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他克莫司通过直接刺激人外周血单核细胞系统抑制特应性皮炎相关细胞因子的产生。(与类固醇的比较)

Tacrolimus suppressed the production of cytokines involved in atopic dermatitis by direct stimulation of human PBMC system. (Comparison with steroids).

作者信息

Sakuma S, Higashi Y, Sato N, Sasakawa T, Sengoku T, Ohkubo Y, Amaya T, Goto T

机构信息

Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd. 1-6, Kashima 2-chome, Yodogawa, Osaka 532-8514, Japan.

出版信息

Int Immunopharmacol. 2001 Jun;1(6):1219-26. doi: 10.1016/s1567-5769(01)00059-5.

Abstract

Tacrolimus (FK506) ointment showed remarkable efficacy against atopic dermatitis in animal models and clinical trials. The suppressive effect of tacrolimus on the production of the cytokines involved in atopic dermatitis (IL-2, IL-3, IL-4, IL-5, IFN-gamma and GM-CSF) from human peripheral blood mononuclear cells (PBMC) was investigated. We constructed a new cytokine production system in which T cells are activated by direct stimulation in vitro with anti-CD3/CD2 or anti-CD3/CD28 antibody combination. Tacrolimus inhibited the production of these cytokines by both stimulations. In a comparative study with steroids (alclometasone dipropionate and betamethason valerate) in anti-CD3/CD2 system, tacrolimus and both steroids inhibited Th1 cytokines (IL-2, IFN-gamma), Th2 cytokines (IL-4, IL-5) and IL-3, GM-CSF (produced by both Th1 and Th2). The suppressive effect of tacrolimus on cytokine production was stronger than that of alclometasone dipropionate and equal to or stronger than that of betamethason valerate. The effective dose of tacrolimus (IC50, 0.02-0.11 ng/ml) is almost the same as for Th1 and Th2 cytokines, and 1 ng/ml of tacrolimus suppressed all cytokines completely. These results suggest that tacrolimus suppresses the allergic cytokines from T cells, and that tacrolimus ointment is effective against atopic dermatitis through the inhibition of cytokine production.

摘要

他克莫司(FK506)软膏在动物模型和临床试验中对特应性皮炎显示出显著疗效。研究了他克莫司对人外周血单个核细胞(PBMC)中参与特应性皮炎的细胞因子(IL-2、IL-3、IL-4、IL-5、IFN-γ和GM-CSF)产生的抑制作用。我们构建了一种新的细胞因子产生系统,其中T细胞通过用抗CD3/CD2或抗CD3/CD28抗体组合在体外直接刺激而被激活。他克莫司通过两种刺激均抑制这些细胞因子的产生。在抗CD3/CD2系统中与类固醇(二丙酸倍氯米松和戊酸倍他米松)的比较研究中,他克莫司和两种类固醇均抑制Th1细胞因子(IL-2、IFN-γ)、Th2细胞因子(IL-4、IL-5)以及IL-3、GM-CSF(由Th1和Th2产生)。他克莫司对细胞因子产生的抑制作用强于二丙酸倍氯米松,且等于或强于戊酸倍他米松。他克莫司的有效剂量(IC50,0.02 - 0.11 ng/ml)对Th1和Th2细胞因子几乎相同,1 ng/ml的他克莫司完全抑制所有细胞因子。这些结果表明他克莫司抑制T细胞产生的过敏性细胞因子,并表明他克莫司软膏通过抑制细胞因子产生对特应性皮炎有效。

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