US2021347887A1PendingUtilityA1

Compositions and methods for modulating an immune response

Assignee: BRIGHAM & WOMENS HOSPITAL INCPriority: Nov 26, 2013Filed: Mar 9, 2021Published: Nov 11, 2021
Est. expiryNov 26, 2033(~7.4 yrs left)· nominal 20-yr term from priority
G01N 33/575A61K 40/42A61K 40/24A61K 40/19A61K 40/11A61K 2239/38A61K 2239/31A61K 2239/55C12N 15/1138G01N 33/6863G01N 2333/525C07K 16/283C07K 16/244A61P 35/04C07K 2317/76C07K 2317/52A61P 37/04G01N 33/6866G01N 2800/52C07K 2317/31C07K 2317/21A61P 43/00C07K 2317/72G01N 33/564G01N 2333/57G01N 33/6854A61K 2039/507G01N 2333/5434C07K 16/00A61P 35/00A61K 2039/505G01N 33/6869A61P 31/00C12N 2310/14G01N 33/574A61K 39/0011
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Claims

Abstract

Described herein are compositions for increasing IL-12 production comprising IgG or a fragment thereof or a variant thereof and uses of said compositions for treating cancer and infectious diseases. Also described herein are compositions for decreasing IL-12 production comprising an agent that inhibits signaling mediated by interaction between FcRn and IgG and uses of said compositions for treating autoimmune diseases. Further described herein are methods for assessing efficacy of treatment by monitoring levels of various cytokines in the subject.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for determining the efficacy of treatment in a subject in need thereof comprising: (a) administering to the subject a treatment comprising a composition comprising an anti-FcRn antibody that inhibits signaling mediated by interaction between FcRn and IgG; (b) providing a sample from the subject, wherein the sample is blood, plasma or tissue; (c) assaying the level of TNF-α in the sample; and (d) determining that the treatment is efficacious if the level of TNF-α in the sample from the subject is lower relative to the level in a reference sample or determining that the treatment is not efficacious if the level of TNF-α in the sample from the subject is higher relative to the level in a reference sample, wherein the subject has an autoimmune disease. 
     
     
         2 . The method of  claim 1 , wherein the antibody is selected from the group consisting of a monoclonal antibody or a fragment thereof, a polyclonal antibody or a fragment thereof, chimeric antibody, humanized antibody and single chain antibody.

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