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7 - Prenatal gene therapy

Published online by Cambridge University Press:  05 February 2014

Khalil Abi-Nader
Affiliation:
University College London
Anna David
Affiliation:
University College London
Sean Kehoe
Affiliation:
John Radcliffe Hospital, Oxford
Lyn Chitty
Affiliation:
University College Hospital, London
Tessa Homfray
Affiliation:
St George’s University of London
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Summary

Summary

Prenatal gene therapy aims to deliver genes to cells and tissues early in prenatal life, allowing correction of a genetic defect before long-term tissue damage has occurred. In contrast to postnatal gene therapy, prenatal application has a number of advantages, including targeting genes to a large population of dividing stem cells, and the smaller fetal size, which allows a higher vector to target cell ratio to be achieved. Early-gestation delivery may result in the fetus developing immune tolerance to the transgenic protein, which would allow postnatal repeat vector administration if needed. Further treatment options include using transduced autologous or allogeneic stem cells to treat congenital fetal disease, or to treat obstetric conditions such as fetal growth restriction by delivering gene therapy to the mother.

Recent advances in vector design and stem cell research have benefited this potential treatment. Although still in the preclinical stage, proof-of-principle studies in animal models of congenital disease, such as the haemophilia mouse, have shown the potential of prenatal gene therapy to cure disease. Investigators have devised delivery strategies in large animals that could be used clinically to apply gene therapy to the human fetus, and prenatal gene therapy may become available for the treatment of certain life-threatening congenital disorders in the near future. In this way, pregnant women and their partners would have a third choice when faced with an affected fetus where currently the only options are either terminating the pregnancy or continuing with an affected fetus with a poor prognosis.

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Chapter
Information
Reproductive Genetics , pp. 101 - 122
Publisher: Cambridge University Press
Print publication year: 2009

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