High Frequencies of Caspase-3 Expressing Mycobacterium tuberculosis-Specific CD4+ T Cells Are Associated With Active Tuberculosis

Abstract

Antigen-specific CD4⁺ T cell responses to <i>Mycobacterium tuberculosis</i> (Mtb) infection are important for host defense against tuberculosis (TB). However, Mtb-specific IFN-γ-producing T cells do not distinguish active tuberculosis (ATB) patients from individuals with asymptomatic latent Mtb infection (LTBI). We reasoned that the immune phenotype of Mtb-specific IFN-γ⁺CD4⁺ T cells could provide an indirect gauge of Mtb antigen load within individuals. We sought to identify immune markers in Mtb-specific IFN-γ⁺CD4⁺ T cells and hypothesized that expression of caspase-3 Mtb-specific CD4⁺ T cells would be associated with ATB. Using polychromatic flow cytometry, we evaluated the expression of caspase-3 in Mtb-specific CD4⁺ T cells from LTBI and ATB as well as from ATB patients undergoing anti-TB treatment. We found significantly higher frequencies of Mtb-specific caspase-3⁺IFN-γ⁺CD4⁺ T cells in ATB compared to LTBI. Caspase-3⁺IFN-γ⁺CD4⁺ T cells were also more activated compared to their caspase-3-negative counterparts. Furthermore, the frequencies of caspase-3⁺IFN-γ⁺CD4⁺ T cells decreased in response to anti-TB treatment. Our studies suggest that the frequencies of caspase-3-expressing antigen-specific CD4⁺ T cells may reflect mycobacterial burden <i>in vivo</i> and may be useful for distinguishing Mtb infection status along with other host biomarkers.