US2016326229A1PendingUtilityA1

Inhibition of il-17 production

Assignee: GENENTECH INCPriority: Oct 30, 2002Filed: Mar 10, 2016Published: Nov 10, 2016
Est. expiryOct 30, 2022(expired)· nominal 20-yr term from priority
Inventors:Austin Gurney
A61P 37/00A61P 37/06A61P 3/10A61P 43/00A61P 9/10A61P 37/02A61P 31/04A61P 25/00A61P 29/02A61P 25/28A61P 29/00C07K 2317/76A61P 19/06C07K 16/244A61P 19/02G01N 2500/02A61K 2039/505A61P 11/00C07K 2319/30A61P 11/06G01N 33/6869A61P 17/06A61K 39/3955A61P 1/04C07K 14/54C07K 2317/21C07K 2317/24A61P 17/00C07K 16/2866C07K 16/24A61P 1/00A61K 39/395C12N 15/09C12N 15/00
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Claims

Abstract

The invention concerns inhibition of the production of proinflammatory cytokine interleukin-17 (IL-17) by T cells, using an antagonist of interleukin-23 (IL-23). The invention further concerns the use of IL-23 antagonists in the treatment of inflammatory diseases characterized by the presence of elevated levels of IL-17. IL-23 antagonists include, without limitation, antibodies specifically binding to a subunit or IL-17 or an IL-17 receptor. The invention additionally concerns induction of IL-7 production by using an IL-23 agonist.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for inhibiting interleukin-17 (IL-17) production by memory T cells, comprising administering to a mammalian subject in need an interleukin-23 (IL-23) antagonist selected from the group consisting of an anti-IL-23 antibody, an anti-IL-23 receptor antibody, an immunoadhesin comprising an IL-23 subunit fused to an immunoglobulin constant region sequence or comprising an IL-23 receptor subunit fused to an immunoglobulin constant region sequence, and an anti-sense oligonucleotide capable of inhibiting translation and/or transcription of a gene encoding a subunit of native IL-23 polypeptide or capable of inhibiting translation and/or transcription of a gene encoding a subunit of a native IL-23 receptor polypeptide. 
     
     
         2 . The method of  claim 1 , wherein the mammalian subject is a human. 
     
     
         3 . The method of  claim 2 , wherein said T cells are activated T cells. 
     
     
         4 . The method of  claim 2 , wherein said antagonist if an anti-IL-23 antibody or an anti-IL-23 receptor antibody. 
     
     
         5 . The method of  claim 4 , wherein said antibody is an antigen-binding antibody fragment. 
     
     
         6 . The method of  claim 5 , wherein said antibody fragment is selected from the group consisting of Fv, Fab, Fab′, and F(ab′) 2  fragments. 
     
     
         7 . The method of  claim 4 , wherein said antibody is a full-length antibody. 
     
     
         8 . The method of  claim 4 , wherein said antibody is chimeric, humanized or human.

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