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促红细胞生成素治疗可改善 MRL/lpr 狼疮肾炎。

Erythropoietin Treatment Ameliorates Lupus Nephritis of MRL/lpr Mice.

机构信息

Department of Rheumatology, Shengjing Hospital of China Medical University, No. 36 Sanhao Street, Heping District, Shenyang, 110004, Liaoning Province, China.

出版信息

Inflammation. 2018 Oct;41(5):1888-1899. doi: 10.1007/s10753-018-0832-5.

Abstract

An increasing body of data has shown that erythropoietin (EPO) plays multiple roles in inflammation control and immunoregulation. However, less attention has been given to its effects on lupus nephritis (LN). In this study, we investigated the therapeutic effects of EPO on LN in MRL/lpr mice, a well-studied animal model for lupus. MRL/lpr mice were randomly divided into an EPO and control group. Mice in the EPO group were treated with EPO; saline was given to the control group. Both groups were treated for 10 weeks. We analyzed the differences of general disease condition, histopathologic changes, Th lymphocytes subsets, and the expression of inflammatory factors of mice between the groups. Compared to the control group, mice in the EPO group showed less spleen hyperplasia, less urinary protein, and lower serum anti-dsDNA antibody; they also had lower renal histopathologic scores and less deposition of IgG/C3 within glomeruli. Moreover, Th1 and Th17 levels were decreased, while Th2 and Treg levels were increased in the spleen, and the expression of inflammatory cytokines decreased in both the spleen and kidneys. EPO increased Th2 and Treg lymphocytes, decreased Th1, Th17 lymphocytes in the spleen, and inhibited the inflammatory reactions in both the spleen and kidneys, thus ameliorating LN of MRL/lpr mice.

摘要

越来越多的证据表明,促红细胞生成素(EPO)在炎症控制和免疫调节中发挥多种作用。然而,人们对其在狼疮肾炎(LN)中的作用关注较少。在这项研究中,我们研究了 EPO 对 MRL/lpr 小鼠 LN 的治疗作用,MRL/lpr 小鼠是一种研究较为深入的狼疮动物模型。MRL/lpr 小鼠被随机分为 EPO 组和对照组。EPO 组小鼠接受 EPO 治疗;对照组给予生理盐水。两组均治疗 10 周。我们分析了两组小鼠的一般疾病状况、组织病理学变化、Th 淋巴细胞亚群以及炎症因子表达的差异。与对照组相比,EPO 组小鼠脾脏增生程度较轻,尿蛋白较少,血清抗 dsDNA 抗体水平较低;肾组织病理学评分较低,肾小球内 IgG/C3 沉积较少。此外,EPO 组小鼠脾脏中 Th1 和 Th17 水平降低,Th2 和 Treg 水平升高,脾脏和肾脏中炎症细胞因子的表达降低。EPO 增加了 Th2 和 Treg 淋巴细胞,减少了脾脏中的 Th1、Th17 淋巴细胞,并抑制了脾脏和肾脏的炎症反应,从而改善了 MRL/lpr 小鼠的 LN。

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