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补体激活凝集素途径对呼吸系统感染的影响。

The Influence of the Lectin Pathway of Complement Activation on Infections of the Respiratory System.

机构信息

Laboratory of Immunobiology of Infections, Institute of Medical Biology, Polish Academy of Sciences, Łódź, Poland.

出版信息

Front Immunol. 2020 Oct 21;11:585243. doi: 10.3389/fimmu.2020.585243. eCollection 2020.

Abstract

Lung diseases are among the leading causes of morbidity and mortality. Complement activation may prevent a variety of respiratory infections, but on the other hand, could exacerbate tissue damage or contribute to adverse side effects. In this review, the associations of factors specific for complement activation the lectin pathway (LP) with infections of the respiratory system, from birth to adulthood, are discussed. The most extensive data concern mannose-binding lectin (MBL) which together with other collectins (collectin-10, collectin-11) and the ficolins (ficolin-1, ficolin-2, ficolin-3) belong to pattern-recognition molecules (PRM) specific for the LP. Those PRM form complexes with MBL-associated serine proteases (MASP-1, MASP-2, MASP-3) and related non-enzymatic factors (MAp19, MAp44). Beside diseases affecting humanity for centuries like tuberculosis or neonatal pneumonia, some recently published data concerning COVID-19 are summarized.

摘要

肺部疾病是导致发病率和死亡率的主要原因之一。补体激活可以预防多种呼吸道感染,但另一方面,也可能加重组织损伤或导致不良反应。在这篇综述中,讨论了补体激活途径(LP)特有的一些因素与从出生到成年的呼吸系统感染之间的关系。最广泛的数据涉及甘露聚糖结合凝集素(MBL),它与其他凝集素(凝集素-10、凝集素-11)和纤维胶凝素(ficolin-1、ficolin-2、ficolin-3)一起属于 LP 特有的模式识别分子(PRM)。这些 PRM 与 MBL 相关的丝氨酸蛋白酶(MASP-1、MASP-2、MASP-3)和相关的非酶因子(MAp19、MAp44)形成复合物。除了几个世纪以来一直影响人类的疾病,如肺结核或新生儿肺炎外,还总结了一些关于 COVID-19 的最新发表的数据。

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