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首页> 外文期刊>Immunology: An Official Journal of the British Society for Immunology >Critical role of M. tuberculosis for dendritic cell maturation to induce collagen-induced arthritis in H-2b background of C57BL/6 mice.
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Critical role of M. tuberculosis for dendritic cell maturation to induce collagen-induced arthritis in H-2b background of C57BL/6 mice.

机译:结核分枝杆菌对树突状细胞成熟在C57BL / 6小鼠的H-2b背景中诱导胶原诱导的关节炎的关键作用。

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摘要

Collagen-induced arthritis (CIA) can be induced even in CIA-resistant H-2(b) background of C57BL/6 mice when these mice are immunized with type II collagen (CII) emulsified in complete Freund's adjuvant (CFA) containing high, but not low, dose of Mycobacterium tuberculosis. Here, we investigated the pathogenesis of CIA in C57BL/6 mice induced by the immunizing protocol. We examined expressions of cytokines, costimulatory molecules and major histocompatibility complex (MHC) class II in draining lymph nodes (DLN) in CIA-induced C57BL/6 mice by quantitative reverse transcription-polymerase chain reaction. We also examined an effect of M. tuberculosis on the expression of these molecules on dendritic cells (DC) in vitro by flow cytometry. We finally examined an effect of M. tuberculosis in CFA used for immunization with CII antigen on priming of CD4+ helper T cells specific to CII in DLN of CIA-induced C57BL/6 mice. The expression of interferon-gamma (IFN-gamma), Interleukin-12p40 (IL-12p40), costimulatory molecules CD40, CD80 and CD86 and MHC class II were up-regulated in DLN of CIA-induced C57BL/6 mice. Expressions of these costimulatory molecules were also up-regulated on DC after stimulation with high, but not low, dose of M. tuberculosis in vitro. Furthermore, priming of CD4+ helper T cells specific to CII antigen in DLN required immunization with CII using CFA containing high, but not low, dose of M. tuberculosis. These results suggested that high dose of M. tuberculosis were required for maturation of DC enough to prime CD4+ helper T cells specific to CII antigen in DLN of H-2b background of C57BL/6 mice.
机译:当这些小鼠用在含有高,低,高,低,高,低,高的弗氏佐剂(FFA)但剂量不低的结核分枝杆菌。在这里,我们调查了由免疫方案诱导的C57BL / 6小鼠中CIA的发病机制。我们通过定量逆转录-聚合酶链反应检查了CIA诱导的C57BL / 6小鼠的引流淋巴结(DLN)中细胞因子,共刺激分子和主要组织相容性复合体(MHC)II类的表达。我们还通过流式细胞术检查了结核分枝杆菌对树突状细胞(DC)上这些分子表达的影响。我们最终检查了用于CII抗原免疫的CFA中的结核分枝杆菌对CIA诱导的C57BL / 6小鼠DLN中CDII +特异于CII的CD4 +辅助性T细胞的启动作用。在CIA诱导的C57BL / 6小鼠的DLN中,干扰素-γ(IFN-γ),白介素12p40(IL-12p40),共刺激分子CD40,CD80和CD86和II类MHC的表达上调。在体外用高剂量但非低剂量的结核分枝杆菌刺激后,这些共刺激分子的表达在DC上也被上调。此外,DLN中CII抗原特异的CD4 +辅助性T细胞的引发需要使用含有高剂量但不低剂量结核分枝杆菌的CFA用CII免疫。这些结果表明,DC的成熟需要高剂量的结核分枝杆菌,以引发C57BL / 6小鼠H-2b背景的DLN中CII抗原特异的CD4 +辅助T细胞。

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