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- Anaerobic Bacterial Fermentation Products Increase Tuberculosis Risk in Antiretroviral-Drug-Treated HIV Patients.
Anaerobic Bacterial Fermentation Products Increase Tuberculosis Risk in Antiretroviral-Drug-Treated HIV Patients.
Citation | “Anaerobic Bacterial Fermentation Products Increase Tuberculosis Risk In Antiretroviral-Drug-Treated Hiv Patients.”. Cell Host & Microbe, pp. 530-537.e4. . |
Center | Albert Einstein College of Medicine |
Author | Leopoldo N Segal, Jose C Clemente, Yonghua Li, Chunhai Ruan, Jane Cao, Mauricio Danckers, Alison Morris, Sarah Tapyrik, Benjamin G Wu, Philip Diaz, Gregory Calligaro, Rodney Dawson, Richard N van Zyl-Smit, Keertan Dheda, William N Rom, Michael D Weiden |
Keywords | FoxP1, Foxp3, HIV, DYSBIOSIS, lung, short-chain fatty acids, Tuberculosis |
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. |
Year of Publication |
2017
|
Journal |
Cell host & microbe
|
Volume |
21
|
Issue |
4
|
Number of Pages |
530-537.e4
|
Date Published |
04/2017
|
ISSN Number |
1934-6069
|
DOI |
10.1016/j.chom.2017.03.003
|
Alternate Journal |
Cell Host Microbe
|
PMID |
28366509
|
PMCID |
PMC5465639
|
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