High Activation of γδ T Cells and the γδ2 T-Cell Subset Is Associated With the Onset of Tuberculosis-Associated Immune Reconstitution Inflammatory Syndrome, ANRS 12153 CAPRI NK.

Human Immunodeficiency Virus 1 (HIV-1) and (Mtb) co-infected patients are commonly at risk of immune reconstitution inflammatory syndrome (IRIS) when initiating antiretroviral treatment (ART). Evidence indicates that innate immunity plays a role in TB-IRIS. Here, we evaluate the phenotype of Gamma-delta (γδ) T cells and invariant Natural Killer (iNK) T cells in tuberculosis-associated IRIS. Forty-eight HIV+/TB+ patients (21 IRIS) and three control groups: HIV-/TB- (HD, = 11), HIV+/TB- ( = 26), and HIV-/TB+ ( = 22) were studied. Samples were taken at ART initiation (week 2 of anti-tuberculosis treatment) and at the diagnosis of IRIS for HIV+/TB+; before ART for HIV+/TB-, and at week 2 of anti-tuberculosis treatment for HIV-/TB+ patients. γδ T cells and Invariant natural killer T (iNKT) cells were analyzed by flow cytometry. Before ART, IRIS, and non-IRIS patients showed a similar proportion of γδ T and iNKT cells. HLA-DR on γδ T cells and δ2γδ T cells was significantly higher in TB-IRIS vs. non-IRIS patients and controls ( < 0.0001). NKG2D expression on γδ T cells and the δ2γδ T cell subset was lower in HIV+/TB+ patients than controls. CD158a expression on γδ T cells was higher in TB-IRIS than non-IRIS ( = 0.02), HIV+/TB-, and HIV-/TB- patients. The higher activation of γδT cells and the γδ2γδ T cell subset suggests that γδ T cells may play a role in the pathogenesis of TB-IRIS.