| Literature DB >> 35357044 |
Muhammad M Mohiuddin1, Corbin E Goerlich1,2, Avneesh K Singh1, Tianshu Zhang1, Ivan Tatarov1, Billeta Lewis1, Faith Sentz1, Alena Hershfeld1, Gheorghe Braileanu1, Patrick Odonkor3, Erik Strauss3, Brittney Williams3, Allen Burke4, Jamie Hittman4, Adnan Bhutta5, Ali Tabatabai6, Anuj Gupta7, Todd Vaught8, Lori Sorrells8, Kasinath Kuravi8, Amy Dandro8, Will Eyestone8, David J Kaczorowski1, David Ayares8, Bartley P Griffith1.
Abstract
We report orthotopic (life-supporting) survival of genetically engineered porcine cardiac xenografts (with six gene modifications) for almost 9 months in baboon recipients. This work builds on our previously reported heterotopic cardiac xenograft (three gene modifications) survival up to 945 days with an anti-CD40 monoclonal antibody-based immunosuppression. In this current study, life-supporting xenografts containing multiple human complement regulatory, thromboregulatory, and anti-inflammatory proteins, in addition to growth hormone receptor knockout (KO) and carbohydrate antigen KOs, were transplanted in the baboons. Selective "multi-gene" xenografts demonstrate survival greater than 8 months without the requirement of adjunctive medications and without evidence of abnormal xenograft thickness or rejection. These data demonstrate that selective "multi-gene" modifications improve cardiac xenograft survival significantly and may be foundational for paving the way to bridge transplantation in humans.Entities:
Keywords: CRISPR; cardiac xenotransplantation; heart failure; pig heart; xenotransplantation
Mesh:
Substances:
Year: 2022 PMID: 35357044 DOI: 10.1111/xen.12744
Source DB: PubMed Journal: Xenotransplantation ISSN: 0908-665X Impact factor: 3.907