IFN-γ independent markers of Mycobacterium tuberculosis exposure among male South African gold miners.

Leela RL Davies ; Malisa T Smith ; Deniz Cizmeci ; Stephanie Fischinger ; Jessica Shih-Lu Lee ; Lenette L Lu ; Erik D Layton ; Alison D Grant ORCID logo ; Katherine Fielding ORCID logo ; Catherine M Stein ; +7 more... W Henry Boom ; Thomas R Hawn ; Sarah M Fortune ; Robert S Wallis ; Gavin J Churchyard ; Galit Alter ; Chetan Seshadri ; (2023) IFN-γ independent markers of Mycobacterium tuberculosis exposure among male South African gold miners. EBioMedicine, 93. 104678-. ISSN 2352-3964 DOI: 10.1016/j.ebiom.2023.104678
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BACKGROUND: The prevalence of tuberculosis among men who work in the gold mines of South Africa is among the highest in the world, but a fraction of miners demonstrate consistently negative results upon tuberculin skin test (TST) and IFN-γ release assay (IGRA). We hypothesized that these "resisters" (RSTRs) may display unconventional immune signatures of exposure to M. tuberculosis (M.tb). METHODS: In a cohort of RSTRs and matched controls with latent TB infection (LTBI), we profiled the functional breadth of M.tb antigen-specific T cell and antibody responses using multi-parameter flow cytometry and systems serology, respectively. FINDINGS: RSTRs and LTBI controls both exhibited IFN-γ independent T-cell and IgG antibody responses to M.tb-specific antigens ESAT-6 and CFP-10. Antigen-specific antibody Fc galactosylation and sialylation were higher among RSTRs. In a combined T-cell and antibody analysis, M.tb lysate-stimulated TNF secretion by T cells correlated positively with levels of purified protein derivative-specific IgG. A multivariate model of the combined data was able to differentiate RSTR and LTBI subjects. INTERPRETATION: IFN-γ independent immune signatures of exposure to M.tb, which are not detected by approved clinical diagnostics, are readily detectable in an occupational cohort uniquely characterized by intense and long-term infection pressure. Further, TNF may mediate a coordinated response between M.tb-specific T-cells and B-cells. FUNDING: This work was supported by the US National Institutes of Health (R01-AI124348 to Boom, Stein, and Hawn; R01-AI125189 and R01-AI146072 to Seshadri; and 75N93019C00071 to Fortune, Alter, Seshadri, and Boom), the Doris Duke Charitable Foundation (Davies), the Bill & Melinda Gates Foundation (OPP1151836 and OPP1109001 to Hawn; and OPP1151840 to Alter), Mass Life Science Foundation (Fortune), and Good Ventures Fund (Fortune).


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