Organ transplants of the future: planning for innovations including xenotransplantation
Summary The future clinical application of animal‐to‐human transplantation (xenotransplantation) is of importance to society as a whole. Favourable preclinical data relevant to cell, tissue and solid organ xenotransplants have been obtained from many animal models utilizing genetic engineering and p...
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Veröffentlicht in: | Transplant international 2021-11, Vol.34 (11), p.2006-2018 |
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container_issue | 11 |
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container_title | Transplant international |
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creator | Cozzi, Emanuele Schneeberger, Stefan Bellini, Maria Irene Berglund, Erik Böhmig, Georg Fowler, Kevin Hoogduijn, Martin Jochmans, Ina Marckmann, Georg Marson, Lorna Neuberger, James Oberbauer, Rainer Pierson, Richard N. Reichart, Bruno Scobie, Linda White, Colin Naesens, Maarten |
description | Summary
The future clinical application of animal‐to‐human transplantation (xenotransplantation) is of importance to society as a whole. Favourable preclinical data relevant to cell, tissue and solid organ xenotransplants have been obtained from many animal models utilizing genetic engineering and protocols of pathogen‐free husbandry. Findings have reached a tipping point, and xenotransplantation of solid organs is approaching clinical evaluation, the process of which now requires close deliberation. Such discussions include considering when there is sufficient evidence from preclinical animal studies to start first‐in‐human xenotransplantation trials. The present article is based on evidence and opinions formulated by members of the European Society for Organ Transplantation who are involved in the Transplantation Learning Journey project. The article includes a brief overview of preclinical concepts and biology of solid organ xenotransplantation, discusses the selection of candidates for first‐in‐human studies and considers requirements for study design and conduct. In addition, the paper emphasizes the need for a regulatory framework for xenotransplantation of solid organs and the essential requirement for input from public and patient stakeholders. |
doi_str_mv | 10.1111/tri.14031 |
format | Article |
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The future clinical application of animal‐to‐human transplantation (xenotransplantation) is of importance to society as a whole. Favourable preclinical data relevant to cell, tissue and solid organ xenotransplants have been obtained from many animal models utilizing genetic engineering and protocols of pathogen‐free husbandry. Findings have reached a tipping point, and xenotransplantation of solid organs is approaching clinical evaluation, the process of which now requires close deliberation. Such discussions include considering when there is sufficient evidence from preclinical animal studies to start first‐in‐human xenotransplantation trials. The present article is based on evidence and opinions formulated by members of the European Society for Organ Transplantation who are involved in the Transplantation Learning Journey project. The article includes a brief overview of preclinical concepts and biology of solid organ xenotransplantation, discusses the selection of candidates for first‐in‐human studies and considers requirements for study design and conduct. In addition, the paper emphasizes the need for a regulatory framework for xenotransplantation of solid organs and the essential requirement for input from public and patient stakeholders.</description><identifier>ISSN: 0934-0874</identifier><identifier>EISSN: 1432-2277</identifier><identifier>DOI: 10.1111/tri.14031</identifier><identifier>PMID: 34459040</identifier><language>eng</language><publisher>Switzerland: Blackwell Publishing Ltd</publisher><subject>Animal husbandry ; Animal models ; Animals ; clinical study design ; Clinical trials ; endpoints ; Genetic engineering ; Heterografts ; Humans ; innovation ; Models, Animal ; organ shortage ; Organ Transplantation ; Organs ; patient centred ; regulation ; Transplantation ; Transplantation, Heterologous ; Transplants ; Transplants & implants ; Xenografts ; Xenotransplantation</subject><ispartof>Transplant international, 2021-11, Vol.34 (11), p.2006-2018</ispartof><rights>2021 Steunstichting ESOT. Published by John Wiley & Sons Ltd</rights><rights>2021 Steunstichting ESOT. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2021 Steunstichting ESOT. Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4261-2323dce421f7f59e77d5ede1ec4030a63765a84729a659939f8ba5983746caaf3</citedby><cites>FETCH-LOGICAL-c4261-2323dce421f7f59e77d5ede1ec4030a63765a84729a659939f8ba5983746caaf3</cites><orcidid>0000-0002-0217-8254 ; 0000-0001-7544-6275 ; 0000-0003-0730-4923 ; 0000-0002-5625-0792 ; 0000-0002-2619-8639 ; 0000-0002-6079-002X ; 0000-0003-4592-2810 ; 0000-0002-7600-912X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftri.14031$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftri.14031$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,550,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34459040$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:147835229$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Cozzi, Emanuele</creatorcontrib><creatorcontrib>Schneeberger, Stefan</creatorcontrib><creatorcontrib>Bellini, Maria Irene</creatorcontrib><creatorcontrib>Berglund, Erik</creatorcontrib><creatorcontrib>Böhmig, Georg</creatorcontrib><creatorcontrib>Fowler, Kevin</creatorcontrib><creatorcontrib>Hoogduijn, Martin</creatorcontrib><creatorcontrib>Jochmans, Ina</creatorcontrib><creatorcontrib>Marckmann, Georg</creatorcontrib><creatorcontrib>Marson, Lorna</creatorcontrib><creatorcontrib>Neuberger, James</creatorcontrib><creatorcontrib>Oberbauer, Rainer</creatorcontrib><creatorcontrib>Pierson, Richard N.</creatorcontrib><creatorcontrib>Reichart, Bruno</creatorcontrib><creatorcontrib>Scobie, Linda</creatorcontrib><creatorcontrib>White, Colin</creatorcontrib><creatorcontrib>Naesens, Maarten</creatorcontrib><creatorcontrib>for ESOT Workstream 1 of the TLJ (Transplantation Learning Journey) Project</creatorcontrib><title>Organ transplants of the future: planning for innovations including xenotransplantation</title><title>Transplant international</title><addtitle>Transpl Int</addtitle><description>Summary
The future clinical application of animal‐to‐human transplantation (xenotransplantation) is of importance to society as a whole. Favourable preclinical data relevant to cell, tissue and solid organ xenotransplants have been obtained from many animal models utilizing genetic engineering and protocols of pathogen‐free husbandry. Findings have reached a tipping point, and xenotransplantation of solid organs is approaching clinical evaluation, the process of which now requires close deliberation. Such discussions include considering when there is sufficient evidence from preclinical animal studies to start first‐in‐human xenotransplantation trials. The present article is based on evidence and opinions formulated by members of the European Society for Organ Transplantation who are involved in the Transplantation Learning Journey project. The article includes a brief overview of preclinical concepts and biology of solid organ xenotransplantation, discusses the selection of candidates for first‐in‐human studies and considers requirements for study design and conduct. In addition, the paper emphasizes the need for a regulatory framework for xenotransplantation of solid organs and the essential requirement for input from public and patient stakeholders.</description><subject>Animal husbandry</subject><subject>Animal models</subject><subject>Animals</subject><subject>clinical study design</subject><subject>Clinical trials</subject><subject>endpoints</subject><subject>Genetic engineering</subject><subject>Heterografts</subject><subject>Humans</subject><subject>innovation</subject><subject>Models, Animal</subject><subject>organ shortage</subject><subject>Organ Transplantation</subject><subject>Organs</subject><subject>patient centred</subject><subject>regulation</subject><subject>Transplantation</subject><subject>Transplantation, Heterologous</subject><subject>Transplants</subject><subject>Transplants & implants</subject><subject>Xenografts</subject><subject>Xenotransplantation</subject><issn>0934-0874</issn><issn>1432-2277</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNp1kVtLxDAQhYMouq4--Aek4Is-dM2tSeObiDcQBFF8DNl2otVusiatl39v1q4KgvMyw8zHYQ4HoR2CJyTVYReaCeGYkRU0IpzRnFIpV9EIK8ZzXEq-gTZjfMIY07LA62iDcV4ozPEI3V-HB-OyLhgX561xXcy8zbpHyGzf9QGOssXWNe4hsz5kjXP-1XSNdzHNVdvXi8s7OP-r8HXeQmvWtBG2l32M7s5Ob08u8qvr88uT46u84lSQnDLK6go4JVbaQoGUdQE1EKiSHWwEk6IwJZdUGVEoxZQtp6ZQJZNcVMZYNkb5oBvfYN5P9Tw0MxM-tDeNXq6e0wQ6GeZEJn5_4OfBv_QQOz1rYgVtehx8HzUthKCCEl4mdO8P-uT74JKbRKlSsJJzkqiDgaqCjzGA_XmBYL1IR6d09Fc6id1dKvbTGdQ_5HccCTgcgLemhY__lfTtzeUg-Qk5Lpnj</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Cozzi, Emanuele</creator><creator>Schneeberger, Stefan</creator><creator>Bellini, Maria Irene</creator><creator>Berglund, Erik</creator><creator>Böhmig, Georg</creator><creator>Fowler, Kevin</creator><creator>Hoogduijn, Martin</creator><creator>Jochmans, Ina</creator><creator>Marckmann, Georg</creator><creator>Marson, Lorna</creator><creator>Neuberger, James</creator><creator>Oberbauer, Rainer</creator><creator>Pierson, Richard N.</creator><creator>Reichart, Bruno</creator><creator>Scobie, Linda</creator><creator>White, Colin</creator><creator>Naesens, Maarten</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-0217-8254</orcidid><orcidid>https://orcid.org/0000-0001-7544-6275</orcidid><orcidid>https://orcid.org/0000-0003-0730-4923</orcidid><orcidid>https://orcid.org/0000-0002-5625-0792</orcidid><orcidid>https://orcid.org/0000-0002-2619-8639</orcidid><orcidid>https://orcid.org/0000-0002-6079-002X</orcidid><orcidid>https://orcid.org/0000-0003-4592-2810</orcidid><orcidid>https://orcid.org/0000-0002-7600-912X</orcidid></search><sort><creationdate>202111</creationdate><title>Organ transplants of the future: planning for innovations including xenotransplantation</title><author>Cozzi, Emanuele ; Schneeberger, Stefan ; Bellini, Maria Irene ; Berglund, Erik ; Böhmig, Georg ; Fowler, Kevin ; Hoogduijn, Martin ; Jochmans, Ina ; Marckmann, Georg ; Marson, Lorna ; Neuberger, James ; Oberbauer, Rainer ; Pierson, Richard N. ; Reichart, Bruno ; Scobie, Linda ; White, Colin ; Naesens, Maarten</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4261-2323dce421f7f59e77d5ede1ec4030a63765a84729a659939f8ba5983746caaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animal husbandry</topic><topic>Animal models</topic><topic>Animals</topic><topic>clinical study design</topic><topic>Clinical trials</topic><topic>endpoints</topic><topic>Genetic engineering</topic><topic>Heterografts</topic><topic>Humans</topic><topic>innovation</topic><topic>Models, Animal</topic><topic>organ shortage</topic><topic>Organ Transplantation</topic><topic>Organs</topic><topic>patient centred</topic><topic>regulation</topic><topic>Transplantation</topic><topic>Transplantation, Heterologous</topic><topic>Transplants</topic><topic>Transplants & implants</topic><topic>Xenografts</topic><topic>Xenotransplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cozzi, Emanuele</creatorcontrib><creatorcontrib>Schneeberger, Stefan</creatorcontrib><creatorcontrib>Bellini, Maria Irene</creatorcontrib><creatorcontrib>Berglund, Erik</creatorcontrib><creatorcontrib>Böhmig, Georg</creatorcontrib><creatorcontrib>Fowler, Kevin</creatorcontrib><creatorcontrib>Hoogduijn, Martin</creatorcontrib><creatorcontrib>Jochmans, Ina</creatorcontrib><creatorcontrib>Marckmann, Georg</creatorcontrib><creatorcontrib>Marson, Lorna</creatorcontrib><creatorcontrib>Neuberger, James</creatorcontrib><creatorcontrib>Oberbauer, Rainer</creatorcontrib><creatorcontrib>Pierson, Richard N.</creatorcontrib><creatorcontrib>Reichart, Bruno</creatorcontrib><creatorcontrib>Scobie, Linda</creatorcontrib><creatorcontrib>White, Colin</creatorcontrib><creatorcontrib>Naesens, Maarten</creatorcontrib><creatorcontrib>for ESOT Workstream 1 of the TLJ (Transplantation Learning Journey) Project</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Transplant international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cozzi, Emanuele</au><au>Schneeberger, Stefan</au><au>Bellini, Maria Irene</au><au>Berglund, Erik</au><au>Böhmig, Georg</au><au>Fowler, Kevin</au><au>Hoogduijn, Martin</au><au>Jochmans, Ina</au><au>Marckmann, Georg</au><au>Marson, Lorna</au><au>Neuberger, James</au><au>Oberbauer, Rainer</au><au>Pierson, Richard N.</au><au>Reichart, Bruno</au><au>Scobie, Linda</au><au>White, Colin</au><au>Naesens, Maarten</au><aucorp>for ESOT Workstream 1 of the TLJ (Transplantation Learning Journey) Project</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Organ transplants of the future: planning for innovations including xenotransplantation</atitle><jtitle>Transplant international</jtitle><addtitle>Transpl Int</addtitle><date>2021-11</date><risdate>2021</risdate><volume>34</volume><issue>11</issue><spage>2006</spage><epage>2018</epage><pages>2006-2018</pages><issn>0934-0874</issn><eissn>1432-2277</eissn><abstract>Summary
The future clinical application of animal‐to‐human transplantation (xenotransplantation) is of importance to society as a whole. Favourable preclinical data relevant to cell, tissue and solid organ xenotransplants have been obtained from many animal models utilizing genetic engineering and protocols of pathogen‐free husbandry. Findings have reached a tipping point, and xenotransplantation of solid organs is approaching clinical evaluation, the process of which now requires close deliberation. Such discussions include considering when there is sufficient evidence from preclinical animal studies to start first‐in‐human xenotransplantation trials. The present article is based on evidence and opinions formulated by members of the European Society for Organ Transplantation who are involved in the Transplantation Learning Journey project. The article includes a brief overview of preclinical concepts and biology of solid organ xenotransplantation, discusses the selection of candidates for first‐in‐human studies and considers requirements for study design and conduct. In addition, the paper emphasizes the need for a regulatory framework for xenotransplantation of solid organs and the essential requirement for input from public and patient stakeholders.</abstract><cop>Switzerland</cop><pub>Blackwell Publishing Ltd</pub><pmid>34459040</pmid><doi>10.1111/tri.14031</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-0217-8254</orcidid><orcidid>https://orcid.org/0000-0001-7544-6275</orcidid><orcidid>https://orcid.org/0000-0003-0730-4923</orcidid><orcidid>https://orcid.org/0000-0002-5625-0792</orcidid><orcidid>https://orcid.org/0000-0002-2619-8639</orcidid><orcidid>https://orcid.org/0000-0002-6079-002X</orcidid><orcidid>https://orcid.org/0000-0003-4592-2810</orcidid><orcidid>https://orcid.org/0000-0002-7600-912X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal husbandry Animal models Animals clinical study design Clinical trials endpoints Genetic engineering Heterografts Humans innovation Models, Animal organ shortage Organ Transplantation Organs patient centred regulation Transplantation Transplantation, Heterologous Transplants Transplants & implants Xenografts Xenotransplantation |
title | Organ transplants of the future: planning for innovations including xenotransplantation |
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