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- W4298120534 abstract "Abstract The liver is a prime target for in vivo gene therapies using recombinant adeno-associated viral vectors (rAAV). Multiple clinical trials have been undertaken for this target in the past 15 years, however we are still to see market approval of the first liver-targeted AAV-based gene therapy. Inefficient expression of the therapeutic transgene, vector-induced liver toxicity and capsid, and/or transgene-mediated immune responses reported at high vector doses are the main challenges to date. One of the contributing factors to the insufficient clinical outcomes, despite highly encouraging preclinical data, is the lack of robust, biologically- and clinically-predictive preclinical models. To this end, this study reports findings of a functional evaluation of six AAV vectors in twelve preclinical models of the human liver, with the aim to uncover which model is the most relevant for the selection of AAV capsid variant for safe and efficient transgene delivery to primary human hepatocytes. The results, generated by studies in models ranging from immortalized cells, iPSC-derived and primary hepatocytes, and primary human hepatic organoids to in vivo models, increased our understanding of the strengths and weaknesses of each system. This should allow the development of novel gene therapies targeting the human liver." @default.
- W4298120534 created "2022-10-01" @default.
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- W4298120534 date "2022-09-30" @default.
- W4298120534 modified "2023-10-18" @default.
- W4298120534 title "Assessment of pre-clinical liver models based on their ability to predict the liver-tropism of AAV vectors" @default.
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- W4298120534 doi "https://doi.org/10.1101/2022.09.28.510021" @default.
- W4298120534 hasPublicationYear "2022" @default.
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