Immune characterization of the HBHA-specific response in Mycobacterium tuberculosisinfected patients with or without HIV infection

RD1-based Interferon-. Release Assays (IGRAs) cannot distinguish latent from active tuberculosis (TB) disease. Conversely, a positive response to heparin-binding haemagglutinin (HBHA)-based IGRAs, among TB-infected subjects, correlates with Mycobacterium tuberculosis (Mtb) containment and low risk of TB progression. The aim of this study was to characterize HBHA-immune responses in HIV-infected and uninfected subjects with active TB or latent TB infection (LTBI). Methods 49 subjects were prospectively enrolled: 22 HIV-uninfected (13 TB, 9 LTBI) and 27 HIVinfected (12 HIV-TB, 15 HIV-LTBI). Whole blood and peripheral blood mononuclear cells were stimulated with HBHA and RD1 antigens. Interferon (IFN). release was evaluated by ELISA whereas cytokine profile [IFN gamma, tumor necrosis (TNF) alpha, interleukin (IL) 2] and phenotype (CD45RA, CCR7) by flow cytometry. Results Among LTBI individuals, HBHA stimulation induced IFN. release in all the HIV-uninfected, while, only 4/ 15 HIV-infected responded. Within the active TB, only 5/ 13 HIV-uninfected and 1/ 12 HIV-TB patients responded. Interestingly, by cytometry we showed that CD4 (+) T-cells response to HBHA was significantly impaired in the HIV-infected subjects with TB or LTBI compared to the HIV-uninfected subjects. The phenotype of HBHA-specific CD4 T-cells showed a predominantly central memory (CM) and effector memory (EM) phenotype without differences among the groups. Differently, HBHA-specific CD8 (+) T-cells, showed mainly a CM and naive phenotype in LTBI group while TB, HIV-LTBI and HIV-TB groups were characterized by EM or terminally differentiated phenotypes. Interestingly, differently than whatobserved for RD1, the cytokine profile of HBHA-specific T-cells evaluated by cytometry showed that the CD4 (+) T-cells were mostly monofunctional. Conversely, CD8-specific Tcells were mostly monofunctional for both HBHA and RD1 stimulations. Conclusions These results characterize the impact of HIV infection in CD4- and CD8-specific response to HBHA in both LTBI and TB patients. HIV infection impairs the CD4 response to HBHA and likely this may lead to an impairment of TB control.