Gene therapy for sickle cell disease: where we are now?

被引:16
|
作者
Kanter, Julie [1 ]
Falcon, Corey [2 ]
机构
[1] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[2] Ochsner Hosp Children, Dept Pediat, Jefferson, LA USA
关键词
PHASE-3;
D O I
10.1182/hematology.2021000250
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
The landscape of sickle cell disease (SCD) treatment continues to evolve rapidly, with new disease-modifying therapies in development and potentially curative options on the horizon. Until recently, allogeneic stem cell transplant has been the only proven cure for SCD. Gene therapy is rising to the forefront of the discussion as a potentially curative or highly disease-modifying option for abating the complications of the disease. Understanding the different types of gene therapy in use, the differences in their end points, and their potential risks and benefits will be key to optimizing the long-term use of this therapy.
引用
收藏
页码:174 / 180
页数:7
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