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dc.contributor.author
Gold, Marielle C.  
dc.contributor.author
McLaren, James E.  
dc.contributor.author
Reistetter, Joseph A.  
dc.contributor.author
Smyk Pearson, Sue  
dc.contributor.author
Ladell, Kristin  
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Swarbrick, Gwendolyn M.  
dc.contributor.author
Yu, Yik Y. L.  
dc.contributor.author
Hansen, Ted H.  
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Lund, Ole  
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Nielsen, Morten  
dc.contributor.author
Gerritsen, Bram  
dc.contributor.author
Kesmir, Can  
dc.contributor.author
Miles, John J.  
dc.contributor.author
Lewinsohn, Deborah A.  
dc.contributor.author
Price, David A.  
dc.contributor.author
Lewinsohn, David M.  
dc.date.available
2017-06-13T16:52:11Z  
dc.date.issued
2014-07  
dc.identifier.citation
Gold, Marielle C.; McLaren, James E.; Reistetter, Joseph A.; Smyk Pearson, Sue; Ladell, Kristin; et al.; MR1-restricted MAIT cells display ligand discrimination and pathogen selectivity through distinct T cell receptor usage; Rockefeller Univ Press; Journal Of Experimental Medicine; 211; 8; 7-2014; 1601-1610  
dc.identifier.issn
0022-1007  
dc.identifier.uri
http://hdl.handle.net/11336/18089  
dc.description.abstract
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 TCRβ 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.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Rockefeller Univ Press  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Mait  
dc.subject
T Cell  
dc.subject
T Cell Receptor  
dc.subject.classification
Otras Ciencias de la Salud  
dc.subject.classification
Ciencias de la Salud  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
MR1-restricted MAIT cells display ligand discrimination and pathogen selectivity through distinct T cell receptor usage  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-06-09T15:01:04Z  
dc.journal.volume
211  
dc.journal.number
8  
dc.journal.pagination
1601-1610  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Birmingham  
dc.description.fil
Fil: Gold, Marielle C.. Oregon Health & Science University; Estados Unidos  
dc.description.fil
Fil: McLaren, James E.. Cardiff University; Reino Unido  
dc.description.fil
Fil: Reistetter, Joseph A.. Oregon Health & Science University; Estados Unidos  
dc.description.fil
Fil: Smyk Pearson, Sue. Oregon Health & Science University; Estados Unidos  
dc.description.fil
Fil: Ladell, Kristin. Cardiff University; Reino Unido  
dc.description.fil
Fil: Swarbrick, Gwendolyn M.. Oregon Health & Science University; Estados Unidos  
dc.description.fil
Fil: Yu, Yik Y. L.. Washington University in St. Louis; Estados Unidos  
dc.description.fil
Fil: Hansen, Ted H.. Washington University in St. Louis; Estados Unidos  
dc.description.fil
Fil: Lund, Ole. Technical University of Denmark; Dinamarca  
dc.description.fil
Fil: Nielsen, Morten. Technical University of Denmark; Dinamarca. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; Argentina  
dc.description.fil
Fil: Gerritsen, Bram. Utrecht Univeristy; Países Bajos  
dc.description.fil
Fil: Kesmir, Can. Utrecht Univeristy; Países Bajos  
dc.description.fil
Fil: Miles, John J.. Cardiff University; Reino Unido  
dc.description.fil
Fil: Lewinsohn, Deborah A.. Oregon Health & Science University; Estados Unidos  
dc.description.fil
Fil: Price, David A.. Cardiff University; Reino Unido. National Institutes of Health; Estados Unidos  
dc.description.fil
Fil: Lewinsohn, David M.. Oregon Health & Science University; Estados Unidos  
dc.journal.title
Journal Of Experimental Medicine  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://jem.rupress.org/content/211/8/1601.long  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1084/jem.20140507  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113934/