Alipogene tiparvovec: gene therapy for lipoprotein lipase deficiency

被引:32
作者
Wierzbicki, Anthony S. [1 ]
Viljoen, Adie [2 ]
机构
[1] Guys & St Thomas Hosp, Dept Metab Med Chem Pathol, London SE1 7EH, England
[2] Lister Hosp, Stevenage SG1 4AB, Herts, England
关键词
alipogene tiparvovec; chylomicronemia; gene therapy; lipoprotein lipase; triglyceride; SEVERE HYPERTRIGLYCERIDEMIA; BENEFICIAL MUTATION; ORLISTAT; S447X;
D O I
10.1517/14712598.2013.738663
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Homozygous lipoprotein lipase (LPL) deficiency is an ultra-orphan disease associated with increased rates of pancreatitis. Current treatments based on acute plasmapheresis allied with ultra-low fat diets are inadequate as responses to fibrates or other triglyceride-lowering therapies tend to be poor. Alipogene tiparvovec is an adeno-associated virus type I (AAV1) gene therapy using a hyper-functional LPL serine(447)-stop (S447X) insert administered intramuscularly under general anaesthetic with allied immunosuppression. Treatment results in histological muscle expression of LPL allied with a transient 40% reduction in triglycerides and improvements in postprandial chylomicron triglyceride content. Alipogene tiparvovec is the first possibly curative treatment for LPL deficiency.
引用
收藏
页码:7 / 10
页数:4
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