Tim-2 regulates T helper type 2 responses and autoimmunity.

Autor: Chakravarti, Sumone, Sabatos, Catherine A., Sheng Xiao, Illes, Zsolt, Cha, Eugene K., Sobel, Raymond A., Zheng, Xin X., Strom, Terry B., Kuchroo, Vijay K.
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Zdroj: Journal of Experimental Medicine; 8/1/2005, Vol. 202 Issue 3, p437-444, 8p, 5 Graphs
Abstrakt: Identification of the T cell immunoglobulin mucin-domain containing (Tim) gene family introduced a new family of cell surface molecules that is involved in the regulation of immune responses. We previously demonstrated that Tim-3 is expressed on terminally differentiated T helper (Th)1 cells, and serves to regulate Th1 immune responses. Here, we describe the identification and function of Tim-2, a novel member of the Tim gene family. In contrast with Tim-3, we demonstrate that Tim-2 is expressed preferentially in differentiated Th2 cells. Blockade of the Tim-2/Tim-2 ligand interaction, by administration of soluble Tim-2 fusion protein (Tim-2 immunogtobulin [Ig]), results in T cell hyperproliferation and the production of Th2 cytokines. Administration of Tim-2 Ig during the induction phase reduces the severity of experimental autoimmune encephalomyelitis, a Thi-mediated autoimmune disease model of multiple sclerosis. We propose that Tim-2, an orthologue of human Tim-1, is critical for the regulation of Th2 responses during autoimmune inflammation. [ABSTRACT FROM AUTHOR]
Databáze: Supplemental Index