Inactivation of porcine endogenous retrovirus in pigs using CRISPR-Cas9

Dong Niu(Genesis Foundation), Hong‐Jiang Wei(Army Medical University), Hong-Jiang Wei(Army Medical University), Lin Lin(Aarhus University), Haydy George(Genesis Foundation), Tao Wang(Genesis Foundation), I‐Hsiu Lee(Yunnan Agricultural University), Hong‐Ye Zhao(Army Medical University), Yong Wang(Army Medical University), Yinan Kan(Harvard University), Ellen Shrock(Harvard University), Emal Lesha(Genesis Foundation), Gang Wang(Aarhus University), Yonglun Luo(Yunnan Agricultural University), Yubo Qing(Yunnan Agricultural University), Deling Jiao(Yunnan Agricultural University), Heng Zhao(Army Medical University), Xiaoyang Zhou(Army Medical University), Shouqi Wang(Army Medical University), Hong Wei(Army Medical University), Hong Wei(Harvard University), Marc Güell(Genesis Foundation), George M. Church(Harvard University), Luhan Yang(Genesis Foundation)
Science
August 11, 2017
Cited by 746

Abstract

Xenotransplantation is a promising strategy to alleviate the shortage of organs for human transplantation. In addition to the concerns about pig-to-human immunological compatibility, the risk of cross-species transmission of porcine endogenous retroviruses (PERVs) has impeded the clinical application of this approach. We previously demonstrated the feasibility of inactivating PERV activity in an immortalized pig cell line. We now confirm that PERVs infect human cells, and we observe the horizontal transfer of PERVs among human cells. Using CRISPR-Cas9, we inactivated all of the PERVs in a porcine primary cell line and generated PERV-inactivated pigs via somatic cell nuclear transfer. Our study highlights the value of PERV inactivation to prevent cross-species viral transmission and demonstrates the successful production of PERV-inactivated animals to address the safety concern in clinical xenotransplantation.


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