淋巴毒素
CXCR5型
CXCL16型
CXCL13型
细胞生物学
滤泡树突状细胞
CCL21型
C-C趋化因子受体7型
CCL19型
XCL2型
淋巴毒素β受体
趋化因子受体
抗原提呈细胞
C-C趋化因子受体6型
淋巴结间质细胞
白细胞介素21
CCL17型
趋化因子受体
白细胞介素12
T细胞
细胞毒性T细胞
生物
免疫学
抗原
趋化因子
细胞因子
免疫系统
体外
生物化学
作者
Beatriz León,André Ballesteros‐Tato,Jeffrey L. Browning,Robert R. Dunn,Troy D. Randall,Frances E. Lund
摘要
In lymph nodes, cellular positioning can dictate the immune response. Lund and colleagues show that nematode infection triggers interactions between lymphotoxin-producing B cells and CXCR5+ dendritic cells and CD4+ T cells to initiate T helper type 2 responses. 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 (TH2 cells), which suggests that TH2 differentiation can initiate outside the T cell zone.
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