Lavelle Ed C, McNeela Edel, Armstrong Michelle E, Leavy Olive, Higgins Sarah C, Mills Kingston H G
Immune Regulation Research Group, Department of Biochemistry, Trinity College, Dublin 2, Ireland.
J Immunol. 2003 Sep 1;171(5):2384-92. doi: 10.4049/jimmunol.171.5.2384.
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-gamma. 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-gamma 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-alpha, MIP-1alpha, MIP-1beta, 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.
先前已有报道称霍乱毒素(CT)是一种有效的黏膜佐剂,可增强对共同给予的外源抗原的Th2或Th1/Th2混合型反应。在此我们证明,CT还能促进针对旁观者抗原的调节性T(Tr)细胞的产生。在CT存在的情况下,用抗原对小鼠进行肠胃外免疫诱导产生了分泌高水平IL-4和IL-10以及低水平IL-5和IFN-γ的T细胞。从这些小鼠产生的抗原特异性CD4(+) T细胞系和克隆具有Th2或1型Tr细胞的细胞因子特征,并且这些T细胞抑制Th1细胞产生IFN-γ。此外,用抗原和CT孵育的骨髓来源的树突状细胞(DC)进行过继转移诱导产生了分泌IL-4和IL-10以及低浓度IL-5的T细胞。先前已表明IL-10可促进1型Tr细胞的分化或扩增。在此我们发现,CT与低剂量LPS协同作用可诱导未成熟DC产生IL-10。CT还增强了DC上CD80、CD86和OX40(CD134)的表达,并诱导趋化因子巨噬细胞炎性蛋白-2(MIP-2)的分泌,但抑制LPS驱动的CD40和ICAM-1表达以及炎性细胞因子/趋化因子IL-12、TNF-α、MIP-1α、MIP-1β和单核细胞趋化蛋白-1的产生。我们的研究结果表明,CT诱导DC成熟,但通过诱导IL-10、抑制IL-12以及选择性地影响表面标志物表达,抑制Th1细胞的产生并促进具有调节活性的T细胞的诱导。