Patent Application
20170275344
The present invention, in at least some aspects, relates to a novel protein, and its variants, fragments and fusion proteins thereof, and methods of use thereof for immunotherapy, and drug development.
Induction of immune tolerance has long been considered the “holy grail” for autoimmune disease therapy. The immune system has the reciprocal tasks to protect the host against invading pathogens, but simultaneously to prevent damage resulting from unwanted reactions to self antigens. The latter part is known as immune tolerance and performed by a complex set of interactive and complementary pathways, which regulate immune responses. T cells have the ability to react to a variety of antigens, both self and nonself. Therefore, there are many mechanisms that exist naturally to eliminate potentially self-reactive responses—this is known as natural tolerance. The main mechanism for eliminating potential autoreactive T cells occurs in the thymus and is known as central tolerance. Some potentially autoreactive T cells escape central tolerance and, therefore, peripheral tolerance mechanisms also exist. Despite these mechanisms, some self-reactive T cells may ‘escape’ and be present in the repertoire; it is believed that their activation may lead to autoimmune disease.
Studies on therapeutic tolerance have attempted to induce and amplify potent physiological mechanisms of tolerance in order to eliminate or neutralize self-reactive T cells and prevent or treat autoimmune diseases. One way to induce tolerance is by manipulation of the interaction between costimulatory ligands and receptors on antigen presenting cells (APCs) and lymphocytes.
CTLA-4 is the most extensively studied costimulatory molecule which down-regulates immune responses. The attributes of immunosuppressive qualities and capacity to induce tolerance have made its recognition as a potential immuno-therapeutic agent for autoimmune mediated inflammatory disorders. Abatacept (commercial name: Orencia) is a fusion protein composed of the ECD (extracellular domain) of CTLA-4 fused to the Fc fragment of hIgG1. Abatacept is believed to induce costimulation blockade, which has been approved for treating patients with rheumatoid arthritis, by effectively interfering with the inflammatory cascade.
Induction of disease control with the current therapies, followed by progressive withdrawal in parallel with re-establishing immune tolerance, may be an attractive approach in the future of autoimmune therapies. Furthermore, due to their immune specificity, in the absence of global immunosuppression, such therapies should be safe for chronic use.
Multiple sclerosis (MS) is a chronic, inflammatory, demyelinating disorder of the central nervous system (CNS), which involves autoimmune responses to myelin antigens. It is characterized by lesions within the CNS and demyelination is a key feature of these lesions. Autoreactive T cells are thought to initiate an autoimmune response directed against components of CNS myelin. The main targets of the autoimmune reactions are thought to be myelin basic protein (MBP), proteolipid protein (PLP) and myelin oligodendrocyte glycoprotein (MOG). Experimental autoimmune encephalomyelitis (EAE), an animal model of MS induced by immunization with myelin components in adjuvant, shows comparable neuronal pathology. Without wishing to be limited by a single hypothesis, studies in EAE have provided convincing evidence that T cells specific for self-antigens mediate pathology in these diseases.
T helper type 1 (Th1) cells are induced by IL-12 and produce IFN-γ, while T helper type 2 (Th2) cells secrete IL-4, IL-5 and IL-13. Th1 cells can mediate proinflammatory or cell-mediated immune responses, whereas Th2 cells mainly promote certain types of humoral immunity. Some immune related diseases, such as autoimmune reactions, inflammation, chronic infection and sepsis, are characterized by a dysregulation of the pro-versus anti-inflammatory tendencies of the immune system, as well as an imbalance in the Th1 versus Th2 cytokine balance. During inflammation, induction of a shift in the balance from Th1 to Th2 protects the organism from systemic ‘overshooting’ with Th1/pro-inflammatory cytokines, by reducing the inflammatory tendencies of the immune system. Immunomodulatory therapies that are associated with a Th1 to Th2 immune shift have protective effects in Th1-mediated autoimmune diseases, such as multiple sclerosis and rheumatoid arthritis. For example, Laquinimod, which has demonstrated efficacy in animal models of several autoimmune diseases including MS, shows immunomodulatory effects through Th1/Th2 shift, and does not lead to immunosuppression. Glatiramer acetate (Copaxone) also induces Th1/Th2 shift with decreased secretion of proinflammatory cytokines, and increased secretion of antiinflammatory cytokines. Furthermore, glatiramer acetate-specific Th2 cells are able to migrate across the blood-brain barrier and cause in situ bystander suppression of autoaggressive Th1 T cells.
FoxP3+ Tregulatory cells (Tregs) are primarily generated in the thymus but also at peripheral sites or induced in cell culture in the presence of TGFβ. Several mechanisms underly the regulatory activity of Tregs, including inhibition of the expansion of differentiated effector T cells, prevention of T cell priming by acting on antigen presenting cells, such as DCs (especially inducible Tregs, iTres), and inhibition of effector T cell trafficking to the target organ (especially thymic Tregs usually designated as tTregs or nTregs). IL-10 plays an important role in the suppressive function of Tregs and/or Bregs by imparing the capacity of DCs to present antigen through increasing MARCH1 and inhibiting CD83 expression and thus controlling the expression of peptide-MHC class II complexes on DC.
Certain immune cells and immune cell signal transduction pathways are promising targets for new agents for treating immune disorders. For example Th1, Th17, Th2 and regulatory T cells (Tregs), regulatory B cells and antigen presenting cells such as monocytes, macrophages and dendridic cells play important roles in modulating autoimmunity and inflammation. Mounting evidence from numerous studies shows the importance of these immune cells in disorders such as rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, psoriasis, lupus erythematosus, type 1 diabetes and uveitis. Most existing therapies target only one pathway at a time.
The background art fails to provide therapies that target multiple cells and pathways involved in autoimmunity, transplant rejection and inflammation, such as Th1, Th17, Th22, Th2, Tregs, Bregs, or other cells that secrete, or influence other cells that secrete, inflammatory molecules such as cytokines, metalloproteases, chemokines and other molecules, and which particularly induce tolerance through the IL-10 and/or TGFβ pathways.
The present invention, in at least some embodiments, is of new uses and methods of treatment for immune related diseases by administering the C1ORF32-ECD protein to a subject in need of treatment thereof to induce immune tolerance, preferably through the IL-10 and/or TGFβ pathways. In the context of immune related diseases, “immune tolerance” refers to reducing, ameliorating or blocking the immune related disease, while leaving intact the disease-fighting abilities of the immune system.
According to at least some embodiments, there is provided a use of an isolated polypeptide comprising a soluble C1ORF32 polypeptide or fragment or variant thereof, for treatment of an immune related disease, by increasing Treg and/or Breg cell population, and/or percentage, and/or activity.
The term “immune related disease (or disorder or condition)” as used herein should be understood to encompass any disease disorder or condition selected from the group including but not limited to autoimmune diseases, inflammatory disorders and immune disorders associated with graft transplantation rejection, such as acute and chronic rejection of organ transplantation, allogenic stem cell transplantation, autologous stem cell transplantation, bone marrow tranplantation, and graft versus host disease.
The term “autoimmune disease” as used herein should be understood to encompass any autoimmune disease and chronic inflammatory conditions. According to at least some embodiments of the invention, the autoimmune diseases should be understood to encompass any disease disorder or condition selected from the group including but not limited to multiple sclerosis, including relapsing-remiting multiple sclerosis, primary progressive multiple sclerosis, and secondary progressive multiple sclerosis; multiple sclerosis, psoriasis; rheumatoid arthritis; psoriatic arthritis, systemic lupus erythematosus (SLE); discoid lupus erythematosus, inflammatory bowel disease, ulcerative colitis; Crohn's disease; benign lymphocytic angiitis, thrombocytopenic purpura, idiopathic thrombocytopenia, idiopathic autoimmune hemolytic anemia, pure red cell aplasia, Sjögren's syndrome, rheumatic disease, connective tissue disease, inflammatory rheumatism, degenerative rheumatism, extra-articular rheumatism, juvenile rheumatoid arthritis, arthritis uratica, muscular rheumatism, chronic polyarthritis, cryoglobulinemic vasculitis, ANCA-associated vasculitis, antiphospholipid syndrome, myasthenia gravis, autoimmune hemolytic anaemia, Guillain-Barré syndrome, chronic immune polyneuropathy, autoimmune thyroiditis, insulin dependent diabetes mellitus, type I diabetes, latent autoimmune diabetes of the adult (LADA), type 2 diabetes with an autoimmune component, Addison's disease, membranous glomerulonephropathy, Goodpasture's disease, autoimmune gastritis, autoimmune atrophic gastritis, pernicious anaemia, pemphigus, pemphigus vulgaris, cirrhosis, primary biliary cirrhosis, dermatomyositis, polymyositis, fibromyositis, myogelosis, celiac disease, immunoglobulin A nephropathy, Henoch-Schönlein purpura, Evans syndrome, dermatitis, atopic dermatitis, psoriasis, psoriasis arthropathica, Graves' disease, Graves' ophthalmopathy, scleroderma, systemic scleroderma, progressive systemic scleroderma, asthma, allergy, primary biliary cirrhosis, Hashimoto's thyroiditis, primary myxedema, sympathetic ophthalmia, autoimmune uveitis, hepatitis, chronic action hepatitis, collagen diseases, ankylosing spondylitis, periarthritis humeroscapularis, panarteritis nodosa, chondrocalcinosis, Wegener's granulomatosis, microscopic polyangiitis, chronic urticaria, bullous skin disorders, pemphigoid, bullous pemphigoid, cicatricial pemphigoid, vitiligo, atopic eczema, eczema, chronic urticaria, autoimmune urticaria, normocomplementemic urticarial vasculitis, hypocomplementemic urticarial vasculitis, autoimmune lymphoproliferative syndrome, Devic's disease, sarcoidosis, pernicious anemia, childhood autoimmune hemolytic anemia, idiopathic autoimmune hemolytic anemia, refractory or chronic autoimmune cytopenias, prevention of development of autoimmune anti-factor viii antibodies in acquired hemophilia a, cold agglutinin disease, neuromyelitis optica, stiff person syndrome, gingivitis, periodontitis, pancreatitis, myocarditis, vasculitis, gastritis, gout, gouty arthritis, and inflammatory skin disorders, selected from the group consisting of psoriasis, atopic dermatitis, eczema, rosacea, urticaria, and acne, normocomplementemic urticarial vasculitis, pericarditis, idiopathic pericarditis, myositis, anti-synthetase syndrome, scleritis, macrophage activation syndrome, Behçet's Syndrome, PAPA syndrome, Blau's syndrome, gout, adult and juvenile Still's disease, cryropyrinopathy, Muckle-Wells syndrome, familial cold-induced auto-inflammatory syndrome, neonatal onset multisystemic inflammatory disease, familial Mediterranean fever, chronic infantile neurologic cutaneous and articular syndrome, a rheumatic disease, polymyalgia rheumatica, mixed connective tissue disease, inflammatory rheumatism, degenerative rheumatism, extra-articular rheumatism, juvenile arthritis, juvenile rheumatoid arthritis, systemic juvenile idiopathic arthritis, arthritis uratica, muscular rheumatism, chronic polyarthritis, reactive arthritis, Reiter's syndrome, rheumatic fever, relapsing polychondritis, Raynaud's phenomenon, vasculitis, cryoglobulinemic vasculitis, temporal arteritis, giant cell arteritis, Takayasu arteritis, chronic inflammatory demyelinating polyneuropathy, Crest syndrome, chronic fatigue and immune dysfunction syndrome (CFIDS), autoimmune inner ear disease, hyper IgD syndrome, Schnitzler's syndrome, autoimmune retinopathy, age-related macular degeneration, atherosclerosis, chronic prostatitis, alopecia, alopecia areata, alopecia universalis, alopecia totalis, utoimmune thrombocytopenic purpura, idiopathic thrombocytopenic purpura, pure red cell aplasia, and TNF receptor-associated periodic syndrome (TRAPS).
Optionally and preferably, the autoimmune disease includes but is not limited to any of the types and subtypes of any of multiple sclerosis, rheumatoid arthritis, type I diabetes, psoriasis, systemic lupus erythematosus, inflammatory bowel disease, uveitis, or Sjogren's syndrome.
As used herein, “multiple sclerosis” comprises one or more of multiple sclerosis, benign multiple sclerosis, relapsing remitting multiple sclerosis, secondary progressive multiple sclerosis, primary progressive multiple sclerosis, progressive relapsing multiple sclerosis, chronic progressive multiple sclerosis, transitional/progressive multiple sclerosis, rapidly worsening multiple sclerosis, clinically-definite multiple sclerosis, malignant multiple sclerosis, also known as Marburg's Variant, and acute multiple sclerosis. Optionally, “conditions relating to multiple sclerosis” include, e.g., Devic's disease, also known as Neuromyelitis Optica; acute disseminated encephalomyelitis, acute demyelinating optic neuritis, demyelinative transverse myelitis, Miller-Fisher syndrome, encephalomyelradiculoneuropathy, acute demyelinative polyneuropathy, tumefactive multiple sclerosis and Balo's concentric sclerosis.
As used herein, “rheumatoid arthritis” comprises one or more of rheumatoid arthritis, gout and pseudo-gout, juvenile idiopathic arthritis, juvenile rheumatoid arthritis, Still's disease, ankylosing spondylitis, rheumatoid vasculitis. Optionally, conditions relating to rheumatoid arthritis include, e.g., osteoarthritis, sarcoidosis, Henoch-Schönlein purpura, psoriatic arthritis, reactive arthritis, spondyloarthropathy, septic arthritis, haemochromatosis, hepatitis, vasculitis, Wegener's granulomatosis, Lyme disease, familial mediterranean fever, hyperimmunoglobulinemia D with recurrent fever, TNF receptor associated periodic syndrome, and enteropathic arthritis associated with inflammatory bowel disease.
As used herein, “Uveitis” comprises one or more of uveitis, anterior uveitis (or iridocyclitis), intermediate uveitis (pars planitis), posterior uveitis (or chorioretinitis) and the panuveitic form.
As used herein, “inflammatory bowel disease” comprises one or more of inflammatory bowel disease, Crohn's disease, ulcerative colitis (UC), collagenous colitis, lymphocytic colitis, ischaemic colitis, diversion colitis, Behçet's disease, indeterminate colitis.
As used herein, “psoriasis” comprises one or more of psoriasis, nonpustular psoriasis including psoriasis vulgaris and psoriatic erythroderma (erythrodermic psoriasis), pustular psoriasis including generalized pustular psoriasis (pustular psoriasis of von Zumbusch), pustulosis palmaris et plantaris (persistent palmoplantar pustulosis, pustular psoriasis of the Barber type, pustular psoriasis of the extremities), annular pustular psoriasis, acrodermatitis continua, impetigo herpetiformis. Optionally, conditions relating to psoriasis include, e.g., drug-induced psoriasis, inverse psoriasis, napkin psoriasis, seborrheic-like psoriasis, guttate psoriasis, nail psoriasis, psoriatic arthritis.
As used herein, “type 1 diabetes” comprises one or more of type 1 diabetes, insulin-dependent diabetes mellitus, idiopathic diabetes, juvenile type 1 diabetes, maturity onset diabetes of the young, latent autoimmune diabetes in adults, gestational diabetes. Conditions relating to type 1 diabetes include, neuropathy including polyneuropathy, mononeuropathy, peripheral neuropathy and autonomicneuropathy; eye complications: glaucoma, cataracts, and/or retinopathy.
As used herein, “Sjogren's syndrome” comprises one or more of Sjogren's syndrome, primary Sjogren's syndrome and secondary Sjogren's syndrome, as well as conditions relating to Sjogren's syndrome including connective tissue disease, such as rheumatoid arthritis, systemic lupus erythematosus, or scleroderma. Other complications include pneumonia, pulmonary fibrosis, interstitial nephritis, inflammation of the tissue around the kidney's filters, glomerulonephritis, renal tubular acidosis, carpal tunnel syndrome, peripheral neuropathy, cranial neuropathy, primary biliary cirrhosis (PBC), cirrhosis, inflammation in the esophagus, stomach, pancreas, and liver (including hepatitis), polymyositis, Raynaud's phenomenon, vasculitis, autoimmune thyroid problems, lymphoma.
As used herein, “systemic lupus erythematosus”, comprises one or more of systemic lupus erythematosus, discoid lupus, lupus arthritis, lupus pneumonitis, lupus nephritis. Conditions relating to systemic lupus erythematosus include osteoarticular tuberculosis, antiphospholipid antibody syndrome, inflammation of various parts of the heart, such as pericarditis, myocarditis, and endocarditis, lung and pleura inflammation, pleuritis, pleural effusion, chronic diffuse interstitial lung disease, pulmonary hypertension, pulmonary emboli, pulmonary hemorrhage, and shrinking lung syndrome, lupus headache, Guillain-Barré syndrome, aseptic meningitis, demyelinating syndrome, mononeuropathy, mononeuritis multiplex, myasthenia gravis, myelopathy, cranial neuropathy, polyneuropathy, vasculitis.
As used herein the term “inflammatory disorders” and/or “inflammation”, used interchangeably, includes inflammatory abnormalities characterized by disregulated immune response to harmful stimuli, such as pathogens, damaged cells, or irritants. Inflammatory disorders underlie a vast variety of human diseases. Non-immune diseases with etiological origins in inflammatory processes include cancer, atherosclerosis, and ischaemic heart disease. Examples of disorders associated with inflammation include: chronic prostatitis, glomerulonephritis, hypersensitivities, pelvic inflammatory disease, reperfusion injury, sarcoidosis, vasculitis, interstitial cystitis, normocomplementemic urticarial vasculitis, pericarditis, myositis, anti-synthetase syndrome, scleritis, macrophage activation syndrome, Bechet's syndrome, PAPA syndrome, Blau's syndrome, gout, adult and juvenile Still's disease, cryropyrinopathy, Muckle-Wells syndrome, familial cold-induced auto-inflammatory syndrome, neonatal onset multisystemic inflammatory disease, familial mediterranean fever, chronic infantile neurologic, cutaneous and articular syndrome, systemic juvenile idiopathic arthritis, hyper IgD syndrome, Schnitzler's syndrome, TNF receptor-associated periodic syndrome (TRAPS), gingivitis, periodontitis, hepatitis, cirrhosis, pancreatitis, myocarditis, vasculitis, gastritis, gout, gouty arthritis, and inflammatory skin disorders, selected from the group consisting of psoriasis, atopic dermatitis, eczema, rosacea, urticaria, and acne.
According to at least some embodiments of the present invention, there are provided C1ORF32-ECD fusion polypeptides having a first fusion partner comprising all or a part of a C1ORF32 soluble polypeptide, such as the ECD of C1ORF32, or a polypeptide comprising all or part of the extracellular domain of ILDR2-WT (SEQ ID NO:1), H19011_1_P8 (SEQ ID NO:2), H19011_1_P8_V1 (SEQ ID NO:3), H19011_1_P9 (SEQ ID NO:4) or H19011_1_P9_V1 (SEQ ID NO:5), or a sequence homologous thereto, and a second fusion partner composed of a heterologous sequence (respectively non-C1ORF32), fused together directly or indirectly via a peptide linker sequence or a chemical linker.
According to at least some embodiments, the isolated polypeptide is at least 80, 90, 95, 96, 97, 98 or 99% (or any integral value in between) homologous to a polypeptide comprising all or part of the extracellular domain of ILDR2-WT (SEQ ID NO:1), H19011_1_P8 (SEQ ID NO:2), H19011_1_P8_V1 (SEQ ID NO:3), H19011_1_P9 (SEQ ID NO:4) or H19011_1_P9_V1 (SEQ ID NO:5). According to at least some embodiments, the isolated polypeptide at least 80, 90, 95, 96, 97, 98 or 99% (or any integral value in between) homologous to a polypeptide comprising all or part of the extracellular domain of ILDR2-WT (SEQ ID NO:1), H19011_1_P8 (SEQ ID NO:2), H19011_1_P8_V1 (SEQ ID NO:3), H19011_1_P9 (SEQ ID NO:4) or H19011_1_P9_V1 (SEQ ID NO:5) has at least one of the SNP variations. The C1ORF32 polypeptide may be of any species of origin. In further embodiments, the C1ORF32 polypeptide is of murine, non-human primate or human origin.
Without wishing to be limited by a single hypothesis, according to at least some embodiments the C1ORF32 fusion protein inhibits the inflammatory activity of Th1, Th17, Th22, or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs. Again without wishing to be limited by a single hypothesis, according to at least some embodiments the C1ORF32 fusion protein can also increase the suppressive capacity of Tregs or Bregs or the immunomodulatory activity of Th2 cells. The C1ORF32 fusion protein can also increase the production of anti-inflammatory molecules such as the cytokine IL-10.
According to at least some embodiments, the C1ORF32 fusion protein modulates the IL-10 and/or TGFβ pathway. As shown herein, the C1ORF32 fusion protein upregulates the IL-10 pathway by upregulating IL-10 secretion and also maintains the TGFβ pathway.
According to at least some embodiments, the C1ORF32 fusion protein induces long term immune tolerance. By “long term” it is meant tolerance which lasts any time period between at least 72 hours to 6 months after cessation of treatment, or even greater than 6 months after cessation of treatment; and/or efficacy at a reduced dosing frequency, including but not limited to a dosing frequency of one dose per any time period from every 72 hours to every 6 months.
According to at least some embodiments, the C1ORF32 fusion protein induces tolerance, and preferably long term tolerance as defined above, to graft tissue with at least one mismatched antigen to the recipient subject. Non-limiting examples of such graft tissue include organs and bone marrow. Preferably, the fusion protein induces graft survival and increase in nTregs and/or iTregs, indicating donor specific tolerance induction (Aaron et al. Journal of Immunology, 2010, 185: 3326-3336). Also preferably, such induction of immune tolerance occurs through the IL-10 pathway and/or the TGF-beta pathway. According to at least some embodiments, the C1ORF32 fusion protein also causes an increase in Bregs or otherwise modulates Breg activity levels. Optionally such a mechanism also occurs for autoimmune disease treatment.
According to at least some embodiments, the C1ORF32 fusion protein may optionally include the full extracellular domain (ECD) of C1ORF32, or a fragment, or a homolog thereof. In one embodiment, the C1ORF32 polypeptide is a soluble fragment of full-length C1ORF32 ECD. Such fragments optionally include those that retain the ability to bind to their natural receptors and incorporate some, or all, of the extracellular domain of the C1ORF32 polypeptide, and lack some or all of the intracellular and/or transmembrane domains. In one embodiment, C1ORF32 polypeptide fragments include the entire extracellular domain of the C1ORF32 polypeptide. In other embodiments, the soluble fragments of C1ORF32 polypeptides are fragments of the extracellular domain that retain C1ORF32 biological activity.
C1ORF32 polypeptide extracellular domains can include 1, 2, 3, 4, 5 or more contiguous amino acids from the transmembrane domain, and/or 1, 2, 3, 4, 5 or more contiguous amino acids from the signal sequence. Alternatively, the extracellular domain can have 1, 2, 3, 4, 5, or more contiguous amino acids removed from the C-terminus; N-terminus, or both. Biologically active variants and/or homologs of C1ORF32 polypeptides and fragments thereof may also be used.
Fragments of C1ORF32 Polypeptides
As used herein the term “soluble C1ORF32” or “soluble C1ORF32 proteins/molecules” refers to fragments of C1ORF32 that include some or all of the IgV and/or ECD domain of the C1ORF32 polypeptide, and lack some or all of the intracellular and/or transmembrane domains, wherein said fragments retain a biological activity of inhibition of T cell activation.
The soluble C1ORF32 molecules used in the methods of the invention may or may not include a signal (leader) peptide sequence.
Particular sequences of interest, according to at least some embodiments of the present invention, include but are not limited to SEQ ID NOs: 6-38.
In particular, the fragments of the extracellular domain of C1ORF32 can include any sequence corresponding to any portion of or comprising the IgV domain of the extracellular domain of C1ORF32, having any sequence corresponding to residues of Human_ILDR2_WT_P8 (SEQ ID NO:2) starting from position 21 and ending at any position between 164 and 170 or corresponding to residues of Human_ILDR2_WT_P8_mut (SEQ ID NO:3) starting from position 21 and ending at any position between 164 and 170, or corresponding to residues of Human_ILDR2_Variant_P9 (SEQ ID NO:4) starting from position 21 and ending at any position between 164 and 170, or corresponding to residues of Human_ILDR2_Variant_P9 (SEQ ID NO:5) starting from position 21 and ending at any position between 164 and 170. The base sequences as given above are with the signal peptide.
The C1ORF32 proteins contain an immunoglobulin domain within the extracellular domain, the IgV domain (or V domain), which is related to the variable domain of antibodies. The IgV domain may be responsible for receptor binding, by analogy to the other B7 family members. The Ig domain of the extracellular domain includes one disulfide bond formed between intradomain cystein residues, as is typical for this fold and may be important for structure-function. In SEQ ID NO: 2 these cysteines are located at residues 42 and 145.
In one embodiment, the first fusion partner is a soluble fragment of C1ORF32. Without wishing to be limited by a single hypothesis, it is believed that useful fragments are those that retain the ability to bind to their natural receptor or receptors and/or retain the ability to inhibit T cell activation. A C1ORF32 polypeptide that is a fragment of full-length C1ORF32 typically has at least 20 percent, 30 percent, 40 percent, 50 percent, 60 percent, 70 percent, 80 percent, 90 percent, 95 percent, 98 percent, 99 percent, 100 percent, or even more than 100 percent of the ability to bind its natural receptor(s) and/or of the ability to inhibit T cell activation as compared to full-length C1ORF32. Soluble C1ORF32 polypeptide fragments are fragments of C1ORF32 polypeptides that may be shed, secreted or otherwise extracted from the producing cells. In other embodiments, the soluble fragments of C1ORF32 polypeptides include fragments of the C1ORF32 extracellular domain that retain C1ORF32 biological activity, such as fragments that retain the ability to bind to their natural receptor or receptors and/or retain the ability to inhibit T cell activation. The extracellular domain can include 1, 2, 3, 4, or 5 contiguous amino acids from the transmembrane domain, and/or 1, 2, 3, 4, or 5 contiguous amino acids from the signal sequence. Alternatively, the extracellular domain can have 1, 2, 3, 4, 5 or more amino acids removed from the C-terminus, N-terminus, or both.
In some embodiments the extracellular domain is only the IgV domain as set forth in SEQ ID NO: 9, or fragments or variants thereof, or the region between the conserved cysteines of the IgV domain which are located at residues 42 and 145 of the full-length protein SEQ ID NO:2, corresponding to the sequence set forth in SEQ ID NO: 38: CHFSTSSHQPAVVQWKFKSYCQDRMGESLGMSSTRAQSLSKRNLEWDPYLDCLDS RRTVRVVASKQGSTVTLGDFYRGREITIVHDADLQIGKLMWGDSGLYYC.
According to at least some embodiments of the present invention, there is provided a pharmaceutical composition comprising an isolated soluble C1ORF32 polypeptide, fragment, variant, or homolog or fusion protein or conjugate containing same, and a pharmaceutically acceptable diluent or carrier, adapted for treatment of immune related disorder.
In one embodiment, the C1ORF32 polypeptide may optionally be fused to one or more domains of an Ig heavy chain constant region, preferably having an amino acid sequence corresponding to the hinge, CH2 and CH3 regions of a human immunoglobulin Cγ1, Cγ2, Cγ3 or Cγ4 chains or to the hinge, CH2 and CH3 regions of a murine immunoglobulin Cγ2a chain.
The fusion proteins may optionally be dimerized or multimerized to form homodimers, heterodimers, homomultimers or heteromultimers. Dimerization/multimerization partners can be arranged either in parallel or antiparallel orientations. Optionally the fusion protein has the sequence set forth in any one of SEQ ID NOs: 42, 43, 62, 64, 66-88.
According to at least some embodiments of the present invention, there is provided a pharmaceutical composition comprising an isolated soluble C1ORF32 polypeptide, or fragment or variant or homolog thereof, or fusion protein containing same, capable of inhibiting T cell activation, and a pharmaceutically acceptable diluent or carrier. Optionally, the pharmaceutical composition comprises the soluble C1ORF32 polypeptide comprising the extracellular domain of ILDR2-WT (SEQ ID NO:1), H19011_1_P8 (SEQ ID NO:2), H19011_1_P8_V1 (SEQ ID NO:3), H19011_1_P9 (SEQ ID NO:4) or H19011_1_P9_V1 (SEQ ID NO:5) or fragment thereof, and a pharmaceutically acceptable diluent or carrier. According to at least some embodiments of the present invention, there is provided a pharmaceutical composition comprising an isolated soluble C1ORF32 polypeptide, or fragment or variant or homolog or fusion protein containing same, and a pharmaceutically acceptable diluent or carrier, adapted for treatment of immune related disorder by any one or more of the following: inhibiting or reducing differentiation of Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules; inhibiting or reducing activity of Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules; inhibiting or reducing the Th1 and/or Th17 pathways; inhibiting or reducing the Th1 and/or Th17 pathways while promoting Th2 pathways/activity/differentiation; inhibiting or reducing inflammatory molecule production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules; inhibiting or reducing proliferation of Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules; interacting with Tregs or Bregs; enhancing Treg or Breg differentiation, enhancing Treg or Breg activity; enhancing IL-10 secretion by Tregs or Bregs; increasing the number of Tregs or Bregs; increasing the suppressive capacity of Tregs or Bregs; interacting with Th2 cells; enhancing Th2 activity, enhancing the immunomodulatory capacity of Th2 cells, increasing the number of Th2 cells, enhancing production of IL-4, IL-5 or IL-10 by Th2 cells; or combinations thereof; limiting the antigen presentation capability of DCs and/or other myeloid cells.
In one embodiment but without wishing to be limited by a single hypothesis, C1ORF32 polypeptides or fusion proteins or pharmaceutical composition containing same, enhance T reg or Breg differentiation, enhance the suppressive activity of Tregs or Bregs on the immune system. Tregs and Bregs can suppress differentiation, proliferation, activity, and/or cytokine production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules. In one embodiment the C1ORF32 polypeptides or fusion proteins or pharmaceutical composition containing same, enhance the suppressive activity of Tregs or Bregs on effector T cells to inhibit or reduce effector functions. In one embodiment the C1ORF32 polypeptides or fusion proteins or pharmaceutical composition containing same, enhance the suppressive activity of Tregs or Bregs on naive T cells to inhibit or reduce naive T cells from differentiating into Th1, Th17, Th22 cells and thereby reduce the number of Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs in a subject.
In one embodiment but without wishing to be limited by a single hypothesis, C1ORF32 polypeptides or fusion proteins or pharmaceutical composition containing same, limits antigen presentation capability of myeloid cells including but not limited to dendritic cells.
In one embodiment, C1ORF32 polypeptides or fusion proteins or pharmaceutical composition containing same, enhance the activity of Th2 immune responses or to increase the number or percentage of Th2 cells. Th2 cells can modulate the differentiation, proliferation, activity, and/or cytokine production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, resulting in inhibition of Th1 and/or Th17 responses, and in immune modulation via a Th1/Th2 shift. In one embodiment the C1ORF32 polypeptides or fusion proteins or pharmaceutical composition containing same, enhance the immunomodulatory activity of Th2 on naive T cells to inhibit or reduce naive T cells from differentiating into Th1, Th17, Th22 cells and thereby reduce the number of Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs in a subject. In one embodiment the C1ORF32 polypeptides or fusion proteins or pharmaceutical composition containing same, promote or enhance production of IL-4, IL-5 or IL-10 by Th2 cells. Optionally the composition is used for treatment of immune related disorders
According to at least some embodiments of the present invention, there is provided a use of an isolated soluble C1ORF32 polypeptide, or fragment or variant or homolog or a fusion protein or conjugate containing same, or a polypeptide comprising the extracellular domain of ILDR2-WT (SEQ ID NO:1), H19011_1_P8 (SEQ ID NO:2), H19011_1_P8_V1 (SEQ ID NO:3), H19011_1_P9 (SEQ ID NO:4) or H19011_1_P9_V1 (SEQ ID NO:5), or fragment or variant or homolog thereof or a fusion protein or conjugate containing same, or a pharmaceutical composition containing any of the foregoing, adapted for treatment of immune related disorder.
Optionally the polypeptide comprises a sequence of amino acid residues having at least 95% sequence identity with amino acid residues depicted in any of SEQ ID NOs:6-41, or a fragment, or a variant, or a homolog thereof, adapted for treatment of immune related disorder. Optionally the polypeptide is attached to a detectable or therapeutic moiety.
According to at least one embodiment there is provided a method to inhibit or reduce epitope spreading in a subject by administering to the subject an effective amount of soluble C1ORF32 polypeptide, fragment, variant, homolog, fusion protein or conjugate thereof, or a pharmaceutical composition thereof. Further embodiments provide a method of administering an effective amount of soluble C1ORF32 polypeptide, fragment, variant, homolog, fusion protein or conjugate thereof, or a pharmaceutical composition thereof to inhibit or reduce epitope spreading in patients with immune related disorder
C1ORF32 polypeptides, fragments, variants, homologs, fusion proteins and/or conjugates thereof can be administered in combination with one or more additional therapeutic agents, including, but not limited to, antibodies against other lymphocyte surface markers (e.g., CD40, alpha-4 integrin) or against cytokines, other fusion proteins, e.g. CTLA4-Ig (Orencia®, belatacept), TNFR-Ig (Enbrel®), TNF-alpha blockers such as Remicade, Cimzia and Humira, CD73-Ig, cyclophosphamide (CTX) (i.e. Endoxan®, Cytoxan®, Neosar®, Procytox®, Revimmune™), methotrexate (MTX) (i.e. Rheumatrex®, Trexall®), belimumab (i.e. Benlysta®), Tysabri or other immunosuppressive drugs, antiproliferatives, cytotoxic agents, or other compounds that may assist in immunosuppression.
In one embodiment, the additional therapeutic agent targets a different pathway involved in immune activation. In a further embodiment, the additional therapeutic agent is a CTLA-4 fusion protein, such as CTLA-4 Ig (abatacept). In a further embodiment, the additional therapeutic agent is a CTLA4-Ig fusion protein known as belatacept that contains two amino acid substitutions (L104E and A29Y) that markedly increases its avidity to CD86 in vivo.
In another embodiment, the second therapeutic agent is cyclophosphamide (CTX). In a further embodiment, C1ORF32 polypeptides, fragments or fusion proteins thereof and CTX are coadministered in an effective amount to treat a chronic autoimmune disease or disorder such as Systemic lupus erythematosus (SLE).
In another embodiment, the second therapeutic agent is methotrexate (MTX). In a further embodiment, C1ORF32 polypeptides, fragments or fusion proteins thereof and MTX are coadministered in an effective amount to treat a chronic autoimmune disease or disorder such as Rheumatoid arthritis (RA). In another embodiment, the second therapeutic agent increases the amount of adenosine in the serum.
In a further embodiment, the second therapeutic is CD73-Ig, recombinant CD73, or another agent (e.g. a cytokine or monoclonal antibody or small molecule) that increases the expression of CD73. In another embodiment the second therapeutic agent is Interferon-beta.
In another embodiment, the second therapeutic is Tysabri or another therapeutic for MS. In a further embodiment, C1ORF32 polypeptides, fragments or fusion proteins thereof is cycled with Tysabri or used during a drug holiday in order to allow less frequent dosing with the second therapeutic and reduce the risk of side effects such as PML and to prevent resistance to the second therapeutic.
In another embodiment, the second therapeutic agent is a small molecule that inhibits or reduces differentiation, proliferation, activity, and/or cytokine production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules. In another embodiment, the second therapeutic agent is a small molecule that interacts with Tregs, enhances Treg activity, promotes or enhances IL-10 secretion by Tregs, increases the number or percentage of Tregs, increases the suppressive capacity of Tregs, or combinations thereof. In one embodiment, the small molecule is retinoic acid or a derivative thereof. In another embodiment, the second therapeutic agent is a small molecule that interacts with Th2 cells, enhances Th2 activity, promotes or enhances IL-10, IL-4 or IL-5 production by Th2 cells, increases the number of Th2 cells, increases the immunomodulatory capacity of Th2 cells, or combinations thereof.
In one embodiment, the small molecule is retinoic acid or a derivative thereof. In another embodiment, the second therapeutic agent is a small molecule that promotes or enhances TGFbeta secretion or responsiveness to TGFbeta.
According to at least some embodiments of the present invention, there is provided use of a combination of a C1ORF32 soluble polypeptide, as recited herein, and a known therapeutic agent effective for treating immune related disorder.
According to at least some embodiments of the present invention, there is provided a method for treating immune related disorder, comprising administering to a subject in need thereof a pharmaceutical composition comprising: a soluble molecule having the extracellular domain of C1ORF32 polypeptide, or a fragment or a variant or a homolog thereof; or a fusion protein or a conjugate thereof; or polypeptide, comprising amino acid residues depicted in any of SEQ D NOs:6-41), or a fragment, or a variant, or a homolog thereof.
According to at least some embodiments of the present invention, there is provided a method for prevention of damage to the myelin coat of neural cells in the central nervous system in MS patients comprising administering to a subject in need thereof a pharmaceutical composition comprising: a soluble molecule having the extracellular domain of C1ORF32 polypeptide, or a fragment, variant, a homolog, a fusion protein or a conjugate thereof; or a polypeptide, comprising amino acid residues depicted in any of SEQ ID NOs 6-41, or a fragment or a variant or a homolog thereof; optionally provided as a pharmaceutical composition.
According to at least some embodiments of the present invention, there is provided a method for treating immune related disorder, wherein the treatment does not cause a global immunosuppression of the immune system in the subject, comprising administering to a subject in need thereof a pharmaceutical composition comprising: a soluble molecule having the extracellular domain of C1ORF32 polypeptide, fragment, variant, homolog, fusion protein or conjugate thereof; or polypeptide, comprising amino acid residues depicted in any of SEQ ID NOs 6-41, or a fragment or a variant or a homolog thereof; optionally provided as a pharmaceutical composition thereof.
According to at least some embodiments of the present invention, there is provided an isolated soluble C1ORF32 polypeptide, fragment, variant, or homolog thereof; optionally as a fusion protein or conjugate, wherein said polypeptide or said fusion protein or conjugate is used for anti-immune related condition immunotherapy for an immune related condition as described herein, optionally provided as a pharmaceutical composition. Optionally treating comprises one or more of curing, managing, reversing, attenuating, alleviating, minimizing, suppressing, managing, or halting the deleterious effects of the above-described diseases.
Treatment as Prevention of Disease and/or Symptom Onset
According to at least some embodiments, treating also includes at least reducing the rate of onset of symptoms and/or etiology of the disease, for example optionally as determined by measurement of one or more diagnostic markers.
Recently such treatment was established by testing of CTLA4-Ig (abatacept), showing that such treatment could reduce the onset of cessation or reduction of insulin production in subjects recently diagnosed with adult onset (Type II) diabetes (Orban et al., Lancet. 2011 Jul. 30; 378(9789):412-9. doi: 10.1016/S0140-6736(11)60886-6. Epub 2011 Jun. 28. Co-stimulation modulation with abatacept in patients with recent-onset type 1 diabetes: a randomised, double-blind, placebo-controlled trial). Another study, by Koura et al (Biol Blood Marrow Transplant. 2013 November; 19(11):1638-49. doi: 10.1016/j.bbmt.2013.09.003. Epub 2013 Sep. 15. In vivo T cell costimulation blockade with abatacept for acute graft-versus-host disease prevention: a first-in-disease trial), showed that graft-vs-host-disease (GVHD) could be prevented through administration of abatacept. Similar detailed studies are planned for rheumatoid arthritis and type I diabetes, to determine whether abatacept can prevent full onset of these diseases in subjects without symptoms of the disease, or with only minor initial symptoms.
With regard to the soluble proteins as described herein, including the fusion proteins as described herein, and without wishing to be limited by a single hypothesis, it is possible that for each disease described herein, prevention or delay of full onset or even symptomatic presentation of these diseases in subjects without symptoms of the disease, or with only minor initial symptoms would be possible by detecting the disease in the subject before full onset or symptomatic presentation, and then administering the soluble proteins (including the fusion proteins) as described herein to the subject according to a suitable dosing regimen.
Optionally, managing comprises reducing the severity of the disease, reducing the frequency of episodes of the disease, reducing the duration of such episodes, or reducing the severity of such episodes or a combination thereof.
Individuals at risk of developing a disease can be identified based on various approaches either before disease development or at very early stages in which disease markers can be identified (i.e. ACPA in rheumatoid arthritis patients, high blood glucose levels in pre-diabetic individuals etc.). The identification of individuals at risk as well as diagnosis of early disease can rely on various approaches including genomics, proteomics, metabolomics, lipidomics, glycomics, secretomics, and serologic approaches Family history can also provide information either in combination with one of the previously described approaches or as a standalone approach. Furthermore, over the past decade microbiome composition is becoming recognized as an important factor in health and disease. The advent of new technologies for interrogating complex microbial communities and in the analysis of microbiome and metagenome will provide another approach for identification of individuals at risk of developing a disease.
Non-limiting examples of such biomarkers and diagnostic methods for specific autoimmune diseases are described below.
For example, various specific biomarkers have been proposed for rheumatoid arthritis, to detect the initiation of the initial disease symptoms before onset of overt (frank) disease symptoms, as described for example in the Orencia clinical trial proposal (“Arthritis Prevention In the Pre-clinical Phase of Rheumatoid Arthritis with Abatacept”, DOI 10.1186/ISRCTN46017566). These biomarkers include a positive test for serum rheumatoid factor (RF) and antibodies to citrullinated protein antigens (ACPA); or alternatively being RF negative, but with high levels of serum ACPA (defined as being equal to 3× upper limit of normal [ULN] for the assay). In addition, joint pain caused by inflammatory tissue processes is considered as a biomarker.
Treatment would optionally prevent or at least slow development of rheumatoid arthritis symptoms, including but not limited to one or more of inflammation, fatigue, joint pain, joint tenderness, joint swelling, joint redness, joint warmth, joint stiffness, loss of joint range of motion, affecting more than one joint (polyarthritis), limping or joint deformity, or a combination thereof.
Other specific biomarkers have been proposed for diabetes, to detect the initiation of the initial disease symptoms before onset of overt (frank) disease symptoms, as described for example in the CTLA4-Ig (Abatacept) clinical trial proposal (“CTLA4-Ig (Abatacept) for Prevention of Abnormal Glucose Tolerance and Diabetes in Relatives At-Risk for Type 1”, ClinicalTrials.gov Identifier: NCT01773707). These biomarkers include the presence of at least one diabetes-related autoantibody, optionally not including mIAA (insulin autoantibodies). Non-limiting examples of such autoantibodies include Islet Cell Cytoplasmic Autoantibodies (ICA); Glutamic Acid Decarboxylase Autoantibodies (GADA); or Insulinoma-Associated-2 Autoantibodies (IA-2A); or a combination thereof.
Although the above biomarkers are generally considered to be related to type 1 diabetes, there is growing evidence that type 2 diabetes may have an autoimmune component and as such, autoantibody biomarkers (as well as non-autoantibody biomarkers) may also optionally be considered as determinants for treatment of patients who would otherwise go on to develop type 2 diabetes, or at least develop it more quickly without treatment (see for example Itariu et al, “Autoimmune Aspects of Type 2 Diabetes Mellitus —A Mini-Review”, Gerontology 2014; 60:189-196, DOI:10.1159/000356747). Non-limiting examples of such biomarkers include the presence of one or more of the above autoantibodies, autoantibodies against β cells, self-reactive T cells, defects in regulatory T cells (Tregs), and/or chronic immune system involved inflammation.
Optionally such autoimmune involvement may indicate the presence of latent autoimmune diabetes of the adult (LADA) as a separate clinical diagnosis.
Treatment would optionally prevent or at least slow development of Abnormal Glucose Tolerance as measured by Oral Glucose Tolerance Test (OGTT). Abnormal Glucose Tolerance is defined as:
a. Fasting plasma glucose≧110 mg/dL (6.1 mmol/L) and <126 mg/dL (7 mmol/L), or
b. 2 hour plasma glucose≧140 mg/dL (7.8 mmol/L) and <200 (11.1 mmol/L), or
c. 30, 60, 90 minute plasma glucose during OGTT≧200 mg/dL (11.1 mmol/L) (or a combination thereof).
Additionally or alternatively, treatment would reduce the level of C-peptide, or at least would slow the rate of increase of C-peptide.
Optionally, treatment would be considered for patients with one or more of the above biomarkers, to induce the above outcomes. Such treatment may optionally be indicated for patients who would otherwise continue to develop type 1 diabetes, type 2 diabetes and/or latent autoimmune diabetes of the adult (LADA).
Other specific biomarkers have been proposed for Sjögren's syndrome, to detect the initiation of the initial disease symptoms before onset of overt (frank) disease symptoms, as described for example in the following reference: Arthritis Rheumatol. 2015 Jun. 24. doi: 10.1002/art.39214. [Epub ahead of print] Autoantibody profiling can predict primary Sjögren's syndrome years before diagnosis and identify those with early onset and severe disease course. Theander E, Jonsson R, Sjöström B, Brokstad K, Olsson P, Henriksson G. Such biomarkers would relate to autoantibodies known to be characteristic of Sjögren's syndrome once overt symptoms have been established, yet which were shown to be present before overt symptoms were established.
Non-limiting examples of such autoantibodies include antinuclear antibodies (ANA), rheumatoid factor (RF), and antibodies against Ro60/SSA, Ro52/SSA and La/SSB. Optionally and preferably, one or more of anti-Ro/SSA and anti-La/SSB antibodies are analyzed to determine a risk of developing the syndrome, particularly primary Sjögren's syndrome (pSS), more preferably to determine a risk of early-onset disease and severe disease course. Optionally and most preferably, one or both of anti-Ro 60/SSA and anti-Ro 52/SSA antibodies are used as biomarkers to determine such risk.
Treatment would optionally prevent or at least slow development of overt symptoms of Sjögren's syndrome, including but not limited to a dry, gritty or burning sensation in the eyes, dry mouth, difficulty talking, chewing or swallowing, a sore or cracked tongue, dry or burning throat, dry or peeling lips, a change in taste or smell, or increased dental decay, or a combination thereof.
Other specific biomarkers have been proposed for psoriasis, to detect the initiation of the initial disease symptoms before onset of overt (frank) disease symptoms, as described for example in the following references: Tsoi et al., Nat Genet. 2012 December; 44(12): 1341-1348. Identification of fifteen new psoriasis susceptibility loci highlights the role of innate immunity; published online 2012 Nov. 11. doi: 10.1038/ng.2467; and Nair et al., Nature Genetics 41, 199-204 (2009) Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways, published online: 25 Jan. 2009|doi:10.1038/ng.311. These biomarkers include genetic markers as described in these references.
Treatment would optionally prevent or at least slow development of overt symptoms of psoriasis, including one or more of red patches of skin covered with silvery scales; small scaling spots; dry, cracked skin that may bleed; itching, burning or soreness; thickened, pitted or ridged nails; or swollen and stiff joints; or a combination thereof.
Twenty SJL/J mice were primed with PLP139-151/CFA, draining lymph nodes were collected on Day +8, reactivated ex vivo with PLP139-151 (20 μg/ml), and on Day 3 of culture cells 3×106 blast cells were transferred i.v. into recipient SJL/J mice (n=10/group). At onset of disease remission (Day +17 post disease induction) mice received three doses (100 μg/dose) per week for two weeks of Control Ig or C1ORF ECD-Fc (SEQ ID NO:42). Mice were followed for disease severity (Mean Clinical Score; A).
On Day +45 after cell transfer spleens and cervical lymph nodes were collected. Total splenocytes and total cervical lymph node cells were used for recall responses, i.e. reactivated ex vivo in the presence of anti-CD3, OVA323-339, PLP139-151, PLP178-191, or MBP84-104. Duplicate cultures were established. One set of cultures were pulsed with 1 μCi tritiated-thymidine at 24 hours and harvested at 72 hours (B and H). The supernatants of the second set of plates were harvested at 72 hours to evaluate the levels of IFN-γ (C and I), IL-17 (D and J), GM-CSF (E and K), IL-4 (F and L), and IL-10 (G and M). The averages of triplicate wells±SEMs are shown.
Statistically significant difference between control and C1ORF ECD-Fc (SEQ ID NO:42) treated groups are indicated (*,**, ***[indicate p<0.05, 0.01, 0.001 respectively).
Twenty SJL/J mice were primed with PLP139-151/CFA, draining lymph nodes were collected on Day +8, reactivated ex vivo with PLP139-151, and on Day +3 of culture 3×106 blast cell were transferred i.v. into recipient SJL/J mice (n=9/group). At onset of disease remission (Day +19 post disease induction) mice received three doses (100 μg/dose) per week for two weeks of Control Ig or C1ORF ECD-Fc (SEQ ID NO:42). Mice were followed for disease severity (Mean Clinical Score, A).
On Day +30 post cell transfer four representative mice from both Control Ig and C1ORF ECD-Fc (SEQ ID NO:42) treatment groups were intravenously injected with AngioSense®750 or with Cat B® 680 FAST imaging agents, 24 hours prior to imaging. At the time of imaging mice were anesthetized by administration of sodium pentobarbital (50 mg/kg) and then imaged using the FMT 2500 fluorescence molecular tomography in vivo imaging system. The data is presented as pmol of CathepsinB or AngioSense present within the brain (B) or spinal cord (C).
Statistically significant differences between control and C1ORF ECD-Fc (SEQ ID NO:42) treated groups are indicated (*,**, *** indicate p<0.05, 0.01, 0.001 respectively).
SJL/J mice were primed with PLP139-151/CFA, draining lymph nodes were collected on Day +8, reactivated ex vivo with PLP139-151, and on Day 3 of culture, cells were labeled with PBSE and 5×106 cells were transferred i.v. into recipient SJL/J mice (n=15/group). Beginning on the day of cell transfer, mice received three doses (100 μg/dose) per week for two weeks of Control Ig or C1ORF ECD-Fc (SEQ ID NO:42). Mice were followed for disease severity (Mean clinical score; A).
On Day +10 spleens, cervical lymph nodes, and CNS were collected and the number of total cells was enumerated (B). The following subpopulations were analyzed: frequency and numbers of PBSE- (C and D) and PBSE (E and F) and total number of T cells in the spleen (G), lymph nodes (H), and CNS (I).
Statistically significant differences between control and C1ORF ECD-Fc (SEQ ID NO:42) treated groups are indicated (*,**, ***, indicate p<0.05, 0.01, 0.001 respectively).
SJL/J-Actin/GFP mice were primed with PLP139-151/CFA, draining lymph nodes were collected on Day +8 reactivated ex vivo with PLP139-151, on Day 3 of culture cells were labeled with PBSE, and 5×106 blast cell were i.v. transferred in to recipient SJL/J mice (n=10/group). Beginning on the day of cell transfer, mice received three doses (100 μg/dose) per week for two weeks of Control Ig or C1ORF ECD-Fc (SEQ ID NO:42) and the mice were followed for disease severity (A). On Day +10 post cell transfer CNS, spleens, and cervical lymph nodes were collected. CNS cells were analyzed for recall responses (B) and the number of CD45hi/GFP+ and CD45hi/PBSE+ cells was evaluated (C and D). Spleen and lymph node were analyzed for total T cells CD3+ GFP+(E and, H), activated T cells CD3+/CD25+ GFP+(F and I) or CD3+/CD4+/CD44+/GFP+ (G and J). Statistically significant difference between control and C1ORF ECD-Fc (SEQ ID NO:42) treated groups are indicated (** indicate p<0.01).
The present invention, in at least some embodiments, relates to any one of the proteins referred to as C1ORF32, fragments, variants and homologs thereof and fusion proteins and conjugates containing same, and pharmaceutical compositions comprising same, and nucleic acid sequences encoding same, and the use thereof as a therapeutic agent for treatment of immune related disorder as described herein, including without limitation use of the ECD (extracellular domain) of a C1ORF32 protein, fragments and/or variants and/or homologs thereof (alone or as part of a fusion protein or conjugate).
Surprisingly, the inventors found that C1ORF ECD-Fc (SEQ ID NOs:42 and 43) had significant and profound effects on various models of human disease, performing at least as well as the current gold standard of care. As noted previously, there are two fusion proteins, a “human-human fusion protein” comprising an amino acid sequence of human C1ORF32 ECD fused to human immunoglobulin Fc (SEQ ID NO:43) and a “human-mouse fusion protein” comprising an amino acid sequence of human C1ORF32 ECD fused to mouse immunoglobulin Fc (SEQ ID NO:42).
For example, as shown in Example 1 (
Similarly, as shown in Example 5 (
Induction of immune tolerance by C1ORF ECD-Fc is further supported by the data presented in Examples 1-3 showing prevention of T1D development in NOD mice following a short course treatment with C1ORF ECD-Fc (SEQ ID NO:42) NOD mice spontaneously develop T1D around the age of 15-30 weeks. Induction of immune tolerance is further supported by example 4 which exemplify abolishment of transplant rejection upon treatment with by C1ORF ECD-Fc (SEQ ID NO:42). In this example, the abolishment of transplant rejection was accompanied by an increase in Tregs supporting a profound biological effect of Tregs in immune tolerance induction by C1ORF ECD-Fc.
As shown in Example 10 (
The beneficial effect of C1ORF ECD-Fc in treatment of autoimmune diseases, particularly rheumatoid arthritis was further supported with data obtained with blood cells taken from human rheumatoid arthritis patients, in which C1ORF ECD-Fc (SEQ ID NO:43) showed a strong beneficial effect similarly to that observed in the related animal models of these diseases (Examples 14-15). Thus, C1ORF ECD-Fc (SEQ ID NO:42 or SEQ ID NO:43) has been shown to provide significant therapeutic benefit in rheumatoid arthritis. Furthermore, in these examples individuals whos blood cells respond in a favorable manner to ex-vivo treatment with C1ORF ECD-Fc (SEQ ID NO:43) (i.e. decrease in Th1, Th17 and other pro-inflammatory cytokines such as for example GM-CSF and increase in Th2 cytokines, IL-10 and TGFbeta) could be identified as individuals with high chances of benefiting from treatment with C1ORF ECD-Fc. Thus, such ex-vivo test for cytokine responses can serve for identifying responsive patients.
Similarly significantly strong effects were seen with the treatment of a humanized psoriatic mouse model with C1ORF ECD-Fc (SEQ ID NO:43) in Example 12 (
Furthermore, C1ORF ECD-Fc (SEQ ID NO:43) was at least as effective as Enbrel in reducing psoriatic disease pathology and symptoms, as well as in terms of the percent of skin grafts which were free of psoriatic disease symptoms. C1ORF ECD-Fc (SEQ ID NO:43) also showed similar strength to dexamethasone in terms of reducing psoriatic disease pathology and symptoms. In addition, C1ORF32 ECD-Fc (SEQ ID NO: 43) and dexamethasone significantly reduced epidermal thickness compared with the vehicle-treated group, while no significant reduction in epidermal thickness was observed with Enbrel.
Example 16 shows an immunomodulatory activity of C1ORF32 ECD-Fc on peripheral blood cells from patients with active (relapsing/remitting) multiple sclerosis, indicating that the fusion protein is able to reduce or stop the immune processes leading to disease symptoms. This data support the therapeutic potential of C1ORF32 ECD-Fc in treating autoimmune diseases and in particular multiple sclerosis. The demonstrated induction of TGF-beta and IL-10 further support the effect of C1ORF32 ECD-Fc on regulatory immune functions including Tregs.
Furthermore such ex-vivo evaluation of the profile of cytokines secreted by patients' peripheral blood cells in response to C1ORF32 ECD-Fc could be used to identify patients that will potentially benefit from treatment with C1ORF32 ECD-Fc.
In order that the present invention may be more readily understood, certain terms are first defined. Additional definitions are set forth throughout the detailed description.
As used herein, if a plurality of serial integral values is given, then the series is assumed to include all integral values in between each integral value.
As used herein the term “isolated” refers to a compound of interest (for example a polynucleotide or a polypeptide) that is in an environment different from that in which the compound naturally occurs e.g. separated from its natural milieu such as by concentrating a peptide to a concentration at which it is not found in nature. “Isolated” includes compounds that are within samples that are substantially enriched for the compound of interest and/or in which the compound of interest is partially or substantially purified.
An “immune cell” refers to any cell from the hemopoietic origin including but not limited to T cells, B cells, monocytes, dendritic cells, and macrophages.
As used herein, the term “polypeptide” refers to a chain of amino acids of any length, regardless of modification (e.g., phosphorylation or glycosylation).
As used herein, a “costimulatory polypeptide” or “costimulatory molecule” is a polypeptide that, upon interaction with a cell-surface molecule on T cells, modulates T cell responses.
As used herein, a “costimulatory signaling” is the signaling activity resulting from the interaction between costimulatory polypeptides on antigen presenting cells and their receptors on T cells during antigen-specific T cell responses. Without wishing to be limited by a single hypothesis, the antigen-specific T cell response is believed to be mediated by two signals: 1) engagement of the T cell Receptor (TCR) with antigenic peptide presented in the context of MHC (signal 1), and 2) a second antigen-independent signal delivered by contact between different costimulatory receptor/ligand pairs (signal 2). Without wishing to be limited by a single hypothesis, this “second signal” is critical in determining the type of T cell response (activation vs inhibition) as well as the strength and duration of that response, and is regulated by both positive and negative signals from costimulatory molecules, such as the B7 family of proteins.
As used herein, the term “B7” polypeptide means a member of the B7 family of proteins that costimulate T cells including, but not limited to B7-1, B7-2, B7-DC, B7-H5, B7-H1, B7-H2, B7-H3, B7-H4, B7-H6, B7-S3 and biologically active fragments and/or variants thereof. Representative biologically active fragments include the extracellular domain or fragments of the extracellular domain that costimulate T cells.
As used herein, “inflammatory molecules” refers to molecules that induce inflammatory responses (directly or indirectly) including, but not limited to, cytokines and metalloproteases such as including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs.
As used herein, a “vector” is a replicon, such as a plasmid, phage, or cosmid, into which another DNA segment may be inserted so as to bring about the replication of the inserted segment. The vectors described herein can be expression vectors. As used herein, an “expression vector” is a vector that includes one or more expression control sequences
As used herein, an “expression control sequence” is a DNA sequence that controls and regulates the transcription and/or translation of another DNA sequence.
“Operably linked” refers to an arrangement of elements wherein the components so described are configured so as to perform their usual or intended function. Thus, two different polypeptides operably linked together retain their respective biological functions while physically linked together.
As used herein, “valency” refers to the number of binding sites available per molecule.
As used herein, a “variant” polypeptide contains at least one amino acid sequence alteration as compared to the amino acid sequence of the corresponding wild-type polypeptide.
As used herein, “conservative” amino acid substitutions are substitutions wherein the substituted amino acid has similar structural or chemical properties. As used herein, the term “host cell” refers to prokaryotic and eukaryotic cells into which a recombinant vector can be introduced.
As used herein, “transformed” and “transfected” encompass the introduction of a nucleic acid (e.g. a vector) into a cell by a number of techniques known in the art.
As used herein, the terms “immunologic”, “immunological” or “immune” response is the development of a beneficial humoral (antibody mediated) and/or a cellular (mediated by antigen-specific T cells or their secretion products) response directed against a peptide in a recipient patient. Such a response can be an active response induced by administration of immunogen or a passive response induced by administration of antibody or primed T-cells. Without wishing to be limited by a single hypothesis, a cellular immune response is elicited by the presentation of polypeptide epitopes in association with Class I or Class II MHC molecules to activate antigen-specific CD4+ T helper cells and/or CD8+ cytotoxic T cells. The response may also involve activation of monocytes, macrophages, NK cells, basophils, dendritic cells, astrocytes, microglia cells, eosinophils, activation or recruitment of neutrophils or other components of innate immunity. The presence of a cell-mediated immunological response can be determined by proliferation assays (CD4+ T cells) or CTL (cytotoxic T lymphocyte) assays. The relative contributions of humoral and cellular responses to the protective or therapeutic effect of an immunogen can be distinguished by separately isolating antibodies and T-cells from an immunized syngeneic animal and measuring protective or therapeutic effect in a second subject.
An “immunogenic agent” or “immunogen” is capable of inducing an immunological response against itself on administration to a mammal, optionally in conjunction with an adjuvant.
As used herein, the term “C1ORF32” refers to the protein as set forth in any one of SEQ ID NOs: 1-5, variants and fragments thereof, plus any soluble ectodomain (ECD) of C1ORF32, and also to C1ORF32-ECD fusion polypeptides having a first fusion partner comprising all or a part of a C1ORF32 soluble polypeptide and a second fusion partner composed of a heterologous sequence (respectively non-C1ORF32), fused together directly or indirectly via a peptide linker sequence or a chemical linker, which can have a therapeutic effect on an immune related disorder. As used herein, the terms C1ORF32 fragments and/or C1ORF32 variants and/or C1ORF32 homologs refer to portions of C1ORF32 comprising amino acid sequence having a biological activity of inhibition of T cell activation.
As used herein the term “soluble C1ORF32” or “soluble ectodomain (ECD)” or “ectodomain” or “soluble C1ORF32 proteins/molecules” refers to fragments of C1ORF32 that include some or all of the extracellular domain of the C1ORF32 polypeptide, and lack some or all of the intracellular and/or transmembrane domains, wherein said fragments retain a biological activity of inhibition of T cell activation. In one embodiment, soluble C1ORF32 polypeptide fragments include the entire extracellular domain of the C1ORF32 polypeptide. In other embodiments, the soluble fragments of C1ORF32 polypeptides include fragments of the extracellular domain.
As used herein, the term “soluble C1ORF32” or “soluble ectodomain (ECD)” or “ectodomain” or “soluble C1ORF32 proteins/molecules” further means non-cell-surface-bound (i.e. circulating) C1ORF32 molecules or any portion of a C1ORF32 molecule including, but not limited to: C1ORF32 polypeptides, fragments or fusion proteins thereof fusion proteins, wherein the extracellular domain of C1ORF32 is fused to an immunoglobulin (Ig) moiety rendering the fusion molecule soluble, or fragments and derivatives thereof, proteins with the extracellular domain of C1ORF32 fused or joined with a portion of a biologically active or chemically active protein such as the papillomavirus E7 gene product, melanoma-associated antigen p97 or HIV env protein, or fragments and derivatives thereof; hybrid (chimeric) fusion proteins such as C1ORF32 polypeptides, fragments or fusion proteins thereof, or fragments and derivatives thereof. “Soluble C1ORF32 proteins/molecules” also include C1ORF32 molecules with the transmembrane domain removed to render the protein soluble, or fragments and derivatives thereof; and soluble C1ORF32 mutant molecules. The soluble C1ORF32 molecules used in the methods of the invention may or may not include a signal (leader) peptide sequence.
The term the “soluble ectodomain (ECD)” or “ectodomain” or “soluble” form of C1ORF32 refers also to the nucleic acid sequences encoding the corresponding proteins of C1ORF32 “soluble ectodomain (ECD)” or “ectodomain” or “soluble C1ORF32 proteins/molecules”).
The C1ORF32 extracellular domain can contain one or more amino acids from the signal peptide or the putative transmembrane domain of C1ORF32. During secretion, the number of amino acids of the signal peptide that are cleaved can vary depending on the expression system and the host. Additionally or alternatively, fragments of C1ORF32 extracellular domain missing one or more amino acids from the C-terminus or the N-terminus that retain the ability to bind to the C1ORF32 receptor can be used as a fusion partner for the disclosed fusion proteins.
Useful variants of such C1ORF32 polypeptides include those that increase biological activity, as indicated by any of the assays described herein, or that increase half life or stability of the protein. Soluble C1ORF32 polypeptides and C1ORF32 fragments, or fusions thereof having C1ORF32 activity, can be engineered to increase biological activity. In a further embodiment, the C1ORF32 polypeptide or fusion protein has been modified with at least one amino acid substitution, deletion, or insertion that increases the binding of the molecule to an immune cell, for example a T cell, and transmits an inhibitory signal into the T cell.
Other optional variants are those C1ORF32 polypetpides that are engineered to selectively bind to one type of T cell versus other immune cells. For example, the C1ORF32 polypeptide can be engineered to bind optionally to Tregs, Th0, Th1, Th17, Th2 or Th22 cells. Preferential binding refers to binding that is at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or greater for one type of cell over another type of cell. Still other variants of C1ORF32 can be engineered to have reduced binding to immune cells relative to wildtype C1ORF32. These variants can be used in combination with variants having stronger binding properties to modulate the immune response with a moderate impact.
Also optionally, variant C1ORF32 polypeptides can be engineered to have an increased half-life relative to wildtype. These variants typically are modified to resist enzymatic degradation. Exemplary modifications include modified amino acid residues and modified peptide bonds that resist enzymatic degradation. Various modifications to achieve this are known in the art.
Protein Modifications
Fusion Proteins
According to at least some embodiments, C1ORF32 fusion polypeptides have a first fusion partner comprising all or a part of a C1ORF32 protein fused to a second polypeptide directly or via a linker peptide sequence or a chemical linker useful to connect the two proteins. The C1ORF32 polypeptide may optionally be fused to a second polypeptide to form a fusion protein as described herein. The presence of the second polypeptide can alter the solubility, stability, affinity and/or valency of the C1ORF32 fusion polypeptide. As used herein, “valency” refers to the number of binding sites available per molecule. In one embodiment the second polypeptide is a polypeptide from a different source or different protein.
According to at least some embodiments, the C1ORF32 protein or fragment is selected for its activity for the treatment of immune related disorder as described herein.
In one embodiment, the second polypeptide contains one or more domains of an immunoglobulin heavy chain constant region, preferably having an amino acid sequence corresponding to the hinge, CH2 and CH3 regions of a human immunoglobulin Cγ1, Cγ2, Cγ3 or Cγ4 chain or to the hinge, CH2 and CH3 regions of a murine immunoglobulin Cγ2a chain. SEQ ID NOs: 45, 46 are exemplary, non-limiting sequences for the hinge, CH2 and CH3 regions of a human immunoglobulin Cγ1.
According to at least some embodiments, the fusion protein is a dimeric fusion protein. In an optional dimeric fusion protein, the dimer results from the covalent bonding of Cys residue in the hinge region of two of the Ig heavy chains that are the same Cys residues that are disulfide linked in dimerized normal Ig heavy chains. Such proteins are referred to as C1ORF32 polypeptides, fragments or fusion proteins thereof.
In one embodiment, the immunoglobulin constant domain may contain one or more amino acid insertions, deletions or substitutions that enhance binding to specific cell types, increase the bioavailability, or increase the stability of the C1ORF32 polypeptides, fusion proteins, or fragments thereof. Suitable amino acid substitutions include conservative and non-conservative substitutions, as described above.
The fusion proteins optionally contain a domain that functions to dimerize or multimerize two or more fusion proteins. The peptide/polypeptide linker domain can either be a separate domain, or alternatively can be contained within one of the other domains (C1ORF32 polypeptide or second polypeptide) of the fusion protein. Similarly, the domain that functions to dimerize or multimerize the fusion proteins can either be a separate domain, or alternatively can be contained within one of the other domains (C1ORF32 polypeptide, second polypeptide or peptide/polypeptide linker domain) of the fusion protein. In one embodiment, the dimerization/multimerization domain and the peptide/polypeptide linker domain are the same. Further specific, illustrative and non-limiting examples of dimerization/multimerization domains and linkers are given below.
Fusion proteins disclosed herein according to at least some embodiments of the present invention are of formula I: N—R1-R2-R3-C wherein “N” represents the N-terminus of the fusion protein, “C” represents the C-terminus of the fusion protein. In the further embodiment, “R1” is a C1ORF32 polypeptide, “R2” is an optional peptide/polypeptide or chemical linker domain, and “R3” is a second polypeptide. Alternatively, R3 may be a C1ORF32 polypeptide and R1 may be a second polypeptide.
Optionally, the fusion protein comprises the C1ORF32 polypeptide fragments as described herein, fused, optionally by a linker peptide of one or more amino acids (e.g. GS) to one or more “half-life extending moieties”. A “half-life extending moiety” is any moiety, for example, a polypeptide, small molecule or polymer, that, when appended to protein, extends the in vivo half-life of that protein in the body of a subject (e.g., in the plasma of the subject). For example, a half-life extending moiety is, in an embodiment of the invention, polyethylene glycol (PEG), monomethoxy PEG (mPEG) or an immunoglobulin (Ig). In an embodiment of the invention, PEG is a 5, 10, 12, 20, 30, 40 or 50 kDa moiety or larger or comprises about 12000 ethylene glycol units (PEG12000).
The fusion protein may also optionally be prepared by chemical synthetic methods and the “join” effected chemically, either during synthesis or post-synthesis. Cross-linking and other such methods may optionally be used (optionally also with the above described genetic level fusion methods), as described for example in U.S. Pat. No. 5,547,853 to Wallner et al, which is hereby incorporated by reference as if fully set forth herein as a non-limiting example only.
According to the present invention, a fusion protein may be prepared from a protein of the invention by fusion with a portion of an immunoglobulin comprising a constant region of an immunoglobulin. More preferably, the portion of the immunoglobulin comprises a heavy chain constant region which is optionally and more preferably a human heavy chain constant region. The heavy chain constant region is most preferably an IgG heavy chain constant region, and optionally and most preferably is an Fc chain, most preferably an IgG Fc fragment that comprises the hinge, CH2 and CH3 domains. The Fc chain may optionally be a known or “wild type” Fc chain, or alternatively may be mutated or truncated. The Fc portion of the fusion protein may optionally be varied by isotype or subclass, may be a chimeric or hybrid, and/or may be modified, for example to improve effector functions, control of half-life, tissue accessibility, augment biophysical characteristics such as stability, and improve efficiency of production (and less costly). Many modifications useful in construction of disclosed fusion proteins and methods for making them are known in the art, see for example Mueller, et al, MoI. Immun, 34(6):441-452 (1997), Swann, et al., Cur. Opin. Immun, 20:493-499 (2008), and Presta, Cur. Opin. Immun 20:460-470 (2008). In some embodiments the Fc region is the native IgG1, IgG2, or IgG4 Fc region. In some embodiments the Fc region is a hybrid, for example a chimeric consisting of IgG2/IgG4 Fc constant regions.
Modifications to the Fc region include, but are not limited to, IgG4 modified to prevent binding to Fc gamma receptors and complement, IgG1 modified to improve binding to one or more Fc gamma receptors, IgG1 modified to minimize effector function (amino acid changes), IgG1 with altered/no glycan (typically by changing expression host or substituting the Asn at position 297), and IgG1 with altered pH-dependent binding to FcRn. The Fc region may include the entire hinge region, or less than the entire hinge region.
In another embodiment, the Fc domain may contain one or more amino acid insertions, deletions or substitutions that reduce binding to the low affinity inhibitory Fc receptor CD32B (FcγRIIB) and retain wild-type levels of binding to or enhance binding to the low affinity activating Fc receptor CD16A (FcγRIIIA).
Another embodiment includes IgG2-4 hybrids and IgG4 mutants that have reduced binding to FcR (Fc receptor) which increase their half life. Representative IgG2-4 hybrids and IgG4 mutants are described in Angal, S. et al., Molecular Immunology, 30(1):105-108 (1993); Mueller, J. et al., Molecular Immunology, 34(6): 441-452 (1997); and U.S. Pat. No. 6,982,323 to Wang et al. In some embodiments the IgG1 and/or IgG2 domain is deleted; for example, Angal et al. describe IgG1 and IgG2 having serine 241 replaced with a proline.
In a further embodiment, the Fc domain contains amino acid insertions, deletions or substitutions that enhance binding to CD16A. A large number of substitutions in the Fc domain of human IgG1 that increase binding to CD16A and reduce binding to CD32B are known in the art and are described in Stavenhagen, et al., Cancer Res., 57(18):8882-90 (2007). Exemplary variants of human IgG1 Fc domains with reduced binding to CD32B and/or increased binding to CD16A contain F243L, R929P, Y300L, V305I or P296L substitutions. These amino acid substitutions may be present in a human IgG1 Fc domain in any combination.
In one embodiment, the human IgG1 Fc domain variant contains a F243L, R929P and Y300L substitution. In another embodiment, the human IgG1 Fc domain variant contains a F243L, R929P, Y300L, V305I and P296L substitution. In another embodiment, the human IgG1 Fc domain variant contains an N297A/Q substitution, as these mutations abolishFcγR binding. Non-limiting, illustrative, exemplary types of mutations are described in US Patent Application No. 20060034852, published on Feb. 16, 2006, hereby incorporated by reference as if fully set forth herein. The term “Fc chain” also optionally comprises any type of Fc fragment.
Several of the specific amino acid residues that are important for antibody constant region-mediated activity in the IgG subclass have been identified. Inclusion, substitution or exclusion of these specific amino acids therefore allows for inclusion or exclusion of specific immunoglobulin constant region-mediated activity. Furthermore, specific changes may result in aglycosylation for example and/or other desired changes to the Fc chain. At least some changes may optionally be made to block a function of Fc which is considered to be undesirable, such as an undesirable immune system effect, as described in greater detail below.
Non-limiting, illustrative examples of mutations to Fc which may be made to modulate the activity of the fusion protein include the following changes (given with regard to the Fc sequence nomenclature as given by Kabat, from Kabat E A et al: Sequences of Proteins of Immunological Interest. US Department of Health and Human Services, NIH, 1991): 220C->S; 233-238 ELLGGP->EAEGAP; 265D->A, preferably in combination with 434N->A; 297N->A (for example to block N-glycosylation); 318-322 EYKCK->AYACA; 330-331AP->SS; or a combination thereof (see for example M. Clark, “Chemical Immunol and Antibody Engineering”, pp 1-31 for a description of these mutations and their effect). The construct for the Fc chain which features the above changes optionally and preferably comprises a combination of the hinge region with the CH2 and CH3 domains.
The above mutations may optionally be implemented to enhance desired properties or alternatively to block non-desired properties. For example, aglycosylation of antibodies was shown to maintain the desired binding functionality while blocking depletion of T-cells or triggering cytokine release, which may optionally be undesired functions (see M. Clark, “Chemical Immunol and Antibody Engineering”, pp 1-31). Substitution of 331proline for serine may block the ability to activate complement, which may optionally be considered an undesired function (see M. Clark, “Chemical Immunol and Antibody Engineering”, pp 1-31). Changing 330 alanine to serine in combination with this change may also enhance the desired effect of blocking the ability to activate complement.
Residues 235 and 237 were shown to be involved in antibody-dependent cell-mediated cytotoxicity (ADCC), such that changing the block of residues from 233-238 as described may also block such activity if ADCC is considered to be an undesirable function.
Residue 220 is normally a cysteine for Fc from IgG1, which is the site at which the heavy chain forms a covalent linkage with the light chain. Optionally, this residue may be changed to another amino acid residue (e.g., serine), to avoid any type of covalent linkage (see M. Clark, “Chemical Immunol and Antibody Engineering”, pp 1-31) or by deletion or truncation.
The above changes to residues 265 and 434 may optionally be implemented to reduce or block binding to the Fc receptor, which may optionally block undesired functionality of Fc related to its immune system functions (see “Binding site on Human IgG1 for Fc Receptors”, Shields et al, Vol 276, pp 6591-6604, 2001).
The above changes are intended as illustrations only of optional changes and are not meant to be limiting in any way. Furthermore, the above explanation is provided for descriptive purposes only, without wishing to be bound by a single hypothesis.
In a further embodiment, the Fc domain is composed of hybridization of hinge, CH1, CH2 and CH3 regions, which are involved in hinge flexibility, binding to Fcgamma and/or FcRn receptors, from different Fc isotypes; wherein the different Fc isotypes optionally and preferably comprise IgD and IgG4. Such “chimeric” Fc enables to control for example, affinity to the counterpart molecule (ligand/receptor), lytic activity (ADCC or CDC) and half-life (Im et al., PLoS One. 2011; 6(9) Natural form of noncytolytic flexible human Fc as a long-acting carrier of agonistic ligand, erythropoietin).
In a further embodiment, the fusion protein includes the extracellular domain of C1ORF32, or a fragment thereof fused to an Ig Fc region. Recombinant Ig-C1ORF32 polypeptides, fragments or fusion proteins thereof fusion proteins can be prepared by fusing the coding region of the extracellular domain of C1ORF32 or a fragment thereof to the Fc region of human IgG1 or mouse IgG2a, as described previously (Chapoval, et al., Methods MoI. Med, 45:247-255 (2000)).
Optionally, C1ORF32 ECD refers also to fusion protein, comprising an amino acid sequence of human C1ORF32 ECD fused to human immunoglobulin Fc (human-human fusion protein). Optionally, said fusion protein comprises the amino acid sequence of the human C1ORF32 ECD set forth in any one of SEQ ID NOs: 6-41 fused to human IgG1 Fc set forth in any one of SEQ ID NOs:45, 46, 47, 65. Optionally, the amino acid sequence of said fusion protein is set forth in any one of SEQ ID NOs: 43, 64.
Optionally, C1ORF32 ECD refers also to a fusion protein comprising an amino acid sequence of human C1ORF32 ECD fused to mouse immunoglobulin Fc (human-mouse fusion protein. Optionally, said fusion protein comprises the amino acid sequence of the human C1ORF32 ECD set forth in any one of SEQ ID NOs: 6-41 fused to mouse IgG2a_Fc set forth in any of SEQ ID NOs:43, 44. Optionally, the amino acid sequence of said fusion protein is set forth in any one of SEQ ID NOs: 42, 62.
The aforementioned exemplary fusion proteins can incorporate any combination of the variants described herein. In another embodiment the terminal lysine of the aforementioned exemplary fusion proteins is deleted.
The disclosed fusion proteins can be isolated using standard molecular biology techniques. For example, an expression vector containing a DNA sequence encoding a C1ORF32 ECD polypeptides, fragments or fusion proteins thereof fusion protein is transfected into 293 cells by calcium phosphate precipitation and cultured in serum-free DMEM. The supernatant is collected at 72 h and the fusion protein is purified by Protein G, or preferably Protein A SEPHAROSE® columns (Pharmacia, Uppsala, Sweden). Optionally, a DNA sequence encoding a C1ORF32 ECD polypeptides, fragments or fusion proteins thereof fusion protein is transfected into GPEx® retrovectors and expressed in CHO—S cells following four rounds of retrovector transduction. The protein is clarified from supernatants using protein A chromatography.
In another embodiment the second polypeptide may have a conjugation domain through which additional molecules can be bound to the C1ORF32 ECD fusion proteins. In one such embodiment, the conjugated molecule is capable of targeting the fusion protein to a particular organ or tissue; further specific, illustrative, non-limiting examples of such targeting domains and/or molecules are given below.
In another such embodiment the conjugated molecule is another immunomodulatory agent that can enhance or augment the effects of the C1ORF32 ECD fusion protein. In another embodiment the conjugated molecule is Polyethylene Glycol (PEG).
Peptide or Polypeptide Linker Domain
The disclosed C1ORF32 ECD fusion proteins optionally contain a peptide or polypeptide linker domain that separates the C1ORF32 ECD polypeptide from the second polypeptide. In one embodiment, the linker domain contains the hinge region of an immunoglobulin. In a further embodiment, the hinge region is derived from a human immunoglobulin. Suitable human immunoglobulins that the hinge can be derived from include IgG, IgD and IgA. In a further embodiment, the hinge region is derived from human IgG Amino acid sequences of immunoglobulin hinge regions and other domains are well known in the art. In one embodiment, C1ORF32 ECD fusion polypeptides contain the hinge, CH2 and CH3 regions of a human immunoglobulin Cγ1 chain, optionally with the Cys at position 220 (according to full length human IgG1, position 5 in SEQ ID NO:45) replaced with a Ser (SEQ ID NO: 46) having at least 85%, 90%, 95%, 99% or 100% sequence homology to amino acid sequence set forth in SEQ ID NO:45:
The hinge can be further shortened to remove amino acids 1, 2, 3, 4, 5, or combinations thereof of any one of SEQ ID NOs: 45, 46. In one embodiment, amino acids 1-5 of any one of SEQ ID NOs: 45, 46 are deleted. Exemplary C1ORF32 ECD fusion polypeptides comprised of the hinge, CH2 and CH3 regions of a human immunoglobulin Cγ1 chain with the Cys at position 220 replaced with a Ser are set forth in SEQ ID NOs:43.
In another embodiment, C1ORF32 ECD fusion polypeptides contain the CH2 and CH3 regions of a human immunoglobulin Cγ1 chain having at least 85%, 90%, 95%, 99% or 100% sequence homology to amino acid sequence set forth in SEQ ID NO:47:
In another embodiment, the C1ORF32 ECD fusion polypeptides contain the CH2 and CH3 regions of a murine immunoglobulin Cγ2a chain at least 85%, 90%, 95%, 99% or 100% sequence homology to amino acid sequence set forth in SEQ ID NO: 44: EPRGPTIKPCPPCKCPAPNLLGGPSVFIFPPKIKDVLMISLSPIVTCVVVDVSEDDPDV QISWFVNNVEVHTAQTQTHREDYNSTLRVVSALPIQHQDWMSGKEFKCKVNNKD LPAPIERTISKPKGSVRAPQVYVLPPPEEEMTKKQVTLTCMVTDFMPEDIYVEWTN NGKTELNYKNTEPVLDSDGSYFMYSKLRVEKKNWVERNSYSCSVVHEGLHNHHT TKSFSRTPGK. In another embodiment, the linker domain contains a hinge region of an immunoglobulin as described above, and further includes one or more additional immunoglobulin domains.
Other suitable peptide/polypeptide linker domains include naturally occurring or non-naturally occurring peptides or polypeptides. Peptide linker sequences are at least 2 amino acids in length. Optionally the peptide or polypeptide domains are flexible peptides or polypeptides. A “flexible linker” herein refers to a peptide or polypeptide containing two or more amino acid residues joined by peptide bond(s) that provides increased rotational freedom for two polypeptides linked thereby than the two linked polypeptides would have in the absence of the flexible linker. Such rotational freedom allows two or more antigen binding sites joined by the flexible linker to each access target antigen(s) more efficiently. Exemplary flexible peptides/polypeptides include, but are not limited to, the amino acid sequences Gly-Ser (SEQ ID NO:48), Gly-Ser-Gly-Ser (SEQ ID NO:49), Ala-Ser (SEQ ID NO:50), Gly-Gly-Gly-Ser (SEQ ID NO:51), Gly4-Ser (SEQ ID NO:52), (Gly4-Ser)2 (SEQ ID NO:53), (Gly4-Ser)3 (SEQ ID NO:54) and (Gly4-Ser)4 (SEQ ID NO: 55). Additional flexible peptide/polypeptide sequences are well known in the art. Other suitable peptide linker domains include the TEV linker ENLYFQG, a linear epitope recognized by the Tobacco Etch Virus protease. Exemplary peptides/polypeptides include, but are not limited to, GSENLYFQGSG (SEQ ID NO: 56). Other suitable peptide linker domains include helix forming linkers such as Ala-(Glu-Ala-Ala-Ala-Lys)n-Ala (n=1-5). Additional helix forming peptide/polypeptide sequences are well known in the art. Non-limiting examples of such linkers are depicted in SEQ ID NOs:57-61.
Dimerization, Multimerization and Targeting Domains
The fusion proteins disclosed herein optionally contain a dimerization or multimerization domain that functions to dimerize or multimerize two or more fusion proteins. The domain that functions to dimerize or multimerize the fusion proteins can either be a separate domain, or alternatively can be contained within one of the other domains (C1ORF32 ECD polypeptide, second polypeptide, or peptide/polypeptide linker domain) of the fusion protein.
Dimerization or multinierization can occur between or among two or more fusion proteins through dimerization or multimerization domains. Alternatively, dimerization or multimerization of fusion proteins can occur by chemical crosslinking. The dimers or multimers that are formed can be homodimeric/homomultimeric or heterodimeric/heteromultimeric. The second polypeptide “partner” in the C1ORF32 ECD fusion polypeptides may be comprised of one or more other proteins, protein fragments or peptides as described herein, including but not limited to any immunoglobulin (Ig) protein or portion thereof, preferably the Fc region, or a portion of a biologically or chemically active protein such as the papillomavirus E7 gene product, melanoma-associated antigen p97), and HIV env protein (gp120). The “partner” is optionally selected to provide a soluble dimer/multimer and/or for one or more other biological activities as described herein.
A “dimerization domain” is formed by the association of at least two amino acid residues or of at least two peptides or polypeptides (which may have the same, or different, amino acid sequences). The peptides or polypeptides may interact with each other through covalent and/or non-covalent associations). Optional dimerization domains contain at least one cysteine that is capable of forming an intermolecular disulfide bond with a cysteine on the partner fusion protein. The dimerization domain can contain one or more cysteine residues such that disulfide bond(s) can form between the partner fusion proteins. In one embodiment, dimerization domains contain one, two or three to about ten cysteine residues. In a further embodiment, the dimerization domain is the hinge region of an immunoglobulin.
Additional exemplary dimerization domains can be any known in the art and include, but not limited to, coiled coils, acid patches, zinc fingers, calcium hands, a CH1-CL pair, an “interface” with an engineered “knob” and/or “protruberance” as described in U.S. Pat. No. 5,821,333, leucine zippers (e.g., from jun and/or fos) (U.S. Pat. No. 5,932,448), and/or the yeast transcriptional activator GCN4, SH2 (src homology 2), SH3 (src Homology 3) (Vidal, et al, Biochemistry, 43, 7336-44 ((2004)), phosphotyrosine binding (PTB) (Zhou, et al., Nature, 378:584-592 (1995)), WW (Sudol, Frog, Biochys. MoL Bio., 65:113-132 (1996)), PDZ (Kim, et al., Nature, 378: 85-88 (1995); Komau, et al, Science, 269.1737-1740 (1995)) 14-3-3, WD40 (Hu5 et al., J Biol Chem., 273, 33489-33494 (1998)) EH, Lim, an isoleucine zipper, a receptor dimer pair (e.g., interleukin-8 receptor (IL-8R); and integrin heterodimers such as LFA-I and GPIIIb/IIIa), or the dimerization region(s) thereof, dimeric ligand polypeptides (e.g. nerve growth factor (NGF), neurotrophin-3 (NT-3), interleukin-8 (IL-8), vascular endothelial growth factor (VEGF), VEGF-C, VEGF-D, PDGF members, and brain-derived neurotrophic factor (BDNF) (Arakawa, et al., J Biol. Chem., 269(45): 27833-27839 (1994) and Radziejewski, et al., Biochem., 32(48): 1350 (1993)) and can also be variants of these domains in which the affinity is altered. The polypeptide pairs can be identified by methods known in the art, including yeast two hybrid screens. Yeast two hybrid screens are described in U.S. Pat. Nos. 5,283,173 and 6,562,576. Affinities between a pair of interacting domains can be determined using methods known in the art, including as described in Katahira, et at, J. Biol Chem, 277, 9242-9246 (2002)). Alternatively, a library of peptide sequences can be screened for heterodimerization, for example, using the methods described in WO 01/00814. Useful methods for protein-protein interactions are also described in U.S. Pat. No. 6,790,624.
A “multimerization domain” is a domain that causes three or more peptides or polypeptides to interact with each other through covalent and/or non-covalent association(s). Suitable multimerization domains include, but are not limited to, coiled-coil domains. A coiled-coil is a peptide sequence with a contiguous pattern of mainly hydrophobic residues spaced 3 and 4 residues apart, usually in a sequence of seven amino acids (heptad repeat) or eleven amino acids (undecad repeat), which assembles (folds) to form a multimeric bundle of helices. Coiled-coils with sequences including some irregular distribution of the 3 and 4 residues spacing are also contemplated. Hydrophobic residues are in particular the hydrophobic amino acids Val, Ile, Leu, Met, Tyr, Phe and Trp. “Mainly hydrophobic” means that at least 50% of the residues must be selected from the mentioned hydrophobic amino acids.
The coiled coil domain may be derived from laminin In the extracellular space, the heterotrimeric coiled coil protein laminin plays an important role in the formation of basement membranes. Apparently, the multifunctional oligomeric structure is required for laminin function. Coiled coil domains may also be derived from the thrombospondins in which three (TSP-I and TSP-2) or five (TSP-3, TSP-4 and TSP-5) chains are connected, or from COMP (COMPcc) (Guo, et at., EMBO J, 1998, 17: 5265-5272) which folds into a parallel five-stranded coiled coil (Malashkevich, et al., Science, 274: 761-765 (1996)). Additional non limiting examples of coiled-coil domains derived from other proteins, and other domains that mediate polypeptide multimerization are known in the art such as the vasodialator-stimulated phosphoprotein (VASP) domain, matrilin-1 (CMP), viral fusion peptides, soluble NSF (N-ethylmaleimide-sensitive factor) Attachment Protein receptor (SNARE) complexes, leucine-rich repeats, certain tRNA synthetases, are suitable for use in the disclosed fusion proteins.
In another embodiment, C1ORF32 ECD polypeptides, fusion proteins, or fragments thereof can be induced to form multimers by binding to a second multivalent polypeptide, such as an antibody. Antibodies suitable for use to multimerize C1ORF32 ECD polypeptides, fusion proteins, or fragments thereof include, but are not limited to, IgM antibodies and cross-linked, multivalent IgG, IgA, IgD, or IgE complexes.
Dimerization or multimerization can occur between or among two or more fusion proteins through dimerization or multimerization domains, including those described above. Alternatively, dimerization or multimerization of fusion proteins can occur by chemical crosslinking. Fusion protein dimers can be homodimers or heterodimers. Fusion protein multimers can be homomultimers or heteromultimers. Fusion protein dimers as disclosed herein are of formula
N—R1-R2-R3-C
N—R4-R5-R6-C
or, alternatively, are of formula
N—R1-R2-R3-C
C—R4-R5-R6-N
wherein the fusion proteins of the dimer provided by formula II are defined as being in a parallel orientation and the fusion proteins of the dimer provided by formula III are defined as being in an antiparallel orientation. Parallel and antiparallel dimers are also referred to as cis and trans dimers, respectively. “N” and “C” represent the N- and C-termini of the fusion protein, respectively. The fusion protein constituents “R1”, “R2” and “R3” are as defined above with respect to formula I. With respect to both formula II and formula III, “R4” is a C1ORF32 ECD polypeptide or a second polypeptide, “R5” is an optional peptide/polypeptide linker domain, and “R6” is a C1ORF32 ECD polypeptide or a second polypeptide, wherein “R6” is a C1ORF32 ECD polypeptide when “R4” is a second polypeptide, and “R6′” is a second polypeptide when “R4” is a C1ORF32 ECD polypeptide. In one embodiment, “R1” is a C1ORF32 ECD polypeptide, “R4” is also a C1ORF32 ECD polypeptide, and “R3” and “R6” are both second polypeptides.
Fusion protein dimers of formula II are defined as homodimers when “R1”=“R4”, “R2”=“R5” and “R3”=“R6”. Similarly, fusion protein dimers of formula III are defined as homodimers when “R1”=“R6”, “R2”=“R5” and “R3”=“R4”. Fusion protein dimers are defined as heterodimers when these conditions are not met for any reason. For example, heterodimers may contain domain orientations that meet these conditions (i.e., for a dimer according to formula II, “R1” and “R4” are both C1ORF32 ECD polypeptides, “R2” and “R5” are both peptide/polypeptide linker domains and “R3” and “R6” are both second polypeptides), however the species of one or more of these domains is not identical. For example, although “R3” and “R6” may both be C1ORF32 ECD polypeptides, one polypeptide may contain a wild-type C1ORF32 ECD amino acid sequence while the other polypeptide may be a variant C1ORF32 ECD polypeptide. An exemplary variant C1ORF32 ECD polypeptide is C1ORF32 ECD, polypeptide that has been modified to have increased or decreased binding to a target cell, increased activity on immune cells, increased or decreased half life or stability. Dimers of fusion proteins that contain either a CHI or CL region of an immunoglobulin as part of the polypeptide linker domain preferably form heterodimers wherein one fusion protein of the dimer contains a CHI region and the other fusion protein of the dimer contains a CL region.
Fusion proteins can also be used to form multimers. As with dimers, multimers may be parallel multimers, in which all fusion proteins of the multimer are aligned in the same orientation with respect to their N- and C-termini Multimers may be antiparallel multimers, in which the fusion proteins of the multimer are alternatively aligned in opposite orientations with respect to their N- and C-termini. Multimers (parallel or antiparallel) can be either homomultimers or heteromultimers. The fusion protein is optionally produced in dimeric form; more preferably, the fusion is performed at the genetic level as described below, by joining polynucleotide sequences corresponding to the two (or more) proteins, portions of proteins and/or peptides, such that a joined or fused protein is produced by a cell according to the joined polynucleotide sequence. A description of preparation for such fusion proteins is described with regard to U.S. Pat. No. 5,851,795 to Linsley et al, which is hereby incorporated by reference as if fully set forth herein as a non-limiting example only.
Targeting Domains
The C1ORF32 ECD polypeptides and fusion proteins can contain a targeting domain to target the molecule to specific sites in the body. Optional targeting domains target the molecule to areas of inflammation. Exemplary targeting domains are antibodies, or antigen binding fragments thereof that are specific for inflamed tissue or to a proinflammatory cytokine including but not limited to IL17, IL-4, IL-6, IL-12, IL-21, IL-22, and IL-23. In the case of neurological disorders such as Multiple Sclerosis, the targeting domain may target the molecule to the CNS or may bind to VCAM-I on the vascular epithelium. Additional targeting domains can be peptide aptamers specific for a proinflammatory molecule. In other embodiments, the C1ORF32 ECD fusion protein can include a binding partner specific for a polypeptide displayed on the surface of an immune cell, for example a T cell. In still other embodiments, the targeting domain specifically targets activated immune cells. Optional immune cells that are targeted include Th0, Th1, Th 17, Th2 and Th22 T cells, other cells that secrete, or cause other cells to secrete inflammatory molecules including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs, and Tregs. For example, a targeting domain for Tregs may bind specifically to CD25. The above changes are intended as illustrations only of optional changes and are not meant to be limiting in any way. Furthermore, the above explanation is provided for descriptive purposes only, without wishing to be bound by a single hypothesis.
Addition of Groups
If a protein according to the present invention is a linear molecule, it is possible to place various functional groups at various points on the linear molecule which are susceptible to or suitable for chemical modification. Functional groups can be added to the termini of linear forms of the protein according to at least some embodiments of the invention. In some embodiments, the functional groups improve the activity of the protein with regard to one or more characteristics, including but not limited to, improvement in stability, penetration (through cellular membranes and/or tissue barriers), tissue localization, efficacy, decreased clearance, decreased toxicity, improved selectivity, improved resistance to expulsion by cellular pumps, and the like. For convenience sake and without wishing to be limiting, the free N-terminus of one of the sequences contained in the compositions according to at least some embodiments of the invention will be termed as the N-terminus of the composition, and the free C-terminal of the sequence will be considered as the C-terminus of the composition. Either the C-terminus or the N-terminus of the sequences, or both, can be linked to a carboxylic acid functional groups or an amine functional group, respectively.
Non-limiting examples of suitable functional groups are described in Green and Wuts, “Protecting Groups in Organic Synthesis”, John Wiley and Sons, Chapters 5 and 7, 1991, the teachings of which are incorporated herein by reference. Preferred protecting groups are those that facilitate transport of the active ingredient attached thereto into a cell, for example, by reducing the hydrophilicity and increasing the lipophilicity of the active ingredient, these being an example for “a moiety for transport across cellular membranes”.
These moieties can optionally and preferably be cleaved in vivo, either by hydrolysis or enzymatically, inside the cell. (Ditter et al., J. Pharm. Sci. 57:783 (1968); Ditter et al., J. Pharm. Sci. 57:828 (1968); Ditter et al., J. Pharm. Sci. 58:557 (1969); King et al., Biochemistry 26:2294 (1987); Lindberg et al., Drug Metabolism and Disposition 17:311 (1989); and Tunek et al., Biochem. Pharm. 37:3867 (1988), Anderson et al., Arch. Biochem. Biophys. 239:538 (1985) and Singhal et al., FASEB J. 1:220 (1987)). Hydroxyl protecting groups include esters, carbonates and carbamate protecting groups Amine protecting groups include alkoxy and aryloxy carbonyl groups, as described above for N-terminal protecting groups. Carboxylic acid protecting groups include aliphatic, benzylic and aryl esters, as described above for C-terminal protecting groups. In one embodiment, the carboxylic acid group in the side chain of one or more glutamic acid or aspartic acid residue in a composition of the present invention is protected, preferably with a methyl, ethyl, benzyl or substituted benzyl ester, more preferably as a benzyl ester.
Non-limiting, illustrative examples of N-terminal protecting groups include acyl groups (—CO—R1) and alkoxy carbonyl or aryloxy carbonyl groups (—CO—O—R1), wherein R1 is an aliphatic, substituted aliphatic, benzyl, substituted benzyl, aromatic or a substituted aromatic group. Specific examples of acyl groups include but are not limited to acetyl, (ethyl)-CO—, n-propyl-CO—, iso-propyl-CO—, n-butyl-CO—, sec-butyl-CO—, t-butyl-CO—, hexyl, lauroyl, palmitoyl, myristoyl, stearyl, oleoyl phenyl-CO—, substituted phenyl-CO—, benzyl-CO— and (substituted benzyl)-CO—. Examples of alkoxy carbonyl and aryloxy carbonyl groups include CH3-O—CO—, (ethyl)-O—CO—, n-propyl-O—CO—, iso-propyl-O—CO—, n-butyl-O—CO—, sec-butyl-O—CO—, t-butyl-O—CO—, phenyl-O— CO—, substituted phenyl-O—CO— and benzyl-O—CO—, (substituted benzyl)-O—CO—, Adamantan, naphtalen, myristoleyl, toluen, biphenyl, cinnamoyl, nitrobenzoy, toluoyl, furoyl, benzoyl, cyclohexane, norbornane, or Z-caproic. In order to facilitate the N-acylation, one to four glycine residues can be present in the N-terminus of the molecule.
The carboxyl group at the C-terminus of the compound can be protected, for example, by a group including but not limited to an amide (i.e., the hydroxyl group at the C-terminus is replaced with —NH2, —NHR2 and —NR2R3) or ester (i.e. the hydroxyl group at the C-terminus is replaced with —OR2). R2 and R3 are optionally independently an aliphatic, substituted aliphatic, benzyl, substituted benzyl, aryl or a substituted aryl group. In addition, taken together with the nitrogen atom, R2 and R3 can optionally form a C4 to C8 heterocyclic ring with from about 0-2 additional heteroatoms such as nitrogen, oxygen or sulfur. Non-limiting suitable examples of suitable heterocyclic rings include piperidinyl, pyrrolidinyl, morpholino, thiomorpholino or piperazinyl. Examples of C-terminal protecting groups include but are not limited to —NH2, —NHCH3, —N(CH3)2, —NH(ethyl), —N(ethyl)2, —N(methyl) (ethyl), —NH(benzyl), —N(C1-C4 alkyl)(benzyl), —NH(phenyl), —N(C1-C4 alkyl) (phenyl), —OCH3, —O-(ethyl), —O-(n-propyl), —O-(n-butyl), —O-(iso-propyl), —O-(sec-butyl), —O-(t-butyl), —O-benzyl and —O-phenyl.
Substitution by Peptidomimetic Moieties
A “peptidomimetic organic moiety” can optionally be substituted for amino acid residues in the composition of this invention both as conservative and as non-conservative substitutions. These moieties are also termed “non-natural amino acids” and may optionally replace amino acid residues, amino acids or act as spacer groups within the peptides in lieu of deleted amino acids. The peptidomimetic organic moieties optionally and preferably have steric, electronic or configurational properties similar to the replaced amino acid and such peptidomimetics are used to replace amino acids in the essential positions, and are considered conservative substitutions. However such similarities are not necessarily required. According to preferred embodiments of the present invention, one or more peptidomimetics are selected such that the composition at least substantially retains its physiological activity as compared to the native protein according to the present invention.
Peptidomimetics may optionally be used to inhibit degradation of the peptides by enzymatic or other degradative processes. The peptidomimetics can optionally and preferably be produced by organic synthetic techniques. Non-limiting examples of suitable peptidomimetics include D amino acids of the corresponding L amino acids, tetrazol (Zabrocki et al., J. Am. Chem. Soc. 110:5875-5880 (1988)); isosteres of amide bonds (Jones et al., Tetrahedron Lett. 29: 3853-3856 (1988)); LL-3-amino-2-propenidone-6-carboxylic acid (LL-Acp) (Kemp et al., J. Org. Chem. 50:5834-5838 (1985)). Similar analogs are shown in Kemp et al., Tetrahedron Lett. 29:5081-5082 (1988) as well as Kemp et al., Tetrahedron Lett. 29:5057-5060 (1988), Kemp et al., Tetrahedron Lett. 29:4935-4938 (1988) and Kemp et al., J. Org. Chem. 54:109-115 (1987). Other suitable but exemplary peptidomimetics are shown in Nagai and Sato, Tetrahedron Lett. 26:647-650 (1985); Di Maio et al., J. Chem. Soc. Perkin Trans., 1687 (1985); Kahn et al., Tetrahedron Lett. 30:2317 (1989); Olson et al., J. Am. Chem. Soc. 112:323-333 (1990); Garvey et al., J. Org. Chem. 56:436 (1990). Further suitable exemplary peptidomimetics include hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylate (Miyake et al., J. Takeda Res. Labs 43:53-76 (1989)); 1,2,3,4-tetrahydro-isoquinoline-3-carboxylate (Kazmierski et al., J. Am. Chem. Soc. 133:2275-2283 (1991)); histidine isoquinolone carboxylic acid (HIC) (Zechel et al., Int. J. Pep. Protein Res. 43 (1991)); (2S, 3S)-methyl-phenylalanine, (2S, 3R)-methyl-phenylalanine, (2R, 3S)-methyl-phenylalanine and (2R, 3R)-methyl-phenylalanine (Kazmierski and Hruby, Tetrahedron Lett. (1991)).
Exemplary, illustrative but non-limiting non-natural amino acids include beta-amino acids (beta3 and beta2), homo-amino acids, cyclic amino acids, aromatic amino acids, Pro and Pyr derivatives, 3-substituted Alanine derivatives, Glycine derivatives, ring-substituted Phe and Tyr Derivatives, linear core amino acids or diamino acids. They are available from a variety of suppliers, such as Sigma-Aldrich (USA) for example.
Protein Chemical Modifications
In the present invention any part of a protein according to at least some embodiments of the invention may optionally be chemically modified, i.e. changed by addition of functional groups. For example the side amino acid residues appearing in the native sequence may optionally be modified, although as described below alternatively other parts of the protein may optionally be modified, in addition to or in place of the side amino acid residues. The modification may optionally be performed during synthesis of the molecule if a chemical synthetic process is followed, for example by adding a chemically modified amino acid. However, chemical modification of an amino acid when it is already present in the molecule (“in situ” modification) is also possible.
The amino acid of any of the sequence regions of the molecule can optionally be modified according to any one of the following exemplary types of modification (in the peptide conceptually viewed as “chemically modified”). Non-limiting exemplary types of modification include carboxymethylation, acylation, phosphorylation, glycosylation or fatty acylation. Ether bonds can optionally be used to join the serine or threonine hydroxyl to the hydroxyl of a sugar. Amide bonds can optionally be used to join the glutamate or aspartate carboxyl groups to an amino group on a sugar (Gang and Jeanloz, Advances in Carbohydrate Chemistry and Biochemistry, Vol. 43, Academic Press (1985); Kunz, Ang. Chem. Int. Ed. English 26:294-308 (1987)). Acetal and ketal bonds can also optionally be formed between amino acids and carbohydrates. Fatty acid acyl derivatives can optionally be made, for example, by acylation of a free amino group (e.g., lysine) (Toth et al., Peptides: Chemistry, Structure and Biology, Rivier and Marshal, eds., ESCOM Publ., Leiden, 1078-1079 (1990)).
As used herein the term “chemical modification”, when referring to a protein or peptide according to the present invention, refers to a protein or peptide where at least one of its amino acid residues is modified either by natural processes, such as processing or other post-translational modifications, or by chemical modification techniques which are well known in the art. Examples of the numerous known modifications typically include, but are not limited to: acetylation, acylation, amidation, ADP-ribosylation, glycosylation, GPI anchor formation, covalent attachment of a lipid or lipid derivative, methylation, myristylation, pegylation, prenylation, phosphorylation, ubiquitination, or any similar process.
Other types of modifications optionally include the addition of a cycloalkane moiety to a biological molecule, such as a protein, as described in PCT Application No. WO 2006/050262, hereby incorporated by reference as if fully set forth herein. These moieties are designed for use with biomolecules and may optionally be used to impart various properties to proteins.
Furthermore, optionally any point on a protein may be modified. For example, pegylation of a glycosylation moiety on a protein may optionally be performed, as described in PCT Application No. WO 2006/050247, hereby incorporated by reference as if fully set forth herein. One or more polyethylene glycol (PEG) groups may optionally be added to 0-linked and/or N-linked glycosylation. The PEG group may optionally be branched or linear. Optionally any type of water-soluble polymer may be attached to a glycosylation site on a protein through a glycosyl linker.
Altered Glycosylation
Proteins according to at least some embodiments of the invention may be modified to have an altered glycosylation pattern (i.e., altered from the original or native glycosylation pattern). As used herein, “altered” means having one or more carbohydrate moieties deleted, and/or having at least one glycosylation site added to the original protein.
Glycosylation of proteins is typically either N-linked or O-linked. N-linked refers to the attachment of the carbohydrate moiety to the side chain of an asparagine residue. The tripeptide sequences, asparagine-X-serine and asparagine-X-threonine, where X is any amino acid except proline, are the recognition sequences for enzymatic attachment of the carbohydrate moiety to the asparagine side chain. Thus, the presence of either of these tripeptide sequences in a polypeptide creates a potential glycosylation site. O-linked glycosylation refers to the attachment of one of the sugars N-acetylgalactosamine, galactose, or xylose to a hydroxyamino acid, most commonly serine or threonine, although 5-hydroxyproline or 5-hydroxylysine may also be used.
Addition of glycosylation sites to proteins according to at least some embodiments of the invention is conveniently accomplished by altering the amino acid sequence of the protein such that it contains one or more of the above-described tripeptide sequences (for N-linked glycosylation sites). The alteration may also be made by the addition of, or substitution by, one or more serine or threonine residues in the sequence of the original protein (for O-linked glycosylation sites). The protein's amino acid sequence may also be altered by introducing changes at the DNA level.
Another means of increasing the number of carbohydrate moieties on proteins is by chemical or enzymatic coupling of glycosides to the amino acid residues of the protein. Depending on the coupling mode used, the sugars may be attached to (a) arginine and histidine, (b) free carboxyl groups, (c) free sulfhydryl groups such as those of cysteine, (d) free hydroxyl groups such as those of serine, threonine, or hydroxyproline, (e) aromatic residues such as those of phenylalanine, tyrosine, or tryptophan, or (f) the amide group of glutamine. These methods are described in WO 87/05330, and in Aplin and Wriston, CRC Crit. Rev. Biochem., 22: 259-306 (1981).
Removal of any carbohydrate moieties present on proteins according to at least some embodiments of the invention may be accomplished chemically or enzymatically. Chemical deglycosylation requires exposure of the protein to trifluoromethanesulfonic acid, or an equivalent compound. This treatment results in the cleavage of most or all sugars except the linking sugar (N-acetylglucosamine or N-acetylgalactosamine), leaving the amino acid sequence intact.
Chemical deglycosylation is described by Hakimuddin et al., Arch. Biochem. Biophys., 259: 52 (1987); and Edge et al., Anal. Biochem., 118: 131 (1981). Enzymatic cleavage of carbohydrate moieties on proteins can be achieved by the use of a variety of endo- and exo-glycosidases as described by Thotakura et al., Meth. Enzymol., 138: 350 (1987).
The terms “individual”, “host”, “subject”, and “patient” are used interchangeably herein, and refer any human or nonhuman animal. The term “nonhuman animal” includes all vertebrates, e.g., mammals and non-mammals, such as nonhuman primates, sheep, dogs, cats, horses, cows chickens, amphibians, reptiles, etc.
Various aspects of the invention are described in further detail in the following subsections.
Peptides
The terms “polypeptide,” “peptide” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues. The terms apply to amino acid polymers in which one or more amino acid residue is an analog or mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers. Polypeptides can be modified, e.g., by the addition of carbohydrate residues to form glycoproteins. The terms “polypeptide,” “peptide” and “protein” include glycoproteins, as well as non-glycoproteins.
Polypeptide products can be biochemically synthesized such as by employing standard solid phase techniques. Such methods include exclusive solid phase synthesis, partial solid phase synthesis methods, fragment condensation, classical solution synthesis. These methods are preferably used when the peptide is relatively short (i.e., 10 kDa) and/or when it cannot be produced by recombinant techniques (i.e., not encoded by a nucleic acid sequence) and therefore involves different chemistry.
Solid phase polypeptide synthesis procedures are well known in the art and further described by John Morrow Stewart and Janis Dillaha Young, Solid Phase Peptide Syntheses (2nd Ed., Pierce Chemical Company, 1984).
Synthetic polypeptides can be purified by preparative high performance liquid chromatography [Creighton T. (1983) Proteins, structures and molecular principles. WH Freeman and Co. N.Y.] and the composition of which can be confirmed via amino acid sequencing.
In cases where large amounts of a polypeptide are desired, it can be generated using recombinant techniques such as described by Bitter et al., (1987) Methods in Enzymol. 153:516-544, Studier et al. (1990) Methods in Enzymol. 185:60-89, Brisson et al. (1984) Nature 310:511-514, Takamatsu et al. (1987) EMBO J. 6:307-311, Coruzzi et al. (1984) EMBO J. 3:1671-1680 and Brogli et al., (1984) Science 224:838-843, Gurley et al. (1986) Mol. Cell. Biol. 6:559-565 and Weissbach & Weissbach, 1988, Methods for Plant Molecular Biology, Academic Press, NY, Section VIII, pp 421-463.
It will be appreciated that peptides identified according to the teachings of the present invention may be degradation products, synthetic peptides or recombinant peptides as well as peptidomimetics, typically, synthetic peptides and peptoids and semipeptoids which are peptide analogs, which may have, for example, modifications rendering the peptides more stable while in a body or more capable of penetrating into cells. Such modifications include, but are not limited to N terminus modification, C terminus modification, peptide bond modification, including, but not limited to, CH2-NH, CH2-S, CH2-S═O, O═C—NH, CH2-O, CH2-CH2, S═C—NH, CH═CH or CF═CH, backbone modifications, and residue modification. Methods for preparing peptidomimetic compounds are well known in the art and are specified, for example, in Quantitative Drug Design, C.A. Ramsden Gd., Chapter 17.2, F. Choplin Pergamon Press (1992), which is incorporated by reference as if fully set forth herein. Further details in this respect are provided hereinunder.
Peptide bonds (—CO—NH—) within the peptide may be substituted, for example, by N-methylated bonds (—N(CH3)-CO—), ester bonds (—C(R)H—C—O—O—C(R)—N—), ketomethylen bonds (—CO—CH2-), α-aza bonds (—NH—N(R)—CO—), wherein R is any alkyl, e.g., methyl, carba bonds (—CH2-NH—), hydroxyethylene bonds (—CH(OH)—CH2-), thioamide bonds (—CS—NH—), olefinic double bonds (—CH═CH—), retro amide bonds (—NH—CO—), peptide derivatives (—N(R)—CH2-CO—), wherein R is the “normal” side chain, naturally presented on the carbon atom.
These modifications can occur at any of the bonds along the peptide chain and even at several (2-3) at the same time.
Natural aromatic amino acids, Trp, Tyr and Phe, may be substituted by synthetic non-natural acid such as Phenylglycine, TIC, naphthylelanine (Nol), ring-methylated derivatives of Phe, halogenated derivatives of Phe or o-methyl-Tyr.
In addition to the above, the peptides of the present invention may also include one or more modified amino acids or one or more non-amino acid monomers (e.g. fatty acids, complex carbohydrates etc).
As used herein in the specification and in the claims section below the term “amino acid” or “amino acids” is understood to include the 20 naturally occurring amino acids; those amino acids often modified post-translationally in vivo, including, for example, hydroxyproline, phosphoserine and phosphothreonine; and other unusual amino acids including, but not limited to, 2-aminoadipic acid, hydroxylysine, isodesmosine, nor-valine, nor-leucine and ornithine. Furthermore, the term “amino acid” includes both D- and L-amino acids.
Since the peptides of the present invention are preferably utilized in therapeutics which require the peptides to be in soluble form, the peptides of the present invention preferably include one or more non-natural or natural polar amino acids, including but not limited to serine and threonine which are capable of increasing peptide solubility due to their hydroxyl-containing side chain.
In cases where large amounts of the peptides of the present invention are desired, the peptides of the present invention can be generated using recombinant techniques such as described by Bitter et al., (1987) Methods in Enzymol. 153:516-544, Studier et al. (1990) Methods in Enzymol. 185:60-89, Brisson et al. (1984) Nature 310:511-514, Takamatsu et al. (1987) EMBO J. 6:307-311, Coruzzi et al. (1984) EMBO J. 3:1671-1680 and Brogli et al., (1984) Science 224:838-843, Gurley et al. (1986) Mol. Cell. Biol. 6:559-565 and Weissbach & Weissbach, 1988, Methods for Plant Molecular Biology, Academic Press, NY, Section VIII, pp 421-463.
Expression Systems
To enable cellular expression of the polynucleotides of the present invention, a nucleic acid construct according to the present invention may be used, which includes at least a coding region of one of the above nucleic acid sequences, and further includes at least one cis acting regulatory element. As used herein, the phrase “cis acting regulatory element” refers to a polynucleotide sequence, preferably a promoter, which binds a trans acting regulator and regulates the transcription of a coding sequence located downstream thereto.
Any suitable promoter sequence can be used by the nucleic acid construct of the present invention.
Preferably, the promoter utilized by the nucleic acid construct of the present invention is active in the specific cell population transformed. Examples of cell type-specific and/or tissue-specific promoters include promoters such as albumin that is liver specific [Pinkert et al., (1987) Genes Dev. 1:268-277], lymphoid specific promoters [Calame et al., (1988) Adv. Immunol. 43:235-275]; in particular promoters of T-cell receptors [Winoto et al., (1989) EMBO J. 8:729-733] and immunoglobulins; [Banerji et al. (1983) Cell 33729-740], neuron-specific promoters such as the neurofilament promoter [Byrne et al. (1989) Proc. Natl. Acad. Sci. USA 86:5473-5477], pancreas-specific promoters [Edlunch et al. (1985) Science 230:912-916] or mammary gland-specific promoters such as the milk whey promoter (U.S. Pat. No. 4,873,316 and European Application Publication No. 264,166). The nucleic acid construct of the present invention can further include an enhancer, which can be adjacent or distant to the promoter sequence and can function in up regulating the transcription therefrom.
The nucleic acid construct of the present invention preferably further includes an appropriate selectable marker and/or an origin of replication. Preferably, the nucleic acid construct utilized is a shuttle vector, which can propagate both in E. coli (wherein the construct comprises an appropriate selectable marker and origin of replication) and be compatible for propagation in cells, or integration in a gene and a tissue of choice. The construct according to the present invention can be, for example, a plasmid, a bacmid, a phagemid, a cosmid, a phage, a virus or an artificial chromosome.
Examples of suitable constructs include, but are not limited to, pcDNA3, pcDNA3.1 (+/−), pGL3, PzeoSV2 (+/−), pDisplay, pEF/myc/cyto, pCMV/myc/cyto each of which is commercially available from Invitrogen Co. (www.invitrogen.com). Examples of retroviral vector and packaging systems are those sold by Clontech, San Diego, Calif., including Retro-X vectors pLNCX and pLXSN, which permit cloning into multiple cloning sites and the transgene is transcribed from CMV promoter. Vectors derived from Mo-MuLV are also included such as pBabe, where the transgene will be transcribed from the 5′ LTR promoter.
Currently preferred in vivo nucleic acid transfer techniques include transfection with viral or non-viral constructs, such as adenovirus, lentivirus, Herpes simplex I virus, or adeno-associated virus (AAV) and lipid-based systems. Useful lipids for lipid-mediated transfer of the gene are, for example, DOTMA, DOPE, and DC-Chol [Tonkinson et al., Cancer Investigation, 14(1): 54-65 (1996)]. The most preferred constructs for use in gene therapy are viruses, most preferably adenoviruses, AAV, lentiviruses, or retroviruses. A viral construct such as a retroviral construct includes at least one transcriptional promoter/enhancer or locus-defining elements, or other elements that control gene expression by other means such as alternate splicing, nuclear RNA export, or post-translational modification of messenger. Such vector constructs also include a packaging signal, long terminal repeats (LTRs) or portions thereof, and positive and negative strand primer binding sites appropriate to the virus used, unless it is already present in the viral construct. In addition, such a construct typically includes a signal sequence for secretion of the peptide from a host cell in which it is placed. Preferably the signal sequence for this purpose is a mammalian signal sequence or the signal sequence of the polypeptides of the present invention. Optionally, the construct may also include a signal that directs polyadenylation, as well as one or more restriction sites and a translation termination sequence. By way of example, such constructs will typically include a 5′ LTR, a tRNA binding site, a packaging signal, an origin of second-strand DNA synthesis, and a 3′ LTR or a portion thereof. Other vectors can be used that are non-viral, such as cationic lipids, polylysine, and dendrimers.
Recombinant Expression Vectors and Host Cells
Another aspect of the invention pertains to vectors, preferably expression vectors, containing a nucleic acid encoding a protein of the invention, or derivatives, fragments, analogs or homologs thereof. As used herein, the term “vector” refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. One type of vector is a “plasmid”, which refers to a circular double stranded DNA loop into which additional DNA segments can be ligated. Another type of vector is a viral vector, wherein additional DNA segments can be ligated into the viral genome. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors having a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. Moreover, certain vectors are capable of directing the expression of genes to which they are operatively-linked. Such vectors are referred to herein as “expression vectors”. In general, expression vectors of utility in recombinant DNA techniques are often in the form of plasmids. In the present specification, “plasmid” and “vector” can be used interchangeably as the plasmid is the most commonly used form of vector. However, the invention is intended to include such other forms of expression vectors, such as viral vectors (e.g., replication defective retroviruses, adenoviruses and adeno-associated viruses), which serve equivalent functions.
The recombinant expression vectors of the invention comprise a nucleic acid of the invention in a form suitable for expression of the nucleic acid in a host cell, which means that the recombinant expression vectors include one or more regulatory sequences, selected on the basis of the host cells to be used for expression, that is operatively-linked to the nucleic acid sequence to be expressed. Within a recombinant expression vector, “operably-linked” is intended to mean that the nucleotide sequence of interest is linked to the regulatory sequences in a manner that allows for expression of the nucleotide sequence (e.g., in an in vitro transcription/translation system or in a host cell when the vector is introduced into the host cell).
The term “regulatory sequence” is intended to include promoters, enhancers and other expression control elements (e.g., polyadenylation signals). Such regulatory sequences are described, for example, in Goeddel, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990). Regulatory sequences include those that direct constitutive expression of a nucleotide sequence in many types of host cell and those that direct expression of the nucleotide sequence only in certain host cells (e.g., tissue-specific regulatory sequences). It will be appreciated by those skilled in the art that the design of the expression vector can depend on such factors as the choice of the host cell to be transformed, the level of expression of protein desired, etc. The expression vectors of the invention can be introduced into host cells to thereby produce proteins or peptides, including fusion proteins or peptides, encoded by nucleic acids as described herein.
The recombinant expression vectors of the invention can be designed for production of variant proteins in prokaryotic or eukaryotic cells. For example, proteins of the invention can be expressed in bacterial cells such as Escherichia coli, insect cells (using baculovirus expression vectors) yeast cells or mammalian cells. Suitable host cells are discussed further in Goeddel, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990). Alternatively, the recombinant expression vector can be transcribed and translated in vitro, for example using T7 promoter regulatory sequences and T7 polymerase.
Expression of proteins in prokaryotes is most often carried out in Escherichia coli with vectors containing constitutive or inducible promoters directing the expression of either fusion or non-fusion proteins. Fusion vectors add a number of amino acids to a protein encoded therein, to the amino or C terminus of the recombinant protein. Such fusion vectors typically serve three purposes: (i) to increase expression of recombinant protein; (ii) to increase the solubility of the recombinant protein; and (iii) to aid in the purification of the recombinant protein by acting as a ligand in affinity purification. Often, in fusion expression vectors, a proteolytic cleavage site is introduced at the junction of the fusion moiety and the recombinant protein to enable separation of the recombinant protein from the fusion moiety subsequent to purification of the fusion protein. Such enzymes, and their cognate recognition sequences, include Factor Xa, thrombin, PreScission, TEV and enterokinase. Typical fusion expression vectors include pGEX (Pharmacia Biotech Inc; Smith and Johnson, 1988. Gene 67: 31-40), pMAL (New England Biolabs, Beverly, Mass.) and pRITS (Pharmacia, Piscataway, N.J.) that fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein.
Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amrann et al., (1988) Gene 69:301-315) and pET 11d (Studier et al., Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990) 60-89)-not accurate, pET11a-d have N terminal T7 tag.
One strategy to maximize recombinant protein expression in E. coli is to express the protein in a host bacterium with an impaired capacity to proteolytically cleave the recombinant protein. See, e.g., Gottesman, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990) 119-128. Another strategy is to alter the nucleic acid sequence of the nucleic acid to be inserted into an expression vector so that the individual codons for each amino acid are those preferentially utilized in E. coli (see, e.g., Wada, et al., 1992. Nucl. Acids Res. 20: 2111-2118). Such alteration of nucleic acid sequences of the invention can be carried out by standard DNA synthesis techniques. Another strategy to solve codon bias is by using BL21-codon plus bacterial strains (Invitrogen) or Rosetta bacterial strain (Novagen), these strains contain extra copies of rare E. coli tRNA genes.
In another embodiment, the expression vector encoding for the protein of the invention is a yeast expression vector. Examples of vectors for expression in yeast Saccharomyces cerevisiae include pYepSecl (Baldari, et al., 1987. EMBO J. 6: 229-234), pMFa (Kurjan and Herskowitz, 1982. Cell 30: 933-943), pJRY88 (Schultz et al., 1987. Gene 54: 113-123), pYES2 (Invitrogen Corporation, San Diego, Calif.), and picZ (InVitrogen Corp, San Diego, Calif.).
Alternatively, polypeptides of the present invention can be produced in insect cells using baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e.g., SF9 cells) include the pAc series (Smith, et al., 1983. Mol. Cell. Biol. 3: 2156-2165) and the pVL series (Lucklow and Summers, 1989. Virology 170: 31-39).
In yet another embodiment, a nucleic acid of the invention is expressed in mammalian cells using a mammalian expression vector. Examples of mammalian expression vectors include pCDM8 (Seed, 1987. Nature 329: 840) and pMT2PC (Kaufman, et al., 1987. EMBO J. 6: 187-195), pIRESpuro (Clontech), pUB6 (Invitrogen), pCEP4 (Invitrogen) pREP4 (Invitrogen), pcDNA3 (Invitrogen). When used in mammalian cells, the expression vector's control functions are often provided by viral regulatory elements. For example, commonly used promoters are derived from polyoma, adenovirus 2, cytomegalovirus, Rous Sarcoma Virus, and simian virus 40. For other suitable expression systems for both prokaryotic and eukaryotic cells see, e.g., Chapters 16 and 17 of Sambrook, et al., Molecular Cloning: A Laboratory Manual. 2nd ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.
In another embodiment, the recombinant mammalian expression vector is capable of directing expression of the nucleic acid preferentially in a particular cell type (e.g., tissue-specific regulatory elements are used to express the nucleic acid). Tissue-specific regulatory elements are known in the art. Non-limiting examples of suitable tissue-specific promoters include the albumin promoter (liver-specific; Pinkert, et al., 1987. Genes Dev. 1: 268-277), lymphoid-specific promoters (Calame and Eaton, 1988. Adv. Immunol. 43: 235-275), in particular promoters of T cell receptors (Winoto and Baltimore, 1989. EMBO J. 8: 729-733) and immunoglobulins (Banerji, et al., 1983. Cell 33: 729-740; Queen and Baltimore, 1983. Cell 33: 741-748), neuron-specific promoters (e.g., the neurofilament promoter; Byrne and Ruddle, 1989. Proc. Natl. Acad. Sci. USA 86: 5473-5477), pancreas-specific promoters (Edlund, et al., 1985. Science 230: 912-916), and mammary gland-specific promoters (e.g., milk whey promoter; U.S. Pat. No. 4,873,316 and European Application Publication No. 264,166). Developmentally-regulated promoters are also encompassed, e.g., the murine hox promoters (Kessel and Gruss, 1990. Science 249: 374-379) and the alpha-fetoprotein promoter (Campes and Tilghman, 1989. Genes Dev. 3: 537-546).
The present invention in at least some embodiments further provides a recombinant expression vector comprising a DNA molecule of the invention cloned into the expression vector in an antisense orientation. That is, the DNA molecule is operatively-linked to a regulatory sequence in a manner that allows for expression (by transcription of the DNA molecule) of an RNA molecule that is antisense to mRNA encoding for protein of the invention. Regulatory sequences operatively linked to a nucleic acid cloned in the antisense orientation can be chosen that direct the continuous expression of the antisense RNA molecule in a variety of cell types, for instance viral promoters and/or enhancers, or regulatory sequences can be chosen that direct constitutive, tissue specific or cell type specific expression of antisense RNA. The antisense expression vector can be in the form of a recombinant plasmid, phagemid or attenuated virus in which antisense nucleic acids are produced under the control of a high efficiency regulatory region, the activity of which can be determined by the cell type into which the vector is introduced. For a discussion of the regulation of gene expression using antisense genes see, e.g., Weintraub, et al., “Antisense RNA as a molecular tool for genetic analysis,” Reviews-Trends in Genetics, Vol. 1(1) 1986.
Another aspect of the invention pertains to host cells into which a recombinant expression vector of the invention has been introduced. The terms “host cell” and “recombinant host cell” are used interchangeably herein. It is understood that such terms refer not only to the particular subject cell but also to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein.
A host cell can be any prokaryotic or eukaryotic cell. For example, protein of the invention can be produced in bacterial cells such as E. coli, insect cells, yeast, plant or mammalian cells (such as Chinese hamster ovary cells (CHO) or COS or 293 cells). Other suitable host cells are known to those skilled in the art.
Vector DNA can be introduced into prokaryotic or eukaryotic cells via conventional transformation or transfection techniques. As used herein, the terms “transformation” and “transfection” are intended to refer to a variety of art-recognized techniques for introducing foreign nucleic acid (e.g., DNA) into a host cell, including calcium phosphate or calcium chloride co-precipitation, DEAE-dextran-mediated transfection, lipofection, or electroporation. Suitable methods for transforming or transfecting host cells can be found in Sambrook, et al. (Molecular Cloning: A Laboratory Manual. 2nd ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989), and other laboratory manuals.
For stable transfection of mammalian cells, it is known that, depending upon the expression vector and transfection technique used, only a small fraction of cells may integrate the foreign DNA into their genome. In order to identify and select these integrants, a gene that encodes a selectable marker (e.g., resistance to antibiotics) is generally introduced into the host cells along with the gene of interest. Various selectable markers include those that confer resistance to drugs, such as G418, hygromycin, puromycin, blasticidin and methotrexate. Nucleic acids encoding a selectable marker can be introduced into a host cell on the same vector as that encoding protein of the invention or can be introduced on a separate vector. Cells stably transfected with the introduced nucleic acid can be identified by drug selection (e.g., cells that have incorporated the selectable marker gene will survive, while the other cells die).
A host cell of the invention, such as a prokaryotic or eukaryotic host cell in culture, can be used to produce (i.e., express) protein of the invention. Accordingly, the present invention in at least some embodiments further provides methods for producing proteins of the invention using the host cells of the invention. In one embodiment, the method comprises culturing the host cell of the present invention (into which a recombinant expression vector encoding protein of the invention has been introduced) in a suitable medium such that the protein of the invention is produced. In another embodiment, the method further comprises isolating protein of the invention from the medium or the host cell.
For efficient production of the protein, it is preferable to place the nucleotide sequences encoding the protein of the invention under the control of expression control sequences optimized for expression in a desired host. For example, the sequences may include optimized transcriptional and/or translational regulatory sequences (such as altered Kozak sequences).
It should be noted, that according to at least some embodiments of the present invention the C1ORF32 polypeptides as described herein may optionally be isolated as naturally-occurring polypeptides, or from any source whether natural, synthetic, semi-synthetic or recombinant. Accordingly, the C1ORF32 proteins may be isolated as naturally-occurring proteins from any species, particularly mammalian, including bovine, ovine, porcine, murine, equine, and preferably human. Alternatively, the C1ORF32 proteins may be isolated as recombinant polypeptides that are expressed in prokaryote or eukaryote host cells, or isolated as a chemically synthesized polypeptide.
A skilled artisan can readily employ standard isolation methods to obtain isolated C1ORF32 proteins. The nature and degree of isolation will depend on the source and the intended use of the isolated molecules.
Protein Chemical Modifications
In the present invention any part of a protein of the invention may optionally be chemically modified, i.e. changed by addition of functional groups. For example the side amino acid residues appearing in the native sequence may optionally be modified, although as described below alternatively other parts of the protein may optionally be modified, in addition to or in place of the side amino acid residues. The modification may optionally be performed during synthesis of the molecule if a chemical synthetic process is followed, for example by adding a chemically modified amino acid. However, chemical modification of an amino acid when it is already present in the molecule (“in situ” modification) is also possible.
The amino acid of any of the sequence regions of the molecule can optionally be modified according to any one of the following exemplary types of modification (in the peptide conceptually viewed as “chemically modified”). Non-limiting exemplary types of modification include carboxymethylation, acylation, phosphorylation, glycosylation or fatty acylation. Ether bonds can optionally be used to join the serine or threonine hydroxyl to the hydroxyl of a sugar. Amide bonds can optionally be used to join the glutamate or aspartate carboxyl groups to an amino group on a sugar (Gang and Jeanloz, Advances in Carbohydrate Chemistry and Biochemistry, Vol. 43, Academic Press (1985); Kunz, Ang. Chem. Int. Ed. English 26:294-308 (1987)). Acetal and ketal bonds can also optionally be formed between amino acids and carbohydrates. Fatty acid acyl derivatives can optionally be made, for example, by acylation of a free amino group (e.g., lysine) (Toth et al., Peptides: Chemistry, Structure and Biology, Rivier and Marshal, eds., ESCOM Publ., Leiden, 1078-1079 (1990)).
As used herein the term “chemical modification”, when referring to a protein or peptide according to the present invention, refers to a protein or peptide where at least one of its amino acid residues is modified either by natural processes, such as processing or other post-translational modifications, or by chemical modification techniques which are well known in the art. Examples of the numerous known modifications typically include, but are not limited to: acetylation, acylation, amidation, ADP-ribosylation, glycosylation, GPI anchor formation, covalent attachment of a lipid or lipid derivative, methylation, myristylation, pegylation, prenylation, phosphorylation, ubiquitination, or any similar process.
Other types of modifications optionally include the addition of a cycloalkane moiety to a biological molecule, such as a protein, as described in PCT Application No. WO 2006/050262, hereby incorporated by reference as if fully set forth herein. These moieties are designed for use with biomolecules and may optionally be used to impart various properties to proteins.
Furthermore, optionally any point on a protein may be modified. For example, pegylation of a glycosylation moiety on a protein may optionally be performed, as described in PCT Application No. WO 2006/050247, hereby incorporated by reference as if fully set forth herein. One or more polyethylene glycol (PEG) groups may optionally be added to 0-linked and/or N-linked glycosylation. The PEG group may optionally be branched or linear. Optionally any type of water-soluble polymer may be attached to a glycosylation site on a protein through a glycosyl linker.
Altered Glycosylation Protein Modification
Proteins of the invention may be modified to have an altered glycosylation pattern (i.e., altered from the original or native glycosylation pattern). As used herein, “altered” means having one or more carbohydrate moieties deleted, and/or having at least one glycosylation site added to the original protein.
Glycosylation of proteins is typically either N-linked or O-linked. N-linked refers to the attachment of the carbohydrate moiety to the side chain of an asparagine residue. The tripeptide sequences, asparagine-X-serine and asparagine-X-threonine, where X is any amino acid except proline, are the recognition sequences for enzymatic attachment of the carbohydrate moiety to the asparagine side chain. Thus, the presence of either of these tripeptide sequences in a polypeptide creates a potential glycosylation site. O-linked glycosylation refers to the attachment of one of the sugars N-acetylgalactosamine, galactose, or xylose to a hydroxyamino acid, most commonly serine or threonine, although 5-hydroxyproline or 5-hydroxylysine may also be used.
Addition of glycosylation sites to proteins of the invention is conveniently accomplished by altering the amino acid sequence of the protein such that it contains one or more of the above-described tripeptide sequences (for N-linked glycosylation sites). The alteration may also be made by the addition of, or substitution by, one or more serine or threonine residues in the sequence of the original protein (for O-linked glycosylation sites). The protein's amino acid sequence may also be altered by introducing changes at the DNA level.
Another means of increasing the number of carbohydrate moieties on proteins is by chemical or enzymatic coupling of glycosides to the amino acid residues of the protein. Depending on the coupling mode used, the sugars may be attached to (a) arginine and histidine, (b) free carboxyl groups, (c) free sulfhydryl groups such as those of cysteine, (d) free hydroxyl groups such as those of serine, threonine, or hydroxyproline, (e) aromatic residues such as those of phenylalanine, tyrosine, or tryptophan, or (f) the amide group of glutamine. These methods are described in WO 87/05330, and in Aplin and Wriston, CRC Crit. Rev. Biochem., 22: 259-306 (1981).
Removal of any carbohydrate moieties present on proteins of the invention may be accomplished chemically, enzymatically or by introducing changes at the DNA level. Chemical deglycosylation requires exposure of the protein to trifluoromethanesulfonic acid, or an equivalent compound. This treatment results in the cleavage of most or all sugars except the linking sugar (N-acetylglucosamine or N-acetylgalactosamine), leaving the amino acid sequence intact.
Chemical deglycosylation is described by Hakimuddin et al., Arch. Biochem. Biophys., 259: 52 (1987); and Edge et al., Anal. Biochem., 118: 131 (1981). Enzymatic cleavage of carbohydrate moieties on proteins can be achieved by the use of a variety of endo- and exo-glycosidases as described by Thotakura et al., Meth. Enzymol., 138: 350 (1987).
METHODS OF TREATMENT
As mentioned hereinabove the C1ORF32 proteins and polypeptides of the present invention as fusion proteins, preferably of the ectodomain or secreted forms of C1ORF32 proteins, can be used to treat any immune related disorder as described herein.
Thus, according to an additional aspect of the present invention there is provided a method of treating immune related disorder.
As used herein the term “treating” refers to preventing, delaying the onset of, curing, reversing, attenuating, alleviating, minimizing, suppressing or halting the deleterious effects of the above-described diseases, disorders or conditions. It also includes managing the disease as described above. By “manage” it is meant reducing the severity of the disease, reducing the frequency of episodes of the disease, reducing the duration of such episodes, reducing the severity of such episodes and the like.
Treating, according to the present invention, can be effected by specifically upregulating the amount and/or the expression of at least one of the polypeptides of the present invention in the subject.
Optionally, upregulation may be effected by administering to the subject at least one of the polypeptides of the present invention (e.g., recombinant or synthetic) or an active portion thereof, as described herein. The polypeptide or peptide may optionally be administered in as part of a pharmaceutical composition, described in more detail below.
It will be appreciated that treatment of the above-described diseases according to at least some embodiments of the present invention may be combined with other treatment methods known in the art useful for treating immune related condition (i.e., combination therapy), as described herein.
The treatment of above-described diseases according to at least some embodiments of the present invention may be combined with identification of individuals at risk for developing an autoimmune disease or condition and treatment according to the present invention initiated prior to full manifestation of disease symptoms.
Optionally the moiety is selected from the group consisting of immunosuppressants such as corticosteroids, cyclosporin, cyclophosphamide, prednisone, azathioprine, methotrexate, rapamycin, tacrolimus, leflunomide or an analog thereof; mizoribine; mycophenolic acid; mycophenolate mofetil; 15-deoxyspergualine or an analog thereof; biological agents such as TNF-alpha blockers or antagonists, or any other biological agent targeting any inflammatory cytokine, nonsteroidal antiinflammatory drugs/Cox-2 inhibitors, hydroxychloroquine, sulphasalazopryine, gold salts, etanercept, infliximab, mycophenolate mofetil, basiliximab, atacicept, rituximab, cytoxan, interferon beta-1a, interferon beta-1b, glatiramer acetate, mitoxantrone hydrochloride, anakinra and/or other biologics and/or intravenous immunoglobulin (IVIG), interferons such as IFN-beta-1a (REBIF®. AVONEX® and CINNOVEX®) and IFN-beta-1b (BETASERON®); EXTAVIA®, BETAFERON®, ZIFERON®); glatiramer acetate (COPAXONE®), a polypeptide; natalizumab (TYSABRI®), mitoxantrone (NOVANTRONE®), a cytotoxic agent, a calcineurin inhibitor, e.g. cyclosporin A or FK506; an immunosuppressive macrolide, e.g. rapamycine or a derivative thereof; e.g. 40-O-(2-hydroxy)ethyl-rapamycin, a lymphocyte homing agent, e.g. FTY720 or an analog thereof, corticosteroids; cyclophosphamide; azathioprene; methotrexate; leflunomide or an analog thereof; mizoribine; mycophenolic acid; mycophenolate mofetil; 15-deoxyspergualine or an analog thereof; immunosuppressive monoclonal antibodies, e.g., monoclonal antibodies to leukocyte receptors, e.g., MHC, CD2, CD3, CD4, CD11a/CD18, CD7, CD25, CD27, B7, CD40, CD45, CD58, CD137, ICOS, CD150 (SLAM), OX40, 4-1BB or their ligands; or other immunomodulatory compounds, e.g. CTLA4-Ig (abatacept, ORENCIA®, belatacept), CD28-Ig, B7-H4-Ig, or other costimulatory agents, or adhesion molecule inhibitors, e.g. mAbs or low molecular weight inhibitors including LFA-1 antagonists, Selectin antagonists and VLA-4 antagonists, or another immunomodulatory agent.
Thus, treatment of multiple sclerosis using the agents according to at least some embodiments of the present invention may be combined with, for example, any known therapeutic agent or method for treating multiple sclerosis. Non-limiting examples of such known therapeutic agent or method for treating multiple sclerosis include interferon class, IFN-beta-1a (REBIF®. AVONEX® and CINNOVEX®) and IFN-beta-1b (BETASERON®, EXTAVIA®, BETAFERON®, ZIFERON®); glatiramer acetate (COPAXONE®), a polypeptide; natalizumab (TYSABRI®); and mitoxantrone (NOVANTRONE®), a cytotoxic agent, Fampridine (AMPYRA®). Other drugs include corticosteroids, methotrexate, cyclophosphamide, azathioprine, and intravenous immunoglobulin (IVIG), inosine, Ocrelizumab (R1594), Mylinax (Caldribine), alemtuzumab (Campath), daclizumab (Zenapax), Panaclar/dimethyl fumarate (BG-12), Teriflunomide (HMR1726), fingolimod (FTY720), laquinimod (ABR216062), as well as Haematopoietic stem cell transplantation, Neurovax, Rituximab (Rituxan) BCG vaccine, low dose naltrexone, helminthic therapy, angioplasty, venous stents, and alternative therapy, such as vitamin D, polyunsaturated fats, medical marijuana.
Thus, treatment of rheumatoid arthritis, using the agents according to at least some embodiments of the present invention may be combined with, for example, any known therapeutic agent or method for treating rheumatoid arthritis. Non-limiting examples of such known therapeutic agents or methods for treating rheumatoid arthritis include glucocorticoids, nonsteroidal anti-inflammatory drug (NSAID) such as salicylates, or cyclooxygenase-2 inhibitors, ibuprofen and naproxen, diclofenac, indomethacin, etodolac Disease-modifying antirheumatic drugs (DMARDs)-Oral DMARDs: Auranofin (Ridaura), Azathioprine (Imuran), Cyclosporine (Sandimmune, Gengraf, Neoral, generic), D-Penicillamine (Cuprimine), Hydroxychloroquine (Plaquenil), IM gold Gold sodium thiomalate (Myochrysine) Aurothioglucose (Solganal), Leflunomide (Arava), Methotrexate (Rheumatrex), Minocycline (Minocin), Staphylococcal protein A immunoadsorption (Prosorba column), Sulfasalazine (Azulfidine). Biologic DMARDs: TNF-α blockers including Adalimumab (Humira), Etanercept (Enbrel), Infliximab (Remicade), golimumab (Simponi), certolizumab pegol (Cimzia), and other Biological DMARDs, such as Anakinra (Kineret), Rituximab (Rituxan), Tocilizumab (Actemra), CD28 inhibitor including Abatacept (Orencia) and Belatacept.
Thus, treatment of IBD, using the agents according to at least some embodiments of the present invention may be combined with, for example, any known therapeutic agent or method for treating IBD. Non-limiting examples of such known therapeutic agents or methods for treating IBD include immunosuppression to control the symptom, such as prednisone, Mesalazine (including Asacol, Pentasa, Lialda, Aspiro), azathioprine (Imuran), methotrexate, or 6-mercaptopurine, steroids, Ondansetron, TNF-α blockers (including infliximab, adalimumab golimumab, certolizumab pegol), Orencia (abatacept), ustekinumab (Stelara®), Briakinumab (ABT-874), Certolizumab pegol (Cimzia®), ITF2357 (givinostat), Natalizumab (Tysabri), Firategrast (SB-683699), Remicade (infliximab), vedolizumab (MLN0002), other drugs including GSK1605786 CCX282-B (Traficet-EN), AJM300, Stelara (ustekinumab), Semapimod (CNI-1493) tasocitinib (CP-690550), LMW Heparin MMX, Budesonide MMX, Simponi (golimumab), MultiStem®, Gardasil HPV vaccine, Epaxal Berna (virosomal hepatitis A vaccine), surgery, such as bowel resection, strictureplasty or a temporary or permanent colostomy or ileostomy; antifungal drugs such as nystatin (a broad spectrum gut antifungal) and either itraconazole (Sporanox) or fluconazole (Diflucan); alternative medicine, prebiotics and probiotics, cannabis, Helminthic therapy or ova of the Trichuris suis helminth.
Thus, treatment of psoriasis, using the agents according to at least some embodiments of the present invention may be combined with, for example, any known therapeutic agent or method for treating psoriasis. Non-limiting examples of such known therapeutics for treating psoriasis include topical agents, typically used for mild disease, phototherapy for moderate disease, and systemic agents for severe disease. Non-limiting examples of topical agents: bath solutions and moisturizers, mineral oil, and petroleum jelly; ointment and creams containing coal tar, dithranol (anthralin), corticosteroids like desoximetasone (Topicort), Betamethasone, fluocinonide, vitamin D3 analogues (for example, calcipotriol), and retinoids. Non-limiting examples of phototherapy: sunlight; wavelengths of 311-313 nm, psoralen and ultraviolet A phototherapy (PUVA). Non-limiting examples of systemic agents: Biologics, such as interleukin antagonists, TNF-α blockers including antibodies such as infliximab (Remicade), adalimumab (Humira), golimumab, certolizumab pegol, and recombinant TNF-α decoy receptor, etanercept (Enbrel); drugs that target T cells, such as efalizumab (Xannelim/Raptiva), alefacept (Ameviv), dendritic cells such Efalizumab; monoclonal antibodies (MAbs) targeting cytokines, including anti-IL-12/IL-23 (ustekinumab (brand name Stelara)) and anti-Interleukin-17; Briakinumab (ABT-874); small molecules, including but not limited to ISA247; Immunosuppressants, such as methotrexate, cyclosporine; vitamin A and retinoids (synthetic forms of vitamin A); and alternative therapy, such as changes in diet and lifestyle, fasting periods, low energy diets and vegetarian diets, diets supplemented with fish oil rich in Vitamin A and Vitamin D (such as cod liver oil), Fish oils rich in the two omega-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) and contain Vitamin E Ichthyotherapy, Hypnotherapy, cannabis.
Thus, treatment of type 1 diabetes, using the agents according to at least some embodiments of the present invention may be combined with, for example, any known therapeutic agent or method for treating type 1 diabetes. Non-limiting examples of such known therapeutics for treating type 1 diabetes include insulin, insulin analogs, islet transplantation, stem cell therapy including PROCHYMAL®, non-insulin therapies such as il-1beta inhibitors including Anakinra (Kineret®), Abatacept (Orencia®), Diamyd, alefacept (Ameviv®), Otelixizumab, DiaPep277 (Hsp60 derived peptide), Alpha 1-Antitrypsin, Prednisone, azathioprine, Ciclosporin, E1-INT (an injectable islet neogenesis therapy comprising an epidermal growth factor analog and a gastrin analog), statins including Zocor®, Simlup®, Simcard®, Simvacor®, Sitagliptin (dipeptidyl peptidase (DPP-4) inhibitor), Anti-CD3 mAb (e.g., Teplizumab); CTLA4-Ig (abatacept), Anti IL-1Beta (Canakinumab), Anti-CD20 mAb (e.g, rituximab).
Thus, treatment of uveitis, using the agents according to at least some embodiments of the present invention may be combined with, for example, any known therapeutic agent or method for treating uveitis. Non-limiting examples of such known therapeutics for treating uveitis include corticosteroids, topical cycloplegics, such as atropine or homatropine, or injection of PSTTA (posterior subtenon triamcinolone acetate), antimetabolite medications, such as methotrexate, TNF-α blockers (including infliximab, adalimumab, etanercept, golimumab, certolizumab pegol).
Thus, treatment for Sjogren's syndrome, using the agents according to at least some embodiments of the present invention may be combined with, for example, any known therapeutic agent or method for treating for Sjogren's syndrome. Non-limiting examples of such known therapeutics for treating for Sjogren's syndrome include Cyclosporine, pilocarpine (Salagen) and cevimeline (Evoxac), Hydroxychloroquine (Plaquenil), cortisone (prednisone and others) and/or azathioprine (Imuran) or cyclophosphamide (Cytoxan), Dexamethasone, Thalidomide, Dehydroepiandrosterone, NGX267, Rebamipide, FID 114657, Etanercept, Raptiva, Belimumab, MabThera (rituximab); Anakinra, intravenous immune globulin (IVIG), Allogeneic Mesenchymal Stem Cells (AlloMSC), Automatic neuro-electrostimulation by “Saliwell Crown”.
Thus, treatment for systemic lupus erythematosus, using the agents according to at least some embodiments of the present invention may be combined with, for example, any known therapeutic agent or method for treating for systemic lupus erythematosus. Non-limiting examples of such known therapeutics for treating for systemic lupus erythematosus include corticosteroids and Disease-modifying antirheumatic drugs (DMARDs), commonly anti-malarial drugs such as plaquenil and immunosuppressants (e.g. methotrexate and azathioprine) Hydroxychloroquine, cytotoxic drugs (e.g., cyclophosphamide and mycophenolate), Hydroxychloroquine (HCQ), Benlysta (belimumab), nonsteroidal anti-inflammatory drugs, Prednisone, Cellcept, Prograf, Atacicept, Lupuzor, Intravenous Immunoglobulins (IVIGs), CellCept (mycophenolate mofetil), Orencia, CTLA4-IgG4m (RG2077), rituximab, Ocrelizumab, Epratuzumab, CNTO 136, Sifalimumab (MEDI-545), A-623 (formerly AMG 623), AMG 557, Rontalizumab, paquinimod (ABR-215757), LY2127399, CEP-33457, Dehydroepiandrosterone, Levothyroxine, abetimus sodium (UP 394), Memantine, Opiates, Rapamycin, Renal transplantation, stem cell transplantation.
The present invention in at least some embodiments also encompasses the use of the compositions of the invention according to at least some embodiments together with other pharmaceutical agents to treat immune system diseases. For example, MS disease may be treated with molecules of the invention in conjunction with, but not limited to, immunosuppressants such as corticosteroids, cyclosporin, prednisone, azathioprine, methotrexate, TNF-alpha blockers or antagonists, or any other biological agent targeting any inflammatory cytokine, nonsteroidal antiinflammatory drugs/Cox-2 inhibitors, hydroxychloroquine, sulphasalazopryine, gold salts, etanercept, infliximab, rapamycin, mycophenolate mofetil, azathioprine, tacrolismus, basiliximab, cytoxan, interferon beta-1a, interferon beta-1b, glatiramer acetate, mitoxantrone hydrochloride, anakinra and/or other biologics. The C1ORF32 polypeptides, fragments or fusion proteins thereof can also be used in combination with one or more of the following agents to regulate an immune response: soluble gp39 (also known as CD40 ligand (CD40L), CD154, T-BAM, TRAP), soluble CD29, soluble CD40, soluble CD80 (e.g. ATCC 68627), soluble CD86, soluble CD28 (e.g. 68628), soluble CD56, soluble Thy-1, soluble CD3, soluble TCR, soluble VLA-4, soluble VCAM-1, soluble LECAM-1, soluble ELAM-1, soluble CD44, antibodies reactive with gp39 (e.g. ATCC HB-10916, ATCC HB-12055 and ATCC HB-12056), antibodies reactive with CD40 (e.g. ATCC HB-9110), antibodies reactive with B7 (e.g. ATCC HB-253, ATCC CRL-2223, ATCC CRL-2226, ATCC HB-301, ATCC HB-11341, etc), antibodies reactive with CD28 (e.g. ATCC HB-11944 or mAb 9.3), antibodies reactive with LFA-1 (e.g. ATCC HB-9579 and ATCC TIB-213), antibodies reactive with LFA-2, antibodies reactive with IL-2, antibodies reactive with IL-12, antibodies reactive with IFN-gamma, antibodies reactive with CD2, antibodies reactive with CD48, antibodies reactive with any ICAM (e.g., ICAM-1 (ATCC CRL-2252), ICAM-2 and ICAM-3), antibodies reactive with CTLA4 (e.g. ATCC HB-304), antibodies reactive with Thy-1, antibodies reactive with CD56, antibodies reactive with CD3, antibodies reactive with CD29, antibodies reactive with TCR, antibodies reactive with VLA-4, antibodies reactive with VCAM-1, antibodies reactive with LECAM-1, antibodies reactive with ELAM-1, antibodies reactive with CD44. In certain embodiments, monoclonal antibodies are preferred. In other embodiments, antibody fragments are preferred. As persons skilled in the art will readily understand, the combination can include the C1ORF32 polypeptides, fragments or fusion proteins thereof with one other immunosuppressive agent, with two other immunosuppressive agents, with three other immunosuppressive agents, etc. The determination of the optimal combination and dosages can be determined and optimized using methods well known in the art.
The C1ORF32 polypeptides, fragments or fusion proteins thereof can also be used in combination with one or more of the following agents: L104EA29YIg, CD80 monoclonal antibodies (mAbs), CD86 mAbs, gp39 mAbs, CD40 mAbs, CD28 mAbs; anti-LFA1 mAbs, antibodies or other agents targeting mechanisms of the immune system such as CD52 (alemtuzumab), CD25 (daclizumab), VLA-4 (natalizumab), CD20 (rituximab), IL2R (daclizumab) and MS4A1 (ocrelizumab); novel oral immunomodulating agents have shown to prevent lymphocyte recirculation from lymphoid organs such as fingolimod (FTY720) or leading to lymphocyte depletion such as mylinax (oral cladribine) or teriflunomide; and agents that prevent immunoactivation such as panaclar (dimethyl fumarate BG-12) or laquinimod (ABR216062). Other combinations will be readily appreciated and understood by persons skilled in the art.
The soluble C1ORF32 polypeptides, fragments or fusion proteins thereof may be administered as the sole active ingredient or together with other drugs in immunomodulating regimens or other anti-inflammatory agents e.g. for the treatment or prevention of allo- or xenograft acute or chronic rejection or inflammatory or autoimmune disorders, or to induce tolerance. For example, it may be used in combination with a calcineurin inhibitor, e.g. cyclosporin A or FK506; an immunosuppressive macrolide, e.g. rapamycine or a derivative thereof; e.g. 40-O-(2-hydroxy)ethyl-rapamycin, a lymphocyte homing agent, e.g. FTY720 or an analog thereof, corticosteroids; cyclophosphamide; azathioprene; methotrexate; leflunomide or an analog thereof; mizoribine; mycophenolic acid; mycophenolate mofetil; 15-deoxyspergualine or an analog thereof; immunosuppressive monoclonal antibodies, e.g., monoclonal antibodies to leukocyte receptors, e.g., MHC, CD2, CD3, CD4, CD 11a/CD18, CD7, CD25, CD 27, B7, CD40, CD45, CD58, CD 137, ICOS, CD150 (SLAM), OX40, 4-1BB or their ligands; or other immunomodulatory compounds, e.g. CTLA4/CD28-Ig, or other adhesion molecule inhibitors, e.g. mAbs or low molecular weight inhibitors including LFA-1 antagonists, Selectin antagonists and VLA-4 antagonists.
Where the C1ORF32 polypeptides, fragments or fusion proteins thereof are administered in conjunction with other immunosuppressive/immunomodulatory or anti-inflammatory therapy, e.g. as hereinabove specified, dosages of the co-administered immunosuppressant, immunomodulatory or anti-inflammatory compound will of course vary depending on the type of co-drug employed, e.g. whether it is a steroid or a cyclosporin, on the specific drug employed, on the condition being treated and so forth.
According to at least some embodiments of the present invention, additional embodiments of combination therapy are provided as described below.
An exemplary embodiment relates to a combination of the C1ORF32 polypeptide, preferably as a fusion protein, with other Treg promoting and/or activating methods for treating the subject. For example, isolation and ex vivo expansion of natural Treg from a subject may optionally be performed, followed by reintroduction to the subject, as an example of a therapy which may optionally be combined with C1ORF32 polypeptide treatment.
Another non-limiting example of such a therapy relates to in vitro induction of Treg from non-Treg (n-Tr) cells from a subject, for example by retinoic acid or by TGF-β and IL-2 treatment, followed by reinfusion into the subject.
Another non-limiting example of such a therapy relates to in vivo induction and expansion of Treg by administration of one or more of anti-CD3 antibodies (αCD3), HADC inhibitors (HADCi) and neuropetides, such as VIP; agents promoting activation and/or expansion of FOXP3+ Tregs: IL-10, TGFb, IL-2, IL-35, IL-30; or agents promoting secretion of these cytokines, retinoic acid, adenosine; or a combination thereof to the subject, preferably concurrently with administration of C1ORF32 polypeptide.
Another non-limiting example of such a therapy relates to potentiation of T cell function, for example by administration of B7-H4-Ig to the subject, preferably concurrently with administration of C1ORF32 polypeptide.
Another non-limiting example of such a therapy relates to mucosal tolerization (tolerance induction) with self-antigen, such as heat shock proteins (HSPs), or HSP-derived peptides, preferably concurrently with administration of C1ORF32 polypeptide.
Another non-limiting example of such a therapy relates to enhancing the responsiveness of effector cells to suppression and blocking pro-inflammatory cytokines.
Another non-limiting example of such a therapy relates to the administration of one or more agents that modulate antigen-presenting cell (APC) through cell-cell contact, for example through reverse signalling via Treg-CTLA-4 engagement of B7 on dendritic cells, preferably concurrently with administration of C1ORF32 polypeptide.
Another non-limiting example of such a therapy relates to the inhibition of co-stimulatory signals for example by administering an anti CD40L or blocking antibody for OX-40, GITR pathways (i.e. to the ligand or to the receptor) to the subject, preferably concurrently with administration of C1ORF32 polypeptide.
Another non-limiting example of such a therapy relates to the promotion of anti-stimulatory signals by administering one or more of PDL-1-Ig or anti PD1, CTLA4-Ig or soluble receptor (fusion protein and the like) to the subject, preferably concurrently with administration of C1ORF32 polypeptide.
Another non-limiting example of such a therapy relates to agents that induce effector cell death: The apoptotic death induced in the targets was shown to be Bcl-2 interacting mediator of cell death (BIM)-dependent. Changing the balance of effector cells and Tregs is one mechanism of enhancing tolerance, thus the combination of treatment with a polypeptide according to the present invention that induces Tregs with a treatment that will induce effector cell death would increase tolerance.
8. Treg function can be modulated by a variety of proinflammatory signals including Toll-like receptor triggering as such triggering can increase Treg number and function (Lu H., Front Immunol. 2014 Mar. 3; 5:83).
Another non-limiting example of such a therapy relates to the administration of one or more agents that activate signaling pathways of Cb1-b, NFATc1, c3, and TRAF6 or to inhibit AKT, PI3-K to the subject, preferably concurrently with administration of C1ORF32 polypeptide.
The C1ORF32 polypeptides, or fragments, or fusions thereof disclosed herein are useful as therapeutic agents. According to at least some embodiments, immune cells, preferably T cells, can be contacted in vivo or ex vivo with C1ORF32 fusion polypeptides to decrease or inhibit immune responses including, but not limited to inflammation. The T cells contacted with C1ORF32 fusion polypeptides can be any cell which expresses the T cell receptor, including α/β and γ/δ T cell receptors. T-cells include all cells which express CD3, including T-cell subsets which also express CD4 and CDS. T-cells include both naive and memory cells and effector cells such as CTL. T-cells also include cells such as Th1, Tc1, Th2, Tc2, Th3, Th17, Th22, Treg, and Tr1 cells. T-cells also include NKT-cells and similar unique classes of the T-cell lineage. For example the compositions can be used to modulate Th1, Th17, Th22, or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs. The compositions can also be used to increase or promote the activity of Tregs, increase the production of cytokines such as IL-10 from Tregs, increase the differentiation of Tregs, increase the number of Tregs, or increase the survival of Tregs. The compositions can also be used to increase or promote the activity of Th2 cells, increase the production of cytokines such as IL-10 or IL-4 from Th2 cells, increase the differentiation of Th2 cells, increase the number of Th2 cells, or increase the survival of Th2 cells.
In some embodiments, the disclosed C1ORF32 polypeptides, or fragments, or fusions thereof are administered in combination with a second therapeutic. Combination therapies may be useful in immune modulation. In some embodiments, C1ORF32 polypeptides, or fragments, or fusions can be used to attenuate or reverse the activity of a pro-inflammatory drug, and/or limit the adverse effects of such drugs. Other immune cells that can be treated with the disclosed C1ORF32 polypeptides, fragments or fusion thereof include T cell precursors, antigen presenting cells such as dendritic cells and monocytes or their precursors, B cells or combinations thereof. The C1ORF32 compositions can be used to modulate the production of antibodies by B cells by contacting the B cells with an effective amount of the C1ORF32 composition to inhibit or reduce antibody production by the B cell relative to a control. The C1ORF32 compositions can also modulate the production of cytokines by the B cells.
According to at least some embodiments, there is provided new uses and methods of treatment for immune related diseases by administering the C1ORF32-ECD protein to a subject in need of treatment thereof to induce immune tolerance, preferably through the IL-10 and/or TGFβ pathways. In the context of immune related diseases, “immune tolerance” refers to reducing, ameliorating or blocking the immune related disease, while leaving intact the disease-fighting abilities of the immune system.
According to at least some embodiments, the C1ORF32 fusion protein modulates the IL-10 and/or TGFβ pathway. As shown herein, the C1ORF32 fusion protein upregulates the IL-10 pathway by upregulating IL-10 secretion and also maintains the TGFβ pathway.
According to at least some embodiments, the C1ORF32 fusion protein induces long term immune tolerance. By “long term” it is meant tolerance which lasts any time period between at least 72 hours to 6 months after cessation of treatment, or even greater than 6 months after cessation of treatment; and/or efficacy at a reduced dosing frequency, including but not limited to a dosing frequency of one dose per any time period from every 72 hours to every 6 months.
According to at least some embodiments, the C1ORF32 fusion protein induces tolerance, and preferably long term tolerance as defined above, to graft tissue with at least one mismatched antigen to the recipient subject. Non-limiting examples of such graft tissue include organs and bone marrow. Preferably, the fusion protein induces graft survival and increase in both nTregs and iTregs, indicating donor specific tolerance induction (Aaron et al. Journal of Immunology, 2010, 185: 3326-3336). Also preferably, such induction of immune tolerance occurs through the IL-10 pathway and/or the TGF-beta pathway.
Methods of Treating Inflammatory Responses
Surprisingly, it was found that inhibition of TGFbeta or of IL10 in the EAE model abolishes C1ORF32-ECD-Fc activity (see Example 6 herein). In addition, C1ORF32-ECD-Fc enhances TGF beta secretion (see Example 15 herein) and also IL10 (as shown previously and herein in Examples 3, 4, 15). Furthermore, it was shown herein that neutralization of Tregs in the EAE model abolishes long-term remission (tolerance) (see Example 5 herein).
According to at least some embodiments, it is therefore provided a method of treatment of immune related conditions by administrating to the subject in need thereof any of the C1ORF32 soluble polypeptides, fragments or fusion proteins thereof or pharmaceutical composition comprising same, which increase TGFbeta and IL10 that are involved in the induction and function of regulatory immune cells, particularly Tregs.
According to further embodiments, it is provided a method of treatment of immune related conditions by administrating to the subject in need thereof any of the C1ORF32 soluble polypeptides, fragments or fusion proteins thereof or pharmaceutical composition comprising same, wherein the treatment results in long-term therapeutic benefit which is associated with regulatory immune cells, particularly Tregs.
The C1ORF32 soluble polypeptides, fragments or fusion proteins thereof or pharmaceutical composition comprising same, that inhibit T cell activation, as manifested by T cell proliferation and cytokine secretion. Specifically, the proteins inhibit Th1 and Th17 responses, while promoting Th2 responses.
The C1ORF32 soluble polypeptides, fragments or fusion proteins thereof or pharmaceutical composition comprising same, are potentially used for therapy of diseases that require down-regulation of costimulatory pathways and or such that require downregulation of Th1 and/or Th17 responses.
A further embodiment provides methods for treating or alleviating one or more symptoms of inflammation. In a further embodiment, the compositions and methods disclosed are useful for treating chronic and persistent inflammation. Inflammation in general can be treated using the disclosed C1ORF32 polypeptides or fragment or fusions thereof.
An immune response including inflammation can be inhibited or reduced in a subject, preferably a human, by administering an effective amount of C1ORF32 polypeptide or fragment, or fusion thereof to inhibit or reduce the biological activity of an immune cell or to reduce the amounts of proinflammatory molecules at a site of inflammation. Exemplary proinflammatory molecules include, but are not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs. Th1 and Th17 are exemplary T cells that can be targeted for inhibition by C1ORF32 polypeptides, fusion proteins or fragments thereof to inhibit or reduce inflammation.
Without wishing to be limited by a single hypothesis for this biological mechanism or any other biological mechanism described herein, the C1ORF32 polypeptides, fragments or fusion proteins thereof are useful for treating inflammation by any or all of the following: inhibiting or reducing differentiation of Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs; inhibiting or reducing activity of Th1, Th 17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs; inhibiting or reducing the Th1 and/or Th17 pathways; inhibiting or reducing cytokine production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs; inhibiting or reducing proliferation of Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs.
Additionally, C1ORF32 polypeptides, fragments or fusion proteins thereof can also enhance Th2 immune responses. C1ORF32 polypeptides, fragments or fusion proteins thereof can also act directly on Th2 cells to promote or enhance production of IL-4, IL-5 or IL-10, or TGFbeta or to increase the number or percentage of Th2 cells, resulting in inhibition of Th1 and/or Th17, and in immune modulation via a Th1/Th2 shift.
Additionally, C1ORF32 polypeptides, fragments or fusion proteins thereof can also enhance TGFbeta secretion or responsiveness to TGFbeta.
Additionally, C1ORF32 polypeptides, fragments or fusion proteins thereof can increase Tregs numbers or percentage.
Additionally, C1ORF32 polypeptides, fragments or fusion proteins thereof can cause Tregs to have an enhanced suppressive effect on an immune response. Tregs can suppress differentiation, proliferation, activity, and/or cytokine production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs. For example, C1ORF32 polypeptides, fragments or fusion proteins thereof can cause Tregs to have an enhanced suppressive effect on Th1 and/or Th17 cells to reduce the level of IFN-gamma and IL-17 produced, respectively. C1ORF32 polypeptides, fragments or fusion proteins thereof can also act directly on Tregs to promote or enhance production of IL-10 to suppress the Th1 and/or Th17 pathway, and/or to increase the number or percentage of Tregs.
Additionally, C1ORF32 polypeptides, fragments or fusion proteins thereof can cause Th2 to have an enhanced modulatory effect on an immune response. Th2 cells can modulate differentiation, proliferation, activity, and/or cytokine production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs. For example, C1ORF32 polypeptides, fragments or fusion proteins thereof can cause Th2 cells to have an enhanced modulatory effect on Th1 and/or Th17 cells to reduce the level of IFN-gamma and IL-17 produced, respectively. C1ORF32 polypeptides, fragments or fusion proteins thereof can also act directly on Th2 cells to promote or enhance production of IL-10 to suppress the Th1 and/or Th17 pathway, and/or to increase the number or percentage of Th2 cells.
Without wishing to be limited by a single hypothesis, it is believed that C1ORF32 polypeptides, fragments or fusion proteins thereof acts at multiple points in multiple T cell pathways. For example, C1ORF32 polypeptides, fragments or fusion proteins thereof can inhibit the differentiation of naive T cells into either Th1 or Th17 cells. Alternatively, C1ORF32 polypeptides, fragments or fusion proteins thereof can interact with Th1 cells or Th17 cells, or both to inhibit or reduce the production of proinflammatory molecules.
Additionally, C1ORF32 polypeptides, fragments or fusion proteins thereof may increase the differentiation of and/or promote Th2 responses resulting in an immunomdulatory effect on the Th1 and/or Th17 pathways to reduce the level of INF-gamma and/or IL-17 produced. C1ORF32 polypeptides, fragments or fusion proteins thereof enhances the production of IL-10 and or TGFbeta from cells such as Th2 and/or Tregs, which in turn inhibits the activity of Th1 and/or Th17 cells and promote immune regulatory activity.
Additionally, C1ORF32 polypeptides, fragments or fusion proteins thereof can affect Tregs to have an enhanced suppressive effect on Th1 and/or Th17 pathways to reduce the level of INF-gamma and/or IL-17 produced. Additionally, C1ORF32 polypeptides, fragments or fusion proteins thereof can enhance the production of IL-10 and/or TGFbeta which inhibits the activity of Th1 and/or Th17 cells and enhance immune regulatory activity.
a. Inhibition of Th1 Development
One method for treating immune related diseases and/or inhibiting or reducing inflammation includes administering an effective amount of a C1ORF32 polypeptide, fusion protein, variants thereof, or fragments thereof to inhibit Th1 development in a subject in need thereof. Inflammation can be inhibited or reduced by blocking naive T cells from differentiating into Th1 cells by administering C1ORF32 polypeptides, fusion proteins, fragments thereof or variants thereof. In one embodiment, the C1ORF32 polypeptides or fusion protein thereof may inhibit or reduce proliferation of Th1 cells. C1ORF32 polypeptides, fragments or fusion proteins thereof may also reduce naive T cells from differentiating into Th1 cells, by blocking antigen presenting cell maturation. Alternatively, C1ORF32 polypeptides, fragments or fusion proteins thereof increase the differentiation of Th2 cells and thereby reduce the number of Th1 cells in a subject. By restricting the number of Th1 cells that can develop in the subject, the amount of proinflammatory molecules such as INF-gamma can be reduced or contained. INF-gamma stimulates the production or release of other proinflammatory molecules including TNF-alpha, and MMPs. Thus, by controlling the number of Th1 cells in a subject, the levels of these other proinflammatory molecules can be controlled, thereby reducing inflammatory responses.
b. Inhibition of Proinflammatory Molecules
Another embodiment provides a method of inhibiting or reducing inflammation in a subject by administering to the subject an effective amount of a C1ORF32 polypeptide, fusion protein thereof, or fragment thereof to inhibit or reduce production of proinflammatory molecules by Th1 cells.
Exemplary proinflammatory molecules produced by Th1 cells includes IFN-gamma. In this embodiment the C1ORF32 polypeptide, fusion protein thereof, or fragment thereof can interact directly with the Th1 cell and inhibit or reduce IFN-gamma production by the Th1 cells. In this embodiment, the amount of proinflammatory molecules is regulated rather than the population of Th1 cells.
Another embodiment provides a method of inhibiting or reducing immune related disease and/or inflammation in a subject by administering to the subject an effective amount of a C1ORF32 polypeptide, fusion protein thereof, or fragment thereof to inhibit or reduce production of disease related proinflammatory molecules including but not limited to cytokines/chemokines such as GM-CSF, CCL3 and CCL5.
a. Inhibition of Th17 Development
Inflammation can also be inhibited or reduced in a subject by administering an effective amount of a C1ORF32 polypeptide, fragment or fusion thereof, to inhibit or block naive T cells from developing into Th17 cells. In one embodiment, the C1ORF32 polypeptide or fusion protein increases the suppressive activity of Tregs on the differentiation of naive T cells into Th17 cells by an amount sufficient to reduce the number of Th17 cells in a subject. Alternatively, the C1ORF32 polypeptide or fusion protein thereof inhibits or reduces proliferation of Th17 cells. C1ORF32 polypeptides or fusion proteins thereof may also reduce naive T cells from differentiating into Th17 cells, by blocking antigen presenting cell maturation. By reducing the population of Th17 cells in a subject, the amount of IL-17 can be reduced, as well as IL-22 and IL-21. IL-17 is a proinflammatory cytokine that causes increases in other proinflammatory molecules such as IL-1beta, TNF-alpha, and MMPs. Thus, by reducing the amount of IL-17 these other proinflammatory molecules can be reduced, thereby reducing or inhibiting immune related disease and/or inflammation.
b. Inhibition of IL-17 Production
Still another embodiment provides a method for treating immune related diseases in a subject by administering an effective amount of C1ORF32 polypeptide, fusion protein thereof, or fragments thereof, to inhibit production of IL-17 by Th17 cells, as well as IL-22 and IL-21. In this embodiment, the C1ORF32 polypeptide or fusion protein can act directly on Th17 cells, for example by binding to Th17 cells resulting in inhibition of IL-17 (or IL-22 and IL-21) production by those Th17 cells. As noted above, inhibition or reduction of IL-17 (and IL-22 or IL-21) leads to the reduction of other proinflammatory molecules, thereby reducing or inhibiting immune related disease and/or inflammation.
The disclosed C1ORF32 polypeptides, fusion proteins, and fragments thereof can be used to inhibit both the Th1 and Th17 pathways simultaneously. Using one anti-inflammatory agent to inhibit two separate pathways provides more robust inhibition or reduction of the immune response.
immune related diseases can also be treated by administering C1ORF32 polypeptides, fusion proteins thereof, or fragments thereof to a subject in an amount effective to enhance Th2 responses, and the suppressive activity of IL-10 producing cells, and to increase TGFbeta secretion, activation or responsiveness and to enhance suppressive or modulatory activity on the Th1 and/or Th17 pathways. In this embodiment the disclosed C1ORF32 polypeptides and fusion proteins cause an increased suppressive effect on IFN-gamma and/or IL-17 production. Another embodiment provides a method for treating immune related diseases by administering an effective amount of C1ORF32 polypeptide, fusion proteins thereof, or fragments thereof to increase production of IL-10 by Th2, Tregs or other immune cells.
Increased production of IL-10 results in the decreased production of IL-17 by Th17 cells and deceased production of IFN-gamma by Th1 cells. In this embodiment, the C1ORF32 polypeptides, fusion proteins, and fragments thereof can interact directly with with immune cells to increase IL-10 production.
Still another embodiment provides a method for treating immune related diseases by administering an effective amount of C1ORF32 polypeptides, fusion proteins thereof, and fragments thereof to inhibit or interfere with the Th1 pathway and Th17 pathway, and to enhance the suppressive effect on the Th1 and/or Th17 pathways by Th2 cells. The C1ORF32 polypeptides, fusion proteins thereof and fragments thereof can also be administered to a subject in an amount effective to increase Th2 cell populations or numbers.
IL-10 production can be increased relative to a control by contacting Th2 cells, Tregs or other immune cells with an effective amount of C1ORF32 polypeptides, C1ORF32 fusion proteins, or fragments thereof having C1ORF32 activity. The increase can occur in vitro or in vivo,
Another embodiment provides a method for treating immune related diseases by administering an effective amount of C1ORF32 polypeptide, fusion proteins thereof, or fragments thereof to increase production and/or secretion of TGFbeta by macrophages or other cell types, or increasing the secretion of serum proteinases such as plasmin that catalyze the release of active TGFbeta from a latent complex or increase the responsiveness to TGFbeta.
Increase in TGFbeta results in increase in regulatory cells including Tregs and Treg17 cells which directly inhibit effector T cell functions.
Treg17 can derive from Th17 cells in an altered differentiation program giving rise to protective and non-pathogenic cells. Treg17 cells can be induced by TGF-beta plus IL-6. Like conventional Treg, induction of regulatory Treg17 cells could play an important role in modulating and preventing certain autoimmune diseases.
Another embodiment provides a method for treating immune related diseases by administering an effective amount of C1ORF32 polypeptide, fusion proteins thereof, or fragments thereof to increase immune regulatory cells including but not limited to Tregs, Treg17, and Bregs.
Immune related diseases and disorders that may be treated using C1ORF32 fusion polypeptides are described herein.
C1ORF32 acts at multiple points in the inflammatory pathway as a master regulator to control the expression and/or activity of effectory cytokines such as IFN-gamma and TNF-alpha. Therefore, the C1ORF32 compositions described herein are particularly useful for treating patients that do not respond to TNF-alpha blockers such as Enbrel, Remicade, Cimzia and Humira, or where TNF-alpha blockers are not safe or effective. In a further embodiment, the C1ORF32 compositions described herein are used to treat autoimmune diseases. In addition, because of its activity as a master regulator in the inflammatory pathway, the C1ORF32 compositions disclosed are particularly useful for treating chronic and persistent inflammation. In a further embodiment, the C1ORF32 compositions described herein are used to treat elapsing and/or remitting multiple sclerosis.
Epitope spreading refers to the ability of B and T cell immune response to diversify both at the level of specificity, from a single determinant to many sites on an auto antigen, and at the level of V gene usage (Monneaux, F. et al., Arthritis & Rheumatism, 46(6): 1430-1438 (2002). Epitope spreading is not restricted to systemic autoimmune disease. It has been described in T cell dependent organ specific diseases such as Diabetes mellitus type 1 and multiple sclerosis in humans, and EAE induced experimental animals with a variety of myelin proteins.
Epitope spreading involves the acquired recognition of new epitopes in the same self molecule as well as epitopes residing in proteins that are associated in the same macromolecular complex. Epitope spreading can be assessed by measuring delayed-type hypersensitivity (DTH) responses, methods of which are known in the art.
One embodiment provides a method for inhibiting or reducing epitope spreading in a subject by administering to the subject an effective amount of C1ORF32 polypeptide, fragment or fusion protein thereof. In a further embodiment the C1ORF32 polypeptide, fragment or fusion protein thereof inhibits epitope spreading in individuals with multiple sclerosis. Preferably, the C1ORF32 polypeptide or fusion thereof inhibits or blocks multiple points of the inflammation pathway.
Yet another embodiment provides a method for inhibiting or reducing epitope spreading in subjects with multiple sclerosis by administering to a subject an effective amount of C1ORF32 polypeptide, fragment or fusion protein thereof to inhibit or reduce differentiation of, proliferation of, activity of, and/or cytokine production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs. Another embodiment provides a method for treating multiple sclerosis by administering to a subject an effective amount of C1ORF32 polypeptide, fragment or fusion protein thereof to interact with Tregs, enhance Treg differentiation, enhance Treg activity, promote or enhances IL-10 secretion by Tregs or other cells, increase the number of Tregs, increase the suppressive capacity of Tregs, or combinations thereof. Another embodiment provides a method for treating multiple sclerosis by administering to a subject an effective amount of C1ORF32 polypeptide, fragment or fusion protein thereof to interact with Th2 cells, enhance Th2 activity, promote or enhance IL-10 secretion by Th2 cells, increase the number of Th2 cells, increase the modulatory capacity of Th2 cells, or combinations thereof.
In one embodiment, the present invention provides a method for inducing or re-establishing immune tolerance in a subject by administering to the subject an effective amount of C1ORF32 polypeptide, fragment or fusion protein thereof. In a further embodiment the C1ORF32 polypeptide, fragment or fusion protein thereof induces tolerance in individuals with immune related diseases. In a specific embodiment the C1ORF32 polypeptide, fragment or fusion protein thereof induces tolerance in individuals with multiple sclerosis. Preferably, the C1ORF32 polypeptide or fusion thereof inhibits or blocks multiple points of the inflammation pathway. In another specific embodiment, the C1ORF32 polypeptide, fragment or fusion protein thereof induces tolerance in individuals with rheumatoid arthritis. Another embodiment provides a method for treating immune related diseases by administering to a subject an effective amount of C1ORF32 polypeptide, fragment or fusion protein thereof to induce immune tolerance by interacting with Tregs, enhancing Treg activity, increasing the number of Tregs, increasing the percentage of Tregs increase the suppressive capacity of Tregs, or combinations thereof. Another embodiment provides a method for treating immune related diseases by administering to a subject an effective amount of C1ORF32 polypeptide, fragment or fusion protein thereof to promote or enhance IL-10 secretion by immune cells. Another embodiment provides a method for treating immune related diseases by administering an effective amount of C1ORF32 polypeptide, fusion proteins thereof, or fragments thereof to increase immune regulatory cells including but not limited to Tregs, Treg17, Bregs.
Combination Therapy
C1ORF32 fusion polypeptides can be used alone or in combination with additional therapeutic agents. The additional therapeutic agents include, but are not limited to, immunosuppressive agents (e.g., antibodies against other lymphocyte surface markers (e.g., CD40, alpha-4 integrin) or against cytokines), other fusion proteins (e.g., CTLA-4-Ig (Orencia®), TNFR-Ig (Enbrel®)), TNF-alpha blockers such as Enbrel, Remicade, Cimzia and Humira, cyclophosphamide (CTX) (i.e. Endoxan®, Cytoxan®, Neosar®, Procytox®, Revimmune™), methotrexate (MTX) (i.e. Rheumatrex®, Trexall®), belimumab (i.e. Benlysta®), or other immunosuppressive drugs (e.g., cyclosporin A, FK506-like compounds, rapamycin compounds, or steroids), anti-proliferatives, cytotoxic agents, or other compounds that may assist in immunosuppression.
In a further embodiment, the additional therapeutic agent functions to inhibit or reduce T cell activation through a separate pathway. In one such embodiment, the additional therapeutic agent is a CTLA-4 fusion protein, such as CTLA-4-Ig (abatacept). CTLA-4-Ig fusion proteins compete with the co-stimulatory receptor, CD28, on T cells for binding to CD80/CD86 (B7-1/B7-2) on antigen presenting cells, and thus function to inhibit T cell activation. In another embodiment, the additional therapeutic agent is a CTLA-4-Ig fusion protein known as belatacept. Belatacept contains two amino acid substitutions (L104E and A29Y) that markedly increase its avidity to CD86 in vivo. In another embodiment, the additional therapeutic agent is Maxy-4.
In another embodiment, the second therapeutic agent is cyclophosphamide (CTX). Cyclophosphamide (the generic name for Endoxan®, Cytoxan®, Neosar®, Procytox®, Revimmune™), also known as cytophosphane, is a nitrogen mustard alkylating agent from the oxazophorines group. It is used to treat various types of cancer and some autoimmune disorders. In a further embodiment, C1ORF32 polypeptides, fragments or fusion proteins thereof and CTX are coadministered in effective amount to prevent or treat a chronic autoimmune disease or disorder such as Systemic lupus erythematosus (SLE). Cyclophosphamide (CTX) is the primary drug used for diffuse proliferative glomerulonephritis in patients with renal lupus. In some embodiments the combination therapy is administered in an effective amount to reduce the blood or serum levels of anti-double stranded DNA (anti-ds DNA) auto antibodies and/or to reduce proteinuria in a patient in need thereof.
In another embodiment, the second therapeutic agent increases the amount of adenosine in the serum, see, for example, WO 08/147482. In a further embodiment, the second therapeutic is CD73-Ig, recombinant CD73, or another agent (e.g. a cytokine or monoclonal antibody or small molecule) that increases the expression of CD73, see for example WO 04/084933. In another embodiment the second therapeutic agent is Interferon-beta.
In another embodiment, the second therapeutic is Tysabri or another therapeutic for MS. In a further embodiment, C1ORF32 polypeptides, fragments or fusion proteins thereof is cycled with Tysabri or used during a drug holiday in order to allow less frequent dosing with the second therapeutic and reduce the risk of side effects such as PML and to prevent resistance to the second therapeutic.
In another embodiment, the second therapeutic agent preferentially treats immune related diseases and/or chronic inflammation, whereby the treatment regimen targets both acute and chronic inflammation. In a further embodiment the second therapeutic is a TNF-alpha blocker.
In another embodiment, the second therapeutic agent is a small molecule that inhibits or reduces differentiation, proliferation, activity, and/or cytokine production and/or secretion by Th1, Th17, Th22, and/or other cells that secrete, or cause other cells to secrete, inflammatory molecules, including, but not limited to, TNF-alpha, IFN-gamma, IL-17, IL-23, IL-22, IL-21, GM-CSF, CCL3, CCL5 and MMPs. In another embodiment, the second therapeutic agent is a small molecule that interacts with Tregs, enhances Treg activity, promotes or enhances IL-10 secretion by Tregs, increases the number of Tregs, increases the suppressive capacity of Tregs, or combinations thereof.
Typically useful small molecules are organic molecules, preferably small organic compounds having a molecular weight of more than 100 and less than about 2,500 daltons, more preferably between 100 and 2000, more preferably between about 100 and about 1250, more preferably between about 100 and about 1000, more preferably between about 100 and about 750, more preferably between about 200 and about 500 daltons. Small molecules comprise functional groups necessary for structural interaction with proteins, particularly hydrogen bonding, and typically include at least an amine, carbonyl, hydroxyl or carboxyl group, preferably at least two of the functional chemical groups. The small molecules often comprise cyclical carbon or heterocyclic structures and/or aromatic or polyaromatic structures substituted with one or more of the above functional groups. Small molecules also include biomolecules including peptides, saccharides, fatty acids, steroids, purines, pyrimidines, derivatives, structural analogs or combinations thereof. In one embodiment, the small molecule is retinoic acid or a derivative thereof. The examples below demonstrate that retinoic acid inhibits or reduces differentiation and/or activity of ThI 7 cells. In a further embodiment, the compositions are used in combination or succession with compounds that increase Treg activity or production. Exemplary Treg enhancing agents include but are not limited to glucocorticoid fluticasone, salmeteroal, antibodies to IL-12, IFN-gamma, and IL-4; vitamin D3, and dexamethasone, and combinations thereof. Antibodies to other proinflammatory molecules can also be used in combination or alternation with the disclosed C1ORF32 polypeptides, fusion proteins, or fragments thereof. Preferred antibodies bind to IL-6, IL-23, IL-22 or IL-21.
As used herein the term “rapamycin compound” includes the neutral tricyclic compound rapamycin, rapamycin derivatives, rapamycin analogs, and other macrolide compounds which are thought to have the same mechanism of action as rapamycin (e.g., inhibition of cytokine function). The language “rapamycin compounds” includes compounds with structural similarity to rapamycin, e.g., compounds with a similar macrocyclic structure, which have been modified to enhance their therapeutic effectiveness. Exemplary Rapamycin compounds are known in the art. The language “FK506-Hke compounds” includes FK506, and FK506 derivatives and analogs, e.g., compounds with structural similarity to FK506, e.g., compounds with a similar macrocyclic structure which have been modified to enhance their therapeutic effectiveness. Examples of FK506-like compounds include, for example, those described in WO 00101385. Preferably, the language “rapamycin compound” as used herein does not include FK506-like compounds. Other suitable therapeutics include, but are not limited to, anti-inflammatory agents. The anti-inflammatory agent can be non-steroidal, steroidal, or a combination thereof. One embodiment provides oral compositions containing about 1% (w/w) to about 5% (w/w), typically about 2.5 (w/w) or an anti-inflammatory agent. Representative examples of non-steroidal anti-inflammatory agents include, without limitation, oxicams, such as piroxicam, isoxicam, tenoxicam, sudoxicam; salicylates, such as aspirin, disalcid, benorylate, trilisate, safapryn, solprin, diflunisal, and fendosal; acetic acid derivatives, such as diclofenac, fenclofenac, indomethacin, sulindac, tolmetin, isoxepac, furofenac, tiopinac, zidometacin, acematacin, fentiazac, zomepirac, clmdanac, oxepinac, felbmac, and ketorolac; fenamates, such as mefenamic, meclofenamic, flufenamic, niflumic, and tolfenamic acids; propionic acid derivatives, such as ibuprofen, naproxen, benoxaprofen, flurbiprofen, ketoprofen, fenoprofen, fenbufen, indopropfen, pirprofen, carprofen, oxaprozin, pranoprofen, miroprofen, tioxaprofen, suprofen, alminoprofen, and tiaprofenic; pyrazoles, such as phenylbutazone, oxyphenbutazone, feprazone, azapropazone, and trimethazone. Mixtures of these non-steroidal anti-inflammatory agents may also be employed. Representative examples of steroidal anti-inflammatory drugs include, without limitation, corticosteroids such as hydrocortisone, hydroxyl-triamcinolone, alpha-methyl dexamethasone, dexamethasone-phosphate, beclomethasone dipropionates, clobetasol valerate, desonide, desoxymethasone, desoxycorticosterone acetate, dexamethasone, dichlorisone, diflorasone diacetate, diflucortolone valerate, fluadrenolone, fluclorolone acetonide, fludrocortisone, flumethasone pivalate, fiuosinolone acetonide, fluocinonide, flucortine butylesters, fluocortolone, fluprednidene (fluprednylidene) acetate, flurandrenolone, halcinonide, hydrocortisone acetate, hydrocortisone butyrate, methylprednisolone, triamcinolone acetonide, cortisone, cortodoxone, flucetonide, fludrocortisone, difluorosone diacetate, fluradrenolone, fludrocortisone, diflurosone diacetate, fluradrenolone acetonide, medrysone, amcinafel, amcinafide, betamethasone and the balance of its esters, chloroprednisone, chlorprednisone acetate, clocortelone, clescinolone, dichlorisone, diflurprednate, flucloronide, flunisolide, fluoromethalone, fluperolone, fluprednisolone, hydrocortisone valerate, hydrocortisone cyclopentylpropionate, hydrocortamate, meprednisone, paramethasone, prednisolones prednisone, beclomethasone dipropionate, triamcinolone, and mixtures thereof.
Pharmaceutical Compositions
The present invention, in some embodiments, features a pharmaceutical composition comprising a therapeutically effective amount of a therapeutic agent according to the present invention. According to the present invention the therapeutic agent could be any one of soluble C1ORF32 protein, C1ORF32 ectodomain, or a fragment or variant thereof, or a fusion protein or a corresponding nucleic acid sequence encoding. The pharmaceutical composition according to the present invention is further used for the treatment of autoimmunity and preferably for treating an immune related disorder as described herein. The therapeutic agents of the present invention can be provided to the subject alone, or as part of a pharmaceutical composition where they are mixed with a pharmaceutically acceptable carrier.
As used herein, “pharmaceutically acceptable carrier” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible. Preferably, the carrier is suitable for intravenous, intramuscular, subcutaneous, parenteral, spinal or epidermal administration (e.g., by injection or infusion). Depending on the route of administration, the active compound, i.e., soluble C1ORF32 protein, C1ORF32 ectodomain, or a fragment or variant thereof, or a fusion protein or a corresponding nucleic acid sequence encoding the pharmaceutical compounds according to at least some embodiments of the present invention may include one or more pharmaceutically acceptable salts. A “pharmaceutically acceptable salt” refers to a salt that retains the desired biological activity of the parent compound and does not impart any undesired toxicological effects (see e.g., Berge, S. M., et al. (1977) J. Pharm. Sci. 66: 1-19). Examples of such salts include acid addition salts and base addition salts. Acid addition salts include those derived from nontoxic inorganic acids, such as hydrochloric, nitric, phosphoric, sulfuric, hydrobromic, hydroiodic, phosphorous and the like, as well as from nontoxic organic acids such as aliphatic mono- and dicarboxylic acids, phenyl-substituted alkanoic acids, hydroxy alkanoic acids, aromatic acids, aliphatic and aromatic sulfonic acids and the like. Base addition salts include those derived from alkaline earth metals, such as sodium, potassium, magnesium, calcium and the like, as well as from nontoxic organic amines, such as N,N′-dibenzylethylenediamine, N-methylglucamine, chloroprocaine, choline, diethanolamine, ethylenediamine, procaine and the like.
A pharmaceutical composition according to at least some embodiments of the present invention also may include a pharmaceutically acceptable anti-oxidants. Examples of pharmaceutically acceptable antioxidants include: (1) water soluble antioxidants, such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite and the like; (2) oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha-tocopherol, and the like; and (3) metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid, and the like. A pharmaceutical composition according to at least some embodiments of the present invention also may include additives such as detergents and solubilizing agents (e.g., TWEEN 20 (polysorbate-20), TWEEN 80 (polysorbate-80)) and preservatives (e.g., Thimersol, benzyl alcohol) and bulking substances (e.g., lactose, mannitol).
Examples of suitable aqueous and nonaqueous carriers that may be employed in the pharmaceutical compositions according to at least some embodiments of the present invention include water, buffered saline of various buffer content (e.g., Tris-HCl, acetate, phosphate), pH and ionic strength, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils, such as olive oil, and injectable organic esters, such as ethyl oleate.
Proper fluidity can be maintained, for example, by the use of coating materials, such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.
These compositions may also contain adjuvants such as preservatives, wetting agents, emulsifying agents and dispersing agents. Prevention of presence of microorganisms may be ensured both by sterilization procedures, supra, and by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents, such as sugars, sodium chloride, and the like into the compositions. In addition, prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption such as aluminum monostearate and gelatin.
Pharmaceutically acceptable carriers include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. The use of such media and agents for pharmaceutically active substances is known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the pharmaceutical compositions according to at least some embodiments of the present invention is contemplated. Supplementary active compounds can also be incorporated into the compositions.
Therapeutic compositions typically must be sterile and stable under the conditions of manufacture and storage. The composition can be formulated as a solution, microemulsion, liposome, or other ordered structure suitable to high drug concentration. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), and suitable mixtures thereof. The proper fluidity 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. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, or sodium chloride in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent that delays absorption, for example, monostearate salts and gelatin. Sterile injectable solutions can be prepared by incorporating the active compound in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by sterilization microfiltration. Generally, dispersions are prepared by incorporating the active compound 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 (lyophilization) that yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
Sterile injectable solutions can be prepared by incorporating the active compound in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by sterilization microfiltration. Generally, dispersions are prepared by incorporating the active compound 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 (lyophilization) that yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
The amount of active ingredient which can be combined with a carrier material to produce a single dosage form will vary depending upon the subject being treated, and the particular mode of administration. The amount of active ingredient which can be combined with a carrier material to produce a single dosage form will generally be that amount of the composition which produces a therapeutic effect. Generally, out of one hundred percent, this amount will range from about 0.01 percent to about ninety-nine percent of active ingredient, preferably from about 0.1 percent to about 70 percent, most preferably from about 1 percent to about 30 percent of active ingredient in combination with a pharmaceutically acceptable carrier.
Dosage regimens are adjusted to provide the optimum desired response (e.g., a therapeutic 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 especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subjects to be treated; each unit contains a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms according to at least some embodiments of the present invention are dictated by and directly dependent on (a) the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and (b) the limitations inherent in the art of compounding such an active compound for the treatment of sensitivity in individuals.
A composition of the present invention can be administered via one or more routes of administration using one or more of a variety of methods known in the art. As will be appreciated by the skilled artisan, the route and/or mode of administration will vary depending upon the desired results. Preferred routes of administration for therapeutic agents according to at least some embodiments of the present invention include intravascular delivery (e.g. injection or infusion), intravenous, intramuscular, intradermal, intraperitoneal, subcutaneous, spinal, oral, enteral, rectal, pulmonary (e.g. inhalation), nasal, topical (including transdermal, buccal and sublingual), intravesical, intravitreal, intraperitoneal, vaginal, brain delivery (e.g. intra-cerebroventricular, intra-cerebral, and convection enhanced diffusion), CNS delivery (e.g. intrathecal, perispinal, and intra-spinal) or parenteral (including subcutaneous, intramuscular, intraperitoneal, intravenous (IV) and intradermal), transdermal (either passively or using iontophoresis or electroporation), transmucosal (e.g., sublingual administration, nasal, vaginal, rectal, or sublingual), administration or administration via an implant, or other parenteral routes of administration, for example by injection or infusion, or other delivery routes and/or forms of administration known in the art. The phrase “parenteral administration” as used herein means modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticular, subcapsular, subarachnoid, intraspinal, epidural and intrasternal injection and infusion or using bioerodible inserts, and can be formulated in dosage forms appropriate for each route of administration. In a specific embodiment, a protein, a therapeutic agent or a pharmaceutical composition according to at least some embodiments of the present invention can be administered intraperitoneally or intravenously.
Compositions of the present invention can be delivered to the lungs while inhaling and traverse across the lung epithelial lining to the blood stream when delivered either as an aerosol or spray dried particles having an aerodynamic diameter of less than about 5 microns. A wide range of mechanical devices designed for pulmonary delivery of therapeutic products can be used, including but not limited to nebulizers, metered dose inhalers, and powder inhalers, all of which are familiar to those skilled in the art. Some specific examples of commercially available devices are the Ultravent nebulizer (Mallinckrodt Inc., St. Louis, Mo.); the Acorn II nebulizer (Marquest Medical Products, Englewood, Colo.); the Ventolin metered dose inhaler (Glaxo Inc., Research Triangle Park, N.C.); and the Spinhaler powder inhaler (Fisons Corp., Bedford, Mass.). Nektar, Alkermes and Mannkind all have inhalable insulin powder preparations approved or in clinical trials where the technology could be applied to the formulations described herein.
In some in vivo approaches, the compositions disclosed herein are administered to a subject in a therapeutically effective amount. As used herein the term “effective amount” or “therapeutically effective amount” means a dosage sufficient to treat, inhibit, or alleviate one or more symptoms of the disorder being treated or to otherwise provide a desired pharmacologic and/or physiologic effect. The precise dosage will vary according to a variety of factors such as subject-dependent variables (e.g., age, immune system health, etc.), the disease, and the treatment being effected. For the polypeptide compositions disclosed herein and nucleic acids encoding the same, as further studies are conducted, information will emerge regarding appropriate dosage levels for treatment of various conditions in various patients, and the ordinary skilled worker, considering the therapeutic context, age, and general health of the recipient, will be able to ascertain proper dosing. The selected dosage depends upon the desired therapeutic effect, on the route of administration, and on the duration of the treatment desired. For polypeptide compositions, generally dosage levels of 0.0001 to 100 mg/kg of body weight daily are administered to mammals and more usually 0.001 to 20 mg/kg. For example dosages can be 0.3 mg/kg body weight, 1 mg/kg body weight, 3 mg/kg body weight, 5 mg/kg body weight or 10 mg/kg body weight or within the range of 1-10 mg/kg. An exemplary treatment regime entails administration once per week, once every two weeks, once every three weeks, once every four weeks, once a month, once every 3 months or once every three to 6 months. Generally, for intravenous injection or infusion, dosage may be lower. Dosage regimens are adjusted to provide the optimum desired response (e.g., a therapeutic 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 especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subjects to be treated; each unit contains a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms according to at least some embodiments of the present invention are dictated by and directly dependent on (a) the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and (b) the limitations inherent in the art of compounding such an active compound for the treatment of sensitivity in individuals.
Optionally the polypeptide formulation may be administered in an amount between 0.0001 to 100 mg/kg weight of the patient/day, preferably between 0.001 to 20.0 mg/kg/day, according to any suitable timing regimen. A therapeutic composition according to at least some embodiments according to at least some embodiments of the present invention can be administered, for example, three times a day, twice a day, once a day, three times weekly, twice weekly or once weekly, once every two weeks or 3, 4, 5, 6, 7 or 8 weeks. Moreover, the composition can be administered over a short or long period of time (e.g., 1 week, 1 month, 1 year, 5 years).
Alternatively, therapeutic agent can be administered as a sustained release formulation, in which case less frequent administration is required. Dosage and frequency vary depending on the half-life of the therapeutic agent in the patient. The half-life for fusion proteins may vary widely. The dosage and frequency of administration can vary depending on whether the treatment is prophylactic or therapeutic. In prophylactic applications, a relatively low dosage is administered at relatively infrequent intervals over a long period of time. Some patients continue to receive treatment for the rest of their lives. In therapeutic applications, a relatively high dosage at relatively short intervals is sometimes required until progression of the disease is reduced or terminated, and preferably until the patient shows partial or complete amelioration of symptoms of disease. Thereafter, the patient can be administered a prophylactic regime.
Actual dosage levels of the active ingredients in the pharmaceutical compositions of the present invention may be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient. The selected dosage level will depend upon a variety of pharmacokinetic factors including the activity of the particular compositions of the present invention employed, the route of administration, the time of administration, the rate of excretion of the particular compound being employed, the duration of the treatment, other drugs, compounds and/or materials used in combination with the particular compositions employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors well known in the medical arts.
A “therapeutically effective dosage” of C1ORF32 soluble protein or C1ORF32 ectodomain or C1ORF32 fusion protein containing same, preferably results in a decrease in severity of disease symptoms, an increase in frequency and duration of disease symptom-free periods, an increase in lifepan, disease remission, or a prevention or reduction of impairment or disability due to the disease affliction.
One of ordinary skill in the art would be able to determine a therapeutically effective amount based on such factors as the subject's size, the severity of the subject's symptoms, and the particular composition or route of administration selected.
In certain embodiments, the polypeptide compositions are administered locally, for example by injection directly into a site to be treated. Typically, the injection causes an increased localized concentration of the polypeptide compositions which is greater than that which can be achieved by systemic administration. For example, in the case of a neurological disorder like Multiple Sclerosis, the protein may be administered locally to a site near the CNS. In another example, as in the case of an arthritic disorder like Rheumatoid Arthritis, the protein may be administered locally to the synovium in the affected joint. The polypeptide compositions can be combined with a matrix as described above to assist in creating a increased localized concentration of the polypeptide compositions by reducing the passive diffusion of the polypeptides out of the site to be treated.
Pharmaceutical compositions of the present invention may be administered with medical devices known in the art. For example, in an optional embodiment, a pharmaceutical composition according to at least some embodiments of the present invention can be administered with a needles hypodermic injection device, such as the devices disclosed in U.S. Pat. Nos. 5,399,163; 5,383,851; 5,312,335; 5,064,413; 4,941,880; 4,790,824; or 4,596,556. Examples of well-known implants and modules useful in the present invention include: U.S. Pat. No. 4,487,603, which discloses an implantable micro-infusion pump for dispensing medication at a controlled rate; U.S. Pat. No. 4,486,194, which discloses a therapeutic device for administering medicaments through the skin; U.S. Pat. No. 4,447,233, which discloses a medication infusion pump for delivering medication at a precise infusion rate; U.S. Pat. No. 4,447,224, which discloses a variable flow implantable infusion apparatus for continuous drug delivery; U.S. Pat. No. 4,439,196, which discloses an osmotic drug delivery system having multi-chamber compartments; and U.S. Pat. No. 4,475,196, which discloses an osmotic drug delivery system. These patents are incorporated herein by reference. Many other such implants, delivery systems, and modules are known to those skilled in the art.
The active compounds can be prepared with carriers that will protect the compound against rapid release, such as a controlled release formulation, including implants, transdermal patches, and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Many methods for the preparation of such formulations are patented or generally known to those skilled in the art. See, e.g., Sustained and Controlled Release Drug Delivery Systems, J. R. Robinson, ed., Marcel Dekker, Inc., New York, 1978.
Therapeutic compositions can be administered with medical devices known in the art. For example, in an optional embodiment, a therapeutic composition according to at least some embodiments of the present invention can be administered with a needles hypodermic injection device, such as the devices disclosed in U.S. Pat. Nos. 5,399,163; 5,383,851; 5,312,335; 5,064,413; 4,941,880; 4,790,824; or 4,596,556. Examples of well-known implants and modules useful in the present invention include: U.S. Pat. No. 4,487,603, which discloses an implantable micro-infusion pump for dispensing medication at a controlled rate; U.S. Pat. No. 4,486,194, which discloses a therapeutic device for administering medicaments through the skin; U.S. Pat. No. 4,447,233, which discloses a medication infusion pump for delivering medication at a precise infusion rate; U.S. Pat. No. 4,447,224, which discloses a variable flow implantable infusion apparatus for continuous drug delivery; U.S. Pat. No. 4,439,196, which discloses an osmotic drug delivery system having multi-chamber compartments; and U.S. Pat. No. 4,475,196, which discloses an osmotic drug delivery system. These patents are incorporated herein by reference. Many other such implants, delivery systems, and modules are known to those skilled in the art.
In certain embodiments, C1ORF32 soluble proteins, C1ORF32 ectodomains, C1ORF32 fusion proteins, other proteins or other therapeutic agents according to at least some embodiments of the present invention can be formulated to ensure proper distribution in vivo. For example, the blood-brain barrier (BBB) excludes many highly hydrophilic compounds. To ensure that the therapeutic compounds according to at least some embodiments of the present invention cross the BBB (if desired), they can be formulated, for example, in liposomes. For methods of manufacturing liposomes, see, e.g., U.S. Pat. Nos. 4,522,811; 5,374,548; and 5,399,331. The liposomes may comprise one or more moieties which are selectively transported into specific cells or organs, thus enhance targeted drug delivery (see, e.g., V. V. Ranade (1989) J. Clin. Pharmacol. 29:685). Exemplary targeting moieties include folate or biotin (see, e.g., U.S. Pat. No. 5,416,016 to Low et al); mannosides (Umezawa et al., (1988) Biochem. Biophys. Res. Commun. 153:1038); antibodies (P. G. Bloeman et al. (1995) FEBS Lett. 357:140; M. Owais et al. (1995) Antimicrob. Agents Chemother. 39:180); surfactant protein A receptor (Briscoe et al. (1995) Am. J Physiol. 1233:134); p120 (Schreier et al. (1994) J. Biol. Chem. 269:9090); see also K. Keinanen; M. L. Laukkanen (1994) FEBS Lett. 346:123; J. J. Killion; I. J. Fidler (1994) Immunomethods 4:273.
Formulations for Parenteral Administration
In a further embodiment, compositions disclosed herein, including those containing peptides and polypeptides, are administered in an aqueous solution, by parenteral injection. The formulation may also be in the form of a suspension or emulsion. In general, pharmaceutical compositions are provided including effective amounts of a peptide or polypeptide, and optionally include pharmaceutically acceptable diluents, preservatives, solubilizers, emulsifiers, adjuvants and/or carriers. Such compositions optionally include one or more for the following: diluents, sterile water, buffered saline of various buffer content (e.g., Tris-HCl, acetate, phosphate), pH and ionic strength; and additives such as detergents and solubilizing agents (e.g., TWEEN 20 (polysorbate-20), TWEEN 80 (polysorbate-80)), anti-oxidants (e.g., water soluble antioxidants such as ascorbic acid, sodium metabisulfite, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite; oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha-tocopherol; and metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid), and preservatives (e.g., Thimersol, benzyl alcohol) and bulking substances (e.g., lactose, mannitol). Examples of non-aqueous solvents or vehicles are ethanol, propylene glycol, polyethylene glycol, vegetable oils, such as olive oil and corn oil, gelatin, and injectable organic esters such as ethyl oleate. The formulations may be freeze dried (lyophilized) or vacuum dried and redissolved/resuspended immediately before use. The formulation may be sterilized by, for example, filtration through a bacteria retaining filter, by incorporating sterilizing agents into the compositions, by irradiating the compositions, or by heating the compositions.
Formulations for Topical Administration
C1ORF32 polypeptides, fragments, fusion polypeptides, nucleic acids, and vectors disclosed herein can be applied topically. Topical administration does not work well for most peptide formulations, although it can be effective especially if applied to the lungs, nasal, oral (sublingual, buccal), vaginal, or rectal mucosa.
Compositions can be delivered to the lungs while inhaling and traverse across the lung epithelial lining to the blood stream when delivered either as an aerosol or spray dried particles having an aerodynamic diameter of less than about 5 microns.
A wide range of mechanical devices designed for pulmonary delivery of therapeutic products can be used, including but not limited to nebulizers, metered dose inhalers, and powder inhalers, all of which are familiar to those skilled in the art. Some specific examples of commercially available devices are the Ultravent nebulizer (Mallinckrodt Inc., St. Louis, Mo.); the Acorn II nebulizer (Marquest Medical Products, Englewood, Colo.); the Ventolin metered dose inhaler (Glaxo Inc., Research Triangle Park, N.C.); and the Spinhaler powder inhaler (Fisons Corp., Bedford, Mass.). Nektar, Alkermes and Mannkind all have inhalable insulin powder preparations approved or in clinical trials where the technology could be applied to the formulations described herein.
Formulations for administration to the mucosa will typically be spray dried drug particles, which may be incorporated into a tablet, gel, capsule, suspension or emulsion. Standard pharmaceutical excipients are available from any formulator. Oral formulations may be in the form of chewing gum, gel strips, tablets or lozenges.
Transdermal formulations may also be prepared. These will typically be ointments, lotions, sprays, or patches, all of which can be prepared using standard technology. Transdermal formulations will require the inclusion of penetration enhancers.
Controlled Delivery Polymeric Matrices
C1ORF32 polypeptides, fragments, fusion polypeptides, nucleic acids, and vectors disclosed herein may also be administered in controlled release formulations. Controlled release polymeric devices can be made for long term release systemically following implantation of a polymeric device (rod, cylinder, film, disk) or injection (microparticles). The matrix can be in the form of microparticles such as microspheres, where peptides are dispersed within a solid polymeric matrix or microcapsules, where the core is of a different material than the polymeric shell, and the peptide is dispersed or suspended in the core, which may be liquid or solid in nature. Unless specifically defined herein, microparticles, microspheres, and microcapsules are used interchangeably. Alternatively, the polymer may be cast as a thin slab or film, ranging from nanometers to four centimeters, a powder produced by grinding or other standard techniques, or even a gel such as a hydrogel. Either non-biodegradable or biodegradable matrices can be used for delivery of polypeptides or nucleic acids encoding the polypeptides, although biodegradable matrices are preferred. These may be natural or synthetic polymers, although synthetic polymers are preferred due to the better characterization of degradation and release profiles. The polymer is selected based on the period over which release is desired. In some cases linear release may be most useful, although in others a pulse release or “bulk release” may provide more effective results. The polymer may be in the form of a hydrogel (typically in absorbing up to about 90% by weight of water), and can optionally be crosslinked with multivalent ions or polymers.
The matrices can be formed by solvent evaporation, spray drying, solvent extraction and other methods known to those skilled in the art. Bioerodible microspheres can be prepared using any of the methods developed for making microspheres for drug delivery, for example, as described by Mathiowitz and Langer, J. Controlled Release, 5:13-22 (1987); Mathiowitz, et al., Reactive Polymers, 6:275-283 (1987); and Mathiowitz, et al., J. Appl Polymer ScL, 35:755-774 (1988).
The devices can be formulated for local release to treat the area of implantation or injection—which will typically deliver a dosage that is much less than the dosage for treatment of an entire body—or systemic delivery. These can be implanted or injected subcutaneously, into the muscle, fat, or swallowed.
The effect of C1ORF32 ECD-Fc treatment on modulation of disease incidence was tested in NOD mice, which spontaneously develop a T1D disease. In NOD mice, autoreactive CD4+ can be observed within the β-islets as early as 2 weeks of age (Yang et al., Immunity 1996 February; 4(2):189-94), and by 10 weeks of age, when the treatment with C1ORF32 ECD-Fc (SEQ ID NO: 42) began in the present experiments, NOD mice develop peri-insulitis and β-cell loss (Jimeno et al., Immunology and Cell Biology. (2010) 88, 734-745).
Materials: C1ORF ECD-Fc (SEQ ID NO:42) was used in these studies, as described below. Control Ig was mouse IgG2a from BioXcell (Cat# BE0085). NOD mice were purchased from Jackson labs, and blood glucose was measured via sampling a small drop of blood from the tail vein.
Methods: Six week old NOD mice were purchased from Jackson labs. At 10 weeks of age, mice were split into groups and treated with either vehicle (PBS) Control Ig or C1ORF ECD-Fc (SEQ ID NO:42) as detailed below. Treatment was given via IP injections 3×/wk/2 wks. Blood glucose levels were monitored weekly from 8 weeks of age until the mice reached 30 or 30 weeks of age as detailed below. Mice were considered diabetic upon having two consecutive blood glucose readings of >250 mg/dL. Diabetic mice were sacrificed on the day of the second high glucose level reading. Blood glucose levels were obtained from the tail vein, and the level of blood glucose measured via use of a OneTouch. UltraSmart. Blood Glocuse Monitoring System (OneTouch; Johnson & Johnson; New Brunswick, N.J.) in a blinded manner. This study was carried out 3 times; For study 3 proteins were provided coded.
Treatment groups (n=5 mice/group):
1. Control Ig (mouse IgG2a), 100 ug/dose
2. C1ORF ECD-Fc (SEQ ID NO:42), 100 ug/dose.
As expected, NOD mice in the Control Ig treated group began to develop T1D at 13 wks of age, and all 5 mice in this control group developed the disease by the age of 17 weeks. In contrast, C1ORF ECD-Fc (SEQ ID NO:42) treatment resulted in inhibition of T1D development: 3 out of 5 mice did not develop T1D, while 2 mice developed the disease considerably later than the control mice—at 17 and 20 wks of age (
All 6 Control Ig treated mice developed T1D by the age of 25 weeks. In contrast, C1ORF ECD-Fc (SEQ ID NO:42) treatment inhibited the development of T1D, and only 1 out of 6 mice developed the disease (
Treatment groups (n=14-15):
1. Control Ig (mouse IgG2a; BioXcell) (100 ug/dose)
2. C1ORF ECD-Fc (SEQ ID NO:42) (100 ug/dose)
All compounds for this study were provided coded.
Only 3 out of 15 mice treated with C1ORF ECD-Fc (SEQ ID NO:42) developed T1D while 13 out of 14 Control Ig treated and 12 out of 15 PBS treated NOD mice developed T1D by the age of 24 weeks. In comparing the various treatment groups statistically via the use of a One-Way ANOVA and a Tukey's Multiple Comparison Post Test, the analyses revealed that the C1ORF ECD-Fc (SEQ ID NO:42) treatment had a significantly decreased incidence of T1D (p<0.001) in comparison to the Control Ig, and PBS treatment groups. Additionally, there was no significant difference in T1D incidence between the Control Ig and the PBS treatment groups. Results are shown in
The effect of C1ORF ECD-Fc (SEQ ID NO:42) treatment on modulation of disease incidence was tested in NOD mice, which spontaneously develop a T1D disease. The data presented herein show that C1ORF ECD-Fc (SEQ ID NO:42) treatment starting before onset of diabetes, significantly decreases the incidence of disease. The combined data from all 3 studies show that C1ORF ECD-Fc (SEQ ID NO:42) treatment inhibited T1D development, as the disease was observed in only 6 out of 26 (23%) of C1ORF ECD-Fc (SEQ ID NO:42) treated NOD mice. In contrast, 24 out of 25 (96%) Control Ig treated NOD mice developed T1D in the same experiments. As early as 2 weeks of age in NOD mice, CD4+ can be observed within the β-islets (1) and by 10 weeks of age, when the treatment schedule began in the present experiments, NOD mice develop peri-insulitis and β-cell loss (2). These published findings suggest that the early stages of the CD4+ cell autoimmune response to antigens present within β-islets of the pancreas are already ongoing at the time of C1ORF ECD-Fc (SEQ ID NO:42) treatment. The highly significant decrease in disease incidence suggests that further analyses are warranted, and that C1ORF ECD-Fc (SEQ ID NO:42) holds promise as a potential therapy for T1D.
The Effect of any One of C1ORF32 Protein Fragments and/or Fusion Proteins Thereof in Modulation of Type 1 Diabetes in Nod Mice, CD28-KO NOD, and B7-2-KO Nod
The effect of any one of C1ORF32 protein fragments and/or fusion proteins thereof is studied in a widely used mouse model of type 1 diabetes: nonobese diabetic (NOD) mice which develop spontaneous In NOD mice, spontaneous insulitis, the hallmark pathologic lesion, evolves through several characteristic stages that begin with peri-insulitis and end with invading and destructive insulitis and overt diabetes. Peri-insulitis is first observed at 3-4 wk of age, invading insulitis at 8-10 wk, and destructive insulitis appears just before the onset of clinical diabetes, with the earliest cases at 10-12 wk. At 20 wk of age, 70-80% of female NOD mice become diabetic (Ansari et al 2003 J. Exp. Med. 198: 63-69).
The study is performed in NOD mice. The efficacy of C1ORF ECD-Fc (SEQ ID NO:42) in T1D model using two KO NOD mice: CD-28-KO NOD mice and B7-1/B7-2 double KO NOD mice, —which develop accelerated diabetes (Lenschow et al 1996 Immunity 5: 285-293; Salomon et al 2000 Immunity 12: 431-440), are also carried out.
Study I: NOD mice are treated with any one of C1ORF32 protein fragments and/or fusion proteins thereof early and late phases during the evolution of diabetes, before or after disease onset, to examine the effects of these compounds on disease pathogenesis and to demonstrate that such treatment reduces disease onset and ameliorates pathogenesis. To study the effect on insulitis, blood glucose levels are measured 3 times/week, for up to 25 weeks (Ansari et al 2003 J. Exp. Med. 198: 63-69).
Mechanism of disease modification and mode of action is studied by experimental evaluation of individual immune cell types: pancreas, pancreatic LNs and spleen are harvested to obtain Tregs, Th subtypes and CD8 T cells, DCs and B cells. Effect on cytokines secretion from cells isolated from pancreas, pancreatic LN and spleen is analysed, focused on IFNg, IL-17, IL-4, IL-10 and TGFb. Upon effect of the tested compounds, the mechanism of disease modification is studied by examination of individual immune cell types (including Tregs, Th subtypes and CD8 T cells, DCs and B cells); cytokines (IFNg, IL-17, IL-4, IL-10 and TGFb) and histology. Histologycal analysis of the pancreas is carried out to compare the onset of insulitis, and the lymphocyte infiltration.
Study II— The effect of any one of C1ORF32 protein fragments and/or fusion proteins thereof in modulation of Type 1 Diabetes in Adoptive transfer model
To further investigate the mode of action of the Ig fusion proteins, an adoptive transfer model of diabetes is used. T cells from diabetic or prediabetic NOD donors are transferred to NOD SCID recipient mice. These mice are monitored for development of diabetes. The urine glucose and blood glucose, and assess histology of the pancreas, and T cell responses are monitored as described in the previous example.
Study III— Diabetes is also induced by the transfer of activated CD4+CD62L+CD25-BDC2.5 T cells (transgenic for TCR recognizing islet specific peptide 1040-p31 activated by incubation with 1040-p31) to NOD recipients. Mice are treated with any one of C1ORF32 protein fragments and/or fusion proteins thereof, control mIgG2a or positive control. Treatments begin 1 day following transfer. Mice are followed for glucose levels 10-28 days post transfer (Bour-Jordan et al., J Clin Invest. 2004; 114(7):979-87).
Seven days post treatment pancreas, spleen, pancreatic LN and peripheral lymph node cells are extracted and examined for different immune cell populations. In addition, recall responses are measured by testing ex-vivo proliferation and cytokine secretion in response to p31 peptide.
C1ORF32 protein fragments and/or fusion proteins thereof prevent or reduce disease onset or the severity thereof in the above studies.
A transplantation model utilizing male bone marrow (BM) cells from C57BL/6 mice transplanted into female mice of the same starin was used to study whether C1ORF32 ECD-Fc induces immune tolerance. In this model BM cells of the male mouse are rejected by the female recipients due to mismatch in the minor histocompatibility antigen encoded by the Y chromosome (Hya). To allow identification of the male cells in the female mice blood, male mice expressing CD45.1 isotype were selected while the female mice carry CD45.2 isotype. This model provides a tool for testing the effect of potential drugs on induction of tolerance towards the grafted cells.
In this model, C1ORF32 ECD-Fc (SEQ ID NO:42) treatment started one week before bone marrow transplantation and continued for five weeks. Female recipient mice were followed for percentage of CD45.1+ and CD45.2+ cells present within the blood.
Female C57BL/6 recipient mice (CD45.2+) were sub-lethally irradiated with 200 rads/cGy 24 hours before transplantation of either female C57Bl/6 (CD45.1+) or male C57Bl/6 (CD45.1+) 5×106 bone marrow cells. Recipient mice were allocated into treatment groups as detailed below (n=6 per group). Treatments were given at 300 ug/dose i.p, 3×/wk starting one week prior to transplantation and continued for 4 weeks following transplantation, giving a total of 15 treatments during this 5 weeks period. Anti-CD40L was used as a positive control, as it has previously been shown to have efficacy in this model (unpublished data).
1. Female CD45.1 into female CD45.2
2. Male CD45.1 into female CD45.2+anti-CD40L (300 ug/dose) (Clone MR-1; BioXCell, Cat#BE0017-1)
3. Male CD45.1 into female CD45.2+C1ORF ECD-Fc (SEQ ID NO:42) (300 ug/dose)2
4. Male CD45.1 into female CD45.2+Control Ig (mouse IgG2a) (300 ug/dose)
Beginning at 2 weeks following bone marrow transplantation, blood samples from the tail were collected from each mouse once a week for 4 weeks. Approximately 2-3 drops of blood were collected per mouse into 200 ul of PBS+EDTA (50 mM), samples were spun down, and RBCs lysed with ammonium chloride. The cells were washed 3× with PBS, stained with the viability dye Aqua Dead Cell Stain (Invitrogen; Cat#L34957), blocked with Fc Receptor block (anti-mouse CD16/32; eBioscience; Cat#14-0161-86), and stained with anti-mouse CD45.1 APC-Cy7 (eBiosciences; Cat#47-0453-80) and anti-mouse CD45.2 FITC (eBioscience; Cat#11-0454-82). The analysis for chimerism was determined by flow cytometric analysis (on total live cells) for the percentage of CD45.1+ versus CD45.2+ cells present in the blood of female recipient mice.
During weeks 6, 7, and 8 the blood samples were also stained to determine the percentage of CD4+ Teff cells and CD4+ Treg cells present within the blood using the cellular markers CD44, CD25, and FoxP3. Details of the Abs used in the flow panels for weeks 6, 7, and 8 are listed below.
These same populations of cells were analyzed at week 8 within the spleen. In addition, the proliferative and secreted cytokine responses of total splenocytes in ex vivo recall cultures were tested in the presence of medium alone, anti-CD3 (1 ug/ml), the HY antigen DBY peptide (NAGFNSNRANSSRSS; Genemed Synthesis; San Antonio, Tex.) (10 ug/ml), irradiated male splenocytes (1:1 ratio), or irradiated female splenocytes (1:1 ratio).
Flow cytometry panels for Weeks 6-8 blood (Panel 1) and Week 8 spleen samples (Panel 2):
Viability Dye (LIVE/DEAD® Fixable Aqua Dead Cell Stain Kit*for 405 nm excitation; Invitrogen; Cat# L34957)
anti-CD45.2 FITC (eBioscience; Cat#11-0454-82)
anti-CD45.1 APC-Cy7 (eBiosciences; Cat#47-0453-80)
anti-CD3 PerCP (BD Bioscience; Cat#553067)
anti-CD4 eFluor 450 (eBiosciences; Cat#48-0042-82)
anti-FoxP3 PE-Cy7 (eBiosciences; Cat#25-5773-82)
anti-CD25 APC (eBiosciences; Cat#17-0251-82)
anti-CD44 PE (eBiosciences; Cat#12-0441-82)
anti-CD45.2 FITC (eBioscience; Cat#11-0454-82)
anti-CD45.1 APC-Cy7 (eBiosciences; Cat#47-0453-80)
anti-CD3 PerCP (BD Bioscience; Cat#553067)
anti-CD4 eFluor 450 (eBiosciences; Cat#48-0042-82)
anti-FoxP3 PE-Cy7 (eBiosciences; Cat#25-5773-82)
anti-Nrp-1 APC (R&D Systems; Cat#FAB566A)
anti-Helios PE (eBiosciences; Cat#12-9883-42)
The data for the weekly percentage of CD45.1+ and CD45.2+ cells present within the blood are shown in
The percentage of CD45.2+ cells in the blood of the female recipients is roughly in inverse correlation to that of grafted CD45.1+ cells, as would be expected.
During weeks 6 and 7 post bone marrow cell transplantation, the CD45.1+ and CD45.2+ cells in the blood of recipient mice were further analyzed to determine if C1ORF ECD-Fc (SEQ ID NO:42) treatment altered the percentage of effector/memory CD4+ T cells (CD4+/CD44hi), activated CD4+ T cells (CD4+/CD25+/FoxP3−), resting CD4+ T cells (CD4+/CD44lo), or Treg cells (CD4+/CD25+/FoxP3+).
The data presented in
No differences were observed in the recipients' CD45.2+ T cell populations among the different treatment groups by week 6 post bone marrow cell transplant (
By week 7, mice receiving male CD45.1+ bone marrow cells plus C1ORF ECD-Fc (SEQ ID NO:42) treatment had significantly lower percentage of activated donor CD4+ T cells (CD45.1+/CD4+/CD25+/FoxP3−) as compared to mice treated with Control Ig (
A similar analysis as that shown in
No differences were observed in the recipients In addition, spleen cells were evaluated for ice treated with C1ORF ECD-Fc (SEQ ID NO:42) as compared to mice treated with Control Ig by week 8 post bone marrow cell transplant (
In contrast to the blood, significant differences within the various CD4+ T cell populations of the recipient's endogenous cells (CD45.2+) were found in the spleen of C1ORF ECD-Fc (SEQ ID NO:42) treated mice compared to those treated with Control Ig. Mice transplanted with male CD45.1+ bone marrow cells and treated with C1ORF ECD-Fc, or with other treatments that lead to successful engraftment (i.e. anti-CD40L or mice transplanted with female CD45.1 cells) had lower percentage and number of CD45.2+, reflective of the increase in CD45.1+ cells, and CD4+ T cells within the spleen compared to mice that were treated with Control Ig and rejected the graft (
The data focused on the donor the data focused on (CD45.1+) show a significant increase in effector/memory CD4+ T cells (CD44hi) and Tregs (FoxP3+CD25+), as well as a decrease in activated CD4+ T cells (FoxP3−CD25+) in the blood of female recipient mice receiving male donor CD45.1+ bone marrow cells and C1ORF ECD-Fc treatment, as compared to the mice with Control Ig treatment (
In addition, C1ORF ECD-Fc (SEQ ID NO:42) treatment resulted in a striking increase in the number of donor-derived (CD45.1+) CD4+/CD25+/FoxP3+ Treg cells, as well as Treg subpopulations: Nrp-1+/Helios+, Nrp-1+/Helios−, and Nrp-1−/Helios−(
Ex vivo reactivation (recall responses) of splenocytes on week 8 was carried out with transplant-related stimuli (HY Ag DBY peptide or irradiated male splenocytes) or transplant-unrelated stimuli (anti-CD3 or irradiated female splenocytes). Compared to cells cultured in medium alone (i.e. without any added stimuli), only the addition of anti-CD3 lead to a substantial increase in cell proliferation (
Parallel splenocytes reactivation cultures were also evaluated for cytokine secretion. The data, presented in
The data from this study show that C1ORF ECD-Fc treatment with a 5 week dosing schedule, beginning one week before bone marrow cell transplant, is effective in preventing graft rejection and induces a tolerogenic environment towards the Hya minor mismatch antigen. This is demonstrated by the presence of donor CD45.1+ chimerism within the blood of CD45.2+ recipient female mice, similar to that obtained following transplantation of female CD45.1+ bone marrow cells or treatment with anti-CD40L, which was used as a positive control.
The increase in the number of donor derived Treg cells present within the spleens of C1ORF ECD-Fc treated mice suggests that tolerance induction by C1ORF ECD-Fc is potentially mediated by its effect on Treg cells. This finding is in agreement with previous in vitro data showing that C1ORF ECD-Fc treatment appears to increase the number of iTreg cells. In the present study C1ORF ECD-Fc treatment resulted in increased number of Treg subtypes, such as Helios+/Nrp-1+ and Helios-/Nrp-1− (which are proposed to represent nTregs and iTregs, respectively) (Thornton et al., J. Immunol. 184: 3433-3441; Yadav et al., J Exp Med. 2012; 209:1713-1722) J Exp Med. 2012 Sep. 24; 209(10):1713-22 J Exp Med. 2012 Sep. 24; 209(10):1713-22.
Functionally, the ex vivo recall data show that splenoctyes isolated from mice receiving C1ORF ECD-Fc treatment produce significantly lower levels of inflammatory cytokines (IFN-gamma, IL-17, GM-CSF, IL-12, IL-2 and TNF-alpha) upon activation with male irradiated splenocytes or DBY peptide compared to Ig control treated mice and an increased level of IL-10 and IL-4 upon activation with irradiated male splenocytes. The latter is supportive of previous similar findings with both splenoctyes and draining lymph node ex vivo recall cultures in the PLP139-151/CFA primed SJL mouse model.
Efficacy and Mode of Action of any One of the C1ORF32 Protein Fragments and/or Fusion Proteins Thereof in Mouse Adoptive Transfer R-Eae Model of Multiple Sclerosis
The therapeutic effect of C1ORF32 ECD-Fc (SEQ ID NO:42) in treatment of autoimmune diseases was tested in a mouse model of multiple sclerosis; Relapsing Remitting Experimental Autoimmune Encephalomyelitis (R-EAE):
Materials and Methods
Animals
Female SJL/J mice˜six week old were purchased from Harlan, and allowed to acclimate at the animal care facility for 1 week before use. SJL-Actin/GFP mice were bred in-house at Northwestern Univeristy and primed at 6-12 weeks of age.
Induction of Adoptive Transfer R-EAE
Female SJL/J mice were primed with 50 ug of PLP139-151/CFA according to the standard laboratory protocol on day 0. On day 8 post disease induction, the inguinal lymph nodes were collected and the total lymph node cells were re-activated in culture in the presence of PLP139-151 for 3 days. At the end of culture, cells were collected and transferred into naive recipient SJL/J mice.
CFA/PLP Emulsion Preparation
a. PLP139-151 peptide stock (Genemed Sythesis Inc) was diluted in PBS (1 mg/ml) in an omni-mixer bucket, followed by addition of an equal volume of CFA.
b. The bucket was mixed in an omnimixer on high speed (setting 4-5) for 5 minutes.
c. The whole emulsion was scooped into 10 ml snap-cap tube, quick spined in a centrifuge (up to 1200 rpm then stopped) and loaded into glass Hamilton syringes. All air bubbles were removed and attached to a 25 G needle.
Priming Donor SJL/J Mice, PLP139-151 Reactivation Cultures, and Blast Cell Transfer
a. Mice were shaved (about a lin.xlin, square on the back between the hind flanks) and injected with CFA/PLP139-151 emulsion at 100 μl per mouse s.c., divided between three spots on the back and flanks. Peptide and final dose given per mouse: 50 μg of PLP139-151 peptide on day 0.
b. On day 8 post priming with PLP139-151/CFA, the draining inguinal lymph nodes were collected, and single cell suspensions were prepared. Total lymph node cells were cultured at a density of 8×106 cells per ml in the HL-1 medium plus PLP139-151 peptide (20 μg/ml) in T75 flasks.
c. After 3 days of culture, the PLP139-151 reactivated cells were collected and counted using an hemacytometer. The number of total viable cells and the number of blast cells was determined. The percentage of blast cells expected following this protocol is 20-30% of the total viable cells.
d. Unless otherwise specified, 3×106 cells were transferred to each recipient mouse by intravenous injection.
e. Mice were split into treatment groups as detailed for each specific experiment.
f. Mice were scored on the indicated days, on a 0-5 disease score scale per standard laboratory protocol: 0, no abnormality; 1, limp tail; 2, limp tail and hind limb weakness; 3, hind limb paralysis; 4, hind limb paralysis and forelimb weakness; and 5, moribund.
Ex vivo recall responses by total splenocytes and lymph node cells from treated mice:
On day 45 (unless otherwise indicated) following cell transfer, spleen and cervical lymph nodes or CNS from 3 representative mice of each group were collected, and the total cells were activated ex vivo at 0.5×106 cells per well with either OVA323-339, PLP139-151, PLP178-191, MBP84-104 (20 ug/ml), or anti-CD3 (1 ug/ml). Two sets of cultures were set up side-by-side. One set was pulsed with 1 uCi of tritiated thymidine at 24 hours and harvested at 72 hours to determine cell proliferation. In the second set of cultures, supernatants were collected at 72 hours and tested for peptide-specific cytokine production as determined by LiquiChip.
Evaluation of BBB Breakdown and Inflammation by Fluorescence Molecular Tomography
Commercially available near infrared (NIR) imaging agents were used to perform tomographic imaging (PerkinElmer Inc., Boston, Mass.). AngioSense®750 was used as a vascular imaging agent, and Cat B® 680 FAST was used to detect regions of increased lysosomal cathepsin B activity. For the in vivo imaging, mice were injected intravenously with 4 nmol of NIR fluorescent agent 24 hrs prior to imaging, and imaged following the last treatment with Control Ig or C1ORF32 ECD-Fc (SEQ ID NO: 42) (Day +30 post-PLP139-151 blast cell transfer). At the time of imaging, mice were anesthetized by administration of sodium pentobarbital (50 mg/kg) and then imaged using the FMT 2500 fluorescence molecular tomography in vivo imaging system (PerkinElmer Inc., Boston, Mass.). For whole body imaging, the anesthetized mice were placed in the supine position, centrally in the imaging cassette to capture the whole body (excluding the head) of the animal within the imaging scan field of the imaging system. For imaging the head, mice were placed in the prone position in the imaging cassette for a separate scan. After positioning the mouse, the imaging cassette was adjusted to the proper depth to gently restrain the mouse and then inserted into the heated docking system (regulated at 37° C.) in the FMT imaging chamber. A FR/NIR laser diode transilluminated (i.e. passed light through the body of the animal to be collected on the opposite side) the animal body, with signal detection occurring via a thermoelectrically cooled CCD camera placed on the opposite side of the imaged animal. Appropriate optical filters allowed the collection of both fluorescence and excitation datasets, and the multiple source-detector fluorescence projections were normalized to the paired collection of laser excitation data. The entire image acquisition sequence took approximately 8-10 min (torso) and 2-3 min (head) per mouse. After image acquisition was complete, mice were perfused with phosphate buffered saline and the CNS was removed to acquire ex vivo images of the tissue to corroborate findings from 3D images. The collected fluorescence data was reconstructed by FMT 2500 system software (TrueQuant, PerkinElmer Inc., Boston, Mass.) which compensates for the effects of tissue heterogeneity on light scattering, allowing for the quantification of fluorescence signal within multiple organ regions. Three-dimensional regions of interest (ROI) were drawn to encompass lung, heart, liver, stomach, kidney, intestine, and bladder tissue regions. For visualization and analysis purposes, FMT 2500 system software provided 3D images and tomographic slices. The total amount of fluorescence (in pmoles) in different organ sites was automatically calculated relative to internal standards generated with known concentrations of appropriate FR/NIR dyes. All data was normalized to fluorescence detected in CFA/saline-immunized healthy control mice.
Proteins Tested:
C1ORF32 ECD-Fc (SEQ ID NO:42) mIgG2a as Ig Control (BioXcell Cat # BE0085).
Statistical Analysis:
Disease course data was analyzed by one-way ANOVA with repeated measures.
Recall Responses Data were Analyzed Using Student's T Test.
C1ORF32 ECD-Fc (SEQ ID NO:42) treatment starting at onset of disease remission results in decrease of disease severity, Th1/Th17 to Th2 shift, and reduced BBB vascular leakage
Two independent studies were performed to evaluate the effect of C1ORF32 ECD-Fc (SEQ ID NO:42) treatment starting at the time of disease remission in the adoptive transfer RR-EAE model (
C1ORF32 ECD-Fc (SEQ ID NO:42) treatment from onset of disease remission also inhibited recall responses of splenocytes and lymph node cells on day 45, as manifested in a decreased level of cellular proliferation (
The effects of C1ORF32 ECD-Fc (SEQ ID NO:42) treatment from onset of remission on vascular leakage in the CNS, as a marker for BBB damage, and on the level of inflammation by monocyte/macrophage activation, were studied in vivo using AngioSense720 and Cat B 680 FAST, respectively, as NIR imaging agents. Four mice were selected from each treatment group and analyzed as described in Materials and Methods. The disease scores in this subgroup of mice were 4, 4, 4, and 4 in the Control Ig treatment group, and 0, 2, 0, and 2 in the C1ORF32 ECD-Fc (SEQ ID NO:42) treatment group. The results, presented on
C1ORF32 ECD-Fc (SEQ ID NO:42) treatment beginning at the time of cell transfer decreases the ability of the transferred cells to induce disease, and decreases the number of transferred cell infiltrates within the CNS.
PLP139-151 sensitized cells were generated as described in Materials and Methods (cell counts in the reactivation culture are presented in Table 2) and labeled with PBSE (4 uM) before transfer to naïve mice. In study “Cgen data” (
An additional experiment (designated “MYC48 FACS”,
Summary
Treatment of SJL/J mice either at the time of PLP139-151-specific reactivated cells transfer or at onset of disease remission resulted in inhibition of disease induction and in a reduction of BBB leakage, as well as CNS inflammation and damage in C1ORF32 ECD-Fc (SEQ ID NO:42) treated mice.
In addition, using the adoptive transfer model described herein, inhibition of recall responses to inducing and spread epitopes and Th1/Th17 to Th2 shift were observed following treatment with C1ORF32 ECD-Fc (SEQ ID NO:42). These effects are similar to the immune effects observed in C1ORF32 ECD-Fc (SEQ ID NO:42) treated mice in the active RR-EAE studies.
When GFP and/or PBSE labeled cells were used for transfer, a reduction of autoreactive cell infiltration into the CNS was detected in the C1ORF32 ECD-Fc (SEQ ID NO:42) treated groups. Reduced CNS infiltration of autoreactive cells might underlie the lower cell numbers that were observed in the active RR-EAE studies, as assessed either by flow cytometry analysis or by immunohistochemical analysis. No reduction was observed in the number of total transferred cells or of T cells in the lymph nodes or in the spleen of C1ORF32 ECD-Fc (SEQ ID NO:42) treated mice. This observation suggests that no general cell depletion is induced by C1ORF32 ECD-Fc (SEQ ID NO:42) treatment.
Altogether the data presented herein support previous observations and further establish the mode of action underlying the beneficial effects of C1ORF32 ECD-Fc (SEQ ID NO:42) in RR-EAE models.
Depletion and/or inactivation of CD4+CD25+FoxP3+ Tregs using anti-CD25 mAb treatment is an accepted strategy to characterize Treg function in vivo.
21.1.1 Study Design
In two studies, EAE was induced in SJL mice via PLP139-151/CFA priming as described under Methods, below. The mice were divided into 4 and 8 groups in Study I and Study II, respectively groups (n=10/treatment group). In both studies, groups 1-4 the mice received two injections separated by one day, of either Control Ab or anti-CD25 (clone 7D4 at 500 μg/injection i.p. (BioXCell Cat# BE0013; West Lebanon, N.H.)) starting at the onset of disease remission (Day +19 and 21 in Study I or Day +20 and 22 in Study II), followed by treatment with either mIgG2a Control Ig or C1ORF32 ECD-Fc (100 ug/dose; 3×/wk; 2 wks) beginning on the day of the second treatment with anti CD25 (Day 21 in study I and day 22 in study II).
To study the importance of Treg function for maintenance of tolerance by C1ORF32 ECD-Fc a second set of mice was set in study II, groups 5-8, in which mice were treated with Control Ig or C1ORF32 ECD-Fc (SEQ ID NO:42) first in a similar regimen as groups 1-4 (beginning on Day +22), and then two weeks following the last C1ORF32 ECD-Fc (SEQ ID NO:42) treatment, on days 46 and 48, mice received either Control Ab or anti-CD25 (500 μg/injection) to inactivate the Treg cells. The mice were followed for the level of disease severity.
C1ORF32 ECD-Fc (SEQ ID NO:42) was diluted in PBS pH 6.0, 0.01% Tween 80, anti-CD25 and control Abs were diluted in PBS.
Study I Treatment Groups (n=10 Mice Per Group)
1. Control Ab (Day +19 and 21) plus Control Ig (100 ug/dose; 3×/wk; 2 wks; beginning on Day +21)
2. Anti-CD25 Ab (Day +19 and 21) plus Control Ig (100 ug/dose; 3×/wk; 2 wks; beginning on Day +21)
3. Control Ab (Day +19 and 21) plus C1ORF ECD-Fc (SEQ ID NO:42) (100 ug/dose; 3×/wk; 2 wks; beginning on Day +21)
4. Anti-CD25 Ab (Day +19 and 21) plus C1ORF ECD-Fc (SEQ ID NO:42) (100 ug/dose; 3×/wk; 2 wks; beginning on Day +21)
Study II Treatment Groups (n=10 Mice Per Group)
1. Control Ab (Day +20 and 22) plus Control Ig (100 ug/dose; 3×/wk; 2 wks; beginning on Day +22)
2. Anti-CD25 Ab (Day +20 and 22) plus Control Ig (100 ug/dose; 3×/wk; 2 wks; beginning on Day +22)
3. Control Ab (Day +20 and 22) plus C1ORF32 ECD-Fc (SEQ ID NO:42) (100 ug/dose; 3×/wk; 2 wks; beginning on Day +22)
4. Anti-CD25 Ab (Day +20 and 22) plus C1ORF32 ECD-Fc (SEQ ID NO:42) (100 ug/dose; 3×/wk; 2 wks; beginning on Day +22)
5. Control Ig (100 ug/dose; 3×/wk; 2 wks; beginning on Day +22) plus Control Ab (Day +46 and 48)
6. Control Ig (100 ug/dose; 3×/wk; 2 wks; beginning on Day +22) plus Anti-CD25 Ab (Day +46 and 48)
7. C1ORF32 ECD-Fc (SEQ ID NO:42) (100 ug/dose; 3×/wk; 2 wks; beginning on Day +22) plus Control Ab (Day +46 and 48)
8. C1ORF32 ECD-Fc (SEQ ID NO:42) (100 ug/dose; 3×/wk; 2 wks; beginning on Day +22) plus Anti-CD25 Ab (Day +46 and 48)
21.1.2 Methods
21.1.2.1 Stock of CFA:
Five 10 ml ampules of Incomplete Freunds Adjuvent (IFA; Difco cat #263910) were combined with two, 100 μg ampules of M. tuberculosis H37RA (Difco cat#231141) in a glass 100 ml bottle. The final concentration of the Complete Freund's Adjuvant was 4 mg/ml. Stored at 4° C.
21.1.2.2 CFA & PLP Emulsion Preparation:
In omni-mixer bucket, peptide stock was diluted in PBS to desired concentration (e.g. 1 mg/ml for PLP139-151) and then equal volume of CFA was added. Before removal of the needed volume from the Complete Freund's Adjuvant it was mixed thoroughly to ensure that the M. tuberculosis is evenly mixed (since M. tuberculosis falls out of solution). Bucket was attached to omnimixer, lowered into ice-filled dish until flush with counter, and mixed on high speed (setting 4-5) for 5 minutes. All the emulsion was scooped into 10 ml snap-cap tube. Quickspin in centrifuge (up to 1200 rpm then stopped) and loaded into glass Hamilton syringes. Removed all air bubbles and attach 25 g needle.
21.1.2.3 Animal Procedures and Treatments:
Naive˜six week old SJL/J mice were purchased from Harlan, and allowed to acclimate to the animal care facility for 1 week. On day of disease induction, day 0, mice were shaved (about a lin.x lin, square on the back between the hind flanks) and injected s.c. with 100 μl of CFA & PLP emulsion per mouse, divided between three spots on back and flanks. PLP139-151 peptide final dose given per mouse was 50 μg.
SJL mice were primed with 50 μg PLP139-151/CFA to induce R-EAE, and followed for disease through the acute phase of disease and into disease remission. At disease remission mice were divided into 4 treatment groups. On Days +19 and 21, mice received either Control Ab or anti-CD25 treatment (500 μg/dose). Beginning on Day +21 mice received Control Ig or C1ORF32 ECD-Fc (SEQ ID NO:42) treatment (100 μg/dose; 3 doses/wk; 2 wks). Clinical results are expressed as the mean clinical score.
Mice were followed for disease and scored on a 0-5 scale per standard lab protocol as follows: 0, no abnormality; 1, limp tail; 2, limp tail and hind limb weakness; 3, hind limb paralysis; 4, hind limb paralysis and forelimb weakness; and 5, moribund.
21.1.3 Results
Study I
In the absence of anti-CD25 treatment a relapsing EAE disease was observed which was abrogated by treatment with C1ORF ECD-Fc (SEQ ID NO:42) (
Study II
In a second study transient inactivation of Tregs in the EAE model by administration of anti-CD25 (antibody) at early stage of the disease, right after the acute phase, did not affect the therapeutic efficacy of C1ORF32 ECD-Fc (SEQ ID NO:42) which completely inhibited diseases symptoms (
This alleviation of disease is probably related to iTregs induced by C1ORF32 ECD-Fc (SEQ ID NO:42) (as previously shown in vitro and in vivo) which are important for the durable effect of C1ORF32 ECD-Fc in R-EAE and are important players in restoration of immune tolerance by C1ORF32 ECD-Fc (SEQ ID NO:42) treatment. The efficacy induced by C1ORF32 ECD-Fc treatment following Treg inactivation at early stage of the disease, right after the acute phase, indicates that at early stages of the disease other mechanisms, probably inhibition of Th1 and Th17 responses, underly the therapeutic effect of C1ORF32 ECD-Fc.
Study Design
SJL/J mice were purchased from Harlan and primed with PLP139-151/CFA per the standard protocol, as described in 21.1.2 Methods, above). At disease remission the mice were split into 6 different treatment groups (n=5) as follows:
Treatment Groups (n=5 mice per group):
1. mIgG2a (control for C1ORF32 ECD-Fc (SEQ ID NO:42)) followed by rIgG1 (control for anti-IL-10)
2. mIgG2a followed by anti-IL-10
3. mIgG2a followed by anti-TGF-β
4. C1ORF32 ECD-Fc (SEQ ID NO:42) followed by rIgG1
5. C1ORF32 ECD-Fc (SEQ ID NO:42) followed by anti-IL-10
6. C1ORF32 ECD-Fc (SEQ ID NO:42) followed by anti-TGF-β
Mice were treated with Control Ig (mouse IgG2a) or C1ORF32 ECD-Fc (SEQ ID NO:42) at 100 ug/dose, each via an i.p. injection. This was followed with a second i.p. injection on the same day of either anti-IL-10 (rat IgG1), rat IgG1 (control Ab), or anti-TGFβ (mouse IgG1) at 100 ug/dose, each. All treatments were given 3×/wk for 2 wks, beginning on day +20 (onset of disease remission) and until day +31 post disease induction. All mice were followed for disease scores until day 44 post disease induction. On day 44, mice were sacrificed and analyzed for total T cell and Treg cell numbers in spleen and CNS.
C1ORF ECD-Fc (SEQ ID NO:42) was diluted in PBS pH 6.0, 0.01% Tween 80, anti-CD25 and control Abs were diluted in PBS.
Materials and Methods
Animal Procedures and Treatments:
EAE was induced in SJL mice as described above.
At onset of disease remission (day +20 post disease induction) mice were allocated into 6 treatment groups (described above) and treated with either C1ORF32 ECD-Fc (SEQ ID NO:42) or control Ig (mIgG2a), and followed on the same day by treatment with anti-IL-10, anti-TGF-β, or rat IgG1 isotype control. All treatments were given at 100 ug/dose in 100 μl of PBS; via i.p. injection, at 3×/week for 2 weeks from onset of remission.
Mice were followed for disease and scored on a 0-5 scale per standard lab protocol as follows: 0, no abnormality; 1, limp tail; 2, limp tail and hind limb weakness; 3, hind limb paralysis; 4, hind limb paralysis and forelimb weakness; and 5, moribund. Dead mice were scored with a score of 5 on the day of death only, and were not further scored on the next days.
On day 44 post disease induction, the rest of the mice were sacrificed and spleens and CNS were taken for cell counts and cell population analysis as described below.
Reagents
Tissue Collection:
1. Mice were deeply anesthetized using Nembutal (500 ug via i.p. injection), and the mice were perfused with 30 ml of sterile 1×PBS.
2. The spleens and CNS were collected.
3. Each tissue was kept separate for each individual mouse, and the tissues were processed individually.
4. The spleens were processed via tissue disruption by mashing the tissues through 100 μm nitex filter. The filters were washed with 10 ml of HBSS+5% FCS.
5. For the spleens, the red blood cells (RBCs) were lysed via ammonium chloride treatment for 4 min at 37 deg C. The cells were pelleted, washed 3 times with HBSS+5% FCS, any cellular debris was removed via the use of 40 μm nitex filter, and counted on a hemocytomter via trypan blue exclusion.
6. The CNS tissue was processed as follows. The CNS tissue was chopped coarsely with scissors, and incubated with 1 ml per CNS of Accutase (Millipore; Cat# SCR005) for 30 min at 37 degC.
7. After the 30 min incubation 5 ml of HBSS+5% FCS was added to each sample, and the sample was transferred to a 40 um nytex mesh cell strainer on top of a 50 ml conical tube, and push CNS through mesh by scraping mesh with the blunt end of a 1 cc-syringe plunger.
8. The cell strainer was washed twice with 10 ml of HBSS+5% FCS.
9. The isolated cells were pelleted by centrifugation at 300×g for 10 min.
10. The pellet was resuspended in 3 ml/CNS 70% Percoll and transfer to 15 ml conical tube.
11. An equal volume of 30% Percoll was layered on top.
12. Tubes were spun at room temp centrifuge at 1600 rpm (600 g) for 30 minutes with no brake.
13. The myelin layer on top was removed by aspiration, and the cells at the 70/30 interface were collected.
14. The collected CNS cells were washed 2× with HBSS+5% FCS, and counted.
Flow Cytometry:
Flow Cytometry Control Tubes and Experimental Sample Tubes
1. Unstained control
2. Single stain controls
3. FMO controls
4. Experimental stains (CD45, CD3, CD4, CD25, FoxP3, Nrp-1, and Helios)
Cells Preparation for Flow Cytometry:
Harvest, wash and count cells, and resuspend at 10×106 cells/mL
1. Plate 50-100 uL (0.5-1×106 cells) in each well, wash cells three times with 1×PBS, and resuspend with 100 uL of LIVE/DEAD® Fixable Aqua Dead Cell Stain Kit*for 405 nm excitation (Invitrogen; Cat# L34957) for 20 minutes on ice.
2. Wash cells three times in 1×PBS+5% FCS.
3. Resuspend cells in 100 ul of mouse Fc Block (anti-CD16/32; eBioscience; Cat#14-0161-86) diluted 1:100 in 1×PBS+5% FCS. Cells were incubated at 4 degC for 20 min.
4. The cells were washed three times in 1×PBS+5% FCS, and then resuspended in the cell surface staining cocktail of antibodies listed below in a final volume of 100 ul. The cells were incubated for 30 min. For the FMO controls, one of the specific antibodies was removed per FMO control.
a. Anti-CD45 APC-Cy7 (eBioscience; Clone 30-F11; Cat#47-0451)
b. Anti-CD3 PE-Cy7 (eBioscience; Clone 145-2C11; Cat#25-0031)
c. Anti-CD4 Pacific Blue (eFluor 450) (eBioscience; Clone GK1.5; Cat#48-0041)
d. Anti-CD25 Fitc (Alexa Fluor 488) (eBioscience; Clone 7D4; Cat#53-0252)
e. Anti-Nrp-1 APC (eBioscience; Clone 3DS304M; Cat#17-3041)
5. The cells were washed three times in 1×PBS, and resuspend 200 uL in freshly made Fix/Perm solution (eBioscience; Cat#00-5523-00) and incubate overnight (or 30 min) at 4 degC.
6. The cells were washed three times in 1× Perm. Buffer, and resuspended in the intracellular staining cocktail of antibodies listed below in a final volume of 100 ul of Perm. buffer.
a. Anti-FoxP3 PercP-Cy5.5 (eBioscience; Clone FJK-16s; Cat#45-5773)
b. Anti-Helios PE (eBioscience; Clone 22F6; Cat#12-9883)
7. Following a 30 min incubation at 4 degC, the cells were washed three times with Perm buffer, and two times with 1×PBS+5% FCS.
8. The cells were resuspended in 400 ul of 1×PBS+5% FCS, and analyzed by flow.
9. Gating scheme for flow: Singlets (FSC-A vs. FSC-H)->Cells (SSC-A vs. FSC-A)->Live (VID stain negative cells)->CD45hi->CD3/CD4+->CD25/FoxP3+->Helios/Nrp-1
Results
Treatment of mice primed with PLP/CFA with C1ORF32 ECD-Fc (SEQ ID NO:42) (followed by rIgG1) resulted in pronounced inhibition of disease progression as compared to mice treated with control Abs only (mIgG2a followed by rIgG1). Neutralization of IL-10 (in the presence of control mIgG2a) did not significantly affect disease severity compared to control Abs only (
In both groups treated with anti-TGFβ, either alone or in combination with C1ORF32 ECD-Fc (SEQ ID NO:42) and in the group treated with anti-IL-10 in combination with C1ORF32 ECD-Fc (SEQ ID NO:42), mice were found dead on days 27-28 of the study. Specifically, in the group treated with mIgG2a and anti-TGFβ, 2 mice were found dead on day 27; 1 dead mouse was found in the group treated with C1ORF32 ECD-Fc (SEQ ID NO:42) and anti-TGFβ on day 28, and 2 dead mice were found on day 28 in the group treated with C1ORF32 ECD-Fc (SEQ ID NO:42) in combination with anti-IL-10. Death of these mice is manifested as a ‘spike’ in the score graph of the respective group on the day of death (
In addition, analysis of the Treg population with Helios and Nrp markers shows a trend of increase in the Nrp+/HeliosLo subpopulation in the spleen following treatment with C1ORF32 ECD-Fc (SEQ ID NO:42) alone or concomitantly with anti-TGFβ. An increase in the NRP+/Helios+ subpopulation was observed when C1ORF32 ECD-Fc (SEQ ID NO:42) and anti-TGFβ were administered concomitantly. C1ORF32 ECD-Fc (SEQ ID NO:42) treatment alone also resulted in upregulation of Nrp−/HeliosLo (
Breg analysis could be performed in a similar manner as described above for Treg: at week 8 post transplantation, blood samples and spleens are analyzed for B cell populations including Breg cells by FACS analysis for CD19, CD24, CD38 and intracellular IL-10. The data shows a generally similar effect as for Treg as described above.
The data presented herein show loss of C1ORF32 ECD-Fc (SEQ ID NO:42) therapeutic effect in the EAE model upon neutralization of TGF-beta or IL-10, and abolishment of C1ORF32 ECD-Fc (SEQ ID NO:42)-induced reduction of CD45+ cells, T cells and Treg cell counts in the CNS. This finding suggests that the therapeutic effect of C1ORF32 ECD-Fc (SEQ ID NO:42) in this model is dependent on TGF-beta and IL-10. Since TGF-beta and IL-10 are important factors in the induction, differentiation and function of Treg cells, this dependency supports an important role for Treg cells in the therapeutic effect of C1ORF32 ECD-Fc (SEQ ID NO:42). In addition, looking at subpopulations of Treg cells in the spleen, a trend towards increase in Nrp+HeliosLo and Nrp-HeliosLo (based on the literature, the latter may be considered as iTreg cells) was observed. Following treatment with C1ORF32 ECD-Fc (SEQ ID NO:42) concomitantly with anti-TGF-beta a trend was observed towards an increase in Nrp+Helios+(based on the literature, these may be considered as nTreg cells). These trends were not observed upon IL-10 neutralization.
Overall, these results demonstrate that C1ORF32 ECD-Fc induces long term efficacy in the EAE and inhibits graft rejection in a model of BM transplantation both of which are accompanied by elevation in Treg counts. Furthermore, the long term efficacy of C1ORF32 ECD-Fc requires functional Treg presence. As C1ORF32 ECD-Fc induces IL-10 secretion, which is a major mediator of Treg function, and as its efficacy in the EAE model seem to depend on IL-10 or on maintenance of iTreg stability by TGFβ, the above described results indicate that the tolerogenic effects of C1ORF32 ECD-Fc are mediated at least in part by IL-10 and/or TGFβ.
Induction of Adoptive Transfer PLP139-151-R-EAE:
a. Donor mice are shaved (about a lin.xlin, square on the back between the hind flanks) and injected with CFA/PLP139-151 emulsion at 100 μl per mouse s.c., divided between three spots on the back and flanks. Peptide and final dose given per mouse: 50 μg of PLP139-151 peptide on day 0.
b. On day 8 post priming with PLP139-151/CFA, the draining inguinal lymph nodes are collected, and single cell suspensions are prepared. Total lymph node cells are cultured at a density of 8×106 cells per ml in the HL-1 medium plus PLP139-151 peptide (20 μg/ml) in T75 flasks.
c. After 3 days of culture, the PLP139-151 reactivated cells are collected and counted using an hemacytometer. The number of total viable cells and the number of blast cells is determined. The percentage of blast cells expected following this protocol is 20-30% of the total viable cells.
d. 3×106 cells are transferred to each recipient mouse by intravenous injection.
e. Mice are treated with Control Ig (mIgG2a) or C1ORF32 ECD-Fc (3×/wk; 2 wks) beginning at the time of cell transfer. The Control Ig or C1ORF32 ECD-Fc treated mice are then primed with PLP139-151/CFA, or OVA323/CFA at 14 days post the final treatment.
f. Mice are scored on a 0-5 disease score scale per standard laboratory protocol: 0, no abnormality; 1, limp tail; 2, limp tail and hind limb weakness; 3, hind limb paralysis; 4, hind limb paralysis and forelimb weakness; and 5, moribund.
If there appears to be a long-lived protection in the specific ability of PLP139-151/CFA priming to induce disease in C1ORF32 ECD-Fc treated mice, indicative of specific tolerance induction, follow up experiments are performed as follows:
I. Similar rechallenge experiments are carried out with other myelin (spread) epitopes (i.e. PLP178-191/CFA and MOG92-106/CFA) in addition to the inducing epitope PLP139-151/CFA
II. Rechallenge with the inducing PLP139-151/CFA at a longer time point (30 or 60 days) after completion of the treatment with C1ORF32 ECD-Fc or control Ig
III. Examining the phenotype of the CD4+ T cell effector and CD4+ T cell regulatory populations via flow cytometric analysis and ex vivo recall responses and suppression assays.
It is possible that due to CFA breaking tolerance during the re-priming, in the first experiment tolerance won't be observed with C1ORF32 ECD-Fc to the inducing PLP139-151/CFA. In such case, the re-challenge is carried out by a 2nd adoptive transfer of lymph node cells taken from SJL mice that have been primed with PLP139-151/CFA, PLP178-191/CFA, or MOG92-106/CFA.
Ag-Specific Tregs, In Vitro
Naïve PLP139-151-specific T cells from 5B6 mice are activated with PLP-pulsed APCs in iTreg promoting conditions and tested for in vitro suppressive activity and ability to inhibit induction and progression of PLP139-151-induced vs. MOG92-106-induced EAE.
Ag-Specific Tregs, In Vivo
Naïve CD4+ T cells are transferred from 5B6 mice (Tg for TCR specific for PLP139-151) into PLP178-191/CFA primed SJL mice at the peak of the acute phase of disease. The recipient mice with EAE are treated from onset of remission with Control Ig or C1ORF32 ECD-Fc, and the number, location (CNS or spleen), and phenotype of the transferred 5B6 T cells are determined via flow cytometry. Analysis is carried out after 1 week of treatment and after the full 2 weeks of treatment.
This experiment can also be completed with 5B6-FoxP3/GFP cells such that the 5B6-FoxP3/GFP Treg cells can be sorted purified, and placed into an in vitro (ex vivo) suppression assay.
General Tregs, In Vitro
Naïve CD4+ T cells from FoxP3-GFP mice are activated in the presence of iTreg cell promoting conditions (100 U/ml IL-2, 10 ng/ml TGF-beta, in the absence or presence of 100 nM retinoic acid) in the presence of either Control Ig (mIgG2a) C1ORF32 ECD-Fc. Following culture, FoxP3/GFP+ cells are sort purified, and the function of the iTreg cells is assessed in an in vitro suppression assay by culture of FoxP3+ Treg cells with effector T cells at different ratios of Tregs vs. effector T cells. The effector T cells are induced by ex-vivo activation of CD4+ T cells with anti-CD3 and anti-CD28 in the presence of irradiated APCs. T cell proliferation is measured by H3-Thymidine incorporation.
If the C1ORF32 ECD-Fc treated iTreg cells do appear to have increased suppressor function, it will be determined whether this suppressor function is cell contact mediated or via secreted factors. For this a combination of trans-well Treg cell suppression assays and conditioned culture medium transfer in the absence or presence of blocking Abs is utilized.
General Tregs, In Vivo
R-EAE is induced in FoxP3-GFP mice on SJL background PLP139-151/CFA. Mice are treated with C1ORF32 ECD-Fc or mIgG2a (100 ug/dose, 3 times/week×2 weeks) and are followed for disease severity. (A) Unseparated total CD4+ T cells and (B) FACS-purified CD4+CD25+Foxp3/GFP+ Treg cells are isolated right after the last treatment and are tested in a ‘suppression assay’ by culturing each of the above T cell populations (A or B) with effector T cells at different ratios of Tregs vs. effector T cells (as described in 23.1.1 above). T cell proliferation is measured by H3-Thymidine incorporation and cytokine production will be evaluated using ELISA.
In addition the ratio of Treg to Teff cells in the spleen and CNS is also evaluated.
Efficacy of any of the C1ORF32 Protein Fragments and/or Fusion Proteins Thereof in Mouse CIA Models of Rheumatoid Arthritis
In brief, this study indicates that C1ORF32 ECD-Fc (SEQ ID NO:42) at 10 mg/kg has a therapeutic effect during experimental arthritis, which is at least similar to, or even greater than that of Enbrel. For certain measurements of rheumatoid arthritis markers in this mouse model, C1ORF32 ECD-Fc (SEQ ID NO:42) had an even greater effect than Enbrel. Indeed in this model, Enbrel appeared far weaker than in previous mouse model studies, perhaps due to the extreme severity of this model. By contrast, C1ORF32 ECD-Fc (SEQ ID NO:42) was able to ameliorate the disease even in this severe model of the disease. However, it should be noted that in three studies, C1ORF32 ECD-Fc (SEQ ID NO:42) showed excellent results in two studies and weak results in one study.
Bovine type II collagen (CII) (RUNMC in house production, batch 03-04-08) at a concentration of 2 mg/ml in acetic acid 0.05M was emulsified in equal volumes of Freund's complete adjuvant (2 mg/ml of Mycobacterium tuberculosis strain H37Ra; Difco, Detroit, Mich.).
On day 0, 10-12 week old male DBA-1 mice (Janvier Elevage, France) (n=95) were immunized i.d. at the base of the tail with 100 μg of bovine CII. On day 21, mice received an intraperitoneal booster injection of 50 μg of CII dissolved in phosphate buffered saline (PBS), and the onset of arthritis occurred a few days after this booster.
Mice were considered to have arthritis when significant changes of redness and/or swelling were noted in the digits or in other parts of the paws. Joint inflammation in each paw was scored visually, using a scale of 0-2 per paw with a maximal score of 8 per animal: 0=non inflamed, 1=mild inflammation, 1.5=marked inflammation, and 2=severe inflammation. Scoring was performed three times a week.
Treatment was started in established CIA early after onset of disease (i.e. therapeutic regimen), when the macroscopic scores per animal were between 0.25 and 1.25 (on a scale of 0-8). The i.p. injections were given three times per week for two weeks, after which the study was terminated and mice were terminally bled to collect serum. Thereafter, the knee and ankle joints were collected and stored in formalin. Histology was scored for inflammation and destruction on an arbitrary scale of 0-3, for five different parameters:
1. Negative control: PBS
2. Negative control mIgG2A (Bioxcell, BE0085): 10 mg/kg
3. C1ORF32 ECD-Fc (SEQ ID NO:42): 10 mg/kg
4. C1ORF32 ECD-Fc (SEQ ID NO:42): 5 mg/kg
5. Positive control: Enbrel (Wyeth, F01421) 5 mg/kg
Joints were fixed for at least 4 days in 4% formaldehyde, decalcified in 5% formic acid, and subsequently dehydrated and embedded in paraffin. Standard frontal sections of 7 μm were mounted on SuperFrost slides (Menzel-Glaser, Braunschweig, Germany). Haematoxylin and eosin (H&E) staining was performed to study joint inflammation. The severity of inflammation in the joints was scored on a scale of 0-3 (0=no cells, 1=mild cellularity, 2=moderate cellularity, and 3=maximal cellularity). To study proteoglycan (PG) depletion from the cartilage matrix, sections were stained with safranin O (SO) followed by counterstaining with fast green. Depletion of PG was determined using an arbitrary scale of 0-3, ranging from normal, fully stained cartilage to destained cartilage, fully depleted of PGs. Chondrocyte death was scored on a scale of 0-3 ranging from no loss of chondrocyte nuclei to complete empty cartilage surface. The degree of cartilage surface erosion was scored on a scale of 0-3, ranging from no damage to complete loss of articular cartilage. Bone destruction was graded separately on a scale of 0-3, ranging from no damage to the complete loss of bone structure. Histopathological changes in the joint were scored on three semiserial sections of the joint spaced 70 μm apart. Scoring was performed in a blindfolded manner.
Statistical analysis: Disease course data was analyzed using one-way ANOVA with repeated measures, with a Bonferroni's post-test of selected pairs to determine statistical differences between C1ORF32 ECD-Fc (SEQ ID NO:42) and Enbrel treated mice, each as compared to Control Ig (IgG2a) treated group.
Effect of Treatment with C1ORF32 ECD-Fc (SEQ ID NO:42) on Macroscopic Scores of CIA
Collagen-induced arthritis in mice treated from disease onset with the negative control PBS or mIgG2A isotype control antibodies showed clear progression of the macroscopic scores of inflammation (
Effect of Treatment with High Dose C1ORF32 ECD-Fc (SEQ ID NO:42) on Histological Scores
To potentially obtain a better differentiation in the effects of high dose C1ORF32 ECD-Fc (SEQ ID NO:42), ankle joints were processed for full histological analysis. As depicted in
Summary
The treatment with C1ORF32 ECD-Fc (SEQ ID NO:42) during collagen-induced arthritis, at the high dose of 10 mg/kg, significantly reduced the macroscopic scores and showed a trend of reduction of the histological scores for inflammation and destruction, although the latter parameters did not reach statistical significance. The treatment with the clinically applied TNF inhibitor Enbrel was not as potent on macroscopic scores as expected, probably due to the fact that this CIA experiment was more severe than previous studies. No therapeutic effect was observed with the low dose C1ORF32 ECD-Fc (SEQ ID NO:42) (5 mg/kg).
Overall, this study indicates that C1ORF32 ECD-Fc (SEQ ID NO:42) at 10 mg/kg has a therapeutic effect during experimental arthritis, which is at least similar to, or even greater than that of Enbrel. Options to consider are (1) an earlier start of treatment, since prophylactic/semi-therapeutic approaches are often less challenging for treatment than the therapeutic regimen, (2) a longer follow-up, since the effects of C1ORF32 ECD-Fc (SEQ ID NO:42) were most obvious in the second week of treatment during this study, (3) use higher dose of C1ORF32 ECD-Fc (SEQ ID NO:42). Although further preclinical research in animal models of arthritis are required, these data suggest that inhibition of costimulation by C1ORF32 ECD-Fc (SEQ ID NO:42) might be a good option to reduce joint pathology in patients suffering from rheumatoid arthritis.
In Vitro Differentiation of iTregs:
iTregs are induced from naïve T cells 96-well flat bottom tissue culture plates (Sigma, Cat. # Z707910) are coated with anti-CD3 mAb (2 ug/mL) and C1ORF ECD-Fc (H:M) or control Ig control (MOPC-173, Biolegend) at 10 ug/ml. Naïve CD4+CD25− T cells are plated at 0.5×105/well in the presence of soluble anti-CD28 (1 ug/ml), TGF-β (Cat#7666-MB; R&D systems) and IL-2 (Cat#202-IL; R&D systems). On Day 5 post stimulation the percentage of CD4+CD25+FoxP3+ cells is assessed by flow cytometry.
Mouse spleens are fragmented and digested for 30 min at 37° C. in complete RPMI 1640 in the presence of Liberase and DNase. After digestion, RBCs are lysed with ACK-lysing buffer. DCs are isolated by labeling cells with CD11c magnetic beads and MACS (>95% purity). DCs are pulsed with 1 mM PCC88-104 or 10 mM HEL48-62 peptides for 37° C. for an hour, washed two times with complete media, and then cultured alone or cocultured with Foxp3+ iTregs from Control Ig or C1ORF ECD-Fc cultures described above or with Teff cells at a ratio of 1:1 for 18 h. The cocultures are treated with 4 mM EDTA to separate DC-iTreg conjugates. Cells are first gated on singlets and then sorted for CD4 CD11c+MHC-II+DC population (Chattopadhyay and Shevach, J Immunol. 2013; 191(12):5875-84).
The Effect of any One of C1ORF32 Protein Fragments and/or Fusion Proteins Thereof in Mouse Model of Psoriasis
The purpose of this study was to evaluate the effectiveness of C1ORF32 ECD-Fc (SEQ ID NO: 43) on the histological parameters of psoriasis in a humanized model of psoriasis. As previously noted, SEQ ID NO:43 is a fusion protein, comprising an amino acid sequence of human C1ORF32 ECD fused to human immunoglobulin Fc (human-human fusion protein). The previous studies related to human C1ORF32 ECD fused to mouse immunoglobulin Fc (human-mouse fusion protein SEQ ID NO:42).
In this model, psoriasis is induced in xenotransplants of healthy human skin transplanted onto beige severe combined immunodeficiency (SCID) mice followed by intradermal (i.d.) injection of IL-2 enriched Peripheral Blood Mononuclear Cells (PBMCs) isolated from blood of psoriasis patients (Nickoloff, 1995; Wrone-Smith, 1996 Gilhar et al., 2002, 2006, 2011). The activity of these compounds was compared to that of Enbrel, a TNF inhibitor which is an approved biological drug for treatment of psoriasis. As a control for model robustness, we used dexamethasone, a steroid with suppressive effects on inflammatory cytokines and chemokines such as TNF-alpha and interferon-gamma which cause severe psoriasis. All treatments were administered intradermally, except for dexamethasone which was given topically.
Patient Demographics: All experiments with human materials were conducted after receiving written informed consent from the participants according to a protocol reviewed and approved by the RAMBAM Medical Center Institutional Review Board in accordance with the Declaration of Helsinki Principles. All experiments using laboratory mice were approved by the Baruch Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, institutional committee on animal use. Ten psoriatic patients were included in this study (8 men and 2 women), mean age 46 years, ranged from 26 to 67 years. All patients had classic plaque psoriasis and none of them had been treated with drugs. Normal skin from 1 healthy volunteer was obtained for grafting.
Study Protocol: A) Healthy human skin pieces with a width of 0.4 mm and surface area of 1.5×1.5 cm were provided from residual skin of routine plastic surgery procedures from the Plastic Surgery Department of the Rambam Medical Center, Israel. In addition, 20 mL blood samples were taken from psoriatic patients. B) Seventy (70) beige-severe combined immunodeficient mice (SCID) (weight˜20-25 g) were included in this study. Normal healthy human donor skin was transplanted onto the beige-SCID mice as previously described (Nickoloff et al., 1995; Wrone-Smith, 1996; Gilhar et al., 2002, 2006, 2011; Kalish et al., 2009) and the mice were divided into 7 groups. C) Peripheral Blood Mononuclear Cells (PBMCs) isolated from psoriatic patients' blood were cultured in the presence of IL-2 [Prospec, 100 U/mL of RPMI 1640 media, 10% human AB serum (Sigma, St. Louis, Mo.), 1% glutamine, 1% antibiotics (media components; Biological Industries, Kibbutz Beit Haemeck, Israel)] for 14 days, as previously described (Gilhar et al, 2002). D) Four weeks following engraftment, each mouse was injected intra-dermally (i.d.) into the grafted skin lesion, with 1×107 activated allogeneic enriched PBMCs from psoriatic patients (
F) Twenty eight days after starting the injections and treatment, skin was harvested (
Determination of Epidermal Thickness:
The entire skin graft was excised and placed in 10% formal saline overnight. Then, the specimens were place in 70% ethanol and were embedded according to the standard H&E protocol. Histological assessment of the skin grafts was performed by light microscopy and evaluated by two blinded observers [the second observer evaluated random slides (about 25% of all slides) to compare the data obtained by the first observer. Rarely, the results were not comparable, and in these cases the first observer re-evaluated the slides]. Epidermal thickness was determined with an ocular micrometer at a minimum of 50 points along the epidermis selected to represent points of maximal and minimal thickness.
IHC
Representative grafts were allocated for IHC analysis. Each analysis was performed on equal samples of affected and healthy grafts. The following markers were evaluated by IHC:
Mouse anti-human HLA-DR (abcam, cat# ab20181), rabbit anti-human ICAM-1 (AbD Serotec, AHP2183), mouse anti-human CD3 (Dako), and mouse anti-human Ki-67 (Life Technologies, cat# ZY-180192Z) were used on deparaffinized and peroxidase blocked slides. Sections were treated with citrate buffer, pH6 for HLA-DR and ICAM-1, and EDTA buffer, pH8 for CD3 and Ki-67, in the microwave oven for 20 minutes, cooled for 30 minutes at room temperature, and blocked for nonspecific binding. All washes were performed with phosphate-buffered saline. All antibodies were applied overnight at 40 C. After washing, slides were incubated with appropriate secondary antibodies (biotinylated horse anti-mouse IgG (Vector Labs, Burlingame, Calif.), and horseradish peroxidase-conjugated donkey anti-rabbit IgG), followed by a wash and incubation with streptavidin-horseradish peroxidase (Jackson ImmunoResearch, West Grove, Pa.) for all the primary mouse antibodies. The markers were revealed by treating sections with 3-amino-9-ethylcarbazole. Samples were examined under light microscopy. Ki-67 index was determined by counting Ki-67 positive cells in the basal layer of the epidermis out of the total number of basal cells. Mean CD3 positive cells was calculated with an ocular micrometer at a minimum of 10 points with an area of 0.66 mm2 each, along the upper dermis.
Statistical Analysis: Data are presented as the mean±standard deviation (STDEV). The study parameters of each group were compared to those of the PBS control group using one-tailed distribution T-Test. Statistical significance was set at p<0.05.
Results
Evaluation of the Human Skin Grafts
Vehicle and Positive Controls Treatment of grafts with vehicle, starting at the time of psoriasis induction, resulted in psoriasis/psoriasiform features as listed in study protocol, section F. Within the vehicle treated group, most grafts (8/10) showed psoriatic or psoriasiform features, including epidermal thickening, massive epidermal proliferation as was observed by Ki-67 immunostaining, high expression of HLA-DR, ICAM-1 and massive infiltration of CD3 positive T cells around and within the epidermis (Table 4 and 5,
Conversely, 7/10 grafts treated with dexamethasone showed lack of psoriasiform features and 1 additional graft showed partial psoriasiform features with tendency toward healthy skin features, while 2 grafts in this group showed psoriasiform features (Table 4). Specifically, the 7/10 dexamethasone-treated grafts displayed normal skin including a low epidermal thickness, low proliferation index, low HLA-DR and ICAM-1 expression and low CD3 positive T cells infiltrate (Tables 4 and 5,
Treatment with Enbrel demonstrated lack of psoriasiform features in 3/9 (33%) grafts (Table 4). These three Enbrel-treated grafts showed features of normal skin including a low epidermal thickness (Table 5,
Mice treated with C1ORF32 ECD-Fc (SEQ ID NO: 43) demonstrated lack of psoriasiform features in 5/9 grafts (55.5%), including features of normal skin, low epidermal thickness, low proliferation index, low HLA-DR and ICAM-1 expression and low CD3 positive T cells infiltrate (Table 4 and 5,
In this study, C1ORF ECD-Fc (SEQ ID NO:43) was tested for its efficacy in the humanized psoriatic SCID mouse model upon prophylactic, intralesional administration of 100 μg per graft, given from the day of PBMCs injection, 3 times a week. Dexamethasone and Enbrel, drugs which are in clinical use for the treatment of psoriatic patients, were used as positive controls.
C1ORF32 ECD-Fc (SEQ ID NO: 43) treatment reduced the occurrence of psoriasiform features in 55% of the grafts. This reduction was also manifested in the immunohistochemical analysis showing decreased expression of HLA-DR (highly expressed in keratinocytes from psoriatic patients), ICAM-1 (an intercellular adhesion molecule, highly expressed in the epidermis and upper dermis of psoriatic patients) and Ki-67 (a marker of cell proliferation which is highly expressed in psoriasis and correlates with the clinical severity of the disease), together with decreased infiltration of T cells (as demonstrated by lower level of CD3- expressing cells).
Furthermore, C1ORF32 ECD-Fc (SEQ ID NO: 43) and dexamethasone significantly reduced epidermal thickness compared with the vehicle-treated group, while no significant reduction in epidermal thickness was observed with Enbrel. In terms of other clinical effects, there is some similarity between the results of the present study and the clinical efficacy of Enbrel. Forty nine percent of psoriasis patients achieved 75% improvement in the psoriasis area-and-severity index (PASI 75) at week 12, while 22% demonstrated PASI 90 (considered almost clear) response (Leonardi et al., 2003). In our study, healthy skin features were observed in 33% grafts, which is comparable to the 22% of PASI 90. PASI score is a tool used to measure the severity and extent of psoriasis. The IHC parameters analyzed in selected grafts are in good correlation with the histological scoring. This demonstrates that this model captures multiple features of psoriatic skin and treatment effects are observed on all of these parameters. The data obtained in this study suggest a potential beneficial effect of C1ORF32 ECD-Fc (SEQ ID NO: 43) in psoriasis.
REFERENCES Batista M D, Ho E L, Kuebler P J, Milush J M, Lanier L L, Kailas E G, York V A, Chang D, Liao W, Unemori P, Leslie K S, Maurer T, Nixon D F Exp Dermatol. 2013; 22:64-6.
Summary
C1ORF32 ECD-Fc (SEQ ID NO: 43) was tested in the humanized skin SCID mouse model of psoriasis along with dexamethasone and Enbrel as positive controls, both of which are treatment options for severe plaque-type psoriasis. Skin grafts from mice treated with vehicle alone displayed histological features of psoriasiform in 8/10 mice. Notably, C1ORF32 ECD-Fc (SEQ ID NO: 43) treatment reduced the occurrence of psoriasiform to only 4/9 mice. Skin grafts from mice treated with dexamethasone reduced the occurrence of psoriasiform to only 2/10 grafts, while treatment with Enbrel resulted in 6/9 grafts displaying psoriasiform features. Furthermore, a significant reduction in epidermal thickness was observed in grafts treated with C1ORF32 ECD-Fc (SEQ ID NO: 43) and dexamethasone (P<0.05, P<0.005, respectively) compared with the vehicle-treated group. None of the other treatment groups including Enbrel significantly affected epidermal thickness. These data suggest a potential beneficial effect of C1ORF32 ECD-Fc (SEQ ID NO: 43) in the treatment of psoriasis. However, the relatively low number of mice included in each group does not permit a definitive conclusion and additional studies are needed to substantiate these results.
In order to demonstrate general efficacy for preventing transplantation rejection with a subject having at least one antigen mismatch, this experiment determines the effects of C1ORF ECD-Fc on the ability to modulate islet transplant rejection across a fully allogeneic MHC barrier. 500 BALB/c pancreatic islets are transplanted under the kidney capsule of recipient C57BL/6 mice rendered diabetic 7 days previously by treatment with streptozotocin. Recipient mice are treated three times per week with control Ig or C1ORF ECD-Fc and monitored for blood glucose levels as a measure of graft acceptance/rejection. Tolerance with ECDI-fixed donor splenocytes is used as the positive control for successful modulation islet graft rejection.
This Example shows the effect of early stage treatment with C1ORF32-P8-V1-ECD-MFC (SEQ ID NO:42) on disease development in collagen induced arthritis (CIA) model of rheumatoid arthritis.
The aim of this study was to estimate the effect of C1ORF32-P8-V1-ECD-mFc (SEQ ID NO:42) on disease development in a type II Collagen induced arthritis (CIA) mouse model upon administration at early stage of disease; i.e., when specific and predictive markers for RA development are present in the serum, but before onset of clinical symptoms.
In the CIA model, arthritis is induced by immunization with type II collagen in CFA on day 1 which is followed by boosting with type II collagen in CFA on day 21. Antibodies against both CII and cyclic citrullinated peptide (CCPs) appear early after immunization, before joint swelling is observed. Kuhn et la., (J Clin Invest. 2006 Apr. 3; 116(4): 961-973) demonstrated that autoantibodies against CII and CCP begin to develop around day 7 after the first immunization and steadily increase while clinical evidence of arthritis are evident 25 days after the initial immunization with CII in CFA.
To evaluate the effect of early stage treatment with C1ORF32-P8-V1-ECD-mFc (SEQ ID NO:42) on disease development treatment started on day 18 and was given IP injection, Q2D to mice from day 18 until day 32.
Male DBA/1O1aHsd mice weighing 16-25 grams (mean 22 g) on day 18 of the study were obtained from Harlan, Inc., Indianapolis, Ind. Mice (10/group) were anaesthetized with Isoflurane, shaved at the base of the tail, and injected intradermally with 150 μl of Freund's Complete Adjuvant (Sigma) containing bovine type II collagen (Elastin Products, Owensville, Mo.) (2 mg/me at the base of the tail on day 0 and again on day 21. On study day 18, mice were randomized by body weight into treatment groups. Treatment was initiated after enrollment and continued every other day (Q2D at 48 h intervals) through study day 33. On study days 23-34, onset of arthritis occurred. Mice were terminated on study day 34. Clinical scores were given for each of the paws (right front, left front, right rear, left rear) on arthritis days 18-34.
Experimental groups were as follows:
Mice were weighed on study days 18, 20, 22, 24, 26, 28, 30, 32 and 34 (prior to necropsy). Daily clinical scores were given for each of the paws (right front, left front, right rear, left rear) on arthritis days 18-34 using the following criteria:
The method for induction of CIA used in this example, which involves a boost of type II collagen in CFA on day 21 after immunization, results in a severe disease which is difficult to inhibit. In this setup, mice develop visual clinical symptoms of arthritis around day 25 post immunization. Early stage treatment (i.e., from day 18, before onset of clinical symptoms) with C1ORF32-P8-V1-ECD-mFc (SEQ ID NO:42) at 10 mg/kg Q2D until day 34 resulted in inhibition of clinical arthritis score compared to groups treated with negative controls (PBS or mIgG2a isotype control) however, this effect did not reach significance. C1ORF32-P8-V1-ECD-mFc (SEQ ID NO:42) treatment at 10 mg/kg also had beneficial effect on body weight loss (measured as percent change from baseline) which was significantly inhibited toward normal beginning on study day 30 and continuing until study termination (data not shown). These results point to improvement in overall wellbeing of mice treated with C1ORF32-P8-V1-ECD-mFc (SEQ ID NO:42). No effect was observed upon treatment with a lower dose of 3.3 mg/kg of C1ORF32-P8-V1-ECD-mFc (SEQ ID NO:42).
The beneficial effect of C1ORF32-P8-V1-ECD-mFc (SEQ ID NO:42) in this model upon treatment from day 18 when autoimmune activity is already established but clinical symptoms are not yet manifested suggest beneficial effect of a human version of this molecule for early stage treatment of autoimmune diseases, particularly RA.
CD4+ T cell are isolated by negative selection from PBMCs using Miltenyi CD4+ T cell Isolation Kit 130-096-533 as per manufactures instructions as follows:
CD4+ T cells (1.5×105 cells/well and 5×104) of healthy volunteers and from RA patients are activated with different concentrations of ConA (0.1, 1, 2, 5 & 10 μg/ml) or PHA (0.1, 1, 5, 10 & 20 μg/ml) for selection of sub-optimal activation conditions.
Following selection of suboptimal activation conditions, C1ORF32 ECD-Fc (SEQ ID NO:43) or control Ig are added each to the above described culture at 1, 3, 10, 30 μg/ml, 1 hour prior to cell stimulation with ConA or PHA.
IL-2 (10 ng/ml) is added to cultures after 24 hours. Following 72 hour incubation, cell culture supernatants removed and stored at −20° C. Supernatants are analyzed for TNFα, IL-6, IL-10, IL-12, IL-23, IL-17 and IL-35 using ELISA as per manufacturer's instructions.
The following experiments will be carried out with blood taken from healthy volunteers as well as from Rheumatoid Arthritis (RA) patients.
The following stains will be performed for each donor:
After 6 days in culture, T cells are washed 3 times in complete medium and counted
TcKs are added to macrophage culture following removal of existing culture media at a ratio of 4:1 (5×104 cells/well/CD4+ T cells plus 2×105 cells/well CD14+ Macrophages). C1ORF32 ECD-Fc (SEQ ID NO:43) or Control IgG are added at 1, 3, 10, 30 μg/ml. For additional controls co-cultures are added with vehicle or with medium only (Wennink et al., 2012).
After 24 hrs of culture, cytokines (IL-10, IFN-α, IL-6, IL-12, CCL5, IL-13, IL-15, IL-17, CCL3, GM-CSF, IFNγ, TNFα, IL-1RA, IL-7, IL-1B, eotaxin, IL-2 IL-4 and IL-2R) are analyzed using ELISA and/or Luminex
The effect of C1ORF32 ECD-Fc (SEQ ID NO:43) on T cells and Macrophages activation during co-culture is also investigated. T cells are gated using CD3/CD4 staining and investigated at 15 minutes and 24 h after compounds addition to the co-cultures. At 15 minutes time point, STAT3 and STATS phosphorylation will be analyzed. At 24 h time point proliferation (CFSE assay), activation marker expression CD69 and chemokine receptors CCR6, CXCR3 (Th17/Th1), CCR4 (TH2) and CCR5 (TH1) are analyzed by FACS. Macrophages are investigated at 24 time point by co-staining for the lineage marker CD64 and for activation markers MHCII, CD86 and CD80.
Differentiated DCs (5×104 cells/well) are co-cultured with CD4+ T cells (2×105 cells/well). C1ORF32 ECD-Fc (SEQ ID NO:43) or Control IgG are added at 1, 3, 10, 30 μg/ml. For additional controls co-cultures are added with vehicle or with medium only.
After 24 hrs of culture, cytokines (IL-10, IFN-α, IL-6, IL-12, CCL5, IL-13, IL-15, IL-17, CCL3, GM-CSF, IFNγ, TNFα, IL-1RA, IL-7, IL-1B, eotaxin, IL-2, IL-4, IL-2R and IL-35) are analyzed using ELISA and/or Luminex.
The effect of C1ORF32 ECD-Fc (SEQ ID NO:43) on T cells and DC activation during co-culture is also investigated. T cells are gated using CD3/CD4 staining and investigated at 15 minutes and 24 h after compounds addition to the co-cultures. At 15 minutes time point, STAT3 and STATS phosphorylation will be analyzed. At 24 h time point proliferation (CFSE assay), activation marker expression CD69 and chemokine receptors CCR6, CXCR3 (Th17/Th1), CCR4 (TH2) and CCR5 (TH1) are analyzed by FACS. The effect of C1ORF32 ECD-Fc (SEQ ID NO:43) on DCs activation is investigated at 24 time point.
Differentiated DCs (5×104 cells/well) are activated with TLR agonists: LPS (1 ng/ml), PAM3 (100 ng/ml), CL097 (1 μg/ml), PolyIC (50 μg/ml), or with 1-2% RA Synovial Fluid.
C1ORF32 ECD-Fc (SEQ ID NO:43) or Control IgG are added prior to cell stimulation at 0.1, 1, 3, 10, 30 μg/ml either during the differentiation phase as well as at day 6 upon dendritic cell stimulation.
Cytokine secretion and cell activation are analyzed as described above.
Purified human peripheral T cells that are cultured ex-vivo in the presence of IL-15, IL-6 and TNFα (TcK) recapitulate the functional properties of synovial T cells of rheumatoid arthritis patients (Wenink et al., 2014). Furthermore, monocytes activated in the presence of GM-CSF exhibit the same characteristics as these of macrophages infiltrating the synovioum during RA.
Co-culture of TcK with autologeuos ex-vivo differentiated macrophages mimics one of the crucial pathways mediating synovial macrophage activation in RA thus serving as a translational tool for evaluating the therapeutic potential of drug candidates. Therefore the effect of C1ORF32 ECD-Fc (SEQ ID NO:43) was tested on the secretion of a range of pro-inflammatory and anti-inflammatory cytokines in such co-cultures. Two studies were carried out, one in which buffy coats from healthy volunteers was used and another study in which the responses of RA patients blood cells responses were compared to that of healthy voluntiers in which blood was used rather than buffy coats.
In co-cultures of TcK and macrophages from healthy volunteers, C1ORF32 ECD-Fc (SEQ ID NO:43) inhibited the secresion of TNFa, CCL5, CCL3, GM-CSF, and IL-5 and to a lesser extent also downregulated the secretion of IFNg, IL-1RA, IL-17, IL-12, IL-13, IL-6 and IL-2R (
Similarly, a marked inhibition of TNFa secretion was observed in co-cultures of TcK and macrophages from RA patients' (n=2) and healthy volunteers blood (n=1) samples (
To study the potential efficacy of C1ORF32 ECD-Fc for treatment of multiple sclerosis, the effect on blood cells taken from MS patients that have had a relapsing remitting disease for years to decades was tested.
PBMCs were taken from eight MS patients with diagnosed relapsing-remitting disease who have experienced a relapse 1-2 days prior to blood drawing.
PBMCs were plated in a flat-bottom 96-well plate at 1e6 cells/well. The cells were cultured in the presence of anti-CD3 (0.5 ug/ml), MS-specific peptide MBP85-96 (10 ug/ml), or tetanus toxoid peptide TT830-843 (10 ug/ml). C1ORF32 ECD-Fc (SEQ ID NO: 43) or Control Ig were added to the cuture at the indicated concentrations. Two replicate plates were set to study for the effect of C1ORF32 ECD-Fc (SEQ ID NO: 43) on proliferation and on pro-inflammatory and anti-inflammatory cytokines secretion. To test for proliferation, the cultures were pulsed on day +1 of culture with 1 uCi of tritiated thymidine and then harvested 3 days later on day +4 of culture. For cytokine analysis, super natantes from a replicate cultures were collected on day +4 of culture and tested using Millipore multiplex assay.
C1ORF32 ECD-Fc (SEQ ID NO: 43) treatment of MS patients' PBMCs that were activated ex-vivo with MBP85-96 resulted in inhibition of cells proliferation, as well as inhibition of IFNg, IL-17, TNFa and increase in IL-4, IL-10, TGFβ and IL-6 (
For example, optionally a C1ORF32 polypeptide, such as C1ORF32 ECD-Fc, is administered if TGF-beta is present at a sufficiently high level. Optionally, additionally or alternatively, the C1ORF32 polypeptide is administered if one or more cytokines are present at a sufficiently high level. Optionally such treatment is initiated even without the presence of any overt symptoms of the disease.
These results are in agreement with previous observations supporting immunomodulatory effects of C1ORF32 ECD-Fc manifested in downregulation of proinflammatory cytokines and upregulation of anti inflammatory cytokines. Such immunomodulatory effects have been previously described in blood cells from mice or from healthy human volunteers that were activated in vitro under Th driving conditions, as well as in lymph node cells and splenocytes from the EAE mouse model of multiple sclerosis, following treatment with C1ORF32 ECD-Fc.
The increase of IL-6, may be part of immunomodulatory effect as this cytokine is known to be involved both in pro- and anti-inflammatory activities. For example, Treg17 cells can be induced in the presense of TGF-beta plus IL-6. Like conventional Treg, induction of regulatory Treg17 cells could play an important role in modulating and preventing certain autoimmune diseases.
It will be appreciated that various features of the invention which are, for clarity, described in the contexts of separate embodiments may also be provided in combination in a single embodiment. Conversely, various features of the invention which are, for brevity, described in the context of a single embodiment may also be provided separately or in any suitable sub-combination. It will also be appreciated by persons skilled in the art that the present invention is not limited by what has been particularly shown and described hereinabove. Rather the scope of the invention is defined only by the claims which follow.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IL2015/050854 | 8/26/2015 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62147000 | Apr 2015 | US | |
| 62042192 | Aug 2014 | US |
