Clonal deletion and the fate of autoreactive thymocytes that survive negative selection.

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2012

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info:eu-repo/semantics/altIdentifier/doi/10.1038/ni.2292

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info:eu-repo/semantics/altIdentifier/pmid/22544394

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info:eu-repo/semantics/altIdentifier/eissn/1529-2916

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_9E7371C181407

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L.A. Pobezinsky et al., « Clonal deletion and the fate of autoreactive thymocytes that survive negative selection. », Serveur académique Lausannois, ID : 10.1038/ni.2292


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Clonal deletion of autoreactive thymocytes is important for self-tolerance, but the intrathymic signals that induce clonal deletion have not been clearly identified. We now report that clonal deletion during negative selection required CD28-mediated costimulation of autoreactive thymocytes at the CD4(+)CD8(lo) intermediate stage of differentiation. Autoreactive thymocytes were prevented from undergoing clonal deletion by either a lack of CD28 costimulation or transgenic overexpression of the antiapoptotic factors Bcl-2 or Mcl-1, with surviving thymocytes differentiating into anergic CD4(-)CD8(-) double-negative thymocytes positive for the T cell antigen receptor αβ subtype (TCRαβ) that 'preferentially' migrated to the intestine, where they re-expressed CD8α and were sequestered as CD8αα(+) intraepithelial lymphocytes (IELs). Our study identifies costimulation by CD28 as the intrathymic signal required for clonal deletion and identifies CD8αα(+) IELs as the developmental fate of autoreactive thymocytes that survive negative selection.

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