Monocyte-Derived IL-5 Reduces TNF Production byMycobacterium tuberculosis–specific CD4 T Cells during SIV/M. tuberculosisCoinfection
Author(s) -
Collin R. Diedrich,
Joshua T. Mattila,
JoAnne L. Flynn
Publication year - 2013
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1202043
Subject(s) - coinfection , tuberculosis , mycobacterium tuberculosis , immunology , ex vivo , virology , monocyte , t cell , biology , mycobacterium , in vivo , macaque , tumor necrosis factor alpha , medicine , immune system , human immunodeficiency virus (hiv) , pathology , paleontology , microbiology and biotechnology
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-γ-producing T cells within 24 h after infection. In vivo, T cell IFN-γ 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.
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