KIM-1 ANTAGONISTS AND USE TO MODULATE IMMUNE SYSTEM
The use of KIM-1 antagonists to inhibit signaling between a T cell and a second cell, e.g., an antigen-presenting cell, is disclosed. Such inhibition is useful for treatment of diseases including various autoimmune diseases and graft-versus-host disease. Also disclosed is the use of a KIM-1 antagonist to inhibit secretion of IFN-γ by lymphocytes or other immune cells in a mammal. Inhibition of IFN-γ is useful for treatment of inflammatory diseases or disorders, e.g., inflammatory bowel disease.
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The field of the invention is medicine, immunology, molecular biology and protein chemistry.
BACKGROUND OF THE INVENTIONKIM-1 (Kidney injury Molecule-1) is a type I cell membrane glycoprotein (Ichimura et al., 1998, J. Biol. Chem. 273:4135-4142). The extracellular portion (ectodomain) of KIM-1 contains a six-cysteine immunoglobulin-like domain and a T/SP rich domain characteristic of mucin-like O-glycosylated proteins. The mucin domain extends the Ig-like domain away from the cell surface like a stalk (Jentoft, 1990, Trends Biochem. Sci. 15:291-294). KIM-1 has been identified as the receptor for hepatitis A virus (Kaplan et al., 1996, EMBO J. 15:4282-4296; WO 96/04376; U.S. Pat. No. 5,622,861). Two human KIM-1 splice variants have been discovered, with one being predominant in the liver (Feigelstock, 1998, J. Virol. 72:6621-6628), and the other being predominant in the kidney (Ichimura et al., supra).
KIM-1 is a member of a gene family known as the TIM (T cell Immunoglobulin and Mucin domain) family. In addition to KIM-1, there are at least two other members of the TIM family in humans. One member was cloned and originally designated the “200 gene” (WO200073498), but subsequently came to be known as TIM-3. Another member was cloned and designated “gene 58” (WO99/38881).
KIM-1 has attracted interest as a clinical diagnostic marker for kidney damage (Bailly et al., 2002, J. Biol. Chem. 277:39739-39748; Han et al., 2002, Kidney Intl. 62:237-244). A mouse homolog of KIM-1 (TIM-1) has been reported to exist within a genetic locus thought to be involved in the development of airway hyperreactivity (McIntire et al., 2001, Nature Immunology 2:1109). A mouse protein known as TIM-2 has been reported to play a role in the in vivo generation of antigen-specific T cells (Kumanogoh et al., 2002, Nature 419:629-633). A mouse protein known as TIM-3 has been associated with immune response regulation in mice (Monney et al., 2002. Nature 415:536-541).
SUMMARY OF THE INVENTIONIt has been discovered that treatment of a mammal with a KIM-1 antagonist alters the interaction of T cells with other immune system cells, e.g., dendritic cells, monocytes macrophages, and B cells, and thereby strongly suppresses an IgG response to an antigen. In addition, it has been discovered that such treatment almost eliminates IgG1 production by memory B cells in response to subsequent challenge with the antigen. In addition, it has been discovered that blockade of the binding of KIM-1 to its receptor reduces secretion of IFN-γ by immune cells engaged in an antigen response in the mixed lymphocyte response (MLR) assay. Based on these discoveries, the invention provides methods for therapeutically modulating immune function in autoimmune diseases and other disorders of the mammalian immune system.
The invention provides a method of inhibiting signaling between a T cell and a second cell, e.g., an antigen-presenting cell (APC), in a mammal. The method includes identifying a mammal, e.g., one with an immune disease or disorder, or one preparing to receive a tissue graft; and administering to the mammal an effective amount of one of the following types of KIM-1 antagonist: (a) a polypeptide comprising a KIM-1 Ig domain, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain; (b) an anti-KIM-1 antibody; and (c) an antigen-binding fragment of an anti-KIM-1 antibody.
The T cell may be an activated T cell, e.g., a T helper cell. It can be a Th2 cell or a Th1 cell. In some embodiments of the invention the T cell is a grafted, donor T cell. The APC can be, but is not limited to, a monocyte, a macrophage, a dendritic cell, or a B cell. In some embodiments of the invention, the APC is presenting an autoantigen.
Preferably, the KIM-1 antagonist is a soluble polypeptide, which can include a KIM-1 mucin domain in addition to the KIM-1 Ig domain. In some embodiments the polypeptide includes a heterologous moiety, e.g., an immunoglobulin (Ig) moiety, a serum albumin moiety, a targeting moiety, a reporter moiety, a multimerization moiety, and a purification-facilitating moiety. A preferred heterologous moiety is an Ig moiety such as an Fc moiety.
In some embodiments the KIM-1 antagonist is a polypeptide conjugated to a polymer such as polyalkylene glycol, a sugar polymer, or a polypeptide. A preferred polymer is a polyalkylene glycol, with polyethylene glycol (PEG) being particularly preferred. The average molecular weight of the polymer preferably is from 2,000 Da to 30,000 Da., and more preferably from 5,000 Da to 20,000 Da., e.g., about 10,000 Da.
The invention provides a method of inhibiting activation of a B cell in a mammal, e.g., by an activated T cell such as a Th2 cell. The method includes contacting the B cell or other APC with an effective amount of a KIM-1 antagonist, or the T cell, if the antagonist is an anti-KIM-1 antibody. In some embodiments of the invention, the activated T cell is a grafted, donor T cell.
The invention provides a method of inhibiting production in a mammal of a subset of antibodies such as IgG, e.g., IgG1, reactive against one or more antigens. The method includes administering an effective amount of a KIM-1 antagonist. In some embodiments the effective amount of the KIM-1 antagonist is administered between 30 minutes and 30 days before the immune system of the mammal first recognizes the one or more antigens. The antigens are autoantigens or autoantigens, depending on the disease, disorder or condition being treated.
The invention provides a method of inhibiting disease relapse in an autoimmune disease. The method includes administering an effective amount of a KIM-1 antagonist.
The invention provides a method of inhibiting epitope spreading in an autoimmune disease. The method includes administering an effective amount of a KIM-1 antagonist.
The invention provides a method of treating a Th2 cell-mediated disease, e.g., systematic lupus erythromatosis, myasthenia gravis, autoimmune hemolytic anemia, Chagas disease, Graves disease, idiopathic thrombocytopenia purpura (ITP), Wegener's granulomatosis, polyarteritis. nodosa, rapidly progressive crescentic glomerulonephritis, or graft-versus-host disease (GVHD), asthma, atopic dermatitis, atopy disorders such as airway hyperresponsive diseases and airway distress syndromes. The method includes administering an effective amount of a KIM-1 antagonist.
The invention provides a method of inhibiting GVHD. The method includes administering an effective amount of a KIM-1 antagonist between 30 minutes and 30 days before the graft.
The invention provides a method of inhibiting secretion of IFN-γ by lymphocytes in a mammal. The method includes administering to the mammal an effective amount of a KIM-1 antagonist.
The invention provides a method of inhibiting the activation of Th1 T cell effector function, and therefore cellular immune responses that occur in inflammatory situations. An example of such an inflammatory situation is inflammatory bowel disease. The method includes administering to the mammal an effective amount of a KIM-1 antagonist.
The invention provides a method of treating an inflammatory disease or disorder in a mammal, e.g., inflammatory bowel diseases such as Crohn's disease, ulcerative colitis, and ileitis. The method includes administering to the mammal an effective amount of a KIM-1 antagonist.
As used herein, “anti-KIM-1 antibody” means an antibody, e.g., an IgG molecule, that binds specifically to the extracellular portion of a full length KIM-1 polypeptide.
As used herein, “full length human KIM-1 polypeptide” means the polypeptide of SEQ ID NO:1 in its entirety or SEQ ID NO:2 in its entirety. These two polypeptides represent splice variants of the human KIM-1 gene.
As used herein, “heterologous moiety” means an amino acid sequence not present in a full-length KIM-1 polypeptide.
As used herein, “KIM-1 antagonist” means (a) a polypeptide comprising a KIM-1 Ig domain, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain; (b) an anti-KIM-1 antibody; or (c) an antigen-binding fragment of an anti-KIM-1 antibody, each of which blocks, inhibits, or interferes with the biological activity of a naturally-occurring KIM-1.
As used herein, “KIM-1 fusion protein” means a fusion protein that includes a KIM-1 moiety fused to a heterologous moiety.
As used herein, “KIM-1 moiety” means a biologically active fragment of a full-length KIM-1 polypeptide.
As used herein, “KIM-1 polypeptide” means a KIM-1 moiety alone or a fusion protein that includes a KIM-1 moiety.
As used herein, “KIM-1 Ig domain” means a portion of SEQ ID NO:1 whose amino terminus is amino acid 29-36, and whose carboxy terminus is amino acid 105-107.
As used herein, “KIM-1 mucin domain” means a portion of SEQ ID NO:1 whose amino terminus is amino acid 126-130, and whose carboxy terminus is amino acid 255-274.
As used herein, “KIM-1 transmembrane domain” means amino acids 290-311 of SEQ ID NO:1.
As used herein, “KIM-1 cytoplasmic domain” means amino acids 312-334 of SEQ ID NO:1, or 312-359 of SEQ ID NO:2.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the invention pertains. In case of conflict, the present specification, including definitions, will control. All publications, patents and other references mentioned herein are incorporated by reference.
Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the invention, the preferred methods and materials are described below. The materials, methods and examples are illustrative only, and are not intended to be limiting. Other features and advantages of the invention will be apparent from the detailed description and from the claims.
The native human KIM-1 gene encodes a polypeptide (
Using a soluble, dimerized, KIM-1 ectodomain-Fc fusion protein (each monomer containing the mouse KIM-1 ectodomain and a human Fc moiety) and a recognized animal model (murine SRBC response), the inventors have achieved a profound alteration of the mammalian immune response. Without intending to be bound by theory, the inventors interpret the observed results as indicating that the fusion protein acts as a KIM-1 antagonist, and that this antagonism interferes with a KIM-1-mediated signaling interaction between T cells and APCs. The downstream effects of this interference include useful modulation of the mammalian immune response. Such modulation can be used to treat autoimmune diseases and other diseases and disorders in which a mammalian immune system attacks an inappropriate target, either through T cell cytotoxicity or through an immunoglobulin response. Examples of diseases or disorders in which immune system modulation would be beneficial include, but are not limited to, arthritis, systemic lupus erythromatosis (also known as SLE or lupus), and graft-versus-host-disease (GVHD).
In methods of the present invention, a soluble KIM-1 antagonist polypeptide or a KIM-1 blocking antibody (or antigen-binding antibody fragment) can be administered directly as a pre-formed polypeptide. Alternatively, it can be administered indirectly through a nucleic acid vector (encoding and expressing the polypeptide). Either way, the result is to antagonize KIM-1-mediated effects on T cells, including T cell activation and stimulation of T cell proliferation. This antagonism of KIM-1 located on T cells can achieve a desired therapeutic effect directly by blocking destructive actions of the T cells themselves. In addition, the antagonism can achieve the desired therapeutic effect indirectly, by blocking activated T cell-mediated activation of B cells, thereby reducing deleterious antibody production.
In various diseases, including autoimmune diseases and certain types of pathogenic infections, damage results from autoantibody responses, i.e., production of antibodies that recognize self-antigens. The present invention provides methods and molecules for reducing such damage by interfering with T cell activation and differentiation. This, in turn, interferes with activated T cell-mediated B cell activation, which interferes with production and secretion of specific immunoglobulins, e.g., IgG1, by the B cells. Accordingly, any disease or disorder characterized by autoantibody responses can be treated by using methods and molecules of the invention.
When certain autoimmune diseases are being treated, exposure to antigens, and the immune system responses, are transient. This results in remissions during which administration of an effective amount of a KIM-1 antagonist would inhibit subsequent reactivation of the immune responses to one or more antigens. In this way the invention can be used to block disease relapse. When certain autoimmune diseases are being treated, the immune system of the mammal first recognizes the one or more antigens as part of an epitope spreading process in the course of an autoimmune disease.
Much of the damage in graft-versus-host disease (GVHD) results directly from actions of donor T cells that become activated in the host (in response to host antigens), once grafted, e.g., in a bone marrow transplant. By virtue of its ability to interfere with T cell activation, the present invention is useful for inhibiting GVHD. In addition to damage from direct actions of activated donor T cells, there is also an antibody-mediated component in GVHD. Because this antibody-mediated component depends on activation of donor T cells, which activate the autoantibody-producing B cells, the invention reduces autoantibody-mediated damage, as well as cellular immunity-mediated damage in GVHD.
Antibody-Mediated Autoimmune DiseasesSystematic lupus erythromatosis (SLE; lupus) is a TH-2 mediated autoimmune disorder characterised by high levels of autoantibodies directed against intracellular antigens such as double stranded DNA, single stranded DNA, and histones. In view of these characteristics, lupus exemplifies an autoimmune disease that can be treated according to the present invention.
Examples of other organ-specific or systemic autoimmune diseases suitable for treatment according to the invention include myasthenia gravis, autoimmune hemolytic anemia, Chagas' disease, Graves disease, idiopathic thrombocytopenia purpura (ITP), Wegener's Granulomatosis, poly-arteritis Nodosa and Rapidly Progressive Crescentic Glomerulonephritis. See, e.g., Benjamin et al., 1996, Immunology, A Short Course, Third Ed. (Wiley-Liss, New York). In addition, rheumatoid arthritis (RA), once thought to be mediated by T cell cytotoxic activity, is now known to have a B cell and/or antibody component (Leandro et al., 2002, Ann. Rheum. Dis., 61:863-866; De Vita et al., Arthritis Rheum. 46:2029-2033; Tsuji et al., 2002, J. Exp. Med. 196:1277-1290), and thus is suitable for treatment according to the invention.
The normal immune response to some pathogenic infectious agents elicits deleterious autoantibody responses. One example is Chagas' disease, an inflammatory cardiomyopathy that develops in humans and experimental animals chronically infected with Trypanosoma cruzi. Anti-self antibodies occur in the sera of Chagas' disease patients (Bach-Elias et al., 1998, Parasitol. Res. 84:796-799; Tibbetts, et al., 1994, J. Immunol. 152:1493-1499), and thus this disease is suitable for treatment according to the invention.
Another example of cell destruction by autoantibodies resulting from infection is idiopathic thrombocytopenia purpura (ITP), in which autoantibodies cause platelet destruction (by complement or phagocytic cells with Fc or C3b receptor) and can lead to bleeding. ITP is suitable for treatment according to the invention.
Graft-Versus Host Disease (GVHD)GVHD exemplifies a T cell-mediated condition that can be treated using methods of the invention. GVHD is initiated when donor T cells recognize host antigens as foreign. GVHD, often a fatal consequence of bone marrow transplantation (BMT) in human patients, can be acute or chronic. Acute and chronic forms of GVHD exemplify the development of antigen specific Th1 and Th2 responses, respectively. Acute GVHD occurs within the first 2 months following BMT, and is characterized by donor cytotoxic T cell-mediated damage to skin, gut, liver, and other organs. Chronic GVHD appears later (over 100 days post-BMT) and is characterized by hyperproduction of immunoglobulin (Ig), including autoantibodies, and damage to the skin, kidney, and other organs caused by Ig-deposition. Nearly 90% of acute GVHD patients go on to develop chronic GVHD. Chronic GVHD appears to be a Th2 T cell mediated disease (De Wit et al., 1993, J. Immunol. 150:361-366). Acute GVHD is a Th1 mediated disease (Krenger et al., 1996, Immunol. Res. 15:50-73; Williamson et al., 1996, J. Immunol. 157:689-699). T cell cytotoxicity is a characteristic of acute GVHD. The consequence of donor anti-host cytotoxicity can be seen in various ways. First, host lymphocytes are rapidly destroyed, such that mice experiencing acute GVHD are profoundly immunosuppressed. Second, donor lymphocytes become engrafted and expand in the host spleen, and their cytotoxic activity can be directly measured in vitro by taking advantage of cell lines that express the host antigens that can be recognized (as foreign) by the donor cells. Third, the disease becomes lethal as additional tissues and cell populations are destroyed.
Chronic GVHD results from antibody-mediated destruction of host tissues and cells and has been called “SLE-like” GVHD. Manifestations include autoantibody formation, Ig-deposition in various organs (kidney, liver), skin rash, lymphoid hyperplasia, Sjögren-like lesions, scleroderma-like lesions, polyarteritis, and other pathologies. This disease is partly mediated by autoantibody formation. In view of the foregoing, chronic GVHD is suitable for treatment according to the invention.
Other Th2-Related DiseasesAtopic disorders are characterized by the expression by immune system cells, including activated T cells and APC, of cytokines, chemokines, and other molecules which are characteristic of Th2 responses, such as the IL-4, IL-5 and IL-13 cytokines, among others. Such atopic disorders therefore will be amenable to treatment by methods that antagonize the development of the Th2 response, such as the KIM-1 antagonists of the invention. Atopic disorders include asthma, the airway hypersensitivity and distress syndromes, and pathologies such as atopic dermatitis. The invention provides a method of inhibiting atopic disorders. The method includes administering an effective amount of a KIM-1 antagonist.
Inflammatory Diseases and Disorders Mediated by Activated Lymphocytes, APC and Pro-Inflammatory CytokinesUsing the mixed lymphocyte reaction assay (MLR) in the mouse and human model systems, the inventors have shown that blockade of KIM-1 binding to its receptor, e.g., using anti-KIM-1 mAbs or a KIM-1-Ig fusion protein, reduces the secretion of IFNγ by responder cells. Accordingly, a KIM-1 antagonist can be used to treat any disease or disorder mediated by IFNγ.
IFNγ is a critical cytokine in immune responses. It has pleotropic effects on the development and extent of inflammatory and immune processes (Boehm et al. 1997, Ann Rev Immunol 15:749-795). Deficiencies in IFNγ production reduce anti-viral and anti-bacterial responses and attenuate inflammatory responses. A KIM-1 antagonist can be used advantageously to reduce IFNγ production in diseases or disorders where IFNγ production is excessive or inappropriate. Examples of such diseases or disorders include autoimmune diseases, colitis and chronic inflammation.
IFNγ is a key component of T cell activation and B cell responses. It influences T cell effector cell development (e.g., via cross regulation with Il-4) and B cell activation (e.g., via regulation of MHC-mediated antigen presentation and expression of B7 molecules). IFNγ is a critical component of Th1 T cell-mediated immune responses. IFNγ has pronounced effects on other immune system components such as macrophages and neutrophils. It stimulates their activation and release of toxic effector molecules.
IFNγ has potent effects on tissue resident cell types. Endothelium is activated by IFNγ. When stimulated with IFNγ, resident cells in diseased tissue, e.g., synoviocytes in rheumatoid arthritis, secrete TNF and other cytokines, MCP-1 and other chemokines, and toxic effector molecules such as nitric oxide. All of these latter functions mediated by IFNγ influence cell trafficking into tissues during inflammation.
As shown in Example 5 (below), blockade of KIM-1 binding to its receptor reduces or eliminates IgG1 production in the SRBC model system. In the MLR assay, the inventor has found that blockade of KIM-1 binding to its receptor reduces IFNγ production by lymphocytes. Without intending to be bound by theory, it is noted that the reduction in IgG1 production and the reduction in IFNγ production may represent two separate effects of KIM-1 blockade, and may not directly related. Therefore, when a KIM-1 antagonist is used to modulate immune function according to the invention, the KIM-1 antagonist may provide a beneficial effect through two separate mechanisms of action.
Fusion Proteins and Conjugated PolypeptidesSome embodiments of the invention involve a KIM-1 antagonist polypeptide wherein a KIM-1 moiety is fused to a heterologous moiety to form a KIM-1 fusion protein. KIM-1 fusion proteins, as opposed to a KIM-1 moiety alone, can be used to accomplish various objectives. Such objectives include, for example, increased serum half-life, improved bioavailability, in vivo targeting to a specific organ or tissue type, improved recombinant expression efficiency, improved host cell secretion, and ease of purification. Depending on the objective(s) to be achieved, the heterologous moiety can be inert or biologically active. Also, it can be chosen to be stably fused to the KIM-1 moiety or to be cleavable, in vitro or in vivo. Heterologous moieties to accomplish different objectives are known in the art.
As an alternative to expression of a KIM-1 fusion protein, a chosen heterologous moiety can be preformed and chemically conjugated to the KIM-1 moiety. In most cases, a chosen heterologous moiety will function similarly, whether fused or conjugated to the KIM-1 moiety. Therefore, in the following discussion of heterologous amino acid sequences, unless otherwise noted, it is to be understood that the heterologous sequence can be joined to the KIM-1 moiety in the form of a fusion protein or as a chemical conjugate.
Pharmacologically active polypeptides such as a KIM-1 polypeptide often exhibit rapid in vivo clearance, necessitating large doses to achieve therapeutically effective concentrations in the body. In addition, polypeptides smaller than about 20 kDa potentially undergo glomerular filtration, which sometimes leads to nephrotoxicity. Fusion or conjugation of relatively small polypeptides such as KIM-1 fragments can be employed to reduce or avoid the risk of such nephrotoxicity. Various heterologous amino acid sequences, i.e., polypeptide moieties or “carriers,” for increasing the in vivo stability, i.e., serum half-life, of therapeutic polypeptides are known.
Due to its long half-life, wide in vivo distribution, and lack of enzymatic or immunological function, essentially full-length human serum albumin (HSA), or an HSA fragment, is a preferred heterologous moiety. Through application of methods and materials such as those taught in Yeh et al., 1992, Proc. Natl. Acad. Sci. USA, 89:1904-1908 and Syed et al., 1997, Blood 89:3243-3252, HSA can be used to form a KIM-1 fusion protein or conjugate that displays pharmacological activity by virtue of the KIM-1 moiety while displaying significantly increased, e.g., 10-fold to 100-fold higher, in vivo stability. Preferably, the N-terminus of the HSA is fused to the C-terminus of the KIM-1 moiety. Since HSA is a naturally secreted protein, the HSA signal sequence can be exploited to obtain secretion of the KIM-1 fusion protein into the cell culture medium, when the fusion protein is produced in a eukaryotic, e.g., mammalian, expression system.
Some embodiments of the invention employ a KIM-1 polypeptide wherein a KIM-1 moiety is fused to an Fc region, i.e., the C-terminal portion of an Ig heavy chain constant region. Potential advantages of a KIM-1-Fc fusion include solubility, in vivo stability, and multivalency, e.g., dimerization. The Fc region used can be an IgA, IgD, or IgG Fc region (hinge-CH2-CH3). Alternatively, it can be an IgE or IgM Fc region (hinge-CH2-CH3-CH4). An IgG Fc region is preferred, e.g., an IgG1 Fc region or IgG4 Fc region. Materials and methods for constructing and expressing DNA encoding Fc fusions are known in the art and can be applied to obtain KIM-1 fusions without undue experimentation.
Preferably, the KIM-1-Fc fusion is constructed with an orientation wherein the KIM-1 moiety forms the amino-terminal portion of the fusion protein. For an example of construction and expression of an Fc fusion with this orientation, see, e.g., Wanner et al., U.S. Pat. No. 5,547,853 (pSAB152). Alternatively, the fusion can be constructed with the opposite orientation, i.e., wherein the KIM-1 moiety forms the carboxy-terminal portion of the fusion. For examples and discussion of this orientation, see, e.g., Lo et al., U.S. Pat. No. 5,541,087.
Some embodiments of the invention employ a KIM-1 fusion protein obtained by constructing a KIM-1 immunofusin DNA in accordance with Lo et al., U.S. Pat. No. 5,541,087. An immunofusin DNA includes a polynucleotide encoding a secretion cassette. The secretion cassette includes sequences encoding (in the 5′ to 3′ direction) a signal sequence, an immunoglobulin Fc region, and a KIM-1 moiety fused to the 3′ end of the secretion cassette. DNA can be expressed at high levels in a host cell, and the fusion protein is efficiently produced and secreted from the host cell. The secreted immunofusin can be collected from the culture media without the need for lysis of the host cell.
In some embodiments the DNA sequence encodes a proteolytic cleavage site between the KIM-1 moiety and the heterologous moiety. A cleavage site provides for the proteolytic cleavage of the encoded fusion protein, thus separating the Fc domain from the target protein. Useful proteolytic cleavage sites include amino acids sequences recognized by proteolytic enzymes such as trypsin, plasmin or enterokinase K.
A KIM-1 polypeptide construct can be incorporated into a replicable expression vector. Useful vectors include linear nucleic acids, plasmids, phagemids, cosmids and the like. An exemplary expression vector is pSAB152 (Wanner et al., U.S. Pat. No. 5,547,853. Another exemplary expression vector is pdC, in which the transcription of the immunofusin DNA is placed under the control of the enhancer and promoter of the human cytomegalovirus (Lo et al., 1991, Biochim. Biophys. Acta 1088:712; and Lo et al., 1998, Protein Engineering 11:495-500). An appropriate host cell can be transformed or transfected with a DNA that encodes a KIM-1 polypeptide, and is used for the expression and secretion of the KIM-1 polypeptide. Preferred host cells include immortal hybridoma cells, myeloma cells, 293 cells, Chinese hamster ovary (CHO) cells, Hela cells, and COS cells.
Fully intact, wild type Fc regions display effector functions that normally are unnecessary and undesired in an Fc fusion protein according to the present invention. Therefore, certain binding sites preferably are deleted from the Fc region during the construction of a KIM-1-Fc fusion protein. For example, since coexpression with the light chain is unnecessary, the binding site for the heavy chain binding protein, Bip (Hendershot et al., 1987, Immunol. Today 8:111-114), is deleted from the Fc region of IgE, such that this site does not interfere with the efficient secretion of the fusion protein. Likewise, the cysteine residues present in the Fc regions which are responsible for binding to the light chain of the immunoglobulin should be deleted or substituted with another amino acid, such that these cysteine residues do not interfere with the proper folding of the Fc region when it is produced as an immunofusin. Transmembrane domain sequences, such as those present in IgM, should be deleted.
The IgG1 Fc region is preferred. Alternatively, the Fc region of the other subclasses of immunoglobulin gamma (gamma-2, gamma-3 and gamma-4) can be used in the secretion cassette. The IgG1 Fc region of immunoglobulin gamma-1 that is preferably used in the secretion cassette includes the hinge region (at least part), the CH2 region, and the CH3 region. In some embodiments, the Fc region of immunoglobulin gamma-1 is a CH2-deleted-Fc, which includes part of the hinge region and the CH3 region, but not the CH2 region. A CH2-deleted-Fc has been described by Gillies et al., 1990, Hum. Antibod Hybridomas, 1:47. In some embodiments, the Fc regions of IgA, IgD, IgE, or IgM, are used.
KIM-1-Fc fusion proteins can be constructed in several different configurations. In one configuration the C-terminus of the KIM-1 moiety is fused directly to the N-terminus of the Fc moiety. In a slightly different configuration, a short linker, e.g., 2-10 amino acids, is incorporated into the fusion between the C-terminus of the KIM-1 moiety and the N-terminus of the Fc moiety. Such a linker provides conformational flexibility, which may improve biological activity in some circumstances. If a sufficient portion of the hinge region is retained in the Fc moiety, the KIM-1-Fc fusion will dimerize, thus forming a divalent molecule. A homogeneous population of monomeric Fc fusions will yield monospecific, bivalent dimers. A mixture of two monomeric Fc fusions each having a different specificity will yield bispecific, bivalent dimers.
KIM-1 conjugates can be constructed using methods known in the art. Any of a number of cross-linkers that contain a corresponding amino reactive group and thiol reactive group can be used to link KIM-1 to serum albumin. Examples of suitable linkers include amine reactive cross-linkers that insert a thiol reactive-maleimide. These include, e.g., SMCC, AMAS, BMPS, MBS, EMCS, SMPB, SMPH, KMUS, or GMBS. Other suitable linkers insert a thiol reactive-haloacetate group. These include, e.g., SBAP, SIA, SLAB and that provide a protected or non protected thiol for reaction with sulfhydryl groups to product a reducible linkage are SPDP, SMPT, SATA, or SAW all of which are commercially available (e.g., Pierce Chemicals). One skilled in the art can similarly envision with alternative strategies that will link the N-terminus of KIM-1 with serum albumin.
One skilled in the art can generate conjugates to serum albumin that are not targeted at the N-terminus of a KIM-1 polypeptide or at the thiol moiety on serum albumin. For example KIM-1-albumin fusions can be generated using genetic engineering techniques, wherein the KIM-1 moiety is fused to the serum albumin gene at its amino-terminus (N-ter), carboxy-terminus (C-ter), or at both ends.
Other derivatives of KIM-1 polypeptides include covalent or aggregate conjugates of modified KIM-1 or its fragments with other proteins or polypeptides, such as by synthesis in recombinant culture as additional N-termini, or C termini. For example, the conjugated peptide may be a signal (or leader) polypeptide sequence at the N-terminal region of the protein which co-translationally or post-translationally directs transfer of the protein from its site of synthesis to its site of function inside or outside of the cell membrane or wall (e.g., the yeast alpha-factor leader). KIM-1 polypeptides can be fused to heterologous peptides to facilitate purification or identification of the KIM-1 moiety (e.g., histidine/KIM-1 fusions). The KIM-1 moiety also can be linked to the peptide Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys (DYKDDDDK) (SEQ ID NO:) (Hopp et al., 1988, Biotechnology 6:1204). This sequence is highly antigenic and provides an epitope reversibly bound by a specific monoclonal antibody. Consequently, it facilitates assay and purification of the expressed recombinant protein. This sequence is specifically cleaved by bovine mucosal enterokinase at the residue immediately following the Asp-Lys pairing.
Expression systems employing gene fusion constructs have been used to enhance the production of proteins in bacteria. Employing a bacterial protein that is normally expressed at a very high level as the amino-terminal fusion partner of a fusion protein helps to ensure efficient transcription and translation of the message, and in some cases the secretion and solubilization of the fusion protein (Smith et al., 1988 Gene 67:31; Hopp et al., supra; La Vallie et al., 1993, Biotechnology 11:187).
Conjugated Polymers (Other Than Polypeptides)Some embodiments of the invention involve a KIM-1 polypeptide wherein one or more polymers are conjugated (covalently linked) to the KIM-1 polypeptide. Examples of polymers suitable for such conjugation include polypeptides (discussed above), sugar polymers and polyalkylene glycol chains. Typically, but not necessarily, a polymer is conjugated to the KIM-1 polypeptide for the purpose of improving one or more of the following: solubility, stability, or bioavailability.
A preferred class of polymer for conjugation to a KIM-1 polypeptide is a polyalkylene glycol. Polyethylene glycol (PEG) is a preferred polyalkylene glycol. PEG moieties, e.g., 1-6 PEG polymers, can be conjugated to each KIM-1 polypeptide to increase serum half life, as compared, to the KIM-1 polypeptide alone. PEG moieties are non-antigenic and essentially biologically inert. PEG moieties used in the practice of the invention may be branched or unbranched.
The number of PEG moieties attached to the KIM-1 polypeptide and the molecular weight of the individual PEG chains can vary. In general, the higher the molecular weight of the polymer, the fewer polymer chains attached to the polypeptide. Preferably, the average molecular weight of PEG is from 2 kDa to 100 kDa. More preferably, the average molecular weight is from 5 kDa to 20 kDa, with 8-12 kDa being most preferred.
The polymer, e.g., PEG, can be linked to the KIM-1 polypeptide through any suitable, exposed reactive group on the polypeptide. The exposed reactive group(s) can be, for example, an N-terminal amino group or the epsilon amino group of an internal lysine residue, or both. Naturally-occurring lysine residues can be exploited for this purpose, or lysine residue(s) can be engineered into the KIM-1 amino acid sequence. An activated polymer can react and covalently link at any free amino group on the KIM-1 polypeptide. Free carboxylic groups, suitably activated carbonyl groups, hydroxyl, guanidyl, imidazole, oxidized carbohydrate moieties and mercapto groups of the KIM-1 (if available) also can be used as reactive groups for polymer attachment.
Preferably, in a conjugation reaction, from about 1.0 to about 10 moles of activated polymer per mole of polypeptide, depending on polypeptide concentration, is employed. Usually, the ratio chosen represents a balance between maximizing the reaction while minimizing side reactions (often non-specific) that can impair the desired pharmacological activity of the KIM-1 moiety. Preferably, at least 50% of the biological activity of the KIM-1 polypeptide is retained, and most preferably nearly 100% is retained.
The polymer can be conjugated to the KIM-1 polypeptide using conventional chemistry. For example, a polyalkylene glycol moiety can be coupled to a lysine epsilon amino group of the KIM-1 polypeptide. Linkage to the lysine side chain can be performed with an N-hydroxylsuccinimide (NHS) active ester such as PEG succinimidyl succinate (SS-PEG) and succinimidyl propionate (SPA-PEG). Suitable polyalkylene glycol moieties include, e.g., carboxymethyl-NHS, norleucine-NHS, SC-PEG, tresylate, aldehyde, epoxide, carbonylimidazole, and PNP carbonate. These reagents are commercially available. Additional amine reactive PEG linkers can be substituted for the succinimidyl moiety. These include, e.g., isothiocyanates, nitrophenylcarbonates, epoxides, and benzotriazole carbonates. Conditions preferably are chosen to maximize the selectivity and extent or reaction. Such optimization of reaction conditions is within ordinary skill in the art.
PEGylation can be carried out by any of the PEGylation reactions known in the art. See, e.g., Focus on Growth Factors, 3:4-10, 1992; published European patent applications EP 0 154 316 and EP 0 401 384. PEGylation may be carried out using an acylation reaction or an alkylation reaction with a reactive polyethylene glycol molecule (or an analogous reactive water-soluble polymer).
PEGylation by acylation generally involves reacting an active ester derivative of polyethylene glycol. Any reactive PEG molecule can be employed in the PEGylation. A preferred activated PEG ester is PEG esterified to N-hydroxysuccinimide (NHS). As used herein, “acylation” includes the following types of linkages between the therapeutic protein and a water soluble polymer such as PEG: amide, carbamate, urethane, and the like. See, e.g., Bioconjugate Chem. 5:133-140, 1994. Reaction parameters should be chosed to avoid temperature, solvent, and pH conditions that would damage or inactivate the KIM-1 polypeptide.
Preferably, the connecting linkage is an amide. Preferably, the at least 95% of the resulting product is mono, di- or tri-PEGylated. However, some species with higher degrees of PEGylation may be formed in amounts depending on the specific reaction conditions used. Optionally, purified PEGylated species are separated from the mixture, particularly unreacted species, by conventional purification methods, including, e.g., dialysis, salting-out, ultrafiltration, ion-exchange chromatography, gel filtration chromatography, and electrophoresis.
PEGylation by alkylation generally involves reacting a terminal aldehyde derivative of PEG with KIM-1 in the presence of a reducing agent. In addition, one can manipulate the reaction conditions to favor PEGylation substantially only at the α-amino group of the N-terminus of KIM-1 (i.e., a mono-PEGylated protein). In either case of mono-PEGylation or poly-PEGylation, the PEG groups are preferably attached to the protein via a —CH2—NH— group. With particular reference to the —CH2— group, this type of linkage is known as an “alkyl” linkage.
Derivatization via reductive alkylation to produce a mono-PEGylated product exploits differential reactivity of different types of primary amino groups (lysine versus the N-terminal) available for derivatization. The reaction is performed at a pH that allows one to take advantage of the pKa differences between the ε-amino groups of the lysine residues and that of the α-amino group of the N-terminal residue of the protein. By such selective derivatization, attachment of a water soluble polymer that contains a reactive group such as an aldehyde, to a protein is controlled: the conjugation with the polymer takes place predominantly at the N-terminus of the protein and no significant modification of other reactive groups, such as the lysine side chain amino groups, occurs. The polymer molecules used in both the acylation and alkylation approaches may be selected from among water soluble polymers as described above. The polymer selected should be modified to have a single reactive group, such as an active ester for acylation or an aldehyde for alkylation, preferably, so that the degree of polymerization may be controlled as provided for in the present methods. An exemplary reactive PEG aldehyde is polyethylene glycol propionaldehyde, which is water stable, or mono C1-C10 alkoxy or aryloxy derivatives thereof (see, U.S. Pat. No. 5,252,714). The polymer may be branched or unbranched. For the acylation reactions, the polymer(s) selected should have a single reactive ester group. For reductive alkylation, the polymer(s) selected should have a single reactive aldehyde group. Generally, the water soluble polymer will not be selected from naturally-occurring glycosyl residues since these are usually made more conveniently by mammalian recombinant expression systems.
Methods for preparing a PEGylated KIM-1 generally includes the steps of (a) reacting a KIM-1 protein or polypeptide with polyethylene glycol (such as a reactive ester or aldehyde derivative of PEG) under conditions whereby the molecule becomes attached to one or more PEG groups, and (b) obtaining the reaction product(s). In general, the optimal reaction conditions for the acylation reactions will be determined case by case based on known parameters and the desired result. For example, the larger the ratio of PEG:protein, the greater the percentage of poly-PEGylated product.
Reductive alkylation to produce a substantially homogeneous population of mono-polymer/KIM-1 generally includes the steps of: (a) reacting a KIM-1 polypeptide with a reactive PEG molecule under reductive alkylation conditions, at a pH suitable to pen-nit selective modification of the α-amino group at the amino terminus of KIM-1; and (b) obtaining the reaction product(s).
For a substantially homogeneous population of mono-polymer/KIM-1 polypeptide, the reductive alkylation reaction conditions are those that permit the selective attachment of the water soluble polymer moiety to the N-terminus of KIM-1. Such reaction conditions generally provide for pKa differences between the lysine amino groups and the α-amino group at the N-terminus (the pKa being the pH at which 50% of the amino groups are protonated and 50% are not). The pH also affects the ratio of polymer to protein to be used. In general, if the pH is lower, a larger excess of polymer to protein will be desired (i.e., the less reactive the N-terminal α-amino group, the more polymer needed to achieve optimal conditions). If the pH is higher, the polymer:protein ratio need not be as large. (Because more reactive groups are available, fewer polymer molecules are needed). For purposes of the present invention, the preferred pH is in the range of 3-9, preferably 3-6.
KIM-1 polypeptides can include a tag, e.g., a moiety that can be subsequently released by proteolysis. Thus, the lysine moiety can be selectively modified by first reacting a His-tag modified with a low molecular weight linker such as Traut's reagent (Pierce) which will react with both the lysine and N-terminus, and then releasing the his tag. The polypeptide will then contain a free SH group that can be selectively modified with a PEG containing a thiol reactive head group such as a maleimide group, a vinylsulfone group, a haloacetate group, or a free or protected SH.
Traut's reagent can be replaced with any linker that will set up a specific site for PEG attachment. By way of example, Traut's reagent could be replaced with SPDP, SMPT, SATA, or SATP (all available from Pierce). Similarly one could react the protein with an amine reactive linker that inserts a maleimide (for example SMCC, AMAS, BMPS, MBS, EMCS, SMPB, SMPH, KMUS, or GMBS), a haloacetate group (SBAP, SIA, SIAB), or a vinylsulfone group and react the resulting product with a PEG that contains a free SH. The only limitation to the size of the linker that is employed is that it cannot block the subsequent removal of the N-terminal tag.
In some embodiments, the polyalkylene glycol moiety is coupled to a cysteine group of the KIM-1 polypeptide. Coupling can be effected using, e.g., a maleimide group, a vinylsulfone group, a haloacetate group, and a thiol group.
Optionally, the KIM-1 polypeptide is conjugated to the polyethylene glycol moiety through a labile bond. The labile bond can be cleaved in, e.g., biochemical hydrolysis, proteolysis, or sulfhydryl cleavage. For example, the bond can be cleaved under in vivo (physiological) conditions.
The reactions may take place by any suitable method used for reacting biologically active materials with inert polymers, preferably at about pH 5-8, e.g., pH 5, 6, 7, or 8, if the reactive groups are on the alpha amino group at the N-terminus. Generally the process involves preparing an activated polymer and thereafter reacting the protein with the activated polymer to produce the soluble protein suitable for formulation.
One or more sites on a KIM-1 polypeptide can be coupled to a polymer. For example, one two, three, four, or five PEG moieties can be attached to the polypeptide. In some embodiments, a PEG moiety is attached at the amino terminus.
Anti-KIM-1 AntibodiesAn anti-KIM-1 antibody or antigen-binding fragment thereof used according to the invention can be any of various types of molecules, including, but not limited to, a polyclonal antibody, monoclonal antibody (mAb), humanized antibody, fully human antibody, chimeric antibody, single-chain antibody, diabody, Fab fragment, Fab′ fragment, F(ab′)2, Fv fragment, Fd fragment, dAb fragment, and complementarity determining region (CDR)-containing fragment.
As used herein: Fd means a fragment that consists of the VH and CH1 domains; Fv means a fragment that consists of the VL and VH domains of a single arm of an antibody; and dAb means a fragment that consists of a VH domain (Ward et al., 1989, Nature 341:544-546). As used herein, single-chain antibody (scFv) means an antibody in which a VL region and a VH region are paired to form a monovalent molecules via a synthetic linker that enables them to be made as a single protein chain (Bird et al., 1988, Science 242:423-426; Huston et al., 1988, Proc. Natl. Acad. Sci. USA 85:5879-5883). As used herein, diabody means a bispecific antibody in which VH and VL domains are expressed on a single polypeptide chain, but using a linker that is too short to allow for pairing between the two domains on the same chain, thereby forcing the domains to pair with complementary domains of another chain and creating two antigen binding sites (see e.g., Holliger, et al., 1993, Proc. Natl. Acad. Sci. USA 90:6444-6448; and Poljak et al., 1994, Structure 2:1121-1123.
Generally applicable methods for obtaining antibodies are known in the art. For a review of methods and materials useful for making anti-KIM-1 antibodies, see e.g., Harlow et al., 1988, Antibodies, A Laboratory Manual; Yelton, et al., 1981, Ann. Rev. Biochem., 50:657-80.; and Ausubel et al., 1989, Current Protocols in Molecular Biology (New York: John Wiley & Sons). Antigen-binding properties of anti-KIM-1 antibodies can be determined by one of ordinary skill in the art, using any of various conventional methods, including, e.g., radioimmunoassay, immunoblot assay and ELISA. Other suitable techniques for producing an antibody of the invention involve in vitro exposure of lymphocytes to a KIM-1 polypeptide, or screening of libraries of antibodies in phage or similar vectors. See, e.g., Huse et al., 1989. Science, 246:1275-1281.
VectorsThe invention provides vectors comprising the nucleic acids encoding KIM-1 polypeptides. The choice of vector and expression control sequences to which the nucleic acids of this invention is operably linked depends on the functional properties desired, e.g., protein expression, and the host cell to be transformed. A vector of the present invention may be at least capable of directing the replication or insertion into the host chromosome, and preferably also expression, of the structural gene included in the rDNA molecule.
Expression control elements useful for regulating the expression of an operably linked coding sequence are known in the art. Examples include, but are not limited to, inducible promoters, constitutive promoters, secretion signals, and other regulatory elements. When an inducible promoter is used, it can be controlled, e.g., by a change in nutrient status, or a change in temperature, in the host cell medium.
The vector can include a prokaryotic replicon, i.e., a DNA sequence having the ability to direct autonomous replication and maintenance of the recombinant DNA molecule extra-chromosomally in a prokaryotic host cell, such as a bacterial host cell, transformed therewith. Such replicons are well known in the art. In addition, vectors that include a prokaryotic replicon may also include a gene whose expression confers a detectable marker such as a drug resistance. Typical of bacterial drug resistance genes are those that confer resistance to ampicillin or tetracycline.
Vectors that include a prokaryotic replicon can further include a prokaryotic or bacteriophage promoter for directing expression of the coding gene sequences in a bacterial host cell. Promoter sequences compatible with bacterial hosts are typically provided in plasmid vectors containing convenient restriction sites for insertion of a DNA segment of the present invention. Examples of such vector plasmids are pUC8, pUC9, pBR322 and pBR329 (BioRad Laboratories), pPL and pKK223 (Pharmacia). Any suitable prokaryotic host can be used to express a recombinant DNA molecule encoding a protein of the invention.
Eukaryotic cell expression vectors are known in the art and are commercially available. Typically, such vectors contain convenient restriction sites for insertion of the desired DNA segment. Exemplary vectors include pSVL and pKSV-10 (Pharmacia), pBPV-1, pML2d (International Biotechnologies), pTDT1 (ATCC 31255).
Eukaryotic cell expression vectors may include a selectable marker, e.g., a drug resistance gene. A preferred drug resistance gene confers neomycin resistance, i.e., the neomycin phosphotransferase (neo) gene (Southern et al., 1982, J. Mol. Anal. Genet. 1:327-341).
To express the antibodies or antibody fragments, DNAs encoding partial or full-length light and heavy chains are inserted into expression vectors. Expression vectors include plasmids, retroviruses, cosmids, YACs, EBV derived episomes, and the like. The expression vector and expression control sequences are chosen to be compatible with the expression host cell used. The antibody light chain gene and the antibody heavy chain gene can be inserted into separate vectors. In some embodiments, both genes are inserted into the same expression vector.
A convenient vector is one that encodes a functionally complete human CH or CL immunoglobulin sequence. Preferably, restriction sites engineered so that any VH or VL sequence can be easily inserted and expressed, as described above. In such vectors, splicing usually occurs between the splice donor site in the inserted J region and the splice acceptor site preceding the human C region, and also at the splice regions that occur within the human CH exons. Polyadenylation and transcription termination occur at native chromosomal sites downstream of the coding regions. The recombinant expression vector can also encode a signal peptide that facilitates secretion of the antibody chain from a host cell.
Preferred regulatory sequences for mammalian host cell expression include viral elements that direct high levels of protein expression in mammalian cells, such as promoters and enhancers derived from retroviral LTRs, cytomegalovirus (CMV) (such as the CMV promoter/enhancer), Simian Virus 40 (SV40) (such as the SV40 promoter/enhancer), adenovirus, (e.g., the adenovirus major late promoter (AdMLP)), polyoma and strong mammalian promoters such as native immunoglobulin and actin promoters. For further description of viral regulatory elements, and sequences thereof, see e.g., U.S. Pat. No. 5,168,062 by Stinski, U.S. Pat. No. 4,510,245 by Bell et al. and U.S. Pat. No. 4,968,615 by Schaffner et al.
The recombinant expression vectors may carry sequences that regulate replication of the vector in host cells (e.g., origins of replication) and selectable marker genes. The selectable marker gene facilitates selection of host cells into which the vector has been introduced (see e.g., U.S. Pat. Nos. 4,399,216, 4,634,665 and 5,179,017, all by Axel et al.). For example, typically the selectable marker gene confers resistance to drugs, such as G418, hygromycin or methotrexate, on a host cell into which the vector has been introduced. Preferred selectable marker genes include the dihydrofolate reductase (DHFR) gene (for use in dhfr− host cells with methotrexate selection/amplification) and the neo gene (for G418 selection).
Nucleic acid molecules encoding KIM-1 polypeptides and anti-KIM-1 antibodies, and vectors comprising these nucleic acid molecules, can be used for transformation of a suitable host cell. Methods for introduction of exogenous DNA into mammalian cells are well known in the art and include dextran-mediated transfection, calcium phosphate precipitation, polybrene-mediated transfection, protoplast fusion, electroporation, encapsulation of the polynucleotide(s) in liposomes, and direct microinjection of the DNA into nuclei. In addition, nucleic acid molecules may be introduced into mammalian cells by viral vectors.
Transformation of host cells can be accomplished by conventional methods suited to the vector and host cell employed. With regard to transformation of prokaryotic host cells, electroporation and salt treatment methods can be employed (Cohen et al., 1972, Proc. Natl. Acad. Sci. USA 69:2110-2114). With regard to transformation of vertebrate cells, electroporation, cationic lipid or salt treatment methods can be employed. See, e.g., Graham et al., 1973, Virology 52:456-467; Wigler et al., 1979, Proc. Natl. Acad. Sci. USA 76:1373-1376).
Host cells can be prokaryotic or eukaryotic. Preferred eukaryotic host cells include, but are not limited to, yeast and mammalian cells. Examples of useful eukaryotic host cells include Chinese hamster ovary (CHO) cells (ATCC Accession No. CCL61), NIH Swiss mouse embryo cells NIH-3T3 (ATCC Accession No. CRL1658), and baby hamster kidney cells (BHK). Mammalian cell lines available as hosts for expression are known in the art and include many immortalized cell lines available from the American Type Culture Collection (ATCC). These include, inter alis, Chinese hamster ovary (CHO) cells, NSO, SP2 cells, HeLa cells, baby hamster kidney (BHK) cells, monkey kidney cells (COS), human hepatocellular carcinoma cells (e.g., Hep G2), A549 cells, and a number of other cell lines.
Expression of polypeptides from production cell lines can be enhanced using known techniques. For example, the glutamine synthetase (GS) system is commonly used for enhancing expression under certain conditions. See, e.g., European Patent Nos. 0216846, 0256055, and 0323997 and European Patent Application No. 89303964.4.
FormulationsCompositions containing KIM-1 polypeptides, anti-KIM-1 antibodies, or antigen binding fragments of anti-KIM-1 antibodies may contain suitable pharmaceutically acceptable carriers. For example, they may contain excipients and/or auxiliaries that facilitate processing of the active compounds into preparations designed for delivery to the site of action. Suitable formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form, for example, water-soluble salts. In addition, suspensions of the active compounds 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 that increase the viscosity of the suspension include, for example, sodium carboxymethyl cellulose, sorbitol and dextran. Optionally, the suspension may also contain stabilizers. Liposomes also can be used to encapsulate the molecules of the invention for delivery into cells or interstitial spaces. Exemplary pharmaceutically acceptable carriers are physiologically compatible solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, water, saline, phosphate buffered saline, dextrose, glycerol, ethanol and the like. In some embodiments, the composition comprises isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, or sodium chloride. In some embodiments, the compositions comprise pharmaceutically acceptable substances such as wetting or minor amounts of auxiliary substances such as wetting or emulsifying agents, preservatives or buffers, which enhance the shelf life or effectiveness of the active ingredients.
Compositions of the invention may be in a variety of forms, including, for example, liquid, semi-solid and solid dosage forms, such as liquid solutions (e.g., injectable and infusible solutions), dispersions or suspensions. The preferred form depends on the intended mode of administration and therapeutic application. In some embodiments, compositions are in the form of injectable or infusible solutions, such as compositions similar to those used for passive immunization of humans.
The composition can be formulated as a solution, micro emulsion, dispersion, liposome, or other ordered structure suitable to high drug concentration. Sterile injectable solutions can be prepared by incorporating the active ingredient in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active ingredient into a sterile vehicle that contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying that yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof, the proper fluidity of a solution can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prolonged absorption of injectable compositions can be brought about by including in the composition an agent that delays absorption, for example, monostearate salts and gelatin.
In some embodiments, the active ingredient is formulated with a controlled-release formulation or device. Examples of such formulations and devices include implants, transdermal patches, and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, for example, ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Methods for the preparation of such formulations and devices are known in the art. See e.g., Sustained and Controlled Release Drug Delivery Systems, 1978, J. R. Robinson, ed., Marcel Dekker, Inc., New York.
Supplementary active compounds also can be incorporated into the compositions.
In some embodiments, a KIM-1 polypeptide, anti-KIM-1 antibody or fragment thereof is coadministered with a second immunomodulatory agent, e.g., BAFF-R-Ig, LTB-R-Ig, CTLA4-Ig, anti-CD40L, or an anti-CD20 monoclonal antibody.
Dosage regimens may be adjusted to provide the optimum desired response. For example, a single bolus may be administered, several divided doses may be administered over time or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation. It is advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the mammalian subjects to be treated, each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
In some embodiments, a therapeutically effective dose for a KIM-1 polypeptide is in the range of 0.1 to 100 mg/kg. In some embodiments the therapeutically effective dose is in the range of 0.5 to 50 mg/kg. In some embodiments, the therapeutically effective dose is in the range of 1.0 to 10 mg/kg, e.g., about 5 mg/kg. Determination of a therapeutically effective dose can also be assessed by performing in vitro experiments that measure the concentration of the modifying agent required to coat target cells (KIM-1 or KIM-1-Receptor-positive cells depending on the modifying agent) for suitable (therapeutic) time periods. FACS and ELISA receptor-ligand binding assays can be used to monitor the cell coating reaction. Based on the results of such in vitro binding assays, a range of suitable modifying agent concentrations can be selected.
Molecules of the invention can be formulated into pharmaceutical compositions by admixture with pharmaceutically acceptable nontoxic excipients or carriers. Such compositions can be prepared for use in parenteral administration, particularly in the form of liquid solutions or suspensions. The composition can be administered in unit dosage form and can be prepared by any suitable method. Such methods are known in the art. For example, see Remington's Pharmaceutical Sciences (Mack Pub. Co., Easton, Pa. 1980).
Liquid dosage forms include pharmaceutically acceptable solutions, emulsions, microemulsions, and suspensions. In addition to the active compound, the liquid dosage form may contain inert ingredients including water, ethyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethylformamide, oils, glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols, fatty acid esters of sorbitan, and mixtures thereof.
Injectable depot formulations can be made by forming microencapsulated matrices of the drug in biodegradable polymers such as polylactide-polyglycolide. Depending on the ratio of drug to polymer, and the nature of the polymer employed, the rate of drug release can be controlled. Other exemplary biodegradable polymers include polyorthoesters and polyanhydrides. Depot injectable formulations also can be prepared by entrapping the drug in liposomes or microemulsions that are compatible with body tissues.
EXAMPLESThe invention is further illustrated by the following experimental examples. The examples are provided for illustrative purposes only, and are not to be construed as limiting the scope or content of the invention in any way.
Example 1 Human KIM-1 Extracellular Domain-Fc Construct (pHI105)The extracellular domain (residues 1-290) of human KIM-1 was fused to the Fc portion of human IgG1 (hinge, CH2, CH3) and cloned into pEAG347, a Biogen mammalian expression plasmid. The plasmid contained a tandem promotor for constitutive expression and the dihydrofolate reductase gene for methotrexate selection of stably expressing cell lines. The amino acid sequence of the encoded fusion polypeptide was as follows:
The signal sequence is indicated by an underline. The Fc hinge is indicated by a box.
DNA encoding residues 1-129 of human KIM-1 fused to the Fc portion of human IgG1 (hinge, CH2, CH3) was cloned into pEAG347, a Biogen mammalian expression plasmid containing a tandem promotor for constitutive expression and the dihydrofolate reductase gene for methotrexate selection of stably expressing cell lines. The amino acid sequence of the encoded fusion polypeptide was as follows:
The extracellular domain (residues 1-290) of human KIM-1 was fused to a short C-terminal peptide [VEHHHHHH] including a repeat of 6 histidine residues and cloned into pCA125, a BIOGEN mammalian expression plasmid containing a CMV promotor for transient constitutive expression in mammalian cells. The amino acid sequence of the encoded fusion polypeptide was as follows:
A PCR-amplified ectodomain of murine kim-1 flanked by NotI and SalI sites was fused with human IgG1Fc (isolated from EAG409 as a SalI-NotI fragment) and cloned into Ebna 293 cell expression vector CH269 (construct PEM073-6) and CHO cell expression vector pV90 (construct PEM078-1). The SalI site is at the junction between kim1 and Fc. The resulting nucleotide sequence of the ORF for the fusion protein was as follows (SalI site in upper case):
The translated sequence of mukim-1 ectodomain-human Fc was as follows. Two junction amino acids contributed by the SalI site are indicated in bold:
The immune response of rodents to sheep red blood cells (SRBC) depends upon competent T cell interaction with APCs and B cells. Therefore the anti-SRBC response is a useful model to examine the role that cellular proteins on lymphocytes and APC play in the development and maturation of the immune response. The anti-SRBC response in mice consists of production of IgM and of the various IgG isotypes, including high levels of the IgG1 isotype, with considerable levels of IgG2a and IgG2b seen as well. IgG1 is considered to be an isotype that is driven by a Th2-mediated immune response, which is characterized by the expression of cytokines such as Il-4, Il-5, and Il-13. IgG2a and IgG2b isotypes are more characteristic of a Th1-driven immune response, and are associated with expression of Il-12. Finally, the IgG3 isotype is typical of T-independent immune responses. All 4 isotypes are represented in the anti-SRBC response.
The course of the anti-SRBC response was followed in mice treated with murine KIM-1-Ig fusion protein (mKIM-1-Ig) to interrupt KIM-1-dependent activity on T cells. Mice were treated the day before challenge (D-1) with 150 ugs/mouse challenged with 100 μl of a 10% solution of SRBC (Colorado Serum Company) in PBS on day 0, then treated again with 150 μg of mKIM-1-Ig on days 3 and 6. The mice were bled for a serum samples on days 7, 14, 21, and 30 following immunization, and anti-SRBC antibody titers were obtained using the hemagglutination assay. This assay relied on the ability of antibodies to crosslink and cluster (“agglutinate”) SRBC based on their pentameric structure (for IgM) or on the presence of a third species anti-idiotypic antisera (for the Ig classes).
In brief, the protocol was as follows. Serum samples were diluted as appropriate (1:15 to 1:200), depending on the isotype being measured, and the day of the response). then titered in 1:2 steps using 96 well assay plates which we obtained from Corning (Costar® #3795). For the IgM assay, the sera samples were assayed in duplicate. 25 μl of 10% SRBC in glucose-PBS (G-PBS) was added to the wells and the agglutination response was allowed to develop for 1 hour at 37° C. For the Ig assays, serum samples were loaded into the plates and diluted in triplicate. 25 μl of 1% 2-mercaptoethanol (Sigma), diluted in G-PBS, was added to each serum sample series, then the plate was incubated for 30 minutes at 37° C. This was done to break all the disulfide bonds which hold together IgM pentamers, and thus to eliminate any IgM background. Then, 25 μl of 10% SRBC in G-PBS, and 25 μl of a 1:250 dilution in G-PBS of anti-idiotypic antisera (goat anti-mouse IgG1, IgG2a, IgG2b, or IgG3, all from Southern Biotechnology Associates) was added to the first 2 of each triplicate to cross-link the anti-SRBC IgGs of that subtype present. The third well of each triplicate was left uncrosslinked to serve as a control for any residual IgM activity that might have survived the 2-mercaptoethanol treatment. The plates were incubated for 1 hour at 37° C. All assay plates were left overnight at 4° C. to stabilize the resulting hemagglutination before being scored and photographed. All titers were scored as the last dilution that gave a positive agglutination readout.
The effect of mKIM-1-Ig treatment on the anti-SRBC response was compared to control groups of mice not challenged with SRBC, or challenged with SRBC but dosed with anti-CD40L, nonspecific polyclonal hIgG, or PBS. The unchallenged and anti-CD40L-treated mice had no anti-SRBC response, as expected. The mice given SRBC and dosed either with PBS or hIgG had robust antibody titers to all classes of Ig tested. The mice treated with mKIM-1-Ig in contrast had a very striking and specific defect in the IgG1 anti-SRBC isotype. In 2 independent experiments using the Balb/c strain of mice, markedly defective levels of IgG1 anti-SBRC were detected (
GVHD is modeled in the mouse using parental into F1 cell transplantation regimens. Splenocytes from the DBA2 strain of mice are injected iv into (DBA2×57B1/6) F1 mice, which are referred to as B6D2F1. The injected splenocytes constitute the graft, and the DBA2 mouse is the donor of that graft. The F1 mouse which receives the graft is the host. Donor T cells present in the graft recognize half of the MHC markers (haplotypes) on host cells as foreign, because they are derived from the other, C57B1/6 parent. This induces a donor T cell response against the host resulting in GVHD. When DBA/2 parental splenocytes are injected into the B6D2F1 host, chronic GVHD develops. In contrast, when C57B1/6 splenocytes are injected into the B6D2F1 host, acute GVHD develops. Although it remains unclear what underlying mechanism is responsible for the distinct disease outcomes using these 2 injection protocols it is believed that the cytokines expressed by the cells contained within the DBA/2 splenocyte graft favor the development of chronic GVHD while the cytokines expressed by the cells contained within the C5781/6 splenocyte graft favor the development of acute GVHD. Reagents which interfere with T cell interactions with antigen presenting cells (e.g., dendritic cells, macrophages, B cells: APC) effectively block both acute and chronic GVHD.
KIM-1 antagonists modify the development of an immunological response in a mouse model of chronic GVHD. The ability to block chronic GVHD includes effects on B cell activation and proliferation, and on the generation of secreted IgG. Mice are treated intraperitoneally (ip) with KIM-1 antagonists or modifying agents, control treatments, or are left untreated. 4 hours later mice receive 1×108 splenocytes isolated from DBA/2 mice, in an 0.5 ml injection given intravenously (iv). The iv injected DBA/2 splenocytes constituted the allograft. 2, 4, and 6 days after the graft is given, the mice are again treated with KIM-1 antagonists or modifying agents or with control treatments. An additional control group of mice receives 1×108 B6D2F1 splenocytes, which cannot induce disease in B6D2F1 recipients. Alternatively, ungrafted and untreated B6D2F1 mice are used as controls. Fourteen days after the graft is given the mice are sacrificed and examined for evidence of disease.
Untreated graft-recipient mice manifest a variety of symptoms that are indicative of the development of chronic GVHD. Splenomegaly, or enlargement of the spleen, is evidence that donor T cells and host B cells have become activated, and are undergoing polyclonal expansion, with dramatic increases in cell number. The appearance of cell surface proteins such as CD69 on a subset of B cells is indicative of B cell activation. The loss of L-selectin molecules from CD4+ and CD8+ T cells is evidence of T cell activation. The secretion of Ig molecules, such as IgG classes, IgA, and IgE, either into the serum, or in in vitro cell culture assays, indicates that B cells have become activated, and have switched their Ig class. In this regard the appearance of anti-self Igs in the serum or in in vitro cell culture assays shows that Igs that are being produced have inappropriate autoantigen recognition. Finally, survivorship can be measured as an outcome of different treatment regimens. Treatment with KIM-1 antagonists (e.g., KIM-1-Ig) or blocks these readouts of the development of chronic GVHD, as shown by reduction in the extent of splenomegaly, reduction in the polyclonal expansion of lymphocyte populations, reduction in the appearance or disappearance of cell surface markers indicating lymphocyte activation, reduction of Ig secretion, and/or reduction in mortality.
We compare control mice to untreated allograft-recipient mice to examine the extent of splenomegaly, B cell activation, and Ig secretion during GVHD. Anti-CD40L mAb MR1 is used as a positive control in these experiments, since it has been previously shown that blocking the CD40L/CD40 interaction is an effective means of interfering with the development of chronic GVHD (Durie et al., 1994, J. Clin. Invest. 94: 1333-1338). To investigate cell populations affected by treatment with KIM-1 antagonists FACS analyses are performed on splenocytes taken from the recipient mice 14 days after graft injection. Spleen cells from 3-4 mice per group are isolated and pooled. Activation of recipient B cells is a defining feature of chronic GVHD. In mice undergoing chronic GVHD a small but readily visible proportion of the B200+ B cells express the activation marker CD69. Therefore CD69 expression is used as a measure of the extent of disease. Total IgG in cultures of splenocytes in mice from different treatment groups is also determined, sice the expression of CD69 by B cells is indicative of their activation state.
In the mouse model the development of the disease is dependent on the Th2 cytokine 114, and can be blocked by treating with anti-114 mAb. Such treatment blocks the expansion of host B cells, and the concomitant hyper-Ig production. The development of GVHD can be followed in a number of ways. The expansion of the donor T cell and host B cell populations is measured by the spleen index, which is the ratio of spleen weight to body weight, normalized to control (non-diseased) mice. The activation of B cells in diseased mice is measured using analyses of B cell activation markers. Finally, the effects of B cell activation is seen in the levels of Ig in circulation (e.g., in serum) or produced by cultures of host splenocytes harvested several weeks after disease induction. Circulating Ig in diseased animals will contain anti-self antibodies. Ultimately, diseased animals succumb to kidney and other organ failure due to accumulated Ig deposition, and therefore survivorship is a relevant measure of disease activity.
Example 7 SCID-hu Mouse ModelsIt is possible to study human immune responses in the SCID-hu mouse. For example, SCID mice are injected intraperitoneally with 2-5×107 human peripheral blood mononuclear cells, and these cells reside and function in the gut for some time, and respond to antigen challenge. NOD-SCID mice are reconstituted with human PBLs and these mice have the additional advantage of the seeding of human cells (T, B, APC) into the spleen, where systemic immune responses may be supported. Appropriate models are discussed in Berney et al., 2001, Transplantation 72:133-140. Other models of immune responses use the SCID/beige mouse and involve cotransplantation of PBLs or fetal cells with fetal mesenteric lymph nodes to provide support for immune responses (Carballido et al., 2000, Nat. Med. 6:103-106.
SCID-hu or NOD-SCID-hu mice are reconstituted with peripheral blood mononuclear cells (PBMCs) isolated from tetanus-toxoid (TT) immunized human donors. SCID-hu mice so reconstituted have human cells residing in various compartments, including the peritoneum. NOD-SOD-hu mice so reconstituted have human T cells residing in various compartments including within their secondary lymphoid organs, such as the spleen. Primary immune responses are induced in these reconstituted mice by immunization with antigen coupled to TT, or to an antigenic portion of TT, or to liposomes, or to liposomes containing TT. Mice so reconstituted and challenged produce a high titer (>1:1000) Ig response to antigen (e.g., NP, DNP, KLH, OVA, HIV gp120 or portions thereof, melanoma-associated antigen GD2, and ovine mucin, are just a few of many examples). Some examples are presented in Ifverson et al., 1995, Immunology 84:111-116. Mice so reconstituted and then treated with KIM-1 antagonists or modifying agents do not produce a high titer to antigen challenge.
In another methodology, SCID-hu mice are reconstituted with fetal human bone, thymus, fragments of skin, and mesenteric lymph nodes (MLN). The presence of MLN is sufficient to support robust immune responses to TT-immunization (and, since all donor tissue is fetal, this is strictly a primary immune response). This model is discussed in detail in Carballido et al., 2000, Nat. Med. 6:103-106. TT-immunization causes human lymphocyte proliferation, and activation, and IgM and IgG-secretion by B cells. Treatment of SCID mice so reconstituted with KIM-1 antagonists or modifying agents reduces the human lymphocyte proliferation, activation, and the secretion of immunoglobulins upon TT-challenge.
In a modification of these models, or other similar NOD-SCID-hu or SCID-hu models, secondary immune responses are measured in a disease setting, e.g., of delayed type hypersensitivity (DTH). In this instance the TT-challenge is given in the footpad of SCID or NOD-SCID mice reconstituted with PBMCs from TT-immune individuals, and the swelling of the footpad is measured in response. The DTH responses relies on the presence of human memory T cells in circulation in the reconstituted mouse. Such models can also be used to detect the possible rejection of donor tissue in transplant patients, as in the “trans vivo” models. An example of this type of approach is discussed in Carrodeguas et al., 1999, Hum. Immunol. 60: 640-651. Treatment of mice so reconstituted with KIM-1 antagonists or modifying agents prevents DTH responses. Other models of human disease responses in the SCID mouse include transfer of splenocytes or PBMCs from autoimmune patients in the mouse, whereby they continue expression of immunoglobulins and other markers of disease (see Martino and Grinaldim 1997, In: Immunology Methods Manual, vol 3. Lefkovits, ed. Academic Press, San Diego). Treatment of these mice with KIM-1 antagonists or modifying agents prior to the transfer of autoimmune cells from patients reduces the expression of immunoglobulins or other markers of the autoimmune pathology.
A very valuable methodology utilizing the SCID mouse involve the xenografting of disease tissue onto the recipient mouse. Methods of transferring skin from psoriasis or atopic dermatitis patients for instance are widely used models of these diseases. Atopic dermatitis is a Th2 mediated cellular immune disease that can be modeled in SCID mice by transferring the PBMCs and biopsies of skin together to the recipient mouse. Treatment of these mice with KIM-1 antagonists or modifiers prevents the cellular accumulation and local cytokine secretion which is evidence of activation of lymphocytes and effector cells (eosinophils, basophils, etc.) in the skin graft. This is evidence of efficacy in preventing dermatitis in the donor patient.
Example 8 Other Murine Models of Atopic DiseaseUseful models of allergy, asthma, airway hypersensitivity (AHR), and other atopic diseases are run in the mouse. For example, allergic skin inflammation is induced by epicutaneous sensitization with antigen. In one example the antigen is ovalbumin (OVA). The Th2 response to this sensitization is shown by the presence of eosinophils in the skin, local expression in the skin of Th2 cytokines, and airway hyperresponsiveness (AHR) to inhaled antigen. Eosinophils are absent from the skin of OVA-sensitized mice that are first treated with KIM-1 antagonists or modifiers, and the level of Th2 cytokines is reduced. Mice that are repeatedly sensitized produce OVA-specific IgE, and their splenocytes secrete the Th2 cytokines IL-4 and IL-5 following in vitro stimulation with OVA. These readouts of the Th2 immune response are blocked upon treatment with KIM-1 antagonists or modifiers. Alternatively, mice (e.g., BALB/c mice) can be sensitized with an i.p. injection of antigen (day 0), then rechallenged with intranasal antigen 3 weeks later (once) and 4 weeks later (3 times: days 26, 27, 28, e.g.). This produces lung hyperresponsiveness (AHR), which is mediated by Th2 cytokines such as IL-13. This Th2 immune response is blocked upon treatment with KIM-1 antagonists or modifiers.
Using the OVA-specific TCR transgenic model (DO11.10), we induce an OVA-specific immune response, then transfer Th20VA-specific T cells to naive recipients, which then are challenged with OVA-aerosal. These mice rapidly develop antigen-specific AHR. This response is blocked when mice are treated with KIM-1 antagonists or modifiers prior to OVA aerosal challenge.
Methacholine aerosol treatment induces the recruitment of eosinophils to the lung, causing AHR in mice. Treatment of mice with KIM-1 antagonists or modifying agents will block AHR development.
Example 9 Collagen-Induced ArthritisIn this murine model of arthritis, collagen is used to trigger T cell-mediated B cell activation and autoantibody production, which attacks the joints, resulting in a condition which resembles rheumatoid arthritis. In various stains of mice this response is dominated by high titers of IgG1. In particular, in mice lacking Il-12 by genetic deficiency (Il-12 knockout mice: Il-12−/−) the IgG1 titer is very high, and these Abs effectively mediate joint destruction.
Mice are treated with collagen in complete freund's adjuvant by injecting intradermally at 2 sites: a small volume delivered to each ear, and a small volume delivered to the skin between the shoulders. Three weeks later the mice are boosted with soluble collagen in saline, using an intraperitoneal route. Within a week, joint damage is assessed by measuring the swelling of the joint with a caliper and by measuring antibody titers. Treatment of mice during the course of disease development ameliorates disease score. In particular, treatment with 0.1-1 mg/kg of KIM-1 antagonists or modifying agents the day prior to disease initiation, followed by treatments thereafter, will block disease development, as assessed by reduced joint swelling and reduced immunolglobulin titers. This is a prophylatic course of treatment.
Treatment with KM-1 a antagonist after induction, and prior to boosting, ameliorates disease development, as assessed by reduced joint swelling and reduced immunolglobulin titers. This is a therapeutic course of treatment. Treatment with KIM-1 antagonists or modifying agents after the boost injection blocks disease development, as assessed by reduced joint swelling and reduced immunolglobulin titers. This is a therapeutic course of treatment.
Example 10 Murine Models of LupusIn the NZB/W model, mice from the NZB strain are mated with mice from the NZW strain, and the F1 progeny develop a lupus like disease over time. Manifestations of disease include the production of auto-antibodies and rheumatoid factor. Ig-deposition in the kidney results from the high amount of Ig and RF produced, leading to decreased kidney function over time, as can be measured by proteinuria in the urine.
The NZB/W F1 progeny begin to manifest symptoms of disease at around 5 months of age, with moderate proteinuria scores at that time (PU of 2). By 9 months of age the mice will have reached a maximum PU=4, and will begin to succomb to disease as a consequence of kidney failure. Another model called SNF1 (SWR×NZB F1 cross) follows similar kinetics.
Mice are treated with 0.1-1 mg/kg of KIM-1 antagonists the day prior to disease initiation, followed by treatments thereafter. This blocks disease development, as measured by the PU score, and/or by measuring titers of immunoglobulin in the serum, and/or by immunohistochemical analysis of hyperplasia in the spleen, and/or by immunohistochemical analysis of immune complex deposition and changes in the structure of the glomeruli in the kidney.
Treatment with KIM-1 antagonists after induction of disease, for example at the 5th month, but prior to severe disease (i.e., PU=2-3, ameliorates disease development or reverses disease damage. This can be measured by the PU score, and/or by measuring titers of immunoglobulin in the serum, and/or by immunohistochemical analysis of hyperplasia in the spleen, and/or by immunohistochemical analysis of immune complex deposition and changes in the structure of the glomeruli in the kidney.
Treatment with KIM-1 antagonists after disease is severe (PU=3-4) blocks disease development or reverses disease damage. This can be measured by the PU score, and/or by measuring titers of immunoglobulin in the serum, and/or by immunohistochemical analysis of hyperplasia in the spleen, and/or by immunohistochemical analysis of immune complex deposition and changes in the structure of the glomeruli in the kidney.
Example 11 Mixed Lymphocyte Reaction (MLR)Mouse MLR assays and antagonism of KIM-1. Mixed lymphocyte reactions (MLR) were run as follows: Spleens were isolated from C57B16 and Balb/c mice using sterile technique, ground roughly to release lymphocytes, then treated with a hypotonic solution (Gey's solution) to lyse red blood cells. The remaining cells were separated from residual tissue by passing them through a cell strainer (BD Falcon, Bedford, Mass. USA), and then were washed with sterile, pyrogen-free PBS, and centrifuged to pellet the cells. The cells were resuspended in the PBS solution a second time, pelleted again, then resuspended in complete RPMI media. The cells were counted and diluted as necessary. The Balb/c lymphocytes were used as the stimulator cells, therefore, these were irradiated at 3000 RAD prior to use.
To set up the assays, stimulator cells were added to the well as varying ratios relative to the number of responder cells (2×105/well). Media was supplemented with rat anti-KIM-1 antibodies, or KIM-1-Ig fusion protein and control-Ig fusion proteins at 20 μg/ml, as indicated. Cultures were set up in three identical plates, and each experimental condition was represented by 3 wells per plate. One plate was used to generate cell proliferation data using an MTS assay (CellTiter 96, Promega, Madison, Wis. USA). The other plates were used to collect supernatant samples for cytokine analyses. ELISAs (Pierce Endogen, Rockford, Ill. USA) were used to measure the levels of mIFNγ, mTNF, and mIl-2 in culture supernatants. Standard errors for values derived from the proliferation assays and ELISAs were less than 10%, and have been omitted from the figures. Large deviations from the positive control values for IFNγ were noted, while the levels of Il-2 and TNF in the cultures were not significantly different between the positive control and treatment groups. Therefore, the Il-2 and TNF data have been omitted; the data for IFNγ and cell proliferation are shown for each representative experiment.
Treatment of the MLR culture with the rat anti-mouse KIM-1 mAbs 3A2.5 and 1H9.11 significantly reduced the level of IFNγ secreted into the supernatant (
Treatment of the MLR culture with KIM-1-Ig fusion protein significantly reduced the level of IFNγ secreted into the supernatant (
Human MLR assays and antagonism of KIM-1. Mixed lymphocyte reactions (MLR) were run as follows: Peripheral blood mononuclear cells were isolated from whole blood taken from normal human donors using Ficoll gradient centrifugation. The cells were then washed with sterile, pyrogen-free PBS, and centrifuged to pellet the cells. The cells were resuspended in the PBS solution a second time, pelleted again, then resuspended in complete RPMI media. The cells were counted and diluted as necessary. JY cells (ATCC, Bethesda, Md. USA) were used as the stimulator cells, therefore, these were irradiated at 10000 RAD prior to use.
To set up the assays, stimulator were added to the well as varying ratios relative to the number of responder cells (2×105/well). Media was supplemented with mouse anti-KIM-1 antibodies, at 20 μg/ml, as indicated. Cultures were set up in three identical plates, and each experimental condition was represented by 3 wells per plate. One plate was used to generate cell proliferation data using an MTS assay (CellTiter 96, Promega, Madison, Wis. USA). The other plates were used to collect supernatant samples for cytokine analyses. ELISAs (Pierce Endogen, Rockford, Ill. USA or R-1-D Systems, Minneapolis, Minn. USA) were used to measure the levels of hIFNγ, hTNF, and hIl-2 in culture supernatants. Standard errors for values derived from the proliferation assays and ELISAs were less than 10%, and have been omitted from the figures. Large deviations from the positive control values for IFNγ were observed, while the levels of Il-2 and TNF in the cultures were not significantly different between the positive control and treatment groups. The TNF data have been omitted. Data for Il-2, IFNγ and cell proliferation are shown for this representative experiment.
Treatment of the MLR culture with the mouse anti-human KIM-1 mAbs AUF1 and AKG7 significantly reduced the level of IFNγ secreted into the supernatant (
The ability of a soluble form of KIM-1-Ig fusion protein to influence the course or severity of symptoms in a model of IBD in experimental mice. In this model, DSS was used to chronically irritate the large bowel (colon), causing inflammation to develop. It was known that pro-inflammatory mediators such as IFNγ, TNF, and 1′-12 are important to the development and severity of IBD, both in mouse models and in human patients (Egger et al., 2000, Digestion 62:240-248; Monteleone et al., 2000, Ann. Med. 32:552-560; Bouma et al., 2003, Nat. Rev. Immunol. 3:521-533). As described above, MLR data had suggested that KIM-1 modulation could influence the production of proinflammatory mediators such as IFNγ. Therefore, a KIM-1-modifying reagent was tested in vivo. It was hypothesized that the KIM-1-Ig fusion protein was acting by interrupting the interaction of one or more ligands with KIM-1 expressed on cells such as activated lymphocytes or other immune cells.
IBD was induced in mice using the dextran sulfate sodium (DSS) model (Copper et al., 1993, Lab. Invest. 69:238-249). A solution of 4.5% DSS (ICN Biomedicals, Aurora Ohio USA) in sterile distilled water was provided as the drinking source. Mice were weighed just prior to introduction to DSS, and weighed daily thereafter. Mice were also scored for extent of diarrhea (1: soft pellet, 2: loose pellet, 3: overtly fluid feces, 4: gross incontinence) and for the presence of blood in the feces (0: none, 1: blood) using the ColoScreen slides (Helena Labs, Beaumont Tex. USA). Small, but detectable, amounts of blood were given an intermediate score of 0.5. Mice were dosed ip with 200 μs of KIM-1-Ig fusion protein or polyclonal hIgG control (S and Immune, Sandoz, Geneva Switzerland) on day 0, day 2, and day 5. On day 8, mice were taken off of DSS-water, and given normal drinking water. Monitoring for weight and clinical scores continued until day 12, at which time the experiment ended.
Treatment of mice during the induction phase of IBD (days 0, 2 and 5) had a significant impact on cumulative weight loss and disease score, up to and including day 8. Therefore, mice were taken off of DSS and returned to normal drinking water, and their recovery was monitored. Mice that had received KIM-1-Ig fusion protein on days 0, 2 and 5 were consistently healthier on day 11 (3 days into recovery) as indicated by the extent of weight loss (
These data suggested that KIM-I modulation in vivo has protective effects in an acute inflammatory context, such as is present after DSS insult to the gut mucosa. These results suggested that KIM-1 antagonists will be efficacious in other acute or chronic inflammatory settings, e.g., in rheumatoid arthritis, multiple sclerosis, psoriasis and pancreatitis.
Other embodiments are within the following claims.
Claims
1. A method of inhibiting signaling between a T cell and a second cell participating in an immune response in a mammal, comprising:
- (a) identifying a mammal selected from the group consisting of a mammal with an immune disease or disorder and a mammal in preparation for a tissue graft; and
- (b) administering to the mammal an effective amount of a KIM-1 antagonist selected from the group consisting of: (i) a polypeptide comprising a KIM-1 Ig domain, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain; (ii) an anti-KIM-1 antibody; and (iii) an antigen-binding fragment of an anti-KIM-1 antibody.
2. The method of claim 1, wherein the second cell is an antigen presenting cell (APC).
3. The method of claim 1, wherein the T cell is an activated T cell.
4. The method of claim 1, wherein the T cell is a T helper cell.
5. The method of claim 4, wherein the T helper cell is a Th2 cell.
6. The method of claim 1, wherein the T cell is a grafted, donor T cell.
7. The method of claim 1, wherein the APC is selected from the group consisting of a monocyte, a macrophage, a dendritic cell, and a B cell.
8. The method of claim 1, wherein the APC is presenting an autoantigen.
9. The method of claim 1, wherein the polypeptide further comprises a KIM-1 mucin domain.
10. The method of claim 1 wherein the polypeptide further comprises a heterologous moiety.
11. The method of claim 10, wherein the heterologous moiety is selected from the group consisting of an immunoglobulin (Ig) moiety, a serum albumin moiety, a targeting moiety, a reporter moiety, and a purification-facilitating moiety.
12. The method of claim 11, wherein the heterologous moiety is an Ig moiety.
13. The method of claim 12, wherein the Ig moiety is an Fc moiety.
14. The method of claim 1, wherein the polypeptide is conjugated to a polymer.
15. The method of claim 14, wherein the polymer is selected from the group consisting of a polyalkylene glycol, a sugar polymer, and a polypeptide.
16. The method of claim 15, wherein the polymer is a polyalkylene glycol.
17. The method of claim 16, wherein the polyalkylene glycol is polyethylene glycol (PEG).
18. The method of claim 17, wherein the average molecular weight of the polymer is from 2,000 Da to 30,000 Da.
19. The method of claim 18, wherein the average molecular weight of the polymer is from 5,000 Da to 20,000 Da.
20. The method of claim 19, wherein the average molecular weight of the polymer is about 10,000 Da.
21. A method of inhibiting activation of a B cell in a mammal, comprising contacting the B cell with an effective amount of a KIM-1 antagonist selected from the group consisting of: (a) a polypeptide comprising a KIM-1 Ig domain, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain; (b) an anti-KIM-1 antibody; and (c) an antigen-binding fragment of an anti-KIM-1 antibody.
22. The method of claim 21, wherein the activation of the B cell is mediated by an activated T cell.
23. The method of claim 22, wherein the activated T cell is a Th2 cell.
24. The method of claim 22, wherein the activated T cell is a grafted, donor T cell.
25. A method of inhibiting production in a mammal of a subset of antibodies against one or more antigens, comprising administering an effective amount of a KIM-1 antagonist selected from the group consisting of: (a) a polypeptide comprising a KIM-1 Ig domain, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain; (b) an anti-KIM-1 antibody; and (c) an antigen-binding fragment of an anti-KIM-1 antibody.
26. The method of claim 25, wherein the antibodies are of the IgG class.
27. The method of claim 26, wherein the antibodies are of IgG1 subclass.
28. The method of claim 27, wherein the effective amount of the polypeptide is administered to the mammal between 30 minutes and 30 days before the immune system of the mammal first recognizes the one or more antigens.
29. The method of claim 28, wherein the one or more antigens are alloantigens.
30. The method of claim 28, wherein the one or more antigens are autoantigens.
31. The method of claim 28, wherein the immune system of the mammal first recognizes the one or more antigens as part of an epitope spreading process in the course of an autoimmune disease.
32. A method of inhibiting epitope spreading in an autoimmune disease, comprising administering an effective amount of a KIM-1 antagonist selected from the group consisting of: (a) a polypeptide comprising a KIM-1 Ig domain, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain; (b) an anti-KIM-1 antibody; and (c) an antigen-binding fragment of an anti-KIM-1 antibody.
33. A method of treating a Th2 cell-mediated disease, comprising administering an effective amount of a KIM-1 antagonist selected from the group consisting of: (a) a polypeptide comprising a KIM-1 Ig domain, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain; (b) an anti-KIM-1 antibody; and (c) an antigen-binding fragment of an anti-KIM-1 antibody.
34. The method of claim 33, wherein the Th2 cell-mediated disease is selected from the group consisting of myasthenia gravis, autoimmune hemolytic anemia, Chagas disease, Graves disease, idiopathic thrombocytopenia purpura (ITP), Wegener's granulomatosis, polyarteritis nodosa, rapidly progressive crescentic glomerulonephritis, graft-versus-host disease (GVHD), and systemic lupus nephritis (SLE).
35. A method of inhibiting GVHD, comprising administering an effective amount of a KIM-1 antagonist selected from the group consisting of: (a) a polypeptide comprising a KIM-1 Ig domain, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain; (b) an anti-KIM-1 antibody; and (c) an antigen-binding fragment of an anti-KIM-1 antibody.
36. A polypeptide comprising a KIM-1 Ig domain and an Fc moiety, and lacking a transmembrane domain and a KIM-1 cytoplasmic domain.
37. A method of inhibiting secretion of IFN-γ by lymphocytes in a mammal, comprising administering to the mammal an effective amount of a KIM-1 antagonist.
38. A method of treating an inflammatory disease or disorder in a mammal, comprising administering to the mammal an effective amount of a KIM-1 antagonist.
39. The method of claim 38, wherein the inflammatory disease or disorder is inflammatory bowel disease.
40. The method of claim 38, wherein the inflammatory disease or disorder is acute or chronic inflammation.
41. The method of claim 4, wherein the T helper cell is a Th1 cell.
Type: Application
Filed: Aug 26, 2009
Publication Date: Apr 1, 2010
Applicant: BIOGEN IDEC MA INC. (Cambridge, MA)
Inventor: Paul D. Rennert (Holliston, MA)
Application Number: 12/548,366
International Classification: A61K 39/395 (20060101);
