CD8 T cells and Mycobacterium tuberculosis infection

被引:153
|
作者
Lin, Philana Ling [1 ]
Flynn, JoAnne L. [2 ,3 ]
机构
[1] Univ Pittsburgh, Childrens Hosp Pittsburgh, Div Infect Dis, Dept Pediat,Med Ctr, Pittsburgh, PA 15224 USA
[2] Univ Pittsburgh, Sch Med, Dept Microbiol & Mol Genet, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Sch Med, Dept Microbiol & Mol Genet, Pittsburgh, PA 15261 USA
关键词
ADAPTIVE IMMUNE-RESPONSE; ANTIMICROBIAL ACTIVITY; CYNOMOLGUS MACAQUES; LATENT TUBERCULOSIS; HIV-1; INFECTION; GRANULYSIN; MICE; LYMPHOCYTES; EXPRESSION; PROTECTION;
D O I
10.1007/s00281-015-0490-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tuberculosis is primarily a respiratory disease that is caused by Mycobacterium tuberculosis. M. tuberculosis can persist and replicate in macrophages in vivo, usually in organized cellular structures called granulomas. There is substantial evidence for the importance of CD4 T cells in control of tuberculosis, but the evidence for a requirement for CD8 T cells in this infection has not been proven in humans. However, animal model data support a non-redundant role for CD8 T cells in control of M. tuberculosis infection. In humans, infection with this pathogen leads to generation of specific CD8 T cell responses. These responses include classical (MHC Class I restricted) and non-classical CD8 T cells. Here, we discuss the potential roles of CD8 T cells in defense against tuberculosis, and our current understanding of the wide range of CD8 T cell types seen in M. tuberculosis infection.
引用
收藏
页码:239 / 249
页数:11
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