霍乱毒素
趋化因子
CD40
CD86
CD80
T细胞
CCL19型
细胞生物学
细胞因子
化学
生物
分子生物学
炎症
免疫学
细胞毒性T细胞
免疫系统
微生物学
趋化因子受体
体外
生物化学
作者
Ed C. Lavelle,Edel A. McNeela,Michelle E. Armstrong,Olive Leavy,Sarah Higgins,Kingston H. G. Mills
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2003-09-01
卷期号:171 (5): 2384-2392
被引量:149
标识
DOI:10.4049/jimmunol.171.5.2384
摘要
Abstract It has previously been reported that cholera toxin (CT) is a potent mucosal adjuvant that enhances Th2 or mixed Th1/Th2 type responses to coadministered foreign Ag. Here we demonstrate that CT also promotes the generation of regulatory T (Tr) cells against bystander Ag. Parenteral immunization of mice with Ag in the presence of CT induced T cells that secreted high levels of IL-4 and IL-10 and lower levels of IL-5 and IFN-γ. Ag-specific CD4+ T cell lines and clones generated from these mice had cytokine profiles characteristic of Th2 or type 1 Tr cells, and these T cells suppressed IFN-γ production by Th1 cells. Furthermore, adoptive transfer of bone marrow-derived dendritic cells (DC) incubated with Ag and CT induced T cells that secreted IL-4 and IL-10 and low concentrations of IL-5. It has previously been shown that IL-10 promotes the differentiation or expansion of type 1 Tr cells. Here we found that CT synergized with low doses of LPS to induce IL-10 production by immature DC. CT also enhanced the expression of CD80, CD86, and OX40 (CD134) on DC and induced the secretion of the chemokine, macrophage inflammatory protein-2 (MIP-2), but inhibited LPS-driven induction of CD40 and ICAM-I expression and production of the inflammatory cytokines/chemokines IL-12, TNF-α, MIP-1α, MIP-1β, and monocyte chemoattractant protein-1. Our findings suggest that CT induces maturation of DC, but, by inducing IL-10, inhibiting IL-12, and selectively affecting surface marker expression, suppresses the generation of Th1 cells and promotes the induction of T cells with regulatory activity.
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