共 50 条
Gene therapy for hemophilia
被引:40
|作者:
Rogers, Geoffrey L.
[1
]
Herzog, Roland W.
[1
]
机构:
[1] Univ Florida, Dept Pediat, Div Cellular & Mol Therapy, Gainesville, FL 32610 USA
来源:
FRONTIERS IN BIOSCIENCE-LANDMARK
|
2015年
/
20卷
关键词:
Gene therapy;
Hemophilia;
Factor IX;
Factor VIII;
AAV;
Lentivirus;
Review;
HUMAN-FACTOR-VIII;
COAGULATION-FACTOR-VIII;
ADENOASSOCIATED VIRAL VECTORS;
SLEEPING-BEAUTY TRANSPOSON;
HEMATOPOIETIC STEM-CELLS;
LONG-TERM EXPRESSION;
HUMAN-FACTOR-IX;
PORCINE FACTOR-VIII;
HIGH-LEVEL EXPRESSION;
SINUSOIDAL ENDOTHELIAL-CELLS;
D O I:
10.2741/4324
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Hemophilia is an X-linked inherited bleeding disorder consisting of two classifications, hemophilia A and hemophilia B, depending on the underlying mutation. Although the disease is currently treatable with intravenous delivery of replacement recombinant clotting factor, this approach represents a significant cost both monetarily and in terms of quality of life. Gene therapy is an attractive alternative approach to the treatment of hemophilia that would ideally provide life-long correction of clotting activity with a single injection. In this review, we will discuss the multitude of approaches that have been explored for the treatment of both hemophilia A and B, including both in vivo and ex vivo approaches with viral and nonviral delivery vectors.
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页码:556 / 603
页数:48
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