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Indoctrinating T cells to attack pathogens through homeschooling.
Parello, Caitlin S; Huseby, Eric S.
Afiliação
  • Parello CS; Department of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
  • Huseby ES; Department of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USA. Electronic address: Eric.Huseby@umassmed.edu.
Trends Immunol ; 36(6): 337-43, 2015 Jun.
Article em En | MEDLINE | ID: mdl-25979654
ABSTRACT
Adaptive immunity is predicated on the ability of the T cell repertoire to have pre-existing specificity for the universe of potential pathogens. Recent findings suggest that T cell receptor (TCR)-self-major histocompatibility protein (pMHC) interactions limit autoimmune responses while enhancing T cell response to foreign antigens. We review these findings here, placing them in context of the current understanding of how TCR-self-pMHC interactions regulate T cell activation thresholds, and suggest that TCR-self-pMHC interactions increase the efficiency of the T cell repertoire by giving a competitive advantage to peptide cross-reactive T cells. We propose that self-reactivity and peptide cross-reactivity are controlled by particular CDR3 sequence motifs, which would allow thymic selection to contribute to solving the feat of broad pathogen specificity by exporting T cells that are pre-screened by positive and negative selection for the ability to be 'moderately' peptide cross-reactive.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T / Linfócitos T / Imunidade Adaptativa / Complexo Principal de Histocompatibilidade / Células Apresentadoras de Antígenos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T / Linfócitos T / Imunidade Adaptativa / Complexo Principal de Histocompatibilidade / Células Apresentadoras de Antígenos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article