补体系统
医学
肾脏疾病
肾小球疾病
疾病
非典型溶血尿毒综合征
免疫学
补语(音乐)
肾病
糖尿病肾病
替代补体途径
伊库利珠单抗
重症监护医学
肾
肾小球肾炎
糖尿病
内科学
免疫系统
生物
内分泌学
生物化学
表型
互补
基因
作者
Marina Vivarelli,Jonathan Barratt,Laurence H. Beck,Fádi Fakhouri,Daniel P. Gale,Elena Goicoechea de Jorge,Marta Mosca,Marina Noris,Matthew C. Pickering,Katalin Suszták,Joshua M. Thurman,Michael Cheung,Jennifer King,Michel Jadoul,Wolfgang C. Winkelmayer,Richard J. Smith,Federico Alberici,Luca Antonucci,Tadej Avčin,Arvind Bagga
标识
DOI:10.1016/j.kint.2024.05.015
摘要
Uncontrolled complement activation can cause or contribute to glomerular injury in multiple kidney diseases. While complement activation plays a causal role in atypical hemolytic uremic syndrome (aHUS) and C3 glomerulopathy (C3G), over the past decade a rapidly accumulating body of evidence has shown a role for complement activation in multiple other kidney diseases, including diabetic nephropathy and several glomerulonephritides. The number of available complement inhibitor therapies has also increased during the same period. In 2022 KDIGO convened a Controversies Conference, The Role of Complement in Kidney Disease, to address the expanding role of complement dysregulation in the pathophysiology, diagnosis, and management of various glomerular diseases, diabetic nephropathy, and other forms of HUS. Conference participants reviewed the evidence for complement playing a primary causal or secondary role in progression for several disease states and considered how evidence of complement involvement might inform management. Participating patients with various complement-mediated diseases and caregivers described concerns related to life planning, implications surrounding genetic testing, and the need for inclusive implementation of effective novel therapies into clinical practice. The value of biomarkers in monitoring disease course and the role of the glomerular microenvironment in complement response were examined, and key gaps in knowledge and research priorities were identified.
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