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感染在自身免疫性疾病发病机制中的作用。

The role of infections in the pathogenesis of autoimmune diseases.

作者信息

Samarkos Michael, Vaiopoulos George

机构信息

5th Department of Internal Medicine, Evangelismos Hospital, Athens, Greece.

出版信息

Curr Drug Targets Inflamm Allergy. 2005 Feb;4(1):99-103. doi: 10.2174/1568010053622821.

Abstract

The autoimmune diseases result from inappropriate responses of the immune system to self antigens. The etiology of autoimmune diseases remains largely unknown but candidate etiologic factors include genetic abnormalities and infections. Although there are considerable data supporting the role of infections in a variety of autoimmune diseases, this role has been unequivocally established in only a few autoimmune diseases. The difficulty in establishing the infectious etiology of autoimmune diseases stems from several factors such as the heterogeneity of clinical manifestations in individual autoimmune diseases and the time interval between infection and autoimmune disease. The data on this association derive from clinical observations, epidemiological studies and research using laboratory techniques, protein sequence database screening and animal models. Infectious agents can cause autoimmune diseases by different mechanisms, which fall into two categories: antigen specific in which pathogen products or elements have a central role e.g. superantigens or epitope (molecular) mimicry, and antigen non-specific in which the pathogen provides the appropriate inflammatory setting for "bystander activation". The most important mechanisms are molecular mimicry and superantigens. As far as molecular mimicry is concerned the recent data on the degeneracy of T cell recognition shifted the focus from searching for linear sequence homology to looking for similarity of antigenic surfaces. Special mention has to be made to retroviruses as they have some unique means of inducing autoimmunity.

摘要

自身免疫性疾病是由免疫系统对自身抗原的不适当反应引起的。自身免疫性疾病的病因在很大程度上仍然未知,但候选病因包括基因异常和感染。尽管有大量数据支持感染在多种自身免疫性疾病中的作用,但这种作用仅在少数自身免疫性疾病中得到明确证实。确定自身免疫性疾病感染病因的困难源于多种因素,如个体自身免疫性疾病临床表现的异质性以及感染与自身免疫性疾病之间的时间间隔。关于这种关联的数据来自临床观察、流行病学研究以及使用实验室技术、蛋白质序列数据库筛选和动物模型的研究。感染因子可通过不同机制导致自身免疫性疾病,这些机制分为两类:抗原特异性机制,其中病原体产物或成分起核心作用,例如超抗原或表位(分子)模拟;以及抗原非特异性机制,其中病原体为“旁观者激活”提供适当的炎症环境。最重要的机制是分子模拟和超抗原。就分子模拟而言,最近关于T细胞识别简并性的数据将重点从寻找线性序列同源性转移到寻找抗原表面的相似性。必须特别提及逆转录病毒,因为它们具有一些独特的诱导自身免疫的方式。

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