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Design and testing of a humanized porcine donor for xenotransplantation

Author

Listed:
  • Ranjith P. Anand

    (eGenesis)

  • Jacob V. Layer

    (eGenesis)

  • David Heja

    (eGenesis)

  • Takayuki Hirose

    (Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • Grace Lassiter

    (Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • Daniel J. Firl

    (eGenesis
    Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • Violette B. Paragas

    (eGenesis)

  • Adam Akkad

    (eGenesis)

  • Sagar Chhangawala

    (eGenesis)

  • Robert B. Colvin

    (Massachusetts General Hospital, Harvard Medical School)

  • Russell J. Ernst

    (eGenesis)

  • Nicholas Esch

    (eGenesis)

  • Kristen Getchell

    (eGenesis)

  • Alexandra K. Griffin

    (eGenesis)

  • Xiaoyun Guo

    (eGenesis)

  • Katherine C. Hall

    (eGenesis)

  • Paula Hamilton

    (eGenesis)

  • Lokesh A. Kalekar

    (eGenesis)

  • Yinan Kan

    (eGenesis)

  • Ahmad Karadagi

    (Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • Feng Li

    (eGenesis)

  • Susan C. Low

    (eGenesis)

  • Rudy Matheson

    (Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • Claudia Nehring

    (eGenesis)

  • Ryo Otsuka

    (Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • Matthew Pandelakis

    (eGenesis)

  • Robert A. Policastro

    (eGenesis)

  • Rebecca Pols

    (eGenesis)

  • Luis Queiroz

    (eGenesis)

  • Ivy A. Rosales

    (Massachusetts General Hospital, Harvard Medical School)

  • William T. Serkin

    (eGenesis)

  • Kathryn Stiede

    (eGenesis)

  • Toshihide Tomosugi

    (Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • Yongqiang Xue

    (eGenesis)

  • Gabriel E. Zentner

    (eGenesis)

  • David Angeles-Albores

    (eGenesis)

  • J. Chris Chao

    (eGenesis)

  • Juliet N. Crabtree

    (eGenesis)

  • Sierra Harken

    (eGenesis)

  • Nicole Hinkle

    (eGenesis)

  • Tania Lemos

    (eGenesis)

  • Mailin Li

    (eGenesis)

  • Lorena Pantano

    (eGenesis)

  • Denise Stevens

    (eGenesis)

  • Omar D. Subedar

    (eGenesis)

  • Xiaoqing Tan

    (eGenesis)

  • Shiyi Yin

    (eGenesis)

  • Imran J. Anwar

    (Duke University Medical Center)

  • David Aufhauser

    (University of Wisconsin)

  • Saverio Capuano

    (Wisconsin National Primate Research Center)

  • Dixon B. Kaufman

    (University of Wisconsin)

  • Stuart J. Knechtle

    (Duke University Medical Center)

  • Jean Kwun

    (Duke University Medical Center)

  • Dhanansayan Shanmuganayagam

    (University of Wisconsin)

  • James F. Markmann

    (Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • George M. Church

    (Harvard Medical School
    Harvard University)

  • Mike Curtis

    (eGenesis)

  • Tatsuo Kawai

    (Center for Transplantation Sciences, Massachusetts General Hospital, Harvard Medical School)

  • Michele E. Youd

    (eGenesis)

  • Wenning Qin

    (eGenesis)

Abstract

Recent human decedent model studies1,2 and compassionate xenograft use3 have explored the promise of porcine organs for human transplantation. To proceed to human studies, a clinically ready porcine donor must be engineered and its xenograft successfully tested in nonhuman primates. Here we describe the design, creation and long-term life-supporting function of kidney grafts from a genetically engineered porcine donor transplanted into a cynomolgus monkey model. The porcine donor was engineered to carry 69 genomic edits, eliminating glycan antigens, overexpressing human transgenes and inactivating porcine endogenous retroviruses. In vitro functional analyses showed that the edited kidney endothelial cells modulated inflammation to an extent that was indistinguishable from that of human endothelial cells, suggesting that these edited cells acquired a high level of human immune compatibility. When transplanted into cynomolgus monkeys, the kidneys with three glycan antigen knockouts alone experienced poor graft survival, whereas those with glycan antigen knockouts and human transgene expression demonstrated significantly longer survival time, suggesting the benefit of human transgene expression in vivo. These results show that preclinical studies of renal xenotransplantation could be successfully conducted in nonhuman primates and bring us closer to clinical trials of genetically engineered porcine renal grafts.

Suggested Citation

  • Ranjith P. Anand & Jacob V. Layer & David Heja & Takayuki Hirose & Grace Lassiter & Daniel J. Firl & Violette B. Paragas & Adam Akkad & Sagar Chhangawala & Robert B. Colvin & Russell J. Ernst & Nichol, 2023. "Design and testing of a humanized porcine donor for xenotransplantation," Nature, Nature, vol. 622(7982), pages 393-401, October.
  • Handle: RePEc:nat:nature:v:622:y:2023:i:7982:d:10.1038_s41586-023-06594-4
    DOI: 10.1038/s41586-023-06594-4
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    Cited by:

    1. Daniel Eisenson & Yu Hisadome & Michelle Santillan & Hayato Iwase & WeiLi Chen & Akira Shimizu & Alex Schulick & Du Gu & Armaan Akbar & Alice Zhou & Kristy Koenig & Kasinath Kuravi & Farzana Rahman & , 2024. "Consistent survival in consecutive cases of life-supporting porcine kidney xenotransplantation using 10GE source pigs," Nature Communications, Nature, vol. 15(1), pages 1-7, December.

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