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细菌IgA蛋白酶对黏膜免疫防御机制的干扰。

Perturbation of mucosal immune defence mechanisms by bacterial IgA proteases.

作者信息

Kilian M, Reinholdt J, Mortensen S B, Sørensen C H

出版信息

Bull Eur Physiopathol Respir. 1983 Mar-Apr;19(2):99-104.

PMID:6347284
Abstract

The secretory IgA system plays an important role in protecting the mucous membranes of the respiratory tract from attacks by microorganisms and potential allergens. We present evidence of in vivo cleavage of S-IgA1 in nasopharyngeal secretions by IgA1 proteases excreted by certain bacteria colonizing the upper respiratory tract. A procedure in two stages, which includes separation of secretion constituents by HPLC and subsequent immunochemical analysis of the fractions by two ELISA systems, identified the S-IgA fragments observed in some nasopharyngeal secretions as intact (FC alpha)2 . SC and Fab alpha, respectively. It is conceivable that colonization of areas of the respiratory tract by increased numbers of IgA1 protease-producing bacteria might cause a local impairment of the mucosal immune barrier. It is hypothesized that such bacterium-induced changes may be a primary event in the pathogenesis of certain inflammatory respiratory diseases and some forms of atopy.

摘要

分泌型IgA系统在保护呼吸道黏膜免受微生物和潜在过敏原的攻击方面发挥着重要作用。我们提供了证据,证明定居在上呼吸道的某些细菌分泌的IgA1蛋白酶可在体内切割鼻咽分泌物中的S-IgA1。一个分两个阶段的程序,包括通过高效液相色谱法分离分泌物成分,以及随后通过两个酶联免疫吸附测定系统对各组分进行免疫化学分析,确定了在一些鼻咽分泌物中观察到的S-IgA片段分别为完整的(FCα)2、分泌片(SC)和Fabα。可以想象,产生IgA1蛋白酶的细菌数量增加,在呼吸道区域定殖,可能会导致黏膜免疫屏障的局部受损。据推测,这种细菌诱导的变化可能是某些炎症性呼吸道疾病和某些特应性形式发病机制中的一个主要事件。

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