US2013296249A1PendingUtilityA1

Methods of blocking tissue destruction by autoreactive t cells

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Assignee: LIU YANGPriority: Mar 29, 2000Filed: May 2, 2013Published: Nov 7, 2013
Est. expiryMar 29, 2020(expired)· nominal 20-yr term from priority
A61P 37/06A61P 37/08A61P 3/10A61P 25/00A61K 38/177C07K 16/2896A61P 17/06A61K 38/00C07K 2319/30C07K 14/70596A61P 19/02C07K 2319/00A61K 39/0008
61
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Abstract

Methods for blocking autoreactive T cell-initiated destruction of tissues in a mammal are provided. In one embodiment, the method comprises administering a purified CD24 polypeptide, a fusion protein comprising such polypeptide, or a biologically active fragment of such polypeptide to a mammalian subject who is suspected of having or predisposed to having an autoimmune disease. In another embodiment, anti-CD24 antibody or anti-CD24 Fab fragments are administered to the subject. In another embodiment, the method comprises administering a CD24 antisense molecule, an expression vector encoding a CD24 antisense molecule, CD24 dsRNAi, or an expression vector encoding CD24 dsRNAi to the subject. The present invention also relates to isolated and purified CD24 fusion proteins employed in the present methods and to transgenic mice that express the human CD24 protein on their T cells and/or their vascular endothelial cells but do not express murine heat shock antigen on any cells.

Claims

exact text as granted — not AI-modified
1 - 28 . (canceled) 
     
     
         29 . A pharmaceutical composition comprising a human HSA/CD24 polypeptide fusion and a physiologically acceptable carrier, wherein the HSA/CD24 polypeptide fusion comprises a HSA/CD24 core region, and wherein the HSA/CD24 polypeptide fusion is glycosylated. 
     
     
         30 . A method for treating a human patient suspected of having, known to have, or predisposed to having multiple sclerosis, said method comprising administering to said patient a pharmaceutical composition comprising a human HSA/CD24 polypeptide fusion and a physiologically acceptable carrier, wherein the HSA/CD24 polypeptide fusion comprises a HSA/CD24 core region, and wherein the HSA/CD24 polypeptide fusion is glycosylated.

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