4.8 Article

Cross-dressed CD8α+/CD103+ dendritic cells prime CD8+ T cells following vaccination

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1203468109

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Funding

  1. Susan G. Komen for the Cure [KG080476]
  2. Department of Defense [W81XWH-06-1-0677]
  3. National Institutes of Health [AI055849]
  4. Howard Hughes Medical Institute
  5. Barnes-Jewish Hospital Foundation

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Activation of naive cluster of differentiation (CD)8(+) cytotoxic T lymphocytes (CTLs) is a tightly regulated process, and specific dendritic cell (DC) subsets are typically required to activate naive CTLs. Potential pathways for antigen presentation leading to CD8(+) T-cell priming include direct presentation, cross-presentation, and cross-dressing. To distinguish between these pathways, we designed single-chain trimer (SCT) peptide-MHC class I complexes that can be recognized as intact molecules but cannot deliver antigen to MHC through conventional antigen processing. We demonstrate that cross-dressing is a robust pathway of antigen presentation following vaccination, capable of efficiently activating both nave and memory CD8(+) T cells and requires CD8 alpha(+)/CD103(+) DCs. Significantly, immune responses induced exclusively by cross-dressing were as strong as those induced exclusively through cross-presentation. Thus, cross-dressing is an important pathway of antigen presentation, with important implications for the study of CD8(+) T-cell responses to viral infection, tumors, and vaccines.

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