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A largely random AAV integration profile after LPLD gene therapy
A largely random AAV integration profile after LPLD gene therapy
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A largely random AAV integration profile after LPLD gene therapy
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A largely random AAV integration profile after LPLD gene therapy
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A largely random AAV integration profile after LPLD gene therapy
A largely random AAV integration profile after LPLD gene therapy
Journal Article

A largely random AAV integration profile after LPLD gene therapy

2013
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Overview
An adeno-associated virus (AAV) vector encoding a variant of human lipoprotein lipase was recently approved in Europe as the first gene therapy for the treatment of LPL deficiency. Here Manfred Schmidt and his colleagues report their analysis of AAV integration sites after injection of the gene therapy construct in LPL-deficient patients and in mice. The clinical application of adeno-associated virus vectors (AAVs) is limited because of concerns about AAV integration–mediated tumorigenicity. We performed integration-site analysis after AAV1-LPL S447X intramuscular injection in five lipoprotein lipase–deficient subjects, revealing random nuclear integration and hotspots in mitochondria. We conclude that AAV integration is potentially safe and that vector breakage and integration may occur from each position of the vector genome. Future viral integration-site analyses should include the mitochondrial genome.