y- 18251(3-对氯苯基)噻唑[3,2-a]苯并咪唑- 2-乙酸)、左旋咪唑和吲哚美辛对体外小鼠T抑制细胞生成的影响。

C M Rogers, T J Rogers, S C Gilman
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引用次数: 9

摘要

体外培养带有葡萄球菌肠毒素B (SEB)的正常BALB/c脾细胞可以激活抗原非特异性抑制T细胞(Ts),这可以通过它们抑制抗体产生的能力在斑块试验中进行检测。实验免疫调节药物wy - 18251(10-100微米)添加到脾细胞和SEB的培养物中,与不添加药物的培养物相比,Ts活性显著增加。左旋咪唑也获得了类似的结果,但相反,吲哚美辛(0.1-10微米)抑制了seb诱导的抑制细胞活性。y- 18251增强Ts活性的能力可能在治疗那些自身免疫性疾病(如类风湿关节炎和系统性红斑狼疮)方面有用,其中过度活跃的B细胞功能是一个特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Wy-18,251 (3-p-chlorophenyl)thiazolo[3,2-a]benzimidazole- 2-acetic acid), levamisole and indomethacin on the generation of murine T suppressor cells in vitro.

In vitro culture of normal BALB/c spleen cells with staphylococcal enterotoxin B (SEB) activates antigen non-specific suppressor T cells (Ts) which can be assayed by their ability to suppress antibody production in a plaque assay. Addition of the experimental immunomodulatory drug Wy-18,251 (10-100 microM) to cultures of spleen cells plus SEB significantly increased Ts activity relative to cultures without the drug. Similar results were obtained with levamisole, but, in contrast, indomethacin (0.1-10 microM) inhibited SEB-induced suppressor cell activity. The ability of Wy-18,251 to augment Ts activity could be therapeutically useful in the treatment of those autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus, in which hyperactive B cell function is a characteristic feature.

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