首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >5R)-5-hydroxytriptolide (LLDT-8), a novel triptolide derivative, prevents experimental autoimmune encephalomyelitis via inhibiting T cell activation.
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5R)-5-hydroxytriptolide (LLDT-8), a novel triptolide derivative, prevents experimental autoimmune encephalomyelitis via inhibiting T cell activation.

机译:5R)-5-羟基雷公藤内酯(LLDT-8)是一种新颖的雷公藤内酯衍生物,可通过抑制T细胞活化来预防实验性自身免疫性脑脊髓炎。

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A novel triptolide derivative (5R)-5-hydroxytriptolide (LLDT-8) has been shown to have potent immunosuppressive activities. Here LLDT-8 was evaluated in experimental autoimmune encephalomyelitis (EAE), the model of multiple sclerosis (MS). LLDT-8 reduced the incidence and severity of EAE, which was associated with the inhibition of the MOG 35-55 lymphocyte recall response, anti-MOG 35-55 T cell responses, interleukin (IL)-2 and interferon (IFN)-gamma production. In vitro, LLDT-8 inhibited primary T cells proliferation, division, IL-2 and IFN-gamma production stimulated with anti-CD3/28. These findings highlight the fact that LLDT-8 prevents EAE by suppressing T cell proliferation and activation, with a potential for treatment of MS.
机译:一种新型雷公藤内酯衍生物(5R)-5-羟基雷公藤内酯(LLDT-8)已显示具有有效的免疫抑制活性。在这里,LLDT-8在实验性自身免疫性脑脊髓炎(EAE)(多发性硬化症(MS)模型)中进行了评估。 LLDT-8降低了EAE的发生率和严重程度,这与抑制MOG 35-55淋巴细胞召回反应,抗MOG 35-55 T细胞反应,白介素(IL)-2和干扰素(IFN)-γ有关生产。在体外,LLDT-8抑制了抗CD3 / 28刺激的原代T细胞增殖,分裂,IL-2和IFN-γ的产生。这些发现凸显了LLDT-8通过抑制T细胞增殖和活化来预防EAE的事实,具有治疗MS的潜力。

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