| Literature DB >> 28366509 |
Leopoldo N Segal1, Jose C Clemente2, Yonghua Li1, Chunhai Ruan3, Jane Cao3, Mauricio Danckers1, Alison Morris4, Sarah Tapyrik5, Benjamin G Wu1, Philip Diaz5, Gregory Calligaro6, Rodney Dawson6, Richard N van Zyl-Smit6, Keertan Dheda6, William N Rom1, Michael D Weiden7.
Abstract
Despite the immune-reconstitution with antiretroviral therapy (ART), HIV-infected individuals remain highly susceptible to tuberculosis (TB) and have an enrichment of oral anaerobes in the lung. Products of bacterial anaerobic metabolism, like butyrate and other short-chain fatty acids (SCFAs), induce regulatory T cells (Tregs). We tested whether SCFAs contribute to poor TB control in a longitudinal cohort of ART-treated HIV-infected South Africans. Increase in serum SCFAs was associated with increased TB susceptibility. SCFAs inhibited IFN-γ and IL-17A production in peripheral blood mononuclear cells from HIV-infected ART-treated individuals in response to M. tuberculosis antigen stimulation. Pulmonary SCFAs correlated with increased oral anaerobes, such as Prevotella in the lung, and with M. tuberculosis antigen-induced Tregs. Metabolites from anaerobic bacterial fermentation may, therefore, increase TB susceptibility by suppressing IFN-γ and IL-17A production during the cellular immune response to M. tuberculosis.Entities:
Keywords: FoxP1; FoxP3; HIV; dysbiosis; lung; short-chain fatty acids; tuberculosis
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Year: 2017 PMID: 28366509 PMCID: PMC5465639 DOI: 10.1016/j.chom.2017.03.003
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023