溶血
血红蛋白
血红素
血红素
结合珠蛋白
化学
生物化学
生物
药理学
免疫学
酶
作者
Florence Vallelian,Paul W. Buehler,Dominik J. Schaer
出处
期刊:Blood
[American Society of Hematology]
日期:2022-06-03
卷期号:140 (17): 1837-1844
被引量:79
标识
DOI:10.1182/blood.2022015596
摘要
During hemolysis, erythrophagocytes dispose damaged red blood cells. This prevents the extracellular release of hemoglobin, detoxifies heme, and recycles iron in a linked metabolic pathway. Complementary to this process, haptoglobin and hemopexin scavenge and shuttle the red blood cell toxins hemoglobin and heme to cellular clearance. Pathological hemolysis outpaces macrophage capacity and scavenger synthesis across a diversity of diseases. This imbalance leads to hemoglobin-driven disease progression. To meet a void in treatment options, scavenger protein-based therapeutics are in clinical development.
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