Evasion and subversion of antigen presentation by Mycobacterium tuberculosis

被引:119
作者
Baena, A. [1 ]
Porcelli, S. A. [1 ,2 ]
机构
[1] Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
来源
TISSUE ANTIGENS | 2009年 / 74卷 / 03期
基金
美国国家卫生研究院;
关键词
antigen presentation; CD1; immune evasion; major histocompatibility complex class II; major histocompatibility complex class I; Mycobacterium tuberculosis; vaccine; MHC-CLASS-II; T-CELL RESPONSES; BACILLUS-CALMETTE-GUERIN; DENDRITIC CELLS; 19-KDA LIPOPROTEIN; HUMAN MACROPHAGES; BOVIS BCG; CROSS-PRESENTATION; IFN-GAMMA; CATHEPSIN-S;
D O I
10.1111/j.1399-0039.2009.01301.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mycobacterium tuberculosis is one of the most successful of human pathogens and has acquired the ability to establish latent or progressive infection and persist even in the presence of a fully functioning immune system. The ability of M. tuberculosis to avoid immune-mediated clearance is likely to reflect a highly evolved and coordinated program of immune evasion strategies, including some that interfere with antigen presentation to prevent or alter the quality of T-cell responses. Here, we review an extensive array of published studies supporting the view that antigen presentation pathways are targeted at many points by pathogenic mycobacteria. These studies show the multiple potential mechanisms by which M. tuberculosis may actively inhibit, subvert or otherwise modulate antigen presentation by major histocompatibility complex class I, class II and CD1 molecules. Unraveling the mechanisms by which M. tuberculosis evades or modulates antigen presentation is of critical importance for the development of more effective new vaccines based on live attenuated mycobacterial strains.
引用
收藏
页码:189 / 204
页数:16
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