实用医学杂志 ›› 2021, Vol. 37 ›› Issue (6): 816-820.doi: 10.3969/j.issn.1006⁃5725.2021.06.026

• 综述 • 上一篇    下一篇

β⁃地中海贫血治疗的研究进展

杨花梅, 孙菲,马燕琳,李崎   

  1. 海南医学院第一附属医院1 海南省人类生殖与遗传重点实验室,2 生殖医学科(海口570100); 3 海南省地方病(地中海贫血)临床医学研究中心(海口570100);4 海南医学院热带转化医学教育部重点实 验室(海口570100);5 海口市人类遗传资源保藏重点实验室(海口570100)

  • 出版日期:2021-03-25 发布日期:2021-03-25
  • 通讯作者: 李崎 E⁃mail:liqi1970@hotmail.com
  • 基金资助:
    国家自然科学基金资助项目(编号:81460034,81960283);海南省重大科技计划资助项目(编号:ZDKJ2017007)

Research progress on treatment of β⁃thalassemia

YANG Huamei*,SUN Fei,MA Yanlin,LI Qi.   

  1. Hainan Pro⁃ vincial Key Laboratory for human reproductive medicine and Genetic Research,the First Affiliated HospitalHainan Medical UniversityHaikou 570100China
  • Online:2021-03-25 Published:2021-03-25
  • Contact: LI Qi E⁃mail:liqi1970@hotmail.com

摘要:

β⁃地中海贫血是由于β⁃珠蛋白基因异常而导致的单基因遗传病,是地中海贫血中最常见的 类型。尽管目前治疗地中海贫血的方法有很多,比如输血、铁螯合、脾切除、异体造血干细胞移植(HSCT 等,但在治愈地中海贫血的道路上仍面临巨大的挑战。本文主要根据β⁃地中海贫血的发病机制系统阐述 其目前的临床治疗策略,并着重叙述基因治疗技术如何治愈β⁃地中海贫血的研究进展。

关键词:

Abstract:

β⁃thalassemia,the most common form of thalassemia,is a monogenic inherited disease caused by the abnormality of β⁃globin gene. Although there are currently many treatments for thalassemia,such as blood transfusion,iron chelation,splenectomy,and allogeneic hematopoietic stem cell transplantation(HSCT),the pathway to cure thalassemia still faces great challenges. In this paper,the current clinical treatment strategies of β⁃thalassemia were systematically described based on the pathogenesis of the disease,and the research progress of how to cure β⁃thalassemia by gene therapy was emphatically described.

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