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白细胞介素-4和白细胞介素-10可减轻小鼠已形成的新月体性肾小球肾炎。

Interleukin-4 and interleukin-10 attenuate established crescentic glomerulonephritis in mice.

作者信息

Kitching A R, Tipping P G, Huang X R, Mutch D A, Holdsworth S R

机构信息

Monash University, Department of Medicine, Monash Medical Centre, Clayton, Victoria, Australia.

出版信息

Kidney Int. 1997 Jul;52(1):52-9. doi: 10.1038/ki.1997.303.

Abstract

Crescentic glomerulonephritis (GN) has immunopathological features of delayed type hypersensitivity (DTH) and results from a T helper cell 1 (Th1) dependent immune response. The current study examined the capacity of Th2 cytokines, interleukin (IL)-4 and IL-10, to alter the outcome of crescentic GN, after injury is established. Sensitized, control treated mice developed crescentic GN with functional renal injury (117 +/- 20 microliters/min, normal mouse 182 +/- 8 microliters/min, P < 0.05) 10 days after an i.v. dose of sheep anti-mouse glomerular basement membrane globulin. Combined treatment with IL-4 and IL-10 starting three days after initiation of disease significantly reduced glomerular crescent formation (5.3 +/- 3.2%, control treatment 23.3 +/- 6.4%, P < 0.02) and preserved renal function (165 +/- 15 microliters/min, P = 0.57 compared to normal mice). Treatment with IL-4 alone did not reduce crescent formation or protect renal function. Mice treated with IL-10 showed trends to decreased crescent formation and preservation of renal function. In all cytokine treated groups, the accumulation of effectors of glomerular injury (CD4+ positive T cells, macrophages and fibrin) was reduced, with the combination treatment having the greatest effect. Administration of Th2 cytokines, IL-4 and IL-10 to mice with established GN attenuates the development of glomerular crescent formation and protects renal function.

摘要

新月体性肾小球肾炎(GN)具有迟发型超敏反应(DTH)的免疫病理特征,由辅助性T细胞1(Th1)依赖性免疫反应引起。本研究在损伤确立后,检测了辅助性T细胞2(Th2)细胞因子白细胞介素(IL)-4和IL-10改变新月体性GN结局的能力。致敏的对照处理小鼠在静脉注射羊抗小鼠肾小球基底膜球蛋白剂量后10天出现伴有功能性肾损伤的新月体性GN(117±20微升/分钟,正常小鼠为182±8微升/分钟,P<0.05)。在疾病开始三天后开始联合使用IL-4和IL-10治疗,显著减少了肾小球新月体形成(5.3±3.2%,对照处理为23.3±6.4%,P<0.02)并保留了肾功能(165±15微升/分钟,与正常小鼠相比P=0.57)。单独使用IL-4治疗并未减少新月体形成或保护肾功能。用IL-10治疗的小鼠显示出新月体形成减少和肾功能保留的趋势。在所有细胞因子治疗组中,肾小球损伤效应细胞(CD4+阳性T细胞、巨噬细胞和纤维蛋白)的积聚减少,联合治疗效果最佳。给已确立GN的小鼠施用Th2细胞因子IL-4和IL-10可减轻肾小球新月体形成的发展并保护肾功能。

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