Your browser doesn't support javascript.
loading
MR1-restricted mucosal associated invariant T (MAIT) cells in the immune response to Mycobacterium tuberculosis.
Gold, Marielle C; Napier, Ruth J; Lewinsohn, David M.
Afiliação
  • Gold MC; Pulmonary and Critical Care Medicine, Oregon Health and Science University, Portland, OR, USA; VA Portland Health Care System (VAPORHCS), Portland, OR, USA; Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR, USA.
Immunol Rev ; 264(1): 154-66, 2015 Mar.
Article em En | MEDLINE | ID: mdl-25703558
The intracellular pathogen Mycobacterium tuberculosis (Mtb) and its human host have long co-evolved. Although the host cellular immune response is critical to the control of the bacterium information on the specific contribution of different immune cell subsets in humans is incomplete. Mucosal associated invariant T (MAIT) cells are a prevalent and unique T-cell population in humans with the capacity to detect intracellular infection with bacteria including Mtb. MAIT cells detect bacterially derived metabolites presented by the evolutionarily conserved major histocompatibility complex-like molecule MR1. Here, we review recent advances in our understanding of this T-cell subset and address the potential roles for MR1-restricted T cells in the control, diagnosis, and therapy of tuberculosis.
Assuntos
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Tuberculose / Antígenos de Histocompatibilidade Classe I / Subpopulações de Linfócitos T / Interações Hospedeiro-Patógeno / Mucosa / Mycobacterium tuberculosis Tipo de estudo: Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Immunol Rev Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Tuberculose / Antígenos de Histocompatibilidade Classe I / Subpopulações de Linfócitos T / Interações Hospedeiro-Patógeno / Mucosa / Mycobacterium tuberculosis Tipo de estudo: Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Immunol Rev Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos