Journal of Clinical Investigation · 1998 · 89 citations · 29 references
Life SciencesCell BiologyImmunologyAutoimmunityCellular ImmunologyImmunopathologyAntigen RecognitionAutoimmune DiseasesCombined ImmunodeficiencyT Cell ActivationT Cell BiologyT Cell DevelopmentT Cell ImmunologyT Cell Repertoire SelectionT Lymphocyte DevelopmentT-cell ImmunophenotypesT-cell Mediated AutoimmunityT-cell Receptor Gene UsageT-cell Repertoire AnalysisTissue Migration
Omenn's syndrome is an inherited human combined immunodeficiency condition characterized by the presence of a large population of activated and tissue-infiltrating T cells. Analysis of the TCRB repertoire revealed a highly restricted TCRBV usage in three patients. More strikingly, T cell clones from the three patients expressed TCRB chains with VDJ junction similarities, suggesting a common antigenic specificity. Analysis of the TCRA repertoire in one patient also revealed a restricted TCRAV usage. Finally, analysis of the TCRBV repertoire of tissue-infiltrating T cells in one patient suggested nonrandom tissue migration. These results suggest that the oligoclonal expansion of T cells observed in Omenn's syndrome could be the consequence of autoimmune proliferation generated by a profound defect in lymphocyte development.
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An αβ T Cell Receptor Structure at 2.5 Å and Its Orientation in the TCR-MHC Complex
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The outline structure of the T‐cell alpha beta receptor.
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