Literature DB >> 22802630

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

Lijin Li1, Sojung Kim, John M Herndon, Peter Goedegebuure, Brian A Belt, Ansuman T Satpathy, Timothy P Fleming, Ted H Hansen, Kenneth M Murphy, William E Gillanders.   

Abstract

Activation of naïve 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 naïve and memory CD8(+) T cells and requires CD8α(+)/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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Year:  2012        PMID: 22802630      PMCID: PMC3411977          DOI: 10.1073/pnas.1203468109

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  21 in total

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5.  Dendritic cells cross-dressed with peptide MHC class I complexes prime CD8+ T cells.

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Journal:  J Immunol       Date:  2006-11-01       Impact factor: 5.422

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Review 6.  The Biology and Underlying Mechanisms of Cross-Presentation of Exogenous Antigens on MHC-I Molecules.

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Review 7.  Antigen presentation in cancer: insights into tumour immunogenicity and immune evasion.

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Review 10.  Specificity through cooperation: BATF-IRF interactions control immune-regulatory networks.

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