[PDF][PDF] Dendritic cells rapidly recruited into epithelial tissues via CCR6/CCL20 are responsible for CD8+ T cell crosspriming in vivo

M Le Borgne, N Etchart, A Goubier, SA Lira, JC Sirard… - Immunity, 2006 - cell.com
M Le Borgne, N Etchart, A Goubier, SA Lira, JC Sirard, N Van Rooijen, C Caux, S Aït-Yahia…
Immunity, 2006cell.com
The nature of dendritic cell (s)(DC [s]) that conditions efficient in vivo priming of CD8+ CTL
after immunization via epithelial tissues remains largely unknown. Here, we show that
myeloid DCs rapidly recruited by adjuvants into the buccal mucosa or skin are essential for
CD8+ T cell crosspriming. Recruitment of circulating DC precursors, including Gr1+
monocytes, precedes the sequential accumulation of CD11c+ MHC class II+ DCs in dermis
and epithelium via a CCR6/CCL20-dependent mechanism. Remarkably, a defect in CCR6 …
Summary
The nature of dendritic cell(s) (DC[s]) that conditions efficient in vivo priming of CD8+ CTL after immunization via epithelial tissues remains largely unknown. Here, we show that myeloid DCs rapidly recruited by adjuvants into the buccal mucosa or skin are essential for CD8+ T cell crosspriming. Recruitment of circulating DC precursors, including Gr1+ monocytes, precedes the sequential accumulation of CD11c+ MHC class II+ DCs in dermis and epithelium via a CCR6/CCL20-dependent mechanism. Remarkably, a defect in CCR6, local neutralization of CCL20, or depletion of monocytes prevents in vivo priming of CD8+ CTL against an innocuous protein antigen administered with adjuvant. In addition, transfer of CCR6-sufficient Gr1+ monocytes restores CD8+ T cell priming in CCR6°/° mice via a direct Ag presentation mechanism. Thus, newly recruited DCs likely derived from circulating monocytes are responsible for efficient crosspriming of CD8+ CTL after mucosal or skin immunization.
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