European Journal of Immunology · 2014 · 60 citations · 46 references
Life SciencesCell BiologyImmunologyCellular ImmunologyVaccine ImmunologyVaccinologyB Cell ActivationB-cell ResponsesGerminal Center ReactionsHumoral ImmunityImmune Response To VaccinationMacrophage BiologyB Cell Response InductionB Cell Response To VaccinationB Cell-mediated ImmunityB-cell Mediated ImmunityFollicular Helper T CellsGerminal Center BiologyVaccination-induced Germinal Center ResponsesWhite Pulp Of Spleen
Ag delivery to specific APCs is an attractive approach in developing strategies for vaccination. CD169(+) macrophages in the marginal zone of the spleen represent a suitable target for delivery of Ag because of their strategic location, which is optimal for the capture of blood-borne Ag and their close proximity to B cells and T cells in the white pulp. Here we show that Ag targeting to CD169(+) macrophages in mice resulted in strong, isotype-switched, high-affinity Ab production and the preferential induction and long-term persistence of Ag-specific GC B cells and follicular Th cells. In agreement with these observations, CD169(+) macrophages retained intact Ag, induced cognate activation of B cells, and increased expression of costimulatory molecules upon activation. In addition, macrophages were required for the production of cytokines that promote B-cell responses. Our results identify CD169(+) macrophages as promoters of high-affinity humoral immune responses and emphasize the value of CD169 as target for Ag delivery to improve vaccine responses.
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