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鉴定诱导 A/J 小鼠自身免疫性心肌炎的肌球蛋白重链-α的新型模拟表位。

Identification of novel mimicry epitopes for cardiac myosin heavy chain-α that induce autoimmune myocarditis in A/J mice.

机构信息

School of Veterinary Medicine and Biomedical Sciences, University of Nebraska-Lincoln, Lincoln, NE 68583, United States.

出版信息

Cell Immunol. 2011;271(2):438-49. doi: 10.1016/j.cellimm.2011.08.013. Epub 2011 Aug 30.

Abstract

Myocarditis is one cause of sudden cardiac death in young adolescents, and individuals affected with myocarditis can develop dilated cardiomyopathy, a frequent reason for heart transplantation. Exposure to environmental microbes has been suspected in the initiation of heart autoimmunity, but the direct causal link is lacking. We report here identification of novel mimicry epitopes that bear sequences similar to those in cardiac myosin heavy chain (MYHC)-α 334-352. These epitopes represent Bacillus spp., Magnetospirillum gryphiswaldense, Cryptococcus neoformans and Zea mays. The mimicry peptides induced varying degrees of myocarditis in A/J mice reminiscent of the disease induced with MYHC-α 334-352. We demonstrate that the mimics induce cross-reactive T cell responses for MYHC-α 334-352 as verified by MHC class II IA(k)/tetramer staining and Th-1 and Th-17 cytokines similar to those of MYHC-α 334-352. The data suggest that exposure to environmental microbes which are otherwise innocuous can predispose to heart autoimmunity by molecular mimicry.

摘要

心肌炎是青少年猝死的一个原因,患有心肌炎的个体可能会发展为扩张型心肌病,这是心脏移植的常见原因。环境微生物的暴露被怀疑是心脏自身免疫的启动因素,但缺乏直接的因果关系。我们在这里报告了新型模拟表位的鉴定,这些表位具有与心肌肌球蛋白重链(MYHC)-α 334-352 相似的序列。这些表位代表了芽孢杆菌属、噬血螺旋菌、新型隐球菌和玉米。模拟肽在 A/J 小鼠中诱导了不同程度的心肌炎,类似于用 MYHC-α 334-352 诱导的疾病。我们证明,模拟物诱导针对 MYHC-α 334-352 的交叉反应性 T 细胞反应,这通过 MHC Ⅱ类 IA(k)/四聚体染色以及与 MYHC-α 334-352 相似的 Th-1 和 Th-17 细胞因子得到证实。数据表明,暴露于原本无害的环境微生物可能通过分子模拟使心脏自身免疫易感性增加。

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