Monocyte-Derived IL-5 Reduces TNF Production by Mycobacterium tuberculosis-specific CD4 T Cells during SIV/M. tuberculosis Coinfection

被引:14
作者
Diedrich, Collin R. [1 ]
Mattila, Joshua T. [1 ]
Flynn, JoAnne L. [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Microbiol & Mol Genet, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
IMMUNODEFICIENCY-VIRUS-INFECTION; CYNOMOLGUS MACAQUES; INTERFERON-GAMMA; PULMONARY TUBERCULOSIS; ALVEOLAR MACROPHAGES; CYTOKINE RESPONSES; HIV-1; INFECTION; IN-VITRO; REPLICATION; ACTIVATION;
D O I
10.4049/jimmunol.1202043
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HIV-infected individuals are significantly more susceptible to tuberculosis (TB) than uninfected individuals. Although it is established that HIV reduces Mycobacterium tuberculosis-specific T cell responses, the causes of this dysfunction are not known. We used the cynomolgus macaque model of TB to demonstrate that ex vivo SIV reduces the frequency of M. tuberculosis-specific TNF and IFN-gamma-producing T cells within 24 h after infection. In vivo, T cell IFN-gamma responses in granulomas from animals with SIV/M. tuberculosis coinfection were lower than SIV-negative animals with active TB. The SIV effects on the inhibition of T cell responses were primarily on APCs and not the T cells directly. Specifically, reductions in the frequency of TNF-producing M. tuberculosis-specific CD4 T cells were caused, at least in part, by SIV-induced production of monocyte derived IL-5.
引用
收藏
页码:6320 / 6328
页数:9
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