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      Cardiac xenotransplantation: from concept to clinic

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          Abstract

          For many patients with terminal/advanced cardiac failure, heart transplantation is the most effective, durable treatment option, and offers the best prospects for a high quality of life. The number of potentially life-saving donated human organs is far fewer than the population who could benefit from a new heart, resulting in increasing numbers of patients awaiting replacement of their failing heart, high waitlist mortality, and frequent reliance on interim mechanical support for many of those deemed among the best candidates but who are deteriorating as they wait. Currently, mechanical assist devices supporting left ventricular or biventricular heart function are the only alternative to heart transplant that is in clinical use. Unfortunately, the complication rate with mechanical assistance remains high despite advances in device design and patient selection and management, and the quality of life of the patients even with good outcomes is only moderately improved. Cardiac xenotransplantation from genetically multi-modified (GM) organ-source pigs is an emerging new option as demonstrated by the consistent long-term success of heterotopic (non-life-supporting) abdominal and life-supporting orthotopic porcine heart transplantation in baboons, and by a recent ‘compassionate use’ transplant of the heart from a GM pig with 10 modifications into a terminally ill patient who survived for 2 months. In this review, we discuss pig heart xenotransplantation as a concept, including pathobiological aspects related to immune rejection, coagulation dysregulation, and detrimental overgrowth of the heart, as well as GM strategies in pigs to prevent or minimize these problems. Additional topics discussed include relevant results of heterotopic and orthotopic heart transplantation experiments in the pig-to-baboon model, microbiological and virologic safety concepts, and efficacy requirements for initiating formal clinical trials. An adequate regulatory and ethical framework as well as stringent criteria for the selection of patients will be critical for the safe clinical development of cardiac xenotransplantation, which we expect will be clinically tested during the next few years.

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          High frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells

          CRISPR RNA-guided endonucleases (RGENs) have rapidly emerged as a facile and efficient platform for genome editing. Here, we use a human cell-based reporter assay to characterize off-target cleavage of Cas9-based RGENs. We find that single and double mismatches are tolerated to varying degrees depending on their position along the guide RNA (gRNA)-DNA interface. We readily detected off-target alterations induced by four out of six RGENs targeted to endogenous loci in human cells by examination of partially mismatched sites. The off-target sites we identified harbor up to five mismatches and many are mutagenized with frequencies comparable to (or higher than) those observed at the intended on-target site. Our work demonstrates that RGENs are highly active even with imperfectly matched RNA-DNA interfaces in human cells, a finding that might confound their use in research and therapeutic applications.
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            Inactivation of porcine endogenous retrovirus in pigs using CRISPR-Cas9

            Xenotransplantation is a promising strategy to alleviate the shortage of organs for human transplantation. In addition to the concern on pig-to-human immunological compatibility, the risk of cross-species transmission of porcine endogenous retroviruses (PERVs) has impeded the clinical application of this approach. Earlier, we demonstrated the feasibility of inactivating PERV activity in an immortalized pig cell line. Here, we confirmed that PERVs infect human cells, and observed the horizontal transfer of PERVs among human cells. Using CRISPR-Cas9, we inactivated all the PERVs in a porcine primary cell line and generated PERV-inactivated pigs via somatic cell nuclear transfer. Our study highlighted the value of PERV inactivation to prevent cross-species viral transmission and demonstrated the successful production of PERV-inactivated animals to address the safety concern in clinical xenotransplantation.
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              Heart Failure With Reduced Ejection Fraction: A Review

              Worldwide, the burden of heart failure has increased to an estimated 23 million people, and approximately 50% of cases are HF with reduced ejection fraction (HFrEF).
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                Author and article information

                Contributors
                Journal
                Cardiovasc Res
                Cardiovasc Res
                cardiovascres
                Cardiovascular Research
                Oxford University Press (US )
                0008-6363
                1755-3245
                December 2022
                03 December 2022
                03 December 2022
                : 118
                : 18 , Spotlight Issue on Heart Failure
                : 3499-3516
                Affiliations
                Walter Brendel Centre for Experimental Medicine, Ludwig-Maximilians-Universität München , Munich 81377, Germany
                Center for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School , Boston, MA 02129, USA
                Division of Cardiac Surgery, Department of Surgery, Massachusetts General Hospital/Harvard Medical School , Boston, MA 02114, USA
                Department of Anaesthesiology, University Hospital, Ludwig-Maximilians-Universität München , Munich 81377, Germany
                Division of Medical Biotechnology, Paul-Ehrlich-Institute , Langen 63225, Germany
                Center for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School , Boston, MA 02129, USA
                Division of Cardiac Surgery, Department of Surgery, Massachusetts General Hospital/Harvard Medical School , Boston, MA 02114, USA
                Gene Centre and Centre for Innovative Medical Models (CiMM), Ludwig-Maximilians-Universität München , Munich 81377, Germany
                Author notes
                Corresponding author. Email: ewolf@ 123456genzentrum.lmu.de

                Conflict of interest: B.R., M.L., and E.W. are cofounders of XTransplant GmbH, Starnberg, Germany. D.K.C.C. is a paid consultant to eGenesis. D.K.C.C. and R.N.P. have previously received research support from Revivicor, Lung Bioengineering PBC, and United Therapeutics; R.N.P. receives research support from eGenesis and Tonix.

                Author information
                https://orcid.org/0000-0003-2859-3664
                https://orcid.org/0000-0002-8899-9431
                https://orcid.org/0000-0003-0996-4941
                https://orcid.org/0000-0001-8727-1935
                https://orcid.org/0000-0003-3764-4590
                https://orcid.org/0000-0002-0430-9510
                Article
                cvac180
                10.1093/cvr/cvac180
                9897693
                36461918
                d19880ad-5855-43c5-a0c6-b03d9e5d364a
                © The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 08 May 2022
                : 17 October 2022
                : 21 October 2022
                : 20 December 2022
                Page count
                Pages: 18
                Funding
                Funded by: Deutsche Forschungsgemeinschaft, doi 10.13039/501100001659;
                Award ID: CRC/TR 127
                Funded by: Swiss National Science Foundation, doi 10.13039/501100001711;
                Award ID: CRSII5_198577/1
                Funded by: NIH, doi 10.13039/100000002;
                Award ID: U19 AI090959
                Categories
                Spotlight Review
                AcademicSubjects/MED00200

                Cardiovascular Medicine
                heart,non-human primate,pig,xenotransplantation experimental,xenotransplantation clinical

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