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狼疮性肾炎中的Th亚群平衡。

Th subset balance in lupus nephritis.

作者信息

Miyake Katsuhisa, Akahoshi Mitsuteru, Nakashima Hitoshi

机构信息

Division of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, Fukuoka 814-0180, Japan.

出版信息

J Biomed Biotechnol. 2011;2011:980286. doi: 10.1155/2011/980286. Epub 2011 Aug 28.

Abstract

Lupus nephritis, which has various histological patterns and variable clinical outcomes, is one of the most important complications of systemic lupus nephritis (SLE). This pathogenetic mechanism in each histologically different type of lupus nephritis (LN) remains unclear. Although SLE is suggested to be a Th2-driven disease, elevation of both Th1 and Th2 cytokines occurs in both humans and mice, suggesting that SLE is a complex disease driven by different lymphocyte subsets with high heterogeneity of clinical manifestations and organ involvement. Recent findings in LN elucidate an essential role for the Th1, IL-17 producing T cells and Th17 cells in the development of diffuse proliferative lupus nephritis (DPLN), and Th2 cytokine in that of membranous lupus nephritis (MLN). These data support the hypothesis that individual Th1/Th2 balance is one of the critical determinants for histopathology of LN.

摘要

狼疮性肾炎具有多种组织学类型和不同的临床结局,是系统性红斑狼疮(SLE)最重要的并发症之一。每种组织学不同类型的狼疮性肾炎(LN)的发病机制仍不清楚。虽然SLE被认为是一种由Th2驱动的疾病,但在人类和小鼠中Th1和Th2细胞因子均会升高,这表明SLE是一种由不同淋巴细胞亚群驱动的复杂疾病,具有临床表现和器官受累的高度异质性。LN的最新研究结果阐明了Th1、产生IL-17的T细胞和Th17细胞在弥漫性增殖性狼疮性肾炎(DPLN)发展中的重要作用,以及Th2细胞因子在膜性狼疮性肾炎(MLN)发展中的作用。这些数据支持了个体Th1/Th2平衡是LN组织病理学关键决定因素之一的假说。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cc8/3163408/dcb1171fa310/JBB2011-980286.001.jpg

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