
CD8 T cells contribute to protective immunity against Mycobacterium tuberculosis. In humans, M. tuberculosis reactive CD8 T cells typically recognize peptides associated to classical MHC class Ia molecules, but little information is available on CD8 T cells recognizing M. tuberculosis Ags presented by nonclassical MHC class Ib molecules. We show here that CD8 T cells from tuberculosis (TB) patients recognize HLA‐E‐binding M. tuberculosis peptides in a CD3/TCR αβ mediated and CD8‐dependent manner, and represent an additional type of effector cells playing a role in immune response to M. tuberculosis during active infection. HLA‐E‐restricted recognition of M. tuberculosis peptides is detectable by a significant enhanced ex vivo frequency of tetramer‐specific circulating CD8 T cells during active TB. These CD8 T cells produce type 2 cytokines upon antigenic in vitro stimulation, help B cells for Ab production, and mediate limited TRAIL‐dependent cytolytic and microbicidal activity toward M. tuberculosis infected target cells. Our results, together with the finding that HLA‐E/M. tuberculosis peptide specific CD8 T cells are detected in TB patients with or without HIV coinfection, suggest that this is a new human T‐cell population that participates in immune response in TB.
Adult, Male, Tetramers, HLA-E, Receptors, Antigen, T-Cell, alpha-beta, Epitopes, T-Lymphocyte, HIV Infections, Humans, Tuberculosis, Cells, Cultured, Antigens, Bacterial, CD8 T lymphocytes; HLA-E; Mycobacterium tuberculosis; TB; Tetramers; Type 2 cytokines; Adult; Antibodies, Bacterial; Antigens, Bacterial; Cells, Cultured; Coinfection; Cytokines; Epitopes, T-Lymphocyte; Female; HIV Infections; Histocompatibility Antigens Class I; Humans; Male; Middle Aged; Mycobacterium tuberculosis; NK Cell Lectin-Like Receptor Subfamily C; NK Cell Lectin-Like Receptor Subfamily D; Protein Binding; Receptors, Antigen, T-Cell, alpha-beta; T-Lymphocytes, Cytotoxic; Tuberculosis; Immunology; Immunology and Allergy; Medicine (all), Type 2 cytokines, Coinfection, Histocompatibility Antigens Class I, Mycobacterium tuberculosis, Middle Aged, Antibodies, Bacterial, CD8 T lymphocytes, TB, Cytokines, Female, NK Cell Lectin-Like Receptor Subfamily C, NK Cell Lectin-Like Receptor Subfamily D, Protein Binding, T-Lymphocytes, Cytotoxic
Adult, Male, Tetramers, HLA-E, Receptors, Antigen, T-Cell, alpha-beta, Epitopes, T-Lymphocyte, HIV Infections, Humans, Tuberculosis, Cells, Cultured, Antigens, Bacterial, CD8 T lymphocytes; HLA-E; Mycobacterium tuberculosis; TB; Tetramers; Type 2 cytokines; Adult; Antibodies, Bacterial; Antigens, Bacterial; Cells, Cultured; Coinfection; Cytokines; Epitopes, T-Lymphocyte; Female; HIV Infections; Histocompatibility Antigens Class I; Humans; Male; Middle Aged; Mycobacterium tuberculosis; NK Cell Lectin-Like Receptor Subfamily C; NK Cell Lectin-Like Receptor Subfamily D; Protein Binding; Receptors, Antigen, T-Cell, alpha-beta; T-Lymphocytes, Cytotoxic; Tuberculosis; Immunology; Immunology and Allergy; Medicine (all), Type 2 cytokines, Coinfection, Histocompatibility Antigens Class I, Mycobacterium tuberculosis, Middle Aged, Antibodies, Bacterial, CD8 T lymphocytes, TB, Cytokines, Female, NK Cell Lectin-Like Receptor Subfamily C, NK Cell Lectin-Like Receptor Subfamily D, Protein Binding, T-Lymphocytes, Cytotoxic
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 68 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
