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炭疽毒素对 T 细胞的靶向作用:同一枚硬币的两面。

T cell targeting by anthrax toxins: two faces of the same coin.

机构信息

Department of Evolutionary Biology, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy.

出版信息

Toxins (Basel). 2011 Jun;3(6):660-71. doi: 10.3390/toxins3060660. Epub 2011 Jun 20.

Abstract

Bacillus anthracis, similar to other bacterial pathogens, has evolved effective immune evasion strategies to prolong its survival in the host, thus ensuring the unchecked spread of the infection. This function is subserved by lethal (LT) and edema (ET) toxins, two exotoxins produced by vegetative anthrax bacilli following germination of the spores. The structure of these toxins and the mechanism of cell intoxication are topics covered by other reviews in this issue. Here we shall discuss how B. anthracis uses LT and ET to suppress the immune defenses of the host, focusing on T lymphocytes, the key players in adaptive immunity. We shall also summarize recent findings showing that, depending on its concentration, ET has the ability not only to suppress T cell activation but also to promote the polarization of CD4(+) T cells to the Th2 and Th17 subsets, highlighting the potential use of this toxin as an immunomodulator.

摘要

炭疽芽孢杆菌与其他细菌病原体类似,已进化出有效的免疫逃避策略,以延长其在宿主体内的存活时间,从而确保感染的不受控制传播。这种功能由致死(LT)和水肿(ET)毒素提供,这两种外毒素是由营养炭疽杆菌在孢子发芽后产生的。这些毒素的结构和细胞中毒的机制是本期其他综述中讨论的主题。在这里,我们将讨论炭疽芽孢杆菌如何利用 LT 和 ET 来抑制宿主的免疫防御,重点是适应性免疫的关键参与者 T 淋巴细胞。我们还将总结最近的发现,表明 ET 不仅能够抑制 T 细胞的激活,而且能够促进 CD4(+)T 细胞向 Th2 和 Th17 亚群的极化,突出了这种毒素作为免疫调节剂的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b6/3202842/17cac3e843b1/toxins-03-00660-g001.jpg

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