a fragment of an IL-37 isoform). In some embodiments, an IL-37 fusion protein includes amino acids 46-206 of isoform B of IL-37. In some embodiments, an IL-37 fusion protein includes SEQ ID NO:2. In some embodiments, the fragment of IL-37 consists of amino acids 46-206 of isoform B of IL-37. In some embodiments, the fragment of IL-37 consists of SEQ ID NO:2.

In some embodiments, an IL-37 fusion protein includes a heavy chain portion of an antibody. In some embodiments, an IL-37 fusion protein includes an IgG-Fc sequence. In some embodiments, the IgG-Fc sequence includes an IgGl-Fc sequence, an IgG2-Fc sequence, an IgG3- Fc sequence, or an IgG4-Fc sequence. In some embodiments, the IgGl-Fc sequence can be a human IgG-Fc sequence. In some embodiments, an IL-37 fusion protein includes SEQ ID NO:4.

In some embodiments, the Fc region includes mutations to the complement (Clq) and/or to

Fc gamma receptor (FcyR) binding sites. In some embodiments, such mutations can render the fusion protein incapable of antibody directed cytotoxicity (ADCC) and complement directed cytotoxicity (CDC). For example, an IgGl-Fc sequence can include L234A and L235A (LALA) substitutions, substitutions that studies have demonstrated greatly reduce binding to Fc gamma receptors (FcyRs). In some embodiments, an IL-37 fusion protein includes SEQ ID NO:5.

Fusing IL-37 to the Fc region of human IgGl is expected to increase half-life in vivo, but the effects of an Fc region on the potency of IL-37 must be determined experimentally. As shown herein, fusion of IL-37 to the Fc region of human IgGl and, in particular, fusion of amino acids 46- 206 of isoform B of IL-37 to the Fc region of human IgGl can produce a construct having beneficial effects on the potency of IL-37.

Surprisingly, although recombinant human IL-37 aa53-206 and recombinant human IL-37 aa46-206 exhibit near similar activities (Figure 2), the respective fusion proteins (IL-37 Fc aa53- 206 and IL-37 Fc aa46-206) do not. For example, when the fusion proteins were tested in the same types of cells at the same time, IL-37 Fc aa53-206 was observed to be less potent in suppressing IFNy than IL-37 Fc aa46-206. Differences between the effects of the fusion proteins were also observed in other experimental models. (See, for example, Figures 15-16 and Examples 5-6.)

IL-37 binds to the IL-18 receptor (IL-18R). The Fc region of human IgGl is a dimer and will, therefore, bring two IL-37 molecules into close proximity, potentially also bringing two IL-18 receptor molecules into close proximity. The effects, if any, of this proximity are unknown.

In some embodiments, an IL-37 fusion protein includes a peptide linker. In some embodiments, the peptide linker connects an IL-37 protein and an Fc sequence. In some

embodiments, the peptide linker can include the amino acid sequence GGGS. In some embodiments, an IL-37 fusion protein includes a signal peptide (sometimes referred to as a signal sequence). In some embodiments, the signal peptide can be a human signal peptide. In some embodiments, the signal peptide can include a CD33 signal peptide. In some embodiments, an IL-37 fusion protein includes SEQ ID NO:6. In some embodiments, a signal peptide can be located at the N-terminus of the IL-37 fusion protein.

Methods of Making IL-37 Fusion Proteins

This disclosure further disclosure describes methods of making an IL-37 fusion protein. In some embodiments, a sequence encoding an IL-37 protein or a fragment of IL-37 protein is fused to a sequence encoding a heavy chain portion of an antibody or a portion or a heavy chain portion of an antibody. In some embodiments, a sequence encoding an IL-37 protein or a fragment of IL-37 protein is operably linked to a sequence encoding a heavy chain portion of an antibody or a portion or a heavy chain portion of an antibody. In some embodiments, a sequence encoding a peptide linker can be included between the sequence encoding an IL-37 protein or a fragment of IL-37 and the sequence encoding a heavy chain portion of an antibody or a portion or a heavy chain portion of an antibody. In some embodiment, the sequence encoding a peptide linker can include a sequence encoding GGGS. In some embodiments, the sequence encoding an IL-37 protein or a fragment of IL-37 can be fused to a peptide encoding a signal peptide. In some embodiments, the signal peptide can include a CD33 signal sequence. In some embodiments, a sequence encoding a signal peptide is connected to and/or operably linked to a sequence encoding a fragment of IL-37.

In some embodiments, the sequence encoding the IL-37 fusion protein is inserted into a vector. In some embodiments, the vector includes a CMV promoter.

In some embodiments, a vector including a sequence encoding the IL-37 fusion protein can be introduced into a cell including, for example, by transfection. In some embodiments, the vector can be stably transfected. In some embodiments, the cell can be an HEK293 cell.

Methods of Using IL-37 Fusion Proteins

This disclosure further disclosure describes methods of using an IL-37 fusion protein. In some embodiments, the method includes administering an effective amount of an IL-37 fusion protein.

In some embodiments, a IL-37 fusion protein described herein can be used to modulate the immune system. For example, modulation of IL-37 has been shown to have a beneficial effect in, for example, subjects having a spinal cord injury (Coll-Miro et al. 2016, PNAS 113(5): 1411-1416), in improvement of a subject's exercise tolerance (Cavalli et al. 2017, Proc Natl Acad Sci USA 114(9):2313-2318), in reducing joint and systemic inflammation (Cavalli et al. 2016, Rheumatology (Oxford) 55(12):2220-2229), in sickle cell anemia patients (Alagbe et al. 2017, Cytokine doi:

10.1016/j .cyto.2017.12.001), in subjects from several different experimental models of

inflammation including arthritis (Cavalli et al. 2018, Immunol Rev. 281(1): 179-190), human lung adenocarcinoma (Chen et al. 2017, Cancer Biomark. doi: 10.3233/CBM-170732), inflammatory bowel disease (Conti et al. 2018, Eur. J. Pharmacol. 818:294-299), osteoarthritis (Ding et al. 2017, Sci. Rep. 7: 11601), alcoholic liver disease (Grabherr et al. 2017, Liver Int. doi: 10.1111/liv.13642), asthma (Huang et al. 2017, Int. Immunopharmacol. 55: 198-204; Lv et al. 2018, Allergy doi:

10.1111/all.13395), allergic rhinitis (Kim et al. 2017, Iran J. Allergy Asthma Immunology 16:404- 417), atherosclerosis related diseases (Liu et al. 2018, Cell Physiol. Biochem. 45: 1034-1050;

McCurdy et al. 2017, J. Immunol. 199(10):3604-3613), and asthma (Zhang et al. 2017, Respir. Res. 18(1): 192).

In some embodiments, a IL-37 fusion protein described herein can be administered to a subject having an IL-37 deficiency and/or low IL-37 expression levels. For example, states in which low IL-37 expression levels have been observed include obesity-induced inflammation and insulin resistance (Ballak et al. 2014, Nat. Commun. 5:4711), allergic airway inflammation and/or asthma (Lunding et al. 2015, Allergy 70(4):366-373), plaque psoriasis (Xu et al. 2015, Autoimmun. Rev. 14: 1170-1175), calcific aortic valve disease (Zeng et al. 2017, PNAS USA 1114: 1631-1636), and alcoholic liver disease (Grabherr et al. 2017, Liver Int. doi: 10.1111/liv.13642).

Pharmaceutical Composition

The present disclosure further provides a pharmaceutical composition that includes an IL-37 fusion protein and a pharmaceutically acceptable carrier. The IL-37 fusion protein is formulated in a pharmaceutical composition and then, in accordance with the method of the invention, administered to a vertebrate, particularly a mammal, such as a human patient, companion animal, or domesticated animal, in a variety of forms adapted to the chosen route of administration. The formulations include those suitable for oral, rectal, vaginal, topical, nasal, ophthalmic, or parenteral (including subcutaneous, intramuscular, intraperitoneal, and intravenous) administration.

The pharmaceutically acceptable carrier can include, for example, an excipient, a diluent, a solvent, an accessory ingredient, a stabilizer, a protein carrier, or a biological compound. Non- limiting examples of a protein carrier includes keyhole limpet hemocyanin (KLH), bovine serum albumin (BSA), ovalbumin, or the like. Non-limiting examples of a biological compound which can serve as a carrier include a glycosaminoglycan, a proteoglycan, and albumin. The carrier can be a synthetic compound, such as dimethyl sulfoxide or a synthetic polymer, such as a

polyalkyleneglycol. Ovalbumin, human serum albumin, other proteins, polyethylene glycol, or the like can be employed as the carrier. In a preferred embodiment, the pharmaceutically acceptable carrier includes at least one compound that is not naturally occurring or a product of nature.

In some embodiments, the IL-37 fusion protein is formulated in combination with one or more additional active agents. Any known therapeutic agent can be included as an additional active agent. The action of the additional active agent in the combination therapy can be cumulative to the IL-37 fusion protein or it can be complementary, for example to manage side effects or other aspects of the patient's medical condition. In one embodiment, the combination therapy includes at least one compound that is not naturally occurring or a product of nature.

The formulations can be conveniently presented in unit dosage form and can be prepared by any of the methods well-known in the art of pharmacy. In some embodiments, a method includes the step of bringing the active agent into association with a pharmaceutical carrier. In general, the formulations are prepared by uniformly and intimately bringing the active compound into association with a liquid carrier, a finely divided solid carrier, or both, and then, if necessary, shaping the product into the desired formulations.

Formulations of the present disclosure suitable for oral administration can be presented as discrete units such as tablets, troches, capsules, lozenges, wafers, or cachets, each containing a predetermined amount of the active agent as a powder or granules, as liposomes, or as a solution or suspension in an aqueous liquor or non-aqueous liquid such as a syrup, an elixir, an emulsion, or a draught. The tablets, troches, pills, capsules, and the like can also contain one or more of the following: a binder such as gum tragacanth, acacia, corn starch or gelatin; an excipient such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid, and the like; a lubricant such as magnesium stearate; a sweetening agent such as sucrose, fructose, lactose, or aspartame; and a natural or artificial flavoring agent. When the unit dosage form is a capsule, it can further contain a liquid carrier, such as a vegetable oil or a polyethylene glycol. Various other materials can be present as coatings or to otherwise modify the physical form of the solid unit dosage form. For instance, tablets, pills, or capsules can be coated with gelatin, wax, shellac, sugar, and the like. A syrup or elixir can contain one or more of a sweetening agent, a preservative such as methyl- or propylparaben, an agent to retard crystallization of the sugar, an agent to increase the solubility of any other ingredient, such as a polyhydric alcohol, for example glycerol or sorbitol, a dye, and flavoring agent. The material used in preparing any unit dosage form is substantially nontoxic in the amounts employed. The active agent can be incorporated into preparations and devices in formulations that may or may not be designed for sustained release.

Formulations suitable for parenteral administration conveniently include a sterile aqueous preparation of the active agent, or dispersions of sterile powders of the active agent, which are preferably isotonic with the blood of the recipient. Parenteral administration of an IL-37 fusion protein (e. g., through an IV. drip) is one form of administration. Isotonic agents that can be included in the liquid preparation include sugars, buffers, and sodium chloride. Solutions of the active agent can be prepared in water, optionally mixed with a nontoxic surfactant. Dispersions of the active agent can be prepared in water, ethanol, a polyol (such as glycerol, propylene glycol, liquid polyethylene glycols, and the like), vegetable oils, or glycerol esters, and mixtures thereof. The ultimate dosage form is sterile, fluid, and stable under the conditions of manufacture and storage. The necessary fluidity can be achieved, for example, by using liposomes, by employing the appropriate particle size in the case of dispersions, or by using surfactants. Sterilization of a liquid preparation can be achieved by any convenient method that preserves the bioactivity of the active agent, preferably by filter sterilization. Preferred methods for preparing powders include vacuum drying and freeze drying of the sterile injectable solutions. Subsequent microbial contamination can be prevented using various antimicrobial agents, for example, antibacterial, antiviral and antifungal agents including parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. Absorption of the active agents over a prolonged period can be achieved by including agents for delaying, for example, aluminum monostearate and gelatin.

Nasal spray formulations include purified aqueous solutions of the active agent with preservative agents and isotonic agents. Such formulations are preferably adjusted to a pH and isotonic state compatible with the nasal mucous membranes. Formulations for rectal or vaginal administration can be presented as a suppository with a suitable carrier such as cocoa butter, or hydrogenated fats or hydrogenated fatty carboxylic acids. Ophthalmic formulations are prepared by a similar method to the nasal spray, except that the pH and isotonic factors are preferably adjusted to match that of the eye. Topical formulations include the active agent dissolved or suspended in one or more media such as mineral oil, petroleum, polyhydroxy alcohols, or other bases used for topical pharmaceutical formulations. Topical formulations can be provided in the form of a bandage, wherein the formulation is incorporated into a gauze or other structure and brought into contact with the skin.

Administration

An IL-37 fusion protein can be administered to a subject alone or in a pharmaceutical composition that includes a pharmaceutically acceptable carrier. The active agent is administered to a vertebrate, more preferably a mammal, such as a human patient, a companion animal, or a domesticated animal, in an amount effective to produce the desired effect. An IL-37 fusion protein can be administered in a variety of routes, including orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery by catheter or stent, subcutaneously, intraadiposally, intraarticularly, intrathecally, or in a slow release dosage form.

The formulations can be administered as a single dose or in multiple doses. Useful dosages of the active agents can be determined by comparing their in vitro activity and the in vivo activity in animal models. Methods for extrapolation of effective dosages in mice, and other animals, to humans are known in the art.

Dosage levels of the active agent in the pharmaceutical compositions of this disclosure can be varied so as to obtain an amount of the active agent which is effective to achieve the desired therapeutic response for a particular subject, composition, and mode of administration, without being toxic to the subject. The selected dosage level will depend upon a variety of factors including the activity of the particular compound of the present disclosure employed, or the ester, salt or amide thereof, the route of administration, the time of administration, the rate of excretion of the particular compound being employed, the duration of the treatment, other drugs, compounds and/or materials used in combination with the IL-37 fusion protein, the age, sex, weight, condition, general health and prior medical history of the subject being treated, and like factors well known in the medical arts.

A physician or veterinarian having ordinary skill in the art can readily determine and prescribe the effective amount of the pharmaceutical composition required. For example, the physician could start doses of the IL-37 fusion protein employed in the pharmaceutical composition at levels lower than that required in order to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved. The present invention is illustrated by the following examples. It is to be understood that the particular examples, materials, amounts, and procedures are to be interpreted broadly in accordance with the scope and spirit of the invention as set forth herein.

EXAMPLES

Example 1

This Example describes the synthesis of IL-37 Fc constructs.

DNA sequences encoding human IL-37 aa 46-218 (SEQ ID NO: l), human IL-37 aa 46-206 (SEQ ID NO:2), and human IL-37 aa 53-206 (SEQ ID NO:3), as shown in Table 1, were fused to a human IgGl sequence (SEQ ID NO:4) via a peptide linker (GGGS) to form Structure A, Structure B, and Structure C (shown in Figure 1C), respectively.

The human CD33 signal sequence was fused to the sequences encoding human IL-37 (SEQ ID NOs: 1-3), and a human Fc region and the resulting constructs (shown in Figure 1C) were incorporated in an expression vector having a CMV promoter. As shown in Table 1, an optional hlgGl-Fc mutations in the Clq binding region to render it non-lytic are bolded and highlighted in gray. The IL-37 Fc aa46-206 construct and IL-37 Fc aa53-206 constructs were expressed in stably transfected HEK293 cells. The IL-37 Fc aa46-218 construct did not express.

For IL-37 Fc aa46-206, a DNA sequence encoding human IL-37 aa 46-218 was fused to human IgG Fc via a peptide linker at the C-terminus (Figure IE). N-terminal sequence analysis suggested that the expressed protein starts at the expected N-terminus, valine 46. The purified protein migrated as a 50 kD or 100 kD band under reducing or non-reducing conditions, respectively.

For IL-37 Fc aa53-206, A DNA sequence encoding the IL-37 sequence comprising amino acids 53-206, accession # Q9NZH6, was fused to human IgG Fc via a peptide linker at the C- terminus (Figure IF). N-terminal sequence analysis suggested that the expressed protein starts at the expected N-terminus, lysine 53. The purified protein migrated as a 52 kD or 105 kD band under reducing or non-reducing conditions, respectively. Table 1.

Example 2

This Example describes the comparison of efficacy of IL-37 proteins.

Results are shown in Figure 2.

Example 3

This Example describes the effect of treating mice with IL-37 fusion proteins including different isoforms of IL-37 on lung function and bronchoalveolar lavage (BAL) fluid eosinophil percentages. These data can provide information regarding the effects of IL-37 fusion proteins on experimental asthma.

Methods were performed as described in, for example, Lunding et al. (Allergy 2015, 70:366- 373; DOI: 10.1111/all.12566) using IL-37Fc. A schematic of the treatment protocol is shown in Figure 3. Results are shown in Figures 4-

5.

Example 4

This Example describes the effect of treating mice with an IL-37 fusion protein including amino acids 46-206 of isoform B of recombinant human IL-37 operably linked to an Fc protein ("IL-37 Fc aa46-206) and an isotype control on tumor growth, lung size, tumor weight, body weight; CD1 lb ⁺ cells, cDCs, K, and CD3 ⁺ T cells cells in the blood; and macrophages and CD3 ⁺ T cells in the tumor.

Mice were treated with IL-37Fc or vehicle and then injected with 4T1 breast cancer tumor cells (Current Protocols in Immunology, Tumor Immunology, 20.2.15, Supplement 39), which spontaneously metastasize in different organs. Mice were treated every 3 days with IL-37Fc (1 μg or 5 μg per mouse). After approximately 28-30 days, liver, lung, spleen, lymph node were removed, cut into small pieces and treated with a 30 minute Collagenase-DNAse digestion at 37°C. After digestion, the organs were passed through a 100 μιη and a 30 μιη cell strainer to obtain single-cell suspensions. After centrifugation, red blood cells were lysed for 2 minutes and the suspension centrifuged one more time.

After the preparation of single cells, 6-Thioguanine, a cytostatic drug that kills normal cells, was added to the single-cell suspension in different ratios with medium. For example, when analyzing the lung, the whole-lung single cell suspension was diluted 1 : 10, 1 : 100, and 1 : 1000 in medium containing the 6-Thioguanine and plated into 6-well plates (3 wells per organ). Cells which lack resistance against the cytostatic drug die, and only the tumor cells proliferate and form macroscopic colonies.

After 7-10 days, the colonies are visible by eye. The wells were stained the crystal violet. After 10 minutes fixation in 70% ethanol, the formed colonies are clearly stained and were counted and the resulting number was normalized.

A schematic of the treatment protocol is shown in Figure 6. Results are show in Figures 7-

14.

Example 5

This Example describes the effect of different IL-37Fc constructs on LPS-induced (10 ng/mL) IL-6 in human blood-monocyte derived Ml differentiated macrophages. The methods were performed as described in Li et al. 2015, PNAS USA 112(8):2497-2502. Results are shown in Figure 15.

Example 6

This Example describes the effect of different IL-37Fc constructs on IL-Ιβ in

J774A.1 cells stimulated with LPS/nigericin. The methods were performed as described in

Marchetti et al. 2018, PNAS USA 115(7):E1530-E1539. Results are shown in Figure 16.

Example 7

This Example describes the effect of IL-37Fc (human IL-37 Fc aa46-206) in models of lung disease including, for example, asthma. In contrast to Example 3 where the IL-37Fc was directly administered into the lung, in this Example, IL-37Fc was administered intraperitoneally as a model of systemic treatment for lung disease. Acute lung injury was simulated using two models: LPS (Figure 17) and Poly I:C (Figure 20). These models of acute lung injury are commonly used as a model for sepsis-related diseases, but they are also relevant for any lung disease in which neutrophils invade the lung and cause damage. Results are shown in Figure 18 and Figure 19 (for LPS) and Figure 21 (for Poly I:C).

The complete disclosure of all patents, patent applications, and publications, and electronically available material (including, for instance, nucleotide sequence submissions in, e.g., GenBank and RefSeq, and amino acid sequence submissions in, e.g., SwissProt, PIR, PRF, PDB, and translations from annotated coding regions in GenBank and RefSeq) cited herein are incorporated by reference. In the event that any inconsistency exists between the disclosure of the present application and the disclosure(s) of any document incorporated herein by reference, the disclosure of the present application shall govern. The foregoing detailed description and examples have been given for clarity of understanding only. No unnecessary limitations are to be understood therefrom. The invention is not limited to the exact details shown and described, for variations obvious to one skilled in the art will be included within the invention defined by the claims.