Open AccessIFNγ‐producing CD4 + T lymphocytes: the double‐edged swords in tuberculosis
Author(s) -
Kumar Pawan
Publication year - 2017
Publication title -
clinical and translational medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
H-Index - 1
ISSN - 2001-1326
DOI - 10.1186/s40169-017-0151-8
Subject(s) - pathogenesis , mycobacterium tuberculosis , immune system , immunology , tuberculosis , autophagy , macrophage , immune reconstitution inflammatory syndrome , t cell , interferon , immunity , medicine , virology , biology , virus , apoptosis , antiretroviral therapy , viral load , in vitro , biochemistry , pathology
IFNγ‐producing CD4 + T cells (IFNγ + CD4 + T cells) are the key orchestrators of protective immunity against Mycobacterium tuberculosis ( Mtb ). Primarily, these cells act by enabling Mtb ‐infected macrophages to enforce phagosome‐lysosome fusion, produce reactive nitrogen intermediates (RNIs), and activate autophagy pathways. However, TB is a heterogeneous disease and a host of clinical and experimental findings has also implicated IFNγ + CD4 + T cells in TB pathogenesis. High frequency of IFNγ + CD4 + T cells is the most invariable feature of the active disease. Active TB patients mount a heightened IFNγ + CD4 + T cell response to mycobacterial antigens and demonstrate an IFNγ‐inducible transcriptomic signature. IFNγ + CD4 + T cells have also been shown to mediate TB‐associated immune reconstitution inflammatory syndrome (TB–IRIS) observed in a subset of antiretroviral therapy (ART)‐treated HIV‐ and Mtb ‐coinfected people. The pathological face of IFNγ + CD4 + T cells during mycobacterial infection is further uncovered by studies in the animal model of TB–IRIS and in Mtb ‐infected PD‐1 −/− mice. This manuscript encompasses the evidence supporting the dual role of IFNγ + CD4 + T cells during Mtb infection and sheds light on immune mechanisms involved in protection versus pathogenesis.