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补体阻断在抗中性粒细胞胞浆抗体相关性血管炎中的作用:一个索引病例、当前概念和未来展望。

Complement blockade in ANCA-associated vasculitis: an index case, current concepts and future perspectives.

机构信息

Unità Operativa Complessa di Nefrologia, Azienda Ospedaliero-Universitaria di Parma, Via Gramsci 14, 43126, Parma, Italy.

出版信息

Intern Emerg Med. 2017 Sep;12(6):727-731. doi: 10.1007/s11739-017-1636-6. Epub 2017 Feb 13.

Abstract

Complement alternative pathway (cAP) hyperactivation seems to be involved in ANCA-associated vasculitis (AAV). We here describe a case of AAV with severe activation of cAP that developed acute renal failure. No mutation predisposing to cAP dysregulation was identified. We treated our patient with the standard immunosuppressive therapy, but disease progression was only reversed after the addition of eculizumab, a monoclonal antibody against C5; the patient eventually achieved an almost complete renal function recovery. A review of the available literature about the role of complement targeted therapies in the treatment of AAV is discussed.

摘要

补体替代途径(cAP)的过度激活似乎与抗中性粒细胞胞质抗体相关性血管炎(AAV)有关。我们在此描述了一例 cAP 严重激活导致急性肾衰竭的 AAV 病例。未发现导致 cAP 失调的易感性突变。我们对患者采用了标准的免疫抑制疗法,但在添加针对 C5 的单克隆抗体依库珠单抗后,疾病才得以逆转;患者最终几乎完全恢复了肾功能。我们还讨论了目前关于补体靶向治疗在 AAV 治疗中的作用的文献综述。

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