Apoptotic modifications affect the autoreactivity of the U1 snRNP autoantigen

被引:26
作者
Hof, D
Raats, JMH
Pruijn, GJM
机构
[1] Radboud Univ Nijmegen, Nijmegen Ctr Mol Life Sci, Dept Biochem, NL-6500 HB Nijmegen, Netherlands
[2] ModiQuest BV, Nijmegen, Netherlands
关键词
apoptosis; autoantibodies; posttranslational modifications; U1; snRNP; U1-70K;
D O I
10.1016/j.autrev.2005.02.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A hallmark of systemic autoimmune diseases is the presence of high titers of serum autoantibodies targeting a diversity of autoantigens. Most components of the U1 snRNP complex are autoantigenic in systemic lupus erythematosus (SLE) and SLE overlap syndrome, which is also called mixed connective tissue disease (MCTD). It is hypothesized that posttranslational modifications, in particular cell death-associated modifications, play an important role in breaking tolerance to self-antigens. Recently, it became clear that the U1 snRNP particle, more specifically its U1-70K protein component, displays a new epitope during apoptosis. This review intends to give an overview of the modifications that occur on the U1 snRNP autoantigens, especially those arising during cell death, to summarize recent data describing autoantibody reactivities with apoptosis-specific epitopes on the U1 snRNP complex, and to provide some insight into the mechanisms that might underlie the immune response to self-antigens. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:380 / 388
页数:9
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