补体系统
狼疮性肾炎
免疫学
凝集素途径
替代补体途径
补体缺乏
系统性红斑狼疮
医学
发病机制
经典补体途径
免疫系统
疾病
内科学
作者
Ruth Fernandez‐Ruiz,H. Michael Belmont
标识
DOI:10.1016/j.trsl.2022.02.001
摘要
The complement system plays crucial roles in homeostasis and host defense against microbes. Deficiency of early complement cascade components has been associated with increased susceptibility to systemic lupus erythematosus (SLE), whereas excessive complement consumption is a hallmark of this disease. Although enhanced classical pathway activation by immune complexes was initially thought to be the main contributor to lupus nephritis (LN) pathogenesis, an increasing body of evidence has suggested the alternative and the lectin pathways are also involved. Therapeutic agents targeting complement activation have been used in LN patients and clinical trials are ongoing. We review the mechanisms by which complement system dysregulation contributes to renal injury in SLE and summarize the latest evidence on the use of anticomplement agents to manage this condition.
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