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百日咳博德特氏菌的补体逃避:对改进现有疫苗的启示

Complement evasion by Bordetella pertussis: implications for improving current vaccines.

作者信息

Jongerius Ilse, Schuijt Tim J, Mooi Frits R, Pinelli Elena

机构信息

Centre for Infectious Disease Control, National Institute for Public Health and the Environment, Antonie van Leeuwenhoeklaan 9, P.O. Box 1, 3720 BA, Bilthoven, The Netherlands.

出版信息

J Mol Med (Berl). 2015 Apr;93(4):395-402. doi: 10.1007/s00109-015-1259-1. Epub 2015 Feb 18.

Abstract

Bordetella pertussis causes whooping cough or pertussis, a highly contagious disease of the respiratory tract. Despite high vaccination coverage, reported cases of pertussis are rising worldwide and it has become clear that the current vaccines must be improved. In addition to the well-known protective role of antibodies and T cells during B. pertussis infection, innate immune responses such as the complement system play an essential role in B. pertussis killing. In order to evade this complement activation and colonize the human host, B. pertussis expresses several molecules that inhibit complement activation. Interestingly, one of the known complement evasion proteins, autotransporter Vag8, is highly expressed in the recently emerged B. pertussis isolates. Here, we describe the current knowledge on how B. pertussis evades complement-mediated killing. In addition, we compare this to complement evasion strategies used by other bacterial species. Finally, we discuss the consequences of complement evasion by B. pertussis on adaptive immunity and how identification of the bacterial molecules and the mechanisms involved in complement evasion might help improve pertussis vaccines.

摘要

百日咳博德特氏菌可引发百日咳,这是一种极具传染性的呼吸道疾病。尽管疫苗接种覆盖率很高,但全球范围内报告的百日咳病例仍在增加,显然当前的疫苗必须加以改进。除了抗体和T细胞在百日咳博德特氏菌感染期间具有众所周知的保护作用外,诸如补体系统等固有免疫反应在杀灭百日咳博德特氏菌方面也起着至关重要的作用。为了逃避这种补体激活并在人类宿主中定殖,百日咳博德特氏菌表达了几种抑制补体激活的分子。有趣的是,已知的补体逃避蛋白之一自转运蛋白Vag8在最近出现的百日咳博德特氏菌分离株中高度表达。在此,我们描述了目前关于百日咳博德特氏菌如何逃避补体介导的杀伤作用的知识。此外,我们将此与其他细菌物种所采用的补体逃避策略进行了比较。最后,我们讨论了百日咳博德特氏菌补体逃避对适应性免疫的影响,以及鉴定参与补体逃避的细菌分子和机制如何有助于改进百日咳疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ca1/4366546/5559ad5ec357/109_2015_1259_Fig1_HTML.jpg

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