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约翰霍普金斯大学的肾缺血再灌注损伤免疫研究。

Immunologic research in kidney ischemia/reperfusion injury at Johns Hopkins University.

机构信息

Division of Nephrology, Department of Medicine, Johns Hopkins University School of Medicine, Ross 965, Baltimore, MD 21205, USA.

出版信息

Immunol Res. 2010 Jul;47(1-3):78-85. doi: 10.1007/s12026-009-8140-7.

DOI:10.1007/s12026-009-8140-7
PMID:20082154
Abstract

Kidney ischemia/reperfusion injury (IRI) is a common and serious problem in hospitalized patients. Immune cell trafficking and leukocyte-endothelial adhesion potentiate kidney IRI. An important immunomodulatory role of T lymphocytes has been elucidated in IRI. Regulatory T cells are a lymphocyte subset that has recently been demonstrated to perform a protective role both in early injury from IRI as well as in later repair. The immune system also participates in distant organ effects during kidney IRI. Studies focusing on immune aspects of kidney IRI have enabled the discovery of promising novel therapeutic and diagnostic approaches.

摘要

肾缺血/再灌注损伤(IRI)是住院患者中常见且严重的问题。免疫细胞迁移和白细胞-内皮细胞黏附加剧了肾 IRI。T 淋巴细胞在 IRI 中具有重要的免疫调节作用,这一点已得到阐明。调节性 T 细胞是一种淋巴细胞亚群,最近的研究表明,它在 IRI 的早期损伤以及后期修复中均发挥保护作用。免疫系统在肾 IRI 期间还参与远处器官的效应。关注肾 IRI 免疫方面的研究使人们发现了有前途的新型治疗和诊断方法。

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本文引用的文献

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Foxp3+ regulatory T cells participate in repair of ischemic acute kidney injury.Foxp3 + 调节性T细胞参与缺血性急性肾损伤的修复。
Kidney Int. 2009 Oct;76(7):717-29. doi: 10.1038/ki.2009.259. Epub 2009 Jul 22.
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The role for T cell repertoire/antigen-specific interactions in experimental kidney ischemia reperfusion injury.T细胞库/抗原特异性相互作用在实验性肾缺血再灌注损伤中的作用。
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Regulatory T cells suppress innate immunity in kidney ischemia-reperfusion injury.
甘露糖结合凝集素参与饮食限制对肾缺血/再灌注损伤的保护作用。
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Expression of p53 and p21(WAF-1), apoptosis, and proliferation of smooth muscle cells in normal myometrium during the menstrual cycle: implication of DNA damage and repair for leiomyoma development.月经周期中正常子宫肌层平滑肌细胞的p53和p21(WAF-1)表达、凋亡及增殖:DNA损伤与修复对平滑肌瘤发生发展的意义
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调节性T细胞在肾脏缺血再灌注损伤中抑制固有免疫。
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