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首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Decreased 4-1BB expression on CD4+CD25 high regulatory T cells in peripheral blood of patients with multiple sclerosis.
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Decreased 4-1BB expression on CD4+CD25 high regulatory T cells in peripheral blood of patients with multiple sclerosis.

机译:多发性硬化症患者外周血CD4 + CD25高调节性T细胞上4-1BB表达降低。

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摘要

As a tumour necrosis factor receptor superfamily member, 4-1BB (CD137) is preferentially expressed in CD4+CD25+ regulatory T cells (Tregs) and has been suggested to play an important role in regulating the generation or function of Tregs. Recent studies of human Tregs have shown that blood CD4+CD25(high) T cells were much closer to Tregs in terms of their functionality. Furthermore, CD4+CD25(high) Tregs have been found to have a decreased effector function in patients with multiple sclerosis (MS). In this study, we examined the expression of 4-1BB and soluble 4-1BB (s4-1BB) protein levels in the peripheral blood of MS patients. Compared with healthy controls, MS patients had decreased 4-1BB expression in their CD4+C25(high) Tregs and increased plasma s4-1BB protein levels. Moreover, the plasma s4-1BB levels of MS patients were shown to be inversely correlated with the 4-1BB surface expression of CD4+CD25(high) Tregs. The down-regulated 4-1BB expression on CD4+CD25(high) Tregs of MS patients may be involved in the impaired immunoactivity of these Tregs. The elevated s4-1BB levels may, at least in part, function as a self-regulatory attempt to inhibit antigen-driven proliferation of Tregs or their immunosuppressive activity.
机译:4-1BB(CD137)作为肿瘤坏死因子受体超家族成员,优先在CD4 + CD25 +调节性T细胞(Tregs)中表达,并被认为在调节Tregs的产生或功能中起重要作用。关于人类Treg的最新研究表明,血液CD4 + CD25(high)T细胞在功能上更接近Treg。此外,已发现多发性硬化症(MS)患者的CD4 + CD25(高)Treg的效应子功能降低。在这项研究中,我们检查了MS患者外周血中4-1BB和可溶性4-1BB(s4-1BB)蛋白的表达。与健康对照相比,MS患者的CD4 + C25(高)Tregs中的4-1BB表达降低,血浆s4-1BB蛋白水平升高。此外,MS患者的血浆s4-1BB水平与CD4 + CD25(高)Tregs的4-1BB表面表达呈负相关。 MS患者CD4 + CD25(高)Treg上的4-1BB表达下调可能与这些Treg的免疫活性受损有关。升高的s4-1BB水平可以至少部分用作抑制Tregs的抗原驱动的增殖或其免疫抑制活性的自我调节尝试。

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