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Beyond memory T cells: mechanisms of protective immunity to tuberculosis infection.
Immunology and Cell Biology ( IF 4 ) Pub Date : 2019-06-23 , DOI: 10.1111/imcb.12278
Pia Steigler 1, 2 , Ayesha J Verrall 3 , Joanna R Kirman 4
Affiliation  

Tuberculosis (TB) is a serious infectious disease caused by infection with Mycobacterium tuberculosis, and kills more people annually than any other single infectious agent. Although a vaccine is available, it is only moderately effective and an improved vaccine is urgently needed. The ability to develop a more effective vaccine has been thwarted by a lack of understanding of the mechanism of vaccine-induced immune protection. Over recent decades, many novel TB vaccines have been developed and almost all have aimed to generate memory CD4 T cells. In this review, we critically evaluate evidence in the literature that supports the contention that memory CD4 T cells are the prime mediators of vaccine-induced protection against TB. Because of the lack of robust evidence supporting memory CD4 T cells in this role, the potential for B-cell antibody and "trained" innate cells as alternative mediators of protective immunity is explored.

中文翻译:

超越记忆T细胞:抵抗结核感染的保护性免疫机制。

结核病(TB)是由结核分枝杆菌感染引起的一种严重的传染病,每年造成的死亡人数超过任何其他单一传染原。尽管有疫苗可用,但它仅是中等有效的,迫切需要改进的疫苗。缺乏对疫苗诱导的免疫保护机制的了解,阻碍了开发更有效疫苗的能力。在最近的几十年中,已经开发了许多新颖的结核病疫苗,并且几乎所有疫苗都旨在产生记忆性CD4 T细胞。在这篇综述中,我们对文献中的证据进行了严格的评估,这些证据支持以下观点:记忆CD4 T细胞是疫苗诱导的抗TB保护作用的主要媒介。由于缺乏有力的证据支持记忆CD4 T细胞发挥这一作用,
更新日期:2019-11-01
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