Monocyte-derived dendritic cells promote T follicular helper cell differentiation

被引:74
|
作者
Chakarov, Svetoslav [1 ,2 ,3 ,4 ]
Fazilleau, Nicolas [1 ,2 ,3 ,4 ]
机构
[1] Ctr Physiopathol Toulouse Purpan, Toulouse, France
[2] Fac Med Toulouse, INSERM, U1043, F-31073 Toulouse, France
[3] CNRS, UMR5282, Toulouse, France
[4] Univ Toulouse 3, F-31062 Toulouse, France
关键词
adjuvant; antibody; dendritic cell; T lymphocyte; Toll-like receptor; IN-VIVO; SWITCH RECOMBINATION; MEDIATED-IMMUNITY; RECEPTOR; ADJUVANTS; ANTIGEN; RESPONSES; INDUCTION; ANTIBODY; BCL6;
D O I
10.1002/emmm.201403841
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To be effective, protein priming must induce the development of a distinct lineage of CD4(+) T cells named T follicular helper (Tfh) cells, which regulate the differentiation of high-affinity memory B cells and long-lived plasma cells. In this context, we tested how adjuvantation with CpG, the Toll-like receptor 9 agonist used in clinics, contributes to antigen-specific T-cell-dependent B-cell responses in vivo. We found that addition of CpG to other vaccine adjuvant increased the differentiation of antigen-specific Tfh cells without changing the overall magnitude of the T-cell response. This phenomenon correlated with an enhancement of the germinal centre reaction, antigen-specific plasma cells and circulating antibodies. We comprehensively demonstrated that, in addition to the classical Tfh-cell differentiation mediated by conventional DC, the promoting effect due to CpG was orchestrated in vivo by antigen presentation and IL-6 secreted by monocyte-derived dendritic cells (DC) as shown in their absence. Thus, while conventional DC initiate T-cell responses, targeting monocyte-derived DC specifically enhances the Tfh programme needed to regulate high-affinity B-cell protection in vivo.
引用
收藏
页码:590 / 603
页数:14
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