Regulation of TH2 development by CXCR5+ dendritic cells and lymphotoxin-expressing B cells

被引:173
作者
Leon, Beatriz [1 ]
Ballesteros-Tato, Andre [1 ]
Browning, Jeffrey L. [2 ]
Dunn, Robert [3 ]
Randall, Troy D. [1 ]
Lund, Frances E. [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Med, Div Allergy Immunol & Rheumatol, Rochester, NY 14642 USA
[2] Biogen Idec Inc, Cambridge, MA USA
[3] Biogen Idec Inc, San Diego, CA USA
基金
美国国家卫生研究院;
关键词
MICE LACKING EXPRESSION; FOLLICULAR HELPER-CELLS; TUMOR-NECROSIS-FACTOR; CD4; T-CELLS; IN-VIVO; LYMPHOID ORGANS; IMMUNE-RESPONSES; CHEMOKINE RECEPTOR; DEPENDENT FASHION; INDUCED ARTHRITIS;
D O I
10.1038/ni.2309
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although cognate encounters between antigen-bearing dendritic cells (DCs) that express the chemokine receptor CCR7 and CCR7(+) naive T cells take place in the T cell zone of lymph nodes, it is unknown whether the colocalization of DCs and T cells in the T cell area is required for the generation of effector cells. Here we found that after infection with an intestinal nematode, antigen-bearing DCs and CD4(+) T cells upregulated the chemokine receptor CXCR5 and localized together outside the T cell zone by a mechanism dependent on the chemokine CXCL13, B cells and lymphotoxin. Notably, lymphotoxin-expressing B cells, CXCR5-expressing DCs and T cells, and CXCL13 were also necessary for development of interleukin 4 (IL-4)-producing type 2 helper T cells (T(H)2 cells), which suggests that T(H)2 differentiation can initiate outside the T cell zone.
引用
收藏
页码:681 / +
页数:11
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