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人类自身免疫性疾病中自身抗体产生的可能机制及病毒感染的关联。

Possible mechanisms of autoantibody production and the connection of viral infections in human autoimmune diseases.

作者信息

Yamamoto K

机构信息

Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo.

出版信息

Tohoku J Exp Med. 1994 May;173(1):75-82. doi: 10.1620/tjem.173.75.

Abstract

The presence of autoantibodies is a characteristic phenomenon in an autoimmune disease. In order to investigate the mechanisms of the autoantibody production, we have performed epitope mappings of the autoantigens. It thus was found that there were multiple epitopes on an autoantigen molecule, and a serum from a patient with an autoimmune disease usually recognizes these multiple epitopes simultaneously, suggesting that autoantibodies are ultimately produced by an antigen-driven mechanism. However, other evidence suggests that tolerance to a self antigen is rather tightly maintained and a simple antigen-driven mechanism cannot easily take place. Based on the results of epitope mappings, it appears that there is a major or a usually recognized epitope on almost every autoantigen molecule. Some patients only recognize this epitope. It is unlikely that only a single epitope can be recognized if a large molecule is immunized to the host. Therefore, the recognition of this universal epitope may play some roles in the induction of the autoantibody production. In fact, some of these epitopes have sequences homologous to those of viral proteins. Thus, it is possible that an immune response to a certain virus might induce by molecular mimicry the recognition of an autoantigen. Possible mechanisms following this molecular mimicry that may induce antigen-driven autoantibody production are discussed.

摘要

自身抗体的存在是自身免疫性疾病中的一个特征性现象。为了研究自身抗体产生的机制,我们对自身抗原进行了表位作图。结果发现,一个自身抗原分子上存在多个表位,自身免疫性疾病患者的血清通常会同时识别这些多个表位,这表明自身抗体最终是由抗原驱动机制产生的。然而,其他证据表明,对自身抗原的耐受性相当严格,简单的抗原驱动机制不易发生。基于表位作图的结果,似乎几乎每个自身抗原分子上都有一个主要的或通常被识别的表位。一些患者只识别这个表位。如果将一个大分子免疫给宿主,不太可能只识别单个表位。因此,对这个普遍表位的识别可能在自身抗体产生的诱导中起一些作用。事实上,这些表位中的一些具有与病毒蛋白序列同源的序列。因此,对某种病毒的免疫反应可能通过分子模拟诱导对自身抗原的识别。本文讨论了这种分子模拟后可能诱导抗原驱动自身抗体产生的机制。

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