US2020369744A1PendingUtilityA1

BSL2v2c2-Ig POLYPEPTIDES

Assignee: BRISTOL MYERS SQUIBB COPriority: Jun 6, 2000Filed: Jan 31, 2020Published: Nov 26, 2020
Est. expiryJun 6, 2020(expired)· nominal 20-yr term from priority
C07K 2319/00A61K 39/39533C07K 2319/40C07K 19/00A61K 38/00C07K 2317/56C07K 2317/73C07K 14/70532C07K 2317/76A61K 2039/505Y02A50/30C07K 2319/10C07K 2319/30C07K 16/2827A61K 38/1774C07K 2319/02G01N 33/5005C07K 2319/03
73
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The present invention provides nucleic acids encoding B7-related factors that modulate the activation of immune or inflammatory response cells, such as T-cells. Also provided are expression vectors and fusion constructs comprising nucleic acids encoding B7-related polypeptides, including BSL1, BSL2, and BSL3. The present invention further provides isolated B7-related polypeptides, isolated fusion proteins comprising B7-related polypeptides, and antibodies that are specifically reactive with B7-related polypeptides, or portions thereof. In addition, the present invention provides assays utilizing B7-related nucleic acids, polypeptides, or peptides. The present invention further provides compositions of B7-related nucleic acids, polypeptides, fusion proteins, or antibodies that are useful for the immunomodulation of a human or animal subject.

Claims

exact text as granted — not AI-modified
1 - 2 . (canceled) 
     
     
         3 . A method of decreasing T-cell proliferation in a subject comprising: administering to the subject a pharmaceutical composition comprising an isolated fusion polypeptide consisting of amino acid sequence SEQ ID NO:9, and a physiologically acceptable carrier, diluent, or excipient, in an amount effective to decrease T-cell proliferation. 
     
     
         4 . The method according to  claim 3 , wherein the subject is affected with a condition selected from the group consisting of tissue rejection, bone marrow rejection, organ transplant rejection, graft versus host disease, psoriasis, chronic obstructive pulmonary disease, asthma, atherosclerosis, rheumatoid arthritis, multiple sclerosis, Lupus erythematosus, Hashimoto's thyroiditis, primary myxedema, Graves' disease, pernicious anemia, autoimmune atrophic gastritis, insulin dependent diabetes mellitus, good pasture's syndrome, myasthenia gravis, pemphigus, Crohn's disease, sympathetic ophthalmia, autoimmune uveitis, autoimmune hemolytic anemia, idiopathic thrombocytopenia, primary biliary cirrhosis, ulcerative colitis, Sjogren's syndrome, polymyositis, and mixed connective tissue disease. 
     
     
         5 . The method according to  claim 3 , wherein the pharmaceutical composition is co-administered with a pharmaceutical composition comprising a monoclonal antibody that binds to a polypeptide consisting of the amino acid sequence SEQ ID NO: 7, and a physiologically acceptable carrier, diluent, or excipient. 
     
     
         6 . The method according to  claim 4 , wherein the pharmaceutical composition is co-administered with a pharmaceutical composition comprising a monoclonal antibody that binds to a polypeptide consisting of the amino acid sequence SEQ ID NO: 7, and a physiologically acceptable carrier, diluent, or excipient. 
     
     
         7 . The method according to  claim 3 , wherein the subject is a human subject. 
     
     
         8 . The method according to  claim 4 , wherein the subject is a human subject. 
     
     
         9 . The method according to  claim 5 , wherein the subject is a human subject. 
     
     
         10 . The method according to  claim 6 , wherein the subject is a human subject.

Join the waitlist — get patent alerts

Track US2020369744A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.