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Updated: Feb 17, 2026

Lentiviral Vector-mediated Gene Therapy of Hepatocytes Ex Vivo for Autologous Transplantation in Swine
Published on: November 4, 2018
Using CRISPR to inactivate endogenous retroviruses in pigs: an important step toward safe xenotransplantation?
Michael J Ross1, P Toby Coates2
1Division of Nephrology, Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, New York, USA; Department of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York, USA.
Abstract:
Xenotransplantation could theoretically provide an unlimited supply of organs for patients living with end-stage kidney disease and other end-stage organ failure, but severe rejection and concerns about possible transmission of zoonotic infections remain important obstacles. In a recent study, investigators used CRISPR-cas9 to generate genetically modified pigs in which all endogenous retroviruses were inactivated. This approach may address one important barrier to the feasibility of clinical trials of xenotransplantation.
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