Safe use of anti‐ CD 154 monoclonal antibody in pig islet xenotransplantation in monkeys
Anti‐ CD 154mAb is a powerful co‐stimulation blockade agent that is efficacious in preventing rejection, even in xenogeneic settings. It has been used in the majority of successful long‐term pig‐to‐non‐human primate islet transplantation models. However, its clinical use was halted as a result of th...
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Veröffentlicht in: | Xenotransplantation (Københaven) 2017-01, Vol.24 (1) |
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container_title | Xenotransplantation (Københaven) |
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creator | Bottino, Rita Knoll, Michael F. Graeme‐Wilson, Joshua Klein, Edwin C. Ayares, David Trucco, Massimo Cooper, David K. C. |
description | Anti‐
CD
154mAb is a powerful co‐stimulation blockade agent that is efficacious in preventing rejection, even in xenogeneic settings. It has been used in the majority of successful long‐term pig‐to‐non‐human primate islet transplantation models. However, its clinical use was halted as a result of thromboembolic complications that were also observed in preclinical and clinical organ transplantation models. An anti‐
CD
154mAb was administered to 14 streptozotocin‐induced diabetic cynomolgus monkey recipients of porcine islets, some of which received the agent for many months. Monkeys were monitored for complications, and blood monitoring was carried out frequently. After euthanasia, multiple biopsies of all organs were examined for histological features of thromboembolism. Anti‐
CD
154mAb prevented rejection of genetically engineered pig islets in all monkeys. No significant complications were attributable specifically to anti‐
CD
154mAb. There was no evidence of thromboembolism in multiple histological sections from all major organs, including the brain. Our data suggest that in diabetic monkeys with pig islet grafts, anti‐
CD
154mAb would appear to be an effective and safe therapy, and is not associated with thromboembolic complications. |
doi_str_mv | 10.1111/xen.12283 |
format | Article |
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CD
154mAb is a powerful co‐stimulation blockade agent that is efficacious in preventing rejection, even in xenogeneic settings. It has been used in the majority of successful long‐term pig‐to‐non‐human primate islet transplantation models. However, its clinical use was halted as a result of thromboembolic complications that were also observed in preclinical and clinical organ transplantation models. An anti‐
CD
154mAb was administered to 14 streptozotocin‐induced diabetic cynomolgus monkey recipients of porcine islets, some of which received the agent for many months. Monkeys were monitored for complications, and blood monitoring was carried out frequently. After euthanasia, multiple biopsies of all organs were examined for histological features of thromboembolism. Anti‐
CD
154mAb prevented rejection of genetically engineered pig islets in all monkeys. No significant complications were attributable specifically to anti‐
CD
154mAb. There was no evidence of thromboembolism in multiple histological sections from all major organs, including the brain. Our data suggest that in diabetic monkeys with pig islet grafts, anti‐
CD
154mAb would appear to be an effective and safe therapy, and is not associated with thromboembolic complications.</description><identifier>ISSN: 0908-665X</identifier><identifier>EISSN: 1399-3089</identifier><identifier>DOI: 10.1111/xen.12283</identifier><language>eng</language><ispartof>Xenotransplantation (Københaven), 2017-01, Vol.24 (1)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c743-f6100d689aa58a31a93f30d87a0da0dc72f6987189656deb08353aee00361e753</citedby><cites>FETCH-LOGICAL-c743-f6100d689aa58a31a93f30d87a0da0dc72f6987189656deb08353aee00361e753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27926,27927</link.rule.ids></links><search><creatorcontrib>Bottino, Rita</creatorcontrib><creatorcontrib>Knoll, Michael F.</creatorcontrib><creatorcontrib>Graeme‐Wilson, Joshua</creatorcontrib><creatorcontrib>Klein, Edwin C.</creatorcontrib><creatorcontrib>Ayares, David</creatorcontrib><creatorcontrib>Trucco, Massimo</creatorcontrib><creatorcontrib>Cooper, David K. C.</creatorcontrib><title>Safe use of anti‐ CD 154 monoclonal antibody in pig islet xenotransplantation in monkeys</title><title>Xenotransplantation (Københaven)</title><description>Anti‐
CD
154mAb is a powerful co‐stimulation blockade agent that is efficacious in preventing rejection, even in xenogeneic settings. It has been used in the majority of successful long‐term pig‐to‐non‐human primate islet transplantation models. However, its clinical use was halted as a result of thromboembolic complications that were also observed in preclinical and clinical organ transplantation models. An anti‐
CD
154mAb was administered to 14 streptozotocin‐induced diabetic cynomolgus monkey recipients of porcine islets, some of which received the agent for many months. Monkeys were monitored for complications, and blood monitoring was carried out frequently. After euthanasia, multiple biopsies of all organs were examined for histological features of thromboembolism. Anti‐
CD
154mAb prevented rejection of genetically engineered pig islets in all monkeys. No significant complications were attributable specifically to anti‐
CD
154mAb. There was no evidence of thromboembolism in multiple histological sections from all major organs, including the brain. Our data suggest that in diabetic monkeys with pig islet grafts, anti‐
CD
154mAb would appear to be an effective and safe therapy, and is not associated with thromboembolic complications.</description><issn>0908-665X</issn><issn>1399-3089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNotUMtOwzAQtBBIhMKBP_CVQ8o6Wzv2EZWnVIkDPSAu0TaxUSC1ozhI5MYn8I18CW5hNdIednZndhg7FzAXqS4_rZ-LotB4wDKBxuQI2hyyDAzoXCn5fMxOYnwDAJRaZuzliZzlH9Hy4Dj5sf35-ubLay7kgm-DD3UXPHX7ySY0E28979tX3sbOjjyJhXEgH_suEWhsg98R0t67neIpO3LURXv232dsfXuzXt7nq8e7h-XVKq_LBeZOCYBGaUMkNaEggw6h0SVBk1CXhVNGl0IbJVVjN6BRIlmbHlDClhJn7OLvbD2EGAfrqn5otzRMlYBql0mVbFb7TPAX9b1VPA</recordid><startdate>201701</startdate><enddate>201701</enddate><creator>Bottino, Rita</creator><creator>Knoll, Michael F.</creator><creator>Graeme‐Wilson, Joshua</creator><creator>Klein, Edwin C.</creator><creator>Ayares, David</creator><creator>Trucco, Massimo</creator><creator>Cooper, David K. C.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201701</creationdate><title>Safe use of anti‐ CD 154 monoclonal antibody in pig islet xenotransplantation in monkeys</title><author>Bottino, Rita ; Knoll, Michael F. ; Graeme‐Wilson, Joshua ; Klein, Edwin C. ; Ayares, David ; Trucco, Massimo ; Cooper, David K. C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c743-f6100d689aa58a31a93f30d87a0da0dc72f6987189656deb08353aee00361e753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bottino, Rita</creatorcontrib><creatorcontrib>Knoll, Michael F.</creatorcontrib><creatorcontrib>Graeme‐Wilson, Joshua</creatorcontrib><creatorcontrib>Klein, Edwin C.</creatorcontrib><creatorcontrib>Ayares, David</creatorcontrib><creatorcontrib>Trucco, Massimo</creatorcontrib><creatorcontrib>Cooper, David K. C.</creatorcontrib><collection>CrossRef</collection><jtitle>Xenotransplantation (Københaven)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bottino, Rita</au><au>Knoll, Michael F.</au><au>Graeme‐Wilson, Joshua</au><au>Klein, Edwin C.</au><au>Ayares, David</au><au>Trucco, Massimo</au><au>Cooper, David K. C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safe use of anti‐ CD 154 monoclonal antibody in pig islet xenotransplantation in monkeys</atitle><jtitle>Xenotransplantation (Københaven)</jtitle><date>2017-01</date><risdate>2017</risdate><volume>24</volume><issue>1</issue><issn>0908-665X</issn><eissn>1399-3089</eissn><abstract>Anti‐
CD
154mAb is a powerful co‐stimulation blockade agent that is efficacious in preventing rejection, even in xenogeneic settings. It has been used in the majority of successful long‐term pig‐to‐non‐human primate islet transplantation models. However, its clinical use was halted as a result of thromboembolic complications that were also observed in preclinical and clinical organ transplantation models. An anti‐
CD
154mAb was administered to 14 streptozotocin‐induced diabetic cynomolgus monkey recipients of porcine islets, some of which received the agent for many months. Monkeys were monitored for complications, and blood monitoring was carried out frequently. After euthanasia, multiple biopsies of all organs were examined for histological features of thromboembolism. Anti‐
CD
154mAb prevented rejection of genetically engineered pig islets in all monkeys. No significant complications were attributable specifically to anti‐
CD
154mAb. There was no evidence of thromboembolism in multiple histological sections from all major organs, including the brain. Our data suggest that in diabetic monkeys with pig islet grafts, anti‐
CD
154mAb would appear to be an effective and safe therapy, and is not associated with thromboembolic complications.</abstract><doi>10.1111/xen.12283</doi></addata></record> |
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title | Safe use of anti‐ CD 154 monoclonal antibody in pig islet xenotransplantation in monkeys |
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