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Pig models of neurodegenerative disorders: Utilization in cell replacement-based preclinical safety and efficacy studies
ABSTRACT An important component for successful translation of cell replacement‐based therapies into clinical practice is the utilization of large animal models to conduct efficacy and/or safety cell dosing studies. Over the past few decades, several large animal models (dog, cat, nonhuman primate) w...
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Published in: | Journal of comparative neurology (1911) 2014-08, Vol.522 (12), p.2784-2801 |
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container_title | Journal of comparative neurology (1911) |
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creator | Dolezalova, Dasa Hruska-Plochan, Marian Bjarkam, Carsten R. Sørensen, Jens Christian H. Cunningham, Miles Weingarten, David Ciacci, Joseph D. Juhas, Stefan Juhasova, Jana Motlik, Jan Hefferan, Michael P. Hazel, Tom Johe, Karl Carromeu, Cassiano Muotri, Alysson Bui, Jack Strnadel, Jan Marsala, Martin |
description | ABSTRACT
An important component for successful translation of cell replacement‐based therapies into clinical practice is the utilization of large animal models to conduct efficacy and/or safety cell dosing studies. Over the past few decades, several large animal models (dog, cat, nonhuman primate) were developed and employed in cell replacement studies; however, none of these models appears to provide a readily available platform to conduct effective and large‐scale preclinical studies. In recent years, numerous pig models of neurodegenerative disorders were developed using both a transgenic approach as well as invasive surgical techniques. The pig model (naïve noninjured animals) was recently used successfully to define the safety and optimal dosing of human spinal stem cells after grafting into the central nervous system (CNS) in immunosuppressed animals. The data from these studies were used in the design of a human clinical protocol used in amyotrophic lateral sclerosis (ALS) patients in a Phase I clinical trial. In addition, a highly inbred (complete major histocompatibility complex [MHC] match) strain of miniature pigs is available which permits the design of comparable MHC combinations between the donor cells and the graft recipient as used in human patients. Jointly, these studies show that the pig model can represent an effective large animal model to be used in preclinical cell replacement modeling. This review summarizes the available pig models of neurodegenerative disorders and the use of some of these models in cell replacement studies. The challenges and potential future directions in more effective use of the pig neurodegenerative models are also discussed. J. Comp. Neurol. 522:2784–2801, 2014. © 2014 Wiley Periodicals, Inc.
Using confocal microscopy, the authors show survival and maturation of pig iPS‐derived neurons after grafting into the lumbar spinal cord of an immunosuppressed pig. The pig is becoming a widely used large animal species in neurodegenerative disease modeling and is being frequently used in preclinical safety and efficacy studies. |
doi_str_mv | 10.1002/cne.23575 |
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An important component for successful translation of cell replacement‐based therapies into clinical practice is the utilization of large animal models to conduct efficacy and/or safety cell dosing studies. Over the past few decades, several large animal models (dog, cat, nonhuman primate) were developed and employed in cell replacement studies; however, none of these models appears to provide a readily available platform to conduct effective and large‐scale preclinical studies. In recent years, numerous pig models of neurodegenerative disorders were developed using both a transgenic approach as well as invasive surgical techniques. The pig model (naïve noninjured animals) was recently used successfully to define the safety and optimal dosing of human spinal stem cells after grafting into the central nervous system (CNS) in immunosuppressed animals. The data from these studies were used in the design of a human clinical protocol used in amyotrophic lateral sclerosis (ALS) patients in a Phase I clinical trial. In addition, a highly inbred (complete major histocompatibility complex [MHC] match) strain of miniature pigs is available which permits the design of comparable MHC combinations between the donor cells and the graft recipient as used in human patients. Jointly, these studies show that the pig model can represent an effective large animal model to be used in preclinical cell replacement modeling. This review summarizes the available pig models of neurodegenerative disorders and the use of some of these models in cell replacement studies. The challenges and potential future directions in more effective use of the pig neurodegenerative models are also discussed. J. Comp. Neurol. 522:2784–2801, 2014. © 2014 Wiley Periodicals, Inc.
Using confocal microscopy, the authors show survival and maturation of pig iPS‐derived neurons after grafting into the lumbar spinal cord of an immunosuppressed pig. The pig is becoming a widely used large animal species in neurodegenerative disease modeling and is being frequently used in preclinical safety and efficacy studies.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.23575</identifier><identifier>PMID: 24610493</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; cell replacement therapy ; Cell- and Tissue-Based Therapy - methods ; Disease Models, Animal ; Humans ; neural precursors ; Neurodegenerative Diseases - surgery ; neurodegenerative models ; pig ; Primates ; stem cells ; Swine</subject><ispartof>Journal of comparative neurology (1911), 2014-08, Vol.522 (12), p.2784-2801</ispartof><rights>2014 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4945-289c8183c823208f1ba23db78e9c673d9e92084d5bc6d7261beb4958eb36af543</citedby><cites>FETCH-LOGICAL-c4945-289c8183c823208f1ba23db78e9c673d9e92084d5bc6d7261beb4958eb36af543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24610493$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dolezalova, Dasa</creatorcontrib><creatorcontrib>Hruska-Plochan, Marian</creatorcontrib><creatorcontrib>Bjarkam, Carsten R.</creatorcontrib><creatorcontrib>Sørensen, Jens Christian H.</creatorcontrib><creatorcontrib>Cunningham, Miles</creatorcontrib><creatorcontrib>Weingarten, David</creatorcontrib><creatorcontrib>Ciacci, Joseph D.</creatorcontrib><creatorcontrib>Juhas, Stefan</creatorcontrib><creatorcontrib>Juhasova, Jana</creatorcontrib><creatorcontrib>Motlik, Jan</creatorcontrib><creatorcontrib>Hefferan, Michael P.</creatorcontrib><creatorcontrib>Hazel, Tom</creatorcontrib><creatorcontrib>Johe, Karl</creatorcontrib><creatorcontrib>Carromeu, Cassiano</creatorcontrib><creatorcontrib>Muotri, Alysson</creatorcontrib><creatorcontrib>Bui, Jack</creatorcontrib><creatorcontrib>Strnadel, Jan</creatorcontrib><creatorcontrib>Marsala, Martin</creatorcontrib><title>Pig models of neurodegenerative disorders: Utilization in cell replacement-based preclinical safety and efficacy studies</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>ABSTRACT
An important component for successful translation of cell replacement‐based therapies into clinical practice is the utilization of large animal models to conduct efficacy and/or safety cell dosing studies. Over the past few decades, several large animal models (dog, cat, nonhuman primate) were developed and employed in cell replacement studies; however, none of these models appears to provide a readily available platform to conduct effective and large‐scale preclinical studies. In recent years, numerous pig models of neurodegenerative disorders were developed using both a transgenic approach as well as invasive surgical techniques. The pig model (naïve noninjured animals) was recently used successfully to define the safety and optimal dosing of human spinal stem cells after grafting into the central nervous system (CNS) in immunosuppressed animals. The data from these studies were used in the design of a human clinical protocol used in amyotrophic lateral sclerosis (ALS) patients in a Phase I clinical trial. In addition, a highly inbred (complete major histocompatibility complex [MHC] match) strain of miniature pigs is available which permits the design of comparable MHC combinations between the donor cells and the graft recipient as used in human patients. Jointly, these studies show that the pig model can represent an effective large animal model to be used in preclinical cell replacement modeling. This review summarizes the available pig models of neurodegenerative disorders and the use of some of these models in cell replacement studies. The challenges and potential future directions in more effective use of the pig neurodegenerative models are also discussed. J. Comp. Neurol. 522:2784–2801, 2014. © 2014 Wiley Periodicals, Inc.
Using confocal microscopy, the authors show survival and maturation of pig iPS‐derived neurons after grafting into the lumbar spinal cord of an immunosuppressed pig. The pig is becoming a widely used large animal species in neurodegenerative disease modeling and is being frequently used in preclinical safety and efficacy studies.</description><subject>Animals</subject><subject>cell replacement therapy</subject><subject>Cell- and Tissue-Based Therapy - methods</subject><subject>Disease Models, Animal</subject><subject>Humans</subject><subject>neural precursors</subject><subject>Neurodegenerative Diseases - surgery</subject><subject>neurodegenerative models</subject><subject>pig</subject><subject>Primates</subject><subject>stem cells</subject><subject>Swine</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkU9v1DAQxS0EotvCgS-ALHGhh7R2_Cc2N7QqC9KqrASFo-XYk8olcRY7gS6fHi_b9oCEOI3m-TdP43kIvaDkjBJSn7sIZzUTjXiEFpRoWWkl6WO0KG-00lo2R-g45xtCiNZMPUVHNZeUcM0W6HYTrvEweugzHjscYU6luYYIyU7hB2Af8pg8pPwGX02hD7-KPEYcInbQ9zjBtrcOBohT1doMHm8TuD7E4GyPs-1g2mEbPYauK5Lb4TzNPkB-hp50ts_w_K6eoKt3F5-X76v1x9WH5dt15bjmoqqVdooq5lTNaqI62tqa-bZRoJ1smNegi8y9aJ30TS1pCy3XQkHLpO0EZyfo9cF3m8bvM-TJDCHvV7cRxjkbKjgnRNJymf-jTHMplKYFffUXejPOKZaP7CnZcE3p3vD0QLk05pygM9sUBpt2hhKzT86U5Myf5Ar78s5xbgfwD-R9VAU4PwA_Qw-7fzuZ5eXFvWV1mAh5gtuHCZu-mXK6Qn69XJnVl_WGMbExn9hvJhOx2A</recordid><startdate>20140815</startdate><enddate>20140815</enddate><creator>Dolezalova, Dasa</creator><creator>Hruska-Plochan, Marian</creator><creator>Bjarkam, Carsten R.</creator><creator>Sørensen, Jens Christian H.</creator><creator>Cunningham, Miles</creator><creator>Weingarten, David</creator><creator>Ciacci, Joseph D.</creator><creator>Juhas, Stefan</creator><creator>Juhasova, Jana</creator><creator>Motlik, Jan</creator><creator>Hefferan, Michael P.</creator><creator>Hazel, Tom</creator><creator>Johe, Karl</creator><creator>Carromeu, Cassiano</creator><creator>Muotri, Alysson</creator><creator>Bui, Jack</creator><creator>Strnadel, Jan</creator><creator>Marsala, Martin</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20140815</creationdate><title>Pig models of neurodegenerative disorders: Utilization in cell replacement-based preclinical safety and efficacy studies</title><author>Dolezalova, Dasa ; Hruska-Plochan, Marian ; Bjarkam, Carsten R. ; Sørensen, Jens Christian H. ; Cunningham, Miles ; Weingarten, David ; Ciacci, Joseph D. ; Juhas, Stefan ; Juhasova, Jana ; Motlik, Jan ; Hefferan, Michael P. ; Hazel, Tom ; Johe, Karl ; Carromeu, Cassiano ; Muotri, Alysson ; Bui, Jack ; Strnadel, Jan ; Marsala, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4945-289c8183c823208f1ba23db78e9c673d9e92084d5bc6d7261beb4958eb36af543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>cell replacement therapy</topic><topic>Cell- and Tissue-Based Therapy - methods</topic><topic>Disease Models, Animal</topic><topic>Humans</topic><topic>neural precursors</topic><topic>Neurodegenerative Diseases - surgery</topic><topic>neurodegenerative models</topic><topic>pig</topic><topic>Primates</topic><topic>stem cells</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dolezalova, Dasa</creatorcontrib><creatorcontrib>Hruska-Plochan, Marian</creatorcontrib><creatorcontrib>Bjarkam, Carsten R.</creatorcontrib><creatorcontrib>Sørensen, Jens Christian H.</creatorcontrib><creatorcontrib>Cunningham, Miles</creatorcontrib><creatorcontrib>Weingarten, David</creatorcontrib><creatorcontrib>Ciacci, Joseph D.</creatorcontrib><creatorcontrib>Juhas, Stefan</creatorcontrib><creatorcontrib>Juhasova, Jana</creatorcontrib><creatorcontrib>Motlik, Jan</creatorcontrib><creatorcontrib>Hefferan, Michael P.</creatorcontrib><creatorcontrib>Hazel, Tom</creatorcontrib><creatorcontrib>Johe, Karl</creatorcontrib><creatorcontrib>Carromeu, Cassiano</creatorcontrib><creatorcontrib>Muotri, Alysson</creatorcontrib><creatorcontrib>Bui, Jack</creatorcontrib><creatorcontrib>Strnadel, Jan</creatorcontrib><creatorcontrib>Marsala, Martin</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dolezalova, Dasa</au><au>Hruska-Plochan, Marian</au><au>Bjarkam, Carsten R.</au><au>Sørensen, Jens Christian H.</au><au>Cunningham, Miles</au><au>Weingarten, David</au><au>Ciacci, Joseph D.</au><au>Juhas, Stefan</au><au>Juhasova, Jana</au><au>Motlik, Jan</au><au>Hefferan, Michael P.</au><au>Hazel, Tom</au><au>Johe, Karl</au><au>Carromeu, Cassiano</au><au>Muotri, Alysson</au><au>Bui, Jack</au><au>Strnadel, Jan</au><au>Marsala, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pig models of neurodegenerative disorders: Utilization in cell replacement-based preclinical safety and efficacy studies</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2014-08-15</date><risdate>2014</risdate><volume>522</volume><issue>12</issue><spage>2784</spage><epage>2801</epage><pages>2784-2801</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>ABSTRACT
An important component for successful translation of cell replacement‐based therapies into clinical practice is the utilization of large animal models to conduct efficacy and/or safety cell dosing studies. Over the past few decades, several large animal models (dog, cat, nonhuman primate) were developed and employed in cell replacement studies; however, none of these models appears to provide a readily available platform to conduct effective and large‐scale preclinical studies. In recent years, numerous pig models of neurodegenerative disorders were developed using both a transgenic approach as well as invasive surgical techniques. The pig model (naïve noninjured animals) was recently used successfully to define the safety and optimal dosing of human spinal stem cells after grafting into the central nervous system (CNS) in immunosuppressed animals. The data from these studies were used in the design of a human clinical protocol used in amyotrophic lateral sclerosis (ALS) patients in a Phase I clinical trial. In addition, a highly inbred (complete major histocompatibility complex [MHC] match) strain of miniature pigs is available which permits the design of comparable MHC combinations between the donor cells and the graft recipient as used in human patients. Jointly, these studies show that the pig model can represent an effective large animal model to be used in preclinical cell replacement modeling. This review summarizes the available pig models of neurodegenerative disorders and the use of some of these models in cell replacement studies. The challenges and potential future directions in more effective use of the pig neurodegenerative models are also discussed. J. Comp. Neurol. 522:2784–2801, 2014. © 2014 Wiley Periodicals, Inc.
Using confocal microscopy, the authors show survival and maturation of pig iPS‐derived neurons after grafting into the lumbar spinal cord of an immunosuppressed pig. The pig is becoming a widely used large animal species in neurodegenerative disease modeling and is being frequently used in preclinical safety and efficacy studies.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>24610493</pmid><doi>10.1002/cne.23575</doi><tpages>18</tpages></addata></record> |
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subjects | Animals cell replacement therapy Cell- and Tissue-Based Therapy - methods Disease Models, Animal Humans neural precursors Neurodegenerative Diseases - surgery neurodegenerative models pig Primates stem cells Swine |
title | Pig models of neurodegenerative disorders: Utilization in cell replacement-based preclinical safety and efficacy studies |
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