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白塞病患者中过度表达白细胞介素-17 和干扰素-γ 的 CD4+T 细胞。

Excessive CD4+ T cells co-expressing interleukin-17 and interferon-γ in patients with Behçet's disease.

机构信息

Department of Immunology and Medicine, St Marianna University School of Medicine, Sugao 2-16-1, Kawasaki, Japan.

出版信息

Clin Exp Immunol. 2012 Apr;168(1):68-74. doi: 10.1111/j.1365-2249.2011.04543.x.

Abstract

Excessive T helper type 1 (Th1) cell activity has been reported in Behçet's disease (BD). Recently, association of Th17 cells with certain autoimmune diseases was reported, and we thus investigated circulating Th17 cells in BD. CD4(+) CD45RO(-) (naive) T cells were cultured with Th0-, Th1-, Th2- and Th17-related cytokines and antibodies, and their mRNA was studied by real-time polymerase chain reaction (PCR). When naive CD4(+) T cells were cultured with Th1- and Th17-related cytokines, interferon (IFN)-γ mRNA and interleukin (IL)-17 mRNA were up-regulated, respectively, in BD patients. Naive CD4(+) T cells cultured in a Th17 cell-inducing condition expressed IL-23 receptor (IL-23R) mRNA excessively. IL-17 mRNA expression was induced only when naive CD4(+) T cells were cultured in the presence of IL-23. CD4(+) T cells cultured with Th17 cytokines expressed excessive RAR-related orphan receptor C (RORC) mRNA. Using intracellular cytokine staining, we found that CD45RO(+) (memory) CD4(+) T cells producing IL-17 and IFN-γ simultaneously were increased significantly. Memory CD4(+) T cells producing IFN-γ but not IL-17 decreased profoundly in BD patients. CD4(+) T cells producing IL-17 and IFN-γ simultaneously were found in BD skin lesions. Collectively, we found excessive CD4(+) T cells producing IL-17 and IFN-γ (Th1/Th17) cells in patients with BD, and possible involvement of IL-23/IL-23R pathway for the appearance of excessive Th1/Th17 cells.

摘要

辅助性 T 细胞 1(Th1)过度活跃已在贝赫切特病(BD)中被报道。最近,有报道称 Th17 细胞与某些自身免疫性疾病有关,因此我们研究了 BD 患者的循环 Th17 细胞。CD4+CD45RO-(幼稚)T 细胞用 Th0、Th1、Th2 和 Th17 相关细胞因子和抗体培养,并通过实时聚合酶链反应(PCR)研究其 mRNA。当幼稚 CD4+T 细胞用 Th1 和 Th17 相关细胞因子培养时,BD 患者的干扰素(IFN)-γ mRNA 和白细胞介素(IL)-17 mRNA 分别上调。在诱导 Th17 细胞的条件下培养的幼稚 CD4+T 细胞过度表达白细胞介素(IL)-23 受体(IL-23R)mRNA。只有当幼稚 CD4+T 细胞在 IL-23 的存在下培养时,才会诱导 IL-17 mRNA 的表达。用 Th17 细胞因子培养的 CD4+T 细胞表达过量的维 A 酸受体相关孤儿受体 C(RORC)mRNA。通过细胞内细胞因子染色,我们发现同时产生 IL-17 和 IFN-γ 的 CD45RO+(记忆)CD4+T 细胞显著增加。BD 患者中同时产生 IFN-γ但不产生 IL-17 的记忆 CD4+T 细胞显著减少。在 BD 皮肤病变中发现了同时产生 IL-17 和 IFN-γ 的 CD4+T 细胞。总之,我们发现 BD 患者中存在过度表达的同时产生 IL-17 和 IFN-γ 的 CD4+T 细胞(Th1/Th17),并且可能涉及 IL-23/IL-23R 途径来产生过多的 Th1/Th17 细胞。

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