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利用小鼠慢性移植物抗宿主(CGVH)病(一种系统性红斑狼疮(SLE)模型)进行药物研发。

The use of the murine chronic graft vs host (CGVH) disease, a model for systemic lupus erythematosus (SLE), for drug discovery.

作者信息

Popovic S, Bartlett R R

机构信息

Department of Microbiology, Technische Hochschule Darmstadt, West Germany.

出版信息

Agents Actions. 1987 Aug;21(3-4):284-6. doi: 10.1007/BF01966492.

Abstract

Studies were conducted to evaluate the use of a murine SLE-like disease for the discovery of novel drugs: This disease is the result of a chronic form of a graft vs host (GVH) reaction. Using prednisolone (Pr), cyclophosphamide (Cy), indomethacin (Indo), and the isoxazol derivative, HWA 486, we found that only Indo was ineffective in inhibiting the SLE symptoms. Interestingly, HWA 486, which did not display any immunosuppressive activity, restored the suppressed T-cell response to the same level as found in healthy mice. We feel that this murine model of SLE could be of value for discovering substances with novel antirheumatic, and/or immunomodulating activities.

摘要

开展了多项研究以评估利用一种小鼠类系统性红斑狼疮疾病来发现新型药物

这种疾病是慢性移植物抗宿主(GVH)反应的结果。使用泼尼松龙(Pr)、环磷酰胺(Cy)、吲哚美辛(Indo)和异恶唑衍生物HWA 486,我们发现只有吲哚美辛在抑制系统性红斑狼疮症状方面无效。有趣的是,不具有任何免疫抑制活性的HWA 486将受抑制的T细胞反应恢复到了与健康小鼠相同的水平。我们认为这种小鼠系统性红斑狼疮模型对于发现具有新型抗风湿和/或免疫调节活性的物质可能具有价值。

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