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夫西地酸,一种功能类似于环孢素A的免疫抑制药物。

Fusidic acid, an immunosuppressive drug with functions similar to cyclosporin A.

作者信息

Bendtzen K, Diamant M, Faber V

机构信息

Department of Medicine TTA, Rigshospitalet University Hospital, Copenhagen, Denmark.

出版信息

Cytokine. 1990 Nov;2(6):423-9. doi: 10.1016/1043-4666(90)90051-t.

Abstract

Fusidic acid, a tetracyclic triterpenoic acid, is used for local and systemic treatment of bacterial infections. Its in vitro effects on the human immune response were tested. Activated blood mononuclear cells released lower levels of interleukin (IL) 1 in the presence of nontoxic and clinically attainable levels of fuscidic acid (15 to 50 micrograms/mL). In contrast, the drug failed to affect the production of two other monocyte-derived cytokines, tumor necrosis factor (TNF)-alpha and IL 6. The production of the T-cell-derived cytokines, IL 2 and interferon-gamma (IFN-gamma), were also suppressed (IC50: 5 to 15 micrograms/mL). The early costimulatory effects of IL 1 and IL 6 on mouse thymocytes and human T cells were suppressed by similar levels of the drug, as was the hybridoma growth-promoting function of IL 6. T-cell proliferation induced by phytohemagglutinin or allogeneic cells was reversibly inhibited (IC50: 15 micrograms/mL). These functions of fusidic acid were strikingly similar to those of cyclosporin A. Because of the low toxicity of the former, it may have a role as a clinically useful suppressor of immunoinflammatory processes.

摘要

夫西地酸是一种四环三萜酸,用于局部和全身细菌感染的治疗。测试了其对人体免疫反应的体外作用。在无毒且临床可达到水平的夫西地酸(15至50微克/毫升)存在下,活化的血液单核细胞释放的白细胞介素(IL)-1水平较低。相比之下,该药物未能影响另外两种单核细胞衍生细胞因子肿瘤坏死因子(TNF)-α和IL-6的产生。T细胞衍生细胞因子IL-2和干扰素-γ(IFN-γ)的产生也受到抑制(半数抑制浓度:5至15微克/毫升)。类似水平的该药物抑制了IL-1和IL-6对小鼠胸腺细胞和人T细胞的早期共刺激作用,以及IL-6的杂交瘤生长促进功能。由植物血凝素或同种异体细胞诱导的T细胞增殖受到可逆抑制(半数抑制浓度:15微克/毫升)。夫西地酸的这些作用与环孢素A的作用惊人地相似。由于前者毒性较低,它可能作为免疫炎症过程的临床有用抑制剂发挥作用。

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