Methods of engineering immune cells for enhanced potency and persistence and uses of engineered cells in immunotherapy
US-2024335536-A1 · Oct 10, 2024 · US
US12043665B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12043665-B2 |
| Application number | US-202117306509-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 3, 2021 |
| Priority date | Jun 30, 2011 |
| Publication date | Jul 23, 2024 |
| Grant date | Jul 23, 2024 |
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The present invention provides a bispecific biologic comprising a ligand specific for CTLA-4 and a ligand specific for a pMHC complex.
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The invention claimed is: 1. A method for treating a subject suffering from a condition selected from an autoimmune disease, comprising administering to the subject an effective amount of the bispecific biologic comprising a ligand specific for CTLA-4 and a ligand specific for a peptide-MHC class II (pMHCII) complex, wherein the ligand specific for CTLA-4 comprises an antibody specific for CTLA-4 and the ligand specific for the pMHCII complex is LAG-3. 2. The method according to claim 1 , wherein the autoimmune disease is selected from type 1 diabetes (T1D), Systemic Lupus Erythematosus (SLE), Rheumatoid Arthritis (RA), inflammatory bowel disease (IBD), ulcerative colitis (UC), Crohn's disease (CD), multiple sclerosis (MS), scleroderma, pemphigus vulgaris (PV), psoriasis, atopic dermatitis, celiac disease, Chronic Obstructive Lung disease, Hashimoto's thyroiditis, Graves' disease (thyroid), Sjogren's syndrome, Guillain-Barre syndrome, Goodpasture's syndrome, Addison's disease, Wegener's granulomatosis, primary biliary sclerosis, sclerosing cholangitis, autoimmune hepatitis, polymyalgia rheumatica, Raynaud's phenomenon, temporal arteritis, giant cell arteritis, autoimmune hemolytic anemia, pernicious anemia, polyarteritis nodosa, Behcet's disease, primary biliary cirrhosis, uveitis, myocarditis, rheumatic fever, ankylosing spondylitis, glomerulonephritis, sarcoidosis, dermatomyositis, myasthenia gravis, polymyositis, alopecia areata, and vitiligo. 3. The method according to claim 1 , wherein LAG-3 is human LAG-3 comprising at least one of mutations R73E, R75A, R75E and R76E. 4. The method according to claim 1 , wherein the ligand specific for CTLA-4 and the ligand specific for the pMHCII complex are spaced apart by a linker. 5. The method according to claim 4 , wherein the linker is one or more of a polyamino acid sequence and an antibody Fc domain. 6. The method according to claim 5 , wherein the polyamino acid sequence is G9 (Gly-9). 7. The method according to claim 1 , wherein the autoimmune disease is type 1 diabetes (T1D). 8. The method according to claim 1 , wherein administration of said bispecific biologic results in induction of regulatory T cells (Tregs). 9. The method according to claim 8 , wherein the Tregs are Foxp3+ Tregs. 10. The method according to claim 1 , wherein the amount of IL-10 and TGF-B in the subject is increased. 11. A method for treating a subject suffering from T1D, comprising administering to the subject an effective amount of the bispecific biologic comprising a ligand specific for CTLA-4 and a ligand specific for a pMHCII complex, wherein the ligand specific for the CTLA-4 comprises an antibody specific for CTLA-4 and the ligand specific for the pMHCII complex is LAG-3. 12. A method of treating a subject in need of regulatory T cell(s) comprising: (i) removing a sample comprising a T cell from a subject; (ii) stimulating said T cell; (iii) treating said T cell with a bispecific biologic comprising a ligand specific for CTLA-4 and a ligand specific for a pMHC complex; (v) reintroducing said T cell to said subject wherein the subject in need of regulatory T cell(s) comprises a subject with an autoimmune disease and wherein the ligand specific for the CTLA-4 comprises an antibody specific for CTLA-4 and the ligand specific for the pMHCII complex is LAG-3.
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