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多发性肌炎与分子模拟——一种自身免疫机制

Polymyositis and molecular mimicry, a mechanism of autoimmunity.

作者信息

Walker E J, Jeffrey P D

出版信息

Lancet. 1986 Sep 13;2(8507):605-7. doi: 10.1016/s0140-6736(86)92429-3.

Abstract

The amino acid sequences of Escherichia coli histidyl-tRNA synthetase and alanyl-tRNA synthetase, two proteins recently identified as autoantigens in polymyositis, were compared by a computer alignment procedure with those of the 3600 proteins tabulated in the National Biomedical Research Foundation protein sequence database. Both proteins contain sequences long enough to function as epitopes that match sequences on viral and muscle proteins. The homology thus revealed not only lends strong support to mechanisms of autoimmunity that invoke the theory of molecular mimicry of viral proteins, but also suggests a rationale for the skeletal muscle target of polymyositis.

摘要

最近在多发性肌炎中被鉴定为自身抗原的两种蛋白质,即大肠杆菌组氨酰 - tRNA合成酶和丙氨酰 - tRNA合成酶的氨基酸序列,通过计算机比对程序与国家生物医学研究基金会蛋白质序列数据库中列出的3600种蛋白质的氨基酸序列进行了比较。这两种蛋白质都含有足够长的序列,可作为与病毒和肌肉蛋白质序列相匹配的表位。由此揭示的同源性不仅有力地支持了援引病毒蛋白质分子模拟理论的自身免疫机制,还为多发性肌炎的骨骼肌靶点提供了一个基本原理。

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