Sustained Rap1 activation in autoantigen-specific T lymphocytes attenuates experimental autoimmune encephalomyelitis

被引:7
|
作者
Salinas, Gabriela Franco
Krausz, Sarah
Dontje, Wendy
Evavold, Brian D. [2 ]
Tak, Paul P.
Baeten, Dominique L. [3 ]
Reedquist, Kris A. [1 ,3 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Div Clin Immunol & Rheumatol, Dept Clin Immunol & Rheumatol, NL-1105 AZ Amsterdam, Netherlands
[2] Emory Univ, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[3] Univ Amsterdam, Acad Med Ctr, Dept Expt Immunol, NL-1105 AZ Amsterdam, Netherlands
关键词
Autoimmunity; T lymphocyte; Tolerance; Experimental autoimmune encephalitis; Rap1; SYSTEMIC-LUPUS-ERYTHEMATOSUS; RHEUMATOID-ARTHRITIS; OXIDATIVE STRESS; CELL DEVELOPMENT; LYMPH-NODES; GTPASE RAP1; ANTIGEN; ADHESION; RASGRP1; MOLECULE;
D O I
10.1016/j.jneuroim.2012.05.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Altered Ras superfamily guanine nucleotide triphosphatase signaling may contribute to the activation of autoreactive T cells in diseases such as rheumatoid arthritis and systemic lupus erythematosus. Here, we show that transgenic expression of activated Rap1, a Ras-related protein which is protective in murine arthritis, in both wildtype (WT) and 2D2 mice, enhances autoreactive T cell activation by myelin oligodendrocyte glycoprotein peptide in vitro and in vivo. However, RapV12 reduces the number of autoreactive T cells in both WT and 2D2 mice, and increases murine survival in experimental autoimmune encephalitis, suggesting Rap1 activation restricts autoimmune T cell-mediated pathology through enhancing tolerance. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:35 / 43
页数:9
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