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pubmed-article:10050679pubmed:abstractTextRecent studies have challenged the long held concept that each T lymphocyte expresses on its surface only a single, unique alphabetaTCR. Dual TCR+ T cells have been recognized, however, their origin and potential to escape screening for self-reactivity remain obscure. We now report the thymic generation of dual alphabetaTCR+ T cells in the H-2Db/H-Y-specific TCR transgenic (Tg) mouse. Dual TCR+ thymocytes were positively selected less efficiently than single TCR+ thymocytes, although a subset attained maturity. Importantly, when TCR Tg mice were bred onto a negatively selecting background, auto-specific cells survived central deletion and matured as CD4+ dual TCR+ cells. These cells were autoreactive when CD8 expression was restored. The existence of autospecific, dual TCR+ T cells may have implications for the maintenance of self tolerance.lld:pubmed
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pubmed-article:10050679pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:10050679pubmed:articleTitleDevelopment and function of autospecific dual TCR+ T lymphocytes.lld:pubmed
pubmed-article:10050679pubmed:affiliationDepartment of Immunology, University of Colorado Health Sciences Center, Denver 80262, USA.lld:pubmed
pubmed-article:10050679pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10050679pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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