Methods of blocking tissue destruction by autoreactive t cells
AssigneeThe Ohio State University Research Foundation
InventorsYang Liu, Pan Zheng, Xue-Feng Bai
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AssigneeThe Ohio State University Research Foundation
InventorsYang Liu, Pan Zheng, Xue-Feng Bai
Estimating the term…
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.
1-28. (canceled)
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.
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.
Dependencies are inferred from the claim text.