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J Exp Med ; 211(8): 1601-10, 2014 Jul 28.
Artículo en Inglés | MEDLINE | ID: mdl-25049333

RESUMEN

Mucosal-associated invariant T (MAIT) cells express a semi-invariant T cell receptor (TCR) that detects microbial metabolites presented by the nonpolymorphic major histocompatibility complex (MHC)-like molecule MR1. The highly conserved nature of MR1 in conjunction with biased MAIT TCRα chain usage is widely thought to indicate limited ligand presentation and discrimination within a pattern-like recognition system. Here, we evaluated the TCR repertoire of MAIT cells responsive to three classes of microbes. Substantial diversity and heterogeneity were apparent across the functional MAIT cell repertoire as a whole, especially for TCRß chain sequences. Moreover, different pathogen-specific responses were characterized by distinct TCR usage, both between and within individuals, suggesting that MAIT cell adaptation was a direct consequence of exposure to various exogenous MR1-restricted epitopes. In line with this interpretation, MAIT cell clones with distinct TCRs responded differentially to a riboflavin metabolite. These results suggest that MAIT cells can discriminate between pathogen-derived ligands in a clonotype-dependent manner, providing a basis for adaptive memory via recruitment of specific repertoires shaped by microbial exposure.


Asunto(s)
Antígenos de Diferenciación de Linfocitos B/metabolismo , Bacterias/inmunología , Antígenos de Histocompatibilidad Clase II/metabolismo , Antígenos de Histocompatibilidad Clase I/metabolismo , Membrana Mucosa/citología , Membrana Mucosa/inmunología , Receptores de Antígenos de Linfocitos T/metabolismo , Linfocitos T/metabolismo , Secuencia de Aminoácidos , Bacterias/efectos de los fármacos , Línea Celular , Células Clonales , Regiones Determinantes de Complementariedad/química , Reordenamiento Génico de la Cadena alfa de los Receptores de Antígenos de los Linfocitos T/genética , Humanos , Ligandos , Antígenos de Histocompatibilidad Menor , Datos de Secuencia Molecular , Membrana Mucosa/efectos de los fármacos , Receptores de Antígenos de Linfocitos T alfa-beta/genética , Homología de Secuencia de Aminoácido , Linfocitos T/efectos de los fármacos , Complejo Vitamínico B/farmacología
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