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The MAIT TCRß chain contributes to discrimination of microbial ligand.
Narayanan, Gitanjali A; McLaren, James E; Meermeier, Erin W; Ladell, Kristin; Swarbrick, Gwendolyn M; Price, David A; Tran, Jessica G; Worley, Aneta H; Vogt, Todd; Wong, Emily B; Lewinsohn, David M.
Afiliação
  • Narayanan GA; Department of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, OR, USA.
  • McLaren JE; Division of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
  • Meermeier EW; Department of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, OR, USA.
  • Ladell K; Division of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
  • Swarbrick GM; Department of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, OR, USA.
  • Price DA; VA Portland Health Care Center, Portland, OR, USA.
  • Tran JG; Division of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
  • Worley AH; Systems Immunity Research Institute, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
  • Vogt T; VA Portland Health Care Center, Portland, OR, USA.
  • Wong EB; VA Portland Health Care Center, Portland, OR, USA.
  • Lewinsohn DM; VA Portland Health Care Center, Portland, OR, USA.
Immunol Cell Biol ; 98(9): 770-781, 2020 10.
Article em En | MEDLINE | ID: mdl-32568415
ABSTRACT
Mucosal-associated invariant T (MAIT) cells are key players in the immune response against microbial infection. The MAIT T-cell receptor (TCR) recognizes a diverse array of microbial ligands, and recent reports have highlighted the variability in the MAIT TCR that could further contribute to discrimination of ligand. The MAIT TCR complementarity determining region (CDR)3ß sequence displays a high level of diversity across individuals, and clonotype usage appears to be dependent on antigenic exposure. To address the relationship between the MAIT TCR and microbial ligand, we utilized a previously defined panel of MAIT cell clones that demonstrated variability in responses against different microbial infections. Sequencing of these clones revealed four pairs, each with shared (identical) CDR3α and different CDR3ß sequences. These pairs demonstrated varied responses against microbially infected dendritic cells as well as against 5-(2-oxopropylideneamino)-6-d-ribitylaminouracil, a ligand abundant in Salmonella enterica serovar Typhimurium, suggesting that the CDR3ß contributes to differences in ligand discrimination. Taken together, these results highlight a key role for the MAIT CDR3ß region in distinguishing between MR1-bound antigens and ligands.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Ativação Linfocitária / Genes Codificadores da Cadeia beta de Receptores de Linfócitos T / Regiões Determinantes de Complementaridade / Células T Invariantes Associadas à Mucosa Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Immunol Cell Biol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Ativação Linfocitária / Genes Codificadores da Cadeia beta de Receptores de Linfócitos T / Regiões Determinantes de Complementaridade / Células T Invariantes Associadas à Mucosa Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Immunol Cell Biol Ano de publicação: 2020 Tipo de documento: Article