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GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation

Wild type (WT) animals cannot be used to objectively assess the immunogenicity of animal tissue-derived biomaterials when used as recipients due to difference with human in α-Gal expression. The purpose of this study is to compare the differences of immunological responses between the GGTA1 gene-kno...

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Autores principales: Mu, Yufeng, Zhang, Yu, Wei, Lina, Chen, Liang, Hao, Feng, Shao, Anliang, Qu, Shuxin, Xu, Liming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719100/
https://www.ncbi.nlm.nih.gov/pubmed/36471894
http://dx.doi.org/10.1016/j.mtbio.2022.100505
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author Mu, Yufeng
Zhang, Yu
Wei, Lina
Chen, Liang
Hao, Feng
Shao, Anliang
Qu, Shuxin
Xu, Liming
author_facet Mu, Yufeng
Zhang, Yu
Wei, Lina
Chen, Liang
Hao, Feng
Shao, Anliang
Qu, Shuxin
Xu, Liming
author_sort Mu, Yufeng
collection PubMed
description Wild type (WT) animals cannot be used to objectively assess the immunogenicity of animal tissue-derived biomaterials when used as recipients due to difference with human in α-Gal expression. The purpose of this study is to compare the differences of immunological responses between the GGTA1 gene-knockout (GTKO) rabbits and WT rabbits after implantation with animal tissue-derived biomaterials. The porcine-derived decellularized bone matrix (natural bone material, NBM) and fresh porcine cancellous bone (PCB) were implanted in GTKO rabbits and WT rabbits, respectively, and sham operation was used as control (Con). At 2- and 6-week post-implantation, the related immunological items including antibody levels, serum-mediated cell lysis, cytokines, lymphocyte subtypes, and histopathological changes were assessed. GTKO rabbits exhibited more sensitive immune responses than WT rabbits after PCB implantation, resulted from a significant increase of antibodies (except total antibodies) and cytokines levels, cell lysis ratios, CD4/CD8 proportions, and inflammatory cells infiltration. Immunological factors and inflammatory cells infiltrate in GTKO rabbits after NBM implantation were significantly lower than those in the PCB group. Among the three groups, the NBM group showed the highest contents of new bone formation elements. In conclusion, the GTKO rabbit is a more sensitive alternative model than WT rabbit for preclinical study of xenografts via in situ implantation. Studies on multiple gene-edited animals are also necessary for more comprehensively evaluating xenoimmunologen risks of animal tissue-derived biomaterials in the future. Additionally, the immunogenicity of NBM was remarkably decreased compared to PCB.
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spelling pubmed-97191002022-12-04 GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation Mu, Yufeng Zhang, Yu Wei, Lina Chen, Liang Hao, Feng Shao, Anliang Qu, Shuxin Xu, Liming Mater Today Bio Full Length Article Wild type (WT) animals cannot be used to objectively assess the immunogenicity of animal tissue-derived biomaterials when used as recipients due to difference with human in α-Gal expression. The purpose of this study is to compare the differences of immunological responses between the GGTA1 gene-knockout (GTKO) rabbits and WT rabbits after implantation with animal tissue-derived biomaterials. The porcine-derived decellularized bone matrix (natural bone material, NBM) and fresh porcine cancellous bone (PCB) were implanted in GTKO rabbits and WT rabbits, respectively, and sham operation was used as control (Con). At 2- and 6-week post-implantation, the related immunological items including antibody levels, serum-mediated cell lysis, cytokines, lymphocyte subtypes, and histopathological changes were assessed. GTKO rabbits exhibited more sensitive immune responses than WT rabbits after PCB implantation, resulted from a significant increase of antibodies (except total antibodies) and cytokines levels, cell lysis ratios, CD4/CD8 proportions, and inflammatory cells infiltration. Immunological factors and inflammatory cells infiltrate in GTKO rabbits after NBM implantation were significantly lower than those in the PCB group. Among the three groups, the NBM group showed the highest contents of new bone formation elements. In conclusion, the GTKO rabbit is a more sensitive alternative model than WT rabbit for preclinical study of xenografts via in situ implantation. Studies on multiple gene-edited animals are also necessary for more comprehensively evaluating xenoimmunologen risks of animal tissue-derived biomaterials in the future. Additionally, the immunogenicity of NBM was remarkably decreased compared to PCB. Elsevier 2022-11-25 /pmc/articles/PMC9719100/ /pubmed/36471894 http://dx.doi.org/10.1016/j.mtbio.2022.100505 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Mu, Yufeng
Zhang, Yu
Wei, Lina
Chen, Liang
Hao, Feng
Shao, Anliang
Qu, Shuxin
Xu, Liming
GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation
title GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation
title_full GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation
title_fullStr GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation
title_full_unstemmed GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation
title_short GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation
title_sort gtko rabbit: a novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719100/
https://www.ncbi.nlm.nih.gov/pubmed/36471894
http://dx.doi.org/10.1016/j.mtbio.2022.100505
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