Ex Vivo Cell Therapy by Ectopic Hepatocyte Transplantation Treats the Porcine Tyrosinemia Model of Acute Liver Failure.

Abstract

The effectiveness of cell-based therapies to treat liver failure is often limited by the diseased liver environment. Here, we provide preclinical proof of concept for hepatocyte transplantation into lymph nodes as a cure for liver failure in a large-animal model with hereditary tyrosinemia type 1 (HT1), a metabolic liver disease caused by deficiency of fumarylacetoacetate hydrolase (FAH) enzyme. Autologous porcine hepatocytes were transduced ex vivo with a lentiviral vector carrying the pig Fah gene and transplanted into mesenteric lymph nodes. Hepatocytes showed early (6 h) and durable (8 months) engraftment in lymph nodes, with reproduction of vascular and hepatic microarchitecture. Subsequently, hepatocytes migrated to and repopulated the native diseased liver. The corrected cells generated sufficient liver mass to clinically ameliorate the acute liver failure and HT1 disease as early as 97 days post-transplantation. Integration site analysis defined the corrected hepatocytes in the liver as a subpopulation of hepatocytes from lymph nodes, indicating that the lymph nodes served as a source for healthy hepatocytes to repopulate a diseased liver. Therefore, ectopic transplantation of healthy hepatocytes cures this pig model of liver failure and presents a promising approach for the development of cures for liver disease in patients.

• Authors: Clara T Nicolas, Robert A Kaiser, Raymond D Hickey, Kari L Allen, Zeji Du, Caitlin J VanLith, Rebekah M Guthman, Bruce Amiot, Lukkana Suksanpaisan, Bing Han, Maria Giovanna Francipane, Amin Cheikhi, Huailei Jiang, Aditya Bansal, Mukesh K Pandey, Ishan Garg, Val Lowe, Aditya Bhagwate, Daniel O'Brien, Jean-Pierre A Kocher, Timothy R DeGrado, Scott L Nyberg, Eric Lagasse, Joseph B Lillegard
• Journal: Molecular therapy. Methods & clinical development (Mol Ther Methods Clin Dev) Vol. 18 Pg. 738-750 (Sep 11 2020) ISSN: 2329-0501 [Print] United States
• PMID: 32913881 (Publication Type: Journal Article)
• Copyright: © 2020 The Author(s).