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理解隐匿性是揭示自身免疫发病机制的关键。

Understanding crypticity is the key to revealing the pathogenesis of autoimmunity.

作者信息

Moudgil Kamal D, Sercarz Eli E

机构信息

University of Maryland School of Medicine, Department of Microbiology and Immunology, BRB 13-019, 655 W. Baltimore St, Baltimore, MD 21201, USA.

出版信息

Trends Immunol. 2005 Jul;26(7):355-9. doi: 10.1016/j.it.2005.05.007.

Abstract

In this opinion, we propose that the hierarchy of antigenic determinants within self-antigens is the major influence in molding the potentially autoreactive T-cell repertoire. The well processed and presented determinants constitute a 'dominant self', whereas the poorly processed and/or presented determinants will be invisible to T cells and comprise a 'cryptic self', which we consider a fundamental cornerstone of a theory of autoimmunity. It accounts for the large repertoire of self-reactive clones because a similar hierarchy is established in the thymus and controls positive and negative selection. Furthermore, this residual T-cell repertoire, largely directed against cryptic determinants, will contain some T cells with sufficient affinity for MHC and antigen that enables them to respond under inflammatory conditions, thus facilitating presentation of previously cryptic determinants.

摘要

在本观点中,我们提出自身抗原内抗原决定簇的层次结构是塑造潜在自身反应性T细胞库的主要影响因素。加工良好且呈递的决定簇构成“显性自身”,而加工不良和/或呈递不佳的决定簇对T细胞不可见,构成“隐蔽自身”,我们认为这是自身免疫理论的一个基本基石。这解释了自身反应性克隆的大量存在,因为在胸腺中建立了类似的层次结构并控制阳性和阴性选择。此外,这个主要针对隐蔽决定簇的残余T细胞库将包含一些对MHC和抗原具有足够亲和力的T细胞,使它们能够在炎症条件下作出反应,从而促进先前隐蔽决定簇的呈递。

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