Plasmacytoid dendritic cells, antigen, and CpG-C license human B cells for plasma cell differentiation and immunoglobulin production in the absence of T-cell help

H Poeck, M Wagner, J Battiany, S Rothenfusser… - Blood, 2004 - ashpublications.org
H Poeck, M Wagner, J Battiany, S Rothenfusser, D Wellisch, V Hornung, B Jahrsdorfer
Blood, 2004ashpublications.org
It has been reported that interferon α (IFN-α) enhances humoral immunity and that dendritic
cells of the myeloid lineage promote B-cell differentiation. Here we studied whether the
plasmacytoid dendritic cell (PDC), a subset of dendritic cells specialized for the production of
IFN-α, is involved in regulating B-cell differentiation and immunoglobulin production. The
recently identified class of CpG oligonucleotides (CpG-C) was used to activate both B cells
and PDCs via Toll-like receptor 9 (TLR9). The presence of PDCs synergistically enhanced …
Abstract
It has been reported that interferon α (IFN-α) enhances humoral immunity and that dendritic cells of the myeloid lineage promote B-cell differentiation. Here we studied whether the plasmacytoid dendritic cell (PDC), a subset of dendritic cells specialized for the production of IFN-α, is involved in regulating B-cell differentiation and immunoglobulin production. The recently identified class of CpG oligonucleotides (CpG-C) was used to activate both B cells and PDCs via Toll-like receptor 9 (TLR9). The presence of PDCs synergistically enhanced CD86 expression, cytokine production (interleukin 6 [IL-6], tumor necrosis factor α, and IL-10) and plasma cell differentiation of isolated human peripheral blood B cells stimulated through CpG-C and B-cell antigen receptor (BCR) ligation. This stimulation protocol was sufficient to drive purified naive B cells into IgM-producing plasma cells and to trigger IgG synthesis in memory B cells. PDCs contributed to B-cell activation via IFN-α secretion. Up-regulation of TLR9 on B cells was not involved. These results demonstrate that CpG-stimulated PDCs induce plasma cell differentiation in naive and memory B cells in the absence of T-cell help, providing an explanation for the excellent activity of CpG oligonucleotides as a humoral vaccine adjuvant. (Blood. 2004;103:3058-3064)
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