Impaired Degranulation and Proliferative Capacity of Mycobacterium tuberculosis-Specific CD8+ T Cells in HIV-Infected Individuals With Latent Tuberculosis

被引:20
|
作者
Kalokhe, Ameeta S. [1 ,2 ]
Adekambi, Toidi [3 ]
Ibegbu, Chris C. [3 ,4 ]
Ray, Susan M. [1 ]
Day, Cheryl L. [2 ,3 ,4 ]
Rengarajan, Jyothi [1 ,3 ]
机构
[1] Emory Univ, Sch Med, Dept Med, Div Infect Dis, Atlanta, GA 30329 USA
[2] Emory Univ, Rollins Sch Publ Hlth, Dept Global Hlth, Atlanta, GA 30329 USA
[3] Emory Univ, Emory Vaccine Ctr, Atlanta, GA 30329 USA
[4] Emory Univ, Yerkes Natl Primate Ctr, Dept Microbiol & Immunol, Atlanta, GA 30329 USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2015年 / 211卷 / 04期
基金
美国国家卫生研究院;
关键词
latent tuberculosis; CD8(+) T cells; HIV; degranulation; proliferation;
D O I
10.1093/infdis/jiu505
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human immunodeficiency virus (HIV)-infected individuals with latent Mycobacterium tuberculosis infection have substantially higher rates of progression to active tuberculosis than HIV-uninfected individuals with latent tuberculosis. To explore HIV-induced deficits in M. tuberculosis-specific CD8(+) T-cell functions, we compared interferon. production, degranulation, and proliferation of CD8(+) T cells in response to M. tuberculosis peptides (ESAT-6/CFP-10) between HIV-infected (median CD4(+) T-cell count, 522 cells/mu L; interquartile range, 318-585 cells/mu L) and HIV-uninfected individuals with latent tuberculosis from South Africa. We found that M. tuberculosis-specific degranulation and proliferative capacities were impaired in the HIV-infected group. Thus, our results suggest that HIV coinfection compromises CD8(+) T-cell functions in latent tuberculosis.
引用
收藏
页码:635 / 640
页数:6
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