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Antigen Persistence Is Required for Dendritic Cell Licensing and CD8+ T Cell Cross-Priming
Author(s) -
Hélène Jusforgues-Saklani,
Martin Uhl,
Nathalie E. Blachère,
Fabrice Lemaı̂tre,
Olivier Lantz,
Philippe Bousso,
Déborah Braun,
James Moon,
Matthew L. Albert
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.181.5.3067
Subject(s) - priming (agriculture) , cytotoxic t cell , cd8 , t cell , microbiology and biotechnology , cross presentation , immunology , antigen presenting cell , biology , major histocompatibility complex , dendritic cell , antigen , mhc class i , immune system , in vitro , genetics , botany , germination
It has been demonstrated that CD4(+) T cells require Ag persistence to achieve effective priming, whereas CD8(+) T cells are on "autopilot" after only a brief exposure. This finding presents a disturbing conundrum as it does not account for situations in which CD8(+) T cells require CD4(+) T cell help. We used a physiologic in vivo model to study the requirement of Ag persistence for the cross-priming of minor histocompatibility Ag-specific CD8(+) T cells. We report inefficient cross-priming in situations in which male cells are rapidly cleared. Strikingly, the failure to achieve robust CD8(+) T cell activation is not due to a problem with cross-presentation. In fact, by providing "extra help" in the form of dendritic cells (DCs) loaded with MHC class II peptide, it was possible to achieve robust activation of CD8(+) T cells. Our data suggest that the "licensing" of cross-presenting DCs does not occur during their initial encounter with CD4(+) T cells, thus accounting for the requirement for Ag persistence and suggesting that DCs make multiple interactions with CD8(+) T cells during the priming phase. These findings imply that long-lived Ag is critical for efficient vaccination protocols in which the CD8(+) T cell response is helper-dependent.

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