阵发性夜间血红蛋白尿
溶血
伊库利珠单抗
血红蛋白尿
医学
骨髓衰竭
免疫学
血液病
骨髓
疾病
溶血性贫血
补体系统
内科学
造血
抗体
生物
干细胞
遗传学
作者
David Dingli,Carlos de Castro,Jamie Koprivnikar,Austin Kulasekararaj,Jaroslaw P. Maciejewski,Brian Mulherin,Jens Panse,Vinod Pullarkat,Alexander Röth,Jamile M. Shammo,Louis Terriou,Ilene C. Weitz,Irina Yermilov,Sarah N. Gibbs,Michael S. Broder,David O. Beenhouwer,David J. Kuter
出处
期刊:Hematology
[Informa]
日期:2024-03-21
卷期号:29 (1)
被引量:3
标识
DOI:10.1080/16078454.2024.2329030
摘要
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired, non-malignant hematologic disease characterized by complement-mediated hemolysis (with or without hemoglobinuria), fatigue, increased susceptibility to thrombosis, and bone marrow dysfunction. The development of complement inhibitors has transformed outcomes for patients with PNH, but patients may still experience pharmacodynamic breakthrough hemolysis (BTH), which can be caused by exposure to a complement amplifying condition (CAC), such as vaccination, infection, or surgery.
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