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抗疟治疗与系统性红斑狼疮中血栓形成、高胆固醇血症及细胞因子的相关性。

The relevance of antimalarial therapy with regard to thrombosis, hypercholesterolemia and cytokines in SLE.

作者信息

Wallace D J, Linker-Israeli M, Metzger A L, Stecher V J

机构信息

Cedars-Sinai Medical Center, Los Angeles.

出版信息

Lupus. 1993 Feb;2 Suppl 1:S13-5.

PMID:8485565
Abstract

Hydroxychloroquine has several less well-known actions that may have clinical relevance in treating systemic lupus erythematosus (SLE). (1) Hydroxychloroquine has a possible anti-thrombotic action. It is a platelet inhibitor and appears to decrease the risk of thromboembolism in patients with anticardiolipin antibodies. (2) Hydroxychloroquine is associated with lower serum cholesterol and low-density lipoprotein levels compared to those present in patients who are taking corticosteroids but not antimalarials for SLE. (3) It may also decrease abnormal levels of cytokines. Interleukin-6 (IL-6), soluble CD8 and soluble IL-2 receptors (sIL-2R) are lower in patients taking antimalarials compared to those on corticosteroids alone or on neither medication. Serum levels of CD8 and sIL-2R decrease after 6 weeks of hydroxychloroquine treatment. These findings may help explain the favorable response of SLE patients treated with antimalarials.

摘要

羟氯喹具有几种不太为人所知的作用,这些作用可能在治疗系统性红斑狼疮(SLE)方面具有临床意义。(1)羟氯喹可能具有抗血栓形成作用。它是一种血小板抑制剂,似乎能降低抗心磷脂抗体患者发生血栓栓塞的风险。(2)与使用皮质类固醇而非抗疟药治疗SLE的患者相比,羟氯喹与较低的血清胆固醇和低密度脂蛋白水平相关。(3)它还可能降低细胞因子的异常水平。与单独使用皮质类固醇或未使用任何药物的患者相比,服用抗疟药的患者白细胞介素-6(IL-6)、可溶性CD8和可溶性IL-2受体(sIL-2R)水平较低。羟氯喹治疗6周后,血清CD8和sIL-2R水平下降。这些发现可能有助于解释接受抗疟药治疗的SLE患者的良好反应。

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