无效红细胞生成:相关因素及其作为β -地中海贫血的潜在治疗靶点

H. Alsaleh, S. Sulong, B. Zilfalil, R. Hassan
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引用次数: 0

摘要

-地中海贫血(b -thal)是一种单基因疾病,表现出很大的临床变异性。b需要。骨髓移植是一种严重的健康问题,唯一的治疗方法是同种异体骨髓移植,这并不是每个人都能得到的,也不是没有风险。b -thal的潜在发病机制。主要是由于无效的红细胞生成(IE),其特点是增殖活动增加,不能产生足够的功能性红细胞。在b -thal。在患者中,IE的严重程度主要负责疾病的表现,后遗症和并发症的标志。本文综述了IE的发病机制、导致IE的因素以及针对这些因素改善患者临床表型的潜在治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ineffective Erythropoiesis: Associated Factors and Their Potential as Therapeutic Targets in Beta-Thalassaemia Major
Beta-thalassaemia ( b -thal.) is single-gene disorder that exhibits much clinical variability. b -thal. major is a major health problem, and the only method of curing is allogenic bone-marrow transplantation, which is not available to everyone and not without risk. The underlying pathogenesis of b -thal. major is due to ineffective erythropoiesis (IE), which is characterized by increased proliferative activity that fails to produce sufficient functional red blood cells. In b -thal. patients, the severity of the IE is mainly responsible for the hallmarks of the disease’s presentation, sequalae and complications. This review discusses the mechanisms of IE, the factors that contribute to it and the potential therapies for targeting these factors to improve patients’ clinical phenotypes.
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