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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Published inMaterials today bio Vol. 18; p. 100505
Main Authors Mu, Yufeng, Zhang, Yu, Wei, Lina, Chen, Liang, Hao, Feng, Shao, Anliang, Qu, Shuxin, Xu, Liming
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.02.2023
Elsevier
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ISSN2590-0064
2590-0064
DOI10.1016/j.mtbio.2022.100505

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Abstract 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. [Display omitted]
AbstractList 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.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.
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.
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. [Display omitted]
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. Image 1
ArticleNumber 100505
Author Chen, Liang
Qu, Shuxin
Shao, Anliang
Zhang, Yu
Mu, Yufeng
Xu, Liming
Wei, Lina
Hao, Feng
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Cites_doi 10.1002/jez.b.21072
10.1155/2022/7950834
10.1002/term.3004
10.1007/s12026-018-8985-8
10.1038/s41598-018-32959-1
10.1002/jbm.b.30951
10.4103/0971-6580.94513
10.1016/j.smim.2007.11.004
10.1155/2020/9680474
10.1097/00007890-199601150-00004
10.1016/j.biomaterials.2016.02.003
10.1080/21691401.2018.1493489
10.1097/TP.0b013e318199c34f
10.1084/jem.160.5.1519
10.1111/j.1365-2362.2005.01441.x
10.1016/j.actbio.2010.11.030
10.1007/s11248-021-00271-w
10.1089/ten.teb.2014.0392
10.1016/j.biomaterials.2017.08.012
10.1084/jem.162.2.573
10.1016/j.smim.2007.11.003
10.1002/jbm.a.33061
10.1016/j.biomaterials.2016.03.024
10.1186/s12863-022-01068-4
10.1016/j.biomaterials.2020.120603
10.4103/1735-3327.92960
10.1016/j.biomaterials.2008.05.006
10.1016/j.biomaterials.2011.05.078
10.1097/00007890-199804270-00020
10.1093/rb/rbaa020
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Keywords Graft material-specific antibody
Xenograft
Immunogenicity evaluation
anti-Gal antibody
α-Gal
GTKO rabbit
In situ implantation
Language English
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This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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These authors contributed equally to this study.
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References Umashankar, Arun, Kumari (bib26) 2011; 97
Wong, Wong, Vapniarsky (bib17) 2016; 92
Galili, Latemple, Radic (bib21) 1998; 65
Anderson, Rodriguez, Chang (bib33) 2008; 20
Shao, Ling, Chen (bib13) 2020; 2020
Umashankar, Mohanan, Kumari (bib25) 2012; 19
Wang, Ruan, Zhang (bib35) 2019; 33
Gates, Xing, Griffiths (bib28) 2019; 13
Konakci K, Bohle, Blumer (bib8) 2005; 35
Shao, Ling, Xu (bib12) 2018; 46
Galili (bib2) 2015; 21
Bayly-Jones, Bubeck, Dunstone (bib31) 2017
Gates, Griffiths (bib27) 2018; 66
Lu, Shao, Shan (bib19) 2018; 8
Galili (bib6) 1999; 32
Ezzelarab M, Garcia B, Azimzadeh A, et al. The innate immune response and activation of coagulation in α1,3-galactosyltransferase gene-knockout xenograft recipients [J]. Transplantation, 87(6): 805-812.
Chen, Wei, Shao (bib10) 2020; 7
Zippel, Wilhelm, Hoene (bib24) 2008; 85
Mu, Wu (bib29) 2021; 25
Franz, Rammelt, Scharnweber (bib32) 2011; 32
Aamodt, Grainger (bib3) 2016; 86
Wei, Mu, Deng (bib18) 2022; 23
Galili, Rachmilewitz, Peleg (bib4) 1984; 160
Kuljanin, Brown, Raleigh (bib22) 2017; 144
Naso, Gandaglia, Iop (bib20) 2011; 7
Galili, Macher, Buehler (bib5) 1985; 162
Shim, Ko, Kim (bib36) 2021; 30
Fang, Qiu, Xia (bib23) 2021; 268
Roy, Jinno-Oue, Shinagawa (bib7) 2006; 306B
Thomas, Bhat, Mapara (bib16) 2012; 9
Mu, Shao, Shi (bib14) 2022; 2022
Griffiths, Choe, Reardon (bib15) 2008; 29
Tearle, Tange, Zannettino (bib11) 1996; 61
Badylak, Gilbert (bib34) 2008; 20
Bilodeau, Goltsis, Rogers (bib1) 2020; 14
Alegre (bib30) 2019
Aamodt (10.1016/j.mtbio.2022.100505_bib3) 2016; 86
Galili (10.1016/j.mtbio.2022.100505_bib5) 1985; 162
Fang (10.1016/j.mtbio.2022.100505_bib23) 2021; 268
Shim (10.1016/j.mtbio.2022.100505_bib36) 2021; 30
Mu (10.1016/j.mtbio.2022.100505_bib29) 2021; 25
Franz (10.1016/j.mtbio.2022.100505_bib32) 2011; 32
Galili (10.1016/j.mtbio.2022.100505_bib6) 1999; 32
Lu (10.1016/j.mtbio.2022.100505_bib19) 2018; 8
Mu (10.1016/j.mtbio.2022.100505_bib14) 2022; 2022
Tearle (10.1016/j.mtbio.2022.100505_bib11) 1996; 61
Umashankar (10.1016/j.mtbio.2022.100505_bib25) 2012; 19
Konakci K (10.1016/j.mtbio.2022.100505_bib8) 2005; 35
Thomas (10.1016/j.mtbio.2022.100505_bib16) 2012; 9
Zippel (10.1016/j.mtbio.2022.100505_bib24) 2008; 85
Gates (10.1016/j.mtbio.2022.100505_bib27) 2018; 66
Badylak (10.1016/j.mtbio.2022.100505_bib34) 2008; 20
Umashankar (10.1016/j.mtbio.2022.100505_bib26) 2011; 97
Shao (10.1016/j.mtbio.2022.100505_bib12) 2018; 46
Galili (10.1016/j.mtbio.2022.100505_bib21) 1998; 65
Galili (10.1016/j.mtbio.2022.100505_bib4) 1984; 160
Wei (10.1016/j.mtbio.2022.100505_bib18) 2022; 23
Chen (10.1016/j.mtbio.2022.100505_bib10) 2020; 7
Naso (10.1016/j.mtbio.2022.100505_bib20) 2011; 7
Kuljanin (10.1016/j.mtbio.2022.100505_bib22) 2017; 144
Alegre (10.1016/j.mtbio.2022.100505_bib30) 2019
Shao (10.1016/j.mtbio.2022.100505_bib13) 2020; 2020
Wong (10.1016/j.mtbio.2022.100505_bib17) 2016; 92
Bilodeau (10.1016/j.mtbio.2022.100505_bib1) 2020; 14
10.1016/j.mtbio.2022.100505_bib9
Wang (10.1016/j.mtbio.2022.100505_bib35) 2019; 33
Anderson (10.1016/j.mtbio.2022.100505_bib33) 2008; 20
Gates (10.1016/j.mtbio.2022.100505_bib28) 2019; 13
Galili (10.1016/j.mtbio.2022.100505_bib2) 2015; 21
Griffiths (10.1016/j.mtbio.2022.100505_bib15) 2008; 29
Bayly-Jones (10.1016/j.mtbio.2022.100505_bib31) 2017
Roy (10.1016/j.mtbio.2022.100505_bib7) 2006; 306B
References_xml – volume: 97
  start-page: 311
  year: 2011
  end-page: 320
  ident: bib26
  article-title: Short duration gluteraldehyde cross linking of decellularized bovine pericardium improves biological response [J]
  publication-title: J. Biomed. Mater. Res.
– volume: 14
  start-page: 521
  year: 2020
  end-page: 538
  ident: bib1
  article-title: Limitations of recellularized biological scaffolds for human transplantation [J]
  publication-title: J Tissue Eng Regen Med
– volume: 25
  start-page: 281
  year: 2021
  end-page: 285
  ident: bib29
  article-title: Development and evaluation of alpha-galactosyl antigen-deficient rabbit model [J]
  publication-title: Chin. J. Tissue Eng. Res.
– start-page: 137
  year: 2019
  end-page: 164
  ident: bib30
  article-title: Monoclonal Antibodies in Transplantation [M]. Antibody Therapeutics
– volume: 2022
  year: 2022
  ident: bib14
  article-title: Immunological risk assessment of xenogeneic dural patch by comparing with raw material via GTKO mice [J]
  publication-title: BioMed Res. Int.
– volume: 92
  start-page: 1
  year: 2016
  end-page: 12
  ident: bib17
  article-title: In vivo xenogeneic scaffold fate is determined by residual antigenicity and extracellular matrix preservation [J]
  publication-title: Biomaterials
– volume: 66
  start-page: 288
  year: 2018
  end-page: 298
  ident: bib27
  article-title: Chronic graft-specific cell-mediated immune response toward candidate xenogeneic biomaterial [J]
  publication-title: Immunol. Res.
– volume: 7
  start-page: 427
  year: 2020
  end-page: 434
  ident: bib10
  article-title: Immune risk assessment of residual alphaGal in xenogeneic decellularized cornea using GTKO mice [J]
  publication-title: Regen Biomater
– volume: 86
  start-page: 68
  year: 2016
  end-page: 82
  ident: bib3
  article-title: Extracellular matrix-based biomaterial scaffolds and the host response [J]
  publication-title: Biomaterials
– volume: 35
  start-page: 17
  year: 2005
  end-page: 23
  ident: bib8
  article-title: Alpha-Gal on bioprostheses: xenograft immune response in cardiac surgery [J]
  publication-title: Eur. J. Clin. Invest.
– volume: 85
  start-page: 334
  year: 2008
  end-page: 342
  ident: bib24
  article-title: Local tissue reaction and differentiation of the prosthesis-specific antibody response following functional implantation of vascular grafts in pigs [J]
  publication-title: J. Biomed. Mater. Res. B Appl. Biomater.
– volume: 268
  year: 2021
  ident: bib23
  article-title: Extracellular matrix scaffold crosslinked with vancomycin for multifunctional antibacterial bone infection therapy
  publication-title: Biomaterials
– volume: 33
  start-page: 235
  year: 2019
  end-page: 243
  ident: bib35
  article-title: Antigenicity of tissues and organs from GGTA1/CMAH/beta 4GalNT2 triple gene knockout pigs [J]
  publication-title: J Biomed Res
– volume: 2020
  year: 2020
  ident: bib13
  article-title: GGTA1/iGb3S double knockout mice: immunological properties and immunogenicity response to xenogeneic bone matrix [J]
  publication-title: BioMed Res. Int.
– volume: 46
  start-page: S359
  year: 2018
  end-page: S369
  ident: bib12
  article-title: Xenogeneic bone matrix immune risk assessment using GGTA1 knockout mice [J]
  publication-title: Artif. Cell Nanomed. Biotechnol.
– volume: 61
  start-page: 13
  year: 1996
  end-page: 19
  ident: bib11
  article-title: The alpha-1,3-galactosyltransferase knockout mouse. Implications for xenotransplantation [J]
  publication-title: Transplantation
– volume: 23
  start-page: 54
  year: 2022
  ident: bib18
  article-title: alpha-Gal antigen-deficient rabbits with GGTA1 gene disruption via CRISPR/Cas9 [J]
  publication-title: BMC Genom Data
– volume: 9
  year: 2012
  ident: bib16
  article-title: Rabbit as an animal model for experimental research [J]
  publication-title: Dent. Res. J.
– volume: 306B
  start-page: 59
  year: 2006
  end-page: 69
  ident: bib7
  article-title: Isolation of the feline α1,3-galactosyltransferase gene, expression in transfected human cells and its phylogenetic analysis [J]
  publication-title: J. Exp. Zool. B Mol. Dev. Evol.
– volume: 19
  start-page: 51
  year: 2012
  ident: bib25
  article-title: Glutaraldehyde treatment elicits toxic response compared to decellularization in bovine pericardium [J]
  publication-title: Toxicol. Int.
– volume: 20
  start-page: 109
  year: 2008
  end-page: 116
  ident: bib34
  article-title: Immune response to biologic scaffold materials [J]
  publication-title: Semin. Immunol.
– volume: 32
  start-page: 1
  year: 1999
  end-page: 23
  ident: bib6
  article-title: Evolution of alpha 1,3galactosyltransferase and of the alpha-Gal epitope [J]
  publication-title: Subcell. Biochem.
– reference: Ezzelarab M, Garcia B, Azimzadeh A, et al. The innate immune response and activation of coagulation in α1,3-galactosyltransferase gene-knockout xenograft recipients [J]. Transplantation, 87(6): 805-812.
– volume: 144
  start-page: 130
  year: 2017
  end-page: 143
  ident: bib22
  article-title: Collagenase treatment enhances proteomic coverage of low-abundance proteins in decellularized matrix bioscaffolds [J]
  publication-title: Biomaterials
– volume: 7
  start-page: 1728
  year: 2011
  end-page: 1734
  ident: bib20
  article-title: First quantitative assay of alpha-Gal in soft tissues: presence and distribution of the epitope before and after cell removal from xenogeneic heart valves [J]
  publication-title: Acta Biomater.
– volume: 8
  year: 2018
  ident: bib19
  article-title: A standardized quantitative method for detecting remnant alpha-Gal antigen in animal tissues or animal tissue-derived biomaterials and its application [J]
  publication-title: Sci. Rep.
– volume: 30
  start-page: 619
  year: 2021
  end-page: 634
  ident: bib36
  article-title: Human immune reactivity of GGTA1/CMAH/A3GALT2 triple knockout Yucatan miniature pigs [J]
  publication-title: Transgenic Res.
– volume: 65
  start-page: 1129
  year: 1998
  end-page: 1132
  ident: bib21
  article-title: A sensitive assay for measuring alpha-Gal epitope expression on cells by a monoclonal anti-Gal antibody [J]
  publication-title: Transplantation
– volume: 21
  start-page: 231
  year: 2015
  end-page: 241
  ident: bib2
  article-title: Avoiding detrimental human immune response against Mammalian extracellular matrix implants [J]
  publication-title: Tissue Eng. B Rev.
– volume: 20
  start-page: 86
  year: 2008
  end-page: 100
  ident: bib33
  article-title: Foreign body reaction to biomaterials [J]
  publication-title: Semin. Immunol.
– volume: 160
  start-page: 1519
  year: 1984
  end-page: 1531
  ident: bib4
  article-title: A unique natural human IgG antibody with anti-alpha-galactosyl specificity [J]
  publication-title: J. Exp. Med.
– volume: 13
  year: 2019
  ident: bib28
  article-title: Immunoproteomic identification of noncarbohydrate antigens eliciting graft-specific adaptive immune responses in patients with bovine pericardial bioprosthetic heart valves [J]
  publication-title: Proteonomics Clin. Appl.
– volume: 162
  start-page: 573
  year: 1985
  end-page: 582
  ident: bib5
  article-title: Human natural anti-alpha-galactosyl IgG. II. The specific recognition of alpha (1----3)-linked galactose residues [J]
  publication-title: J. Exp. Med.
– volume: 29
  start-page: 3514
  year: 2008
  end-page: 3520
  ident: bib15
  article-title: Immunoproteomic identification of bovine pericardium xenoantigens [J]
  publication-title: Biomaterials
– start-page: 372
  year: 2017
  ident: bib31
  article-title: The mystery behind membrane insertion: a review of the complement membrane attack complex [J]
  publication-title: Philos. Trans. R. Soc. Lond. B Biol. Sci.
– volume: 32
  start-page: 6692
  year: 2011
  end-page: 6709
  ident: bib32
  article-title: Immune responses to implants–a review of the implications for the design of immunomodulatory biomaterials [J]
  publication-title: Biomaterials
– volume: 306B
  start-page: 59
  issue: 1
  year: 2006
  ident: 10.1016/j.mtbio.2022.100505_bib7
  article-title: Isolation of the feline α1,3-galactosyltransferase gene, expression in transfected human cells and its phylogenetic analysis [J]
  publication-title: J. Exp. Zool. B Mol. Dev. Evol.
  doi: 10.1002/jez.b.21072
– volume: 32
  start-page: 1
  year: 1999
  ident: 10.1016/j.mtbio.2022.100505_bib6
  article-title: Evolution of alpha 1,3galactosyltransferase and of the alpha-Gal epitope [J]
  publication-title: Subcell. Biochem.
– volume: 2022
  year: 2022
  ident: 10.1016/j.mtbio.2022.100505_bib14
  article-title: Immunological risk assessment of xenogeneic dural patch by comparing with raw material via GTKO mice [J]
  publication-title: BioMed Res. Int.
  doi: 10.1155/2022/7950834
– volume: 14
  start-page: 521
  issue: 3
  year: 2020
  ident: 10.1016/j.mtbio.2022.100505_bib1
  article-title: Limitations of recellularized biological scaffolds for human transplantation [J]
  publication-title: J Tissue Eng Regen Med
  doi: 10.1002/term.3004
– volume: 66
  start-page: 288
  issue: 2
  year: 2018
  ident: 10.1016/j.mtbio.2022.100505_bib27
  article-title: Chronic graft-specific cell-mediated immune response toward candidate xenogeneic biomaterial [J]
  publication-title: Immunol. Res.
  doi: 10.1007/s12026-018-8985-8
– volume: 8
  issue: 1
  year: 2018
  ident: 10.1016/j.mtbio.2022.100505_bib19
  article-title: A standardized quantitative method for detecting remnant alpha-Gal antigen in animal tissues or animal tissue-derived biomaterials and its application [J]
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-018-32959-1
– volume: 85
  start-page: 334
  issue: 2
  year: 2008
  ident: 10.1016/j.mtbio.2022.100505_bib24
  article-title: Local tissue reaction and differentiation of the prosthesis-specific antibody response following functional implantation of vascular grafts in pigs [J]
  publication-title: J. Biomed. Mater. Res. B Appl. Biomater.
  doi: 10.1002/jbm.b.30951
– volume: 19
  start-page: 51
  issue: 1
  year: 2012
  ident: 10.1016/j.mtbio.2022.100505_bib25
  article-title: Glutaraldehyde treatment elicits toxic response compared to decellularization in bovine pericardium [J]
  publication-title: Toxicol. Int.
  doi: 10.4103/0971-6580.94513
– volume: 13
  issue: 4
  year: 2019
  ident: 10.1016/j.mtbio.2022.100505_bib28
  article-title: Immunoproteomic identification of noncarbohydrate antigens eliciting graft-specific adaptive immune responses in patients with bovine pericardial bioprosthetic heart valves [J]
  publication-title: Proteonomics Clin. Appl.
– start-page: 372
  issue: 1726
  year: 2017
  ident: 10.1016/j.mtbio.2022.100505_bib31
  article-title: The mystery behind membrane insertion: a review of the complement membrane attack complex [J]
  publication-title: Philos. Trans. R. Soc. Lond. B Biol. Sci.
– volume: 20
  start-page: 86
  issue: 2
  year: 2008
  ident: 10.1016/j.mtbio.2022.100505_bib33
  article-title: Foreign body reaction to biomaterials [J]
  publication-title: Semin. Immunol.
  doi: 10.1016/j.smim.2007.11.004
– volume: 2020
  year: 2020
  ident: 10.1016/j.mtbio.2022.100505_bib13
  article-title: GGTA1/iGb3S double knockout mice: immunological properties and immunogenicity response to xenogeneic bone matrix [J]
  publication-title: BioMed Res. Int.
  doi: 10.1155/2020/9680474
– volume: 33
  start-page: 235
  issue: 4
  year: 2019
  ident: 10.1016/j.mtbio.2022.100505_bib35
  article-title: Antigenicity of tissues and organs from GGTA1/CMAH/beta 4GalNT2 triple gene knockout pigs [J]
  publication-title: J Biomed Res
– volume: 61
  start-page: 13
  issue: 1
  year: 1996
  ident: 10.1016/j.mtbio.2022.100505_bib11
  article-title: The alpha-1,3-galactosyltransferase knockout mouse. Implications for xenotransplantation [J]
  publication-title: Transplantation
  doi: 10.1097/00007890-199601150-00004
– volume: 86
  start-page: 68
  year: 2016
  ident: 10.1016/j.mtbio.2022.100505_bib3
  article-title: Extracellular matrix-based biomaterial scaffolds and the host response [J]
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2016.02.003
– volume: 46
  start-page: S359
  issue: sup3
  year: 2018
  ident: 10.1016/j.mtbio.2022.100505_bib12
  article-title: Xenogeneic bone matrix immune risk assessment using GGTA1 knockout mice [J]
  publication-title: Artif. Cell Nanomed. Biotechnol.
  doi: 10.1080/21691401.2018.1493489
– ident: 10.1016/j.mtbio.2022.100505_bib9
  doi: 10.1097/TP.0b013e318199c34f
– volume: 160
  start-page: 1519
  issue: 5
  year: 1984
  ident: 10.1016/j.mtbio.2022.100505_bib4
  article-title: A unique natural human IgG antibody with anti-alpha-galactosyl specificity [J]
  publication-title: J. Exp. Med.
  doi: 10.1084/jem.160.5.1519
– volume: 35
  start-page: 17
  issue: 1
  year: 2005
  ident: 10.1016/j.mtbio.2022.100505_bib8
  article-title: Alpha-Gal on bioprostheses: xenograft immune response in cardiac surgery [J]
  publication-title: Eur. J. Clin. Invest.
  doi: 10.1111/j.1365-2362.2005.01441.x
– volume: 7
  start-page: 1728
  issue: 4
  year: 2011
  ident: 10.1016/j.mtbio.2022.100505_bib20
  article-title: First quantitative assay of alpha-Gal in soft tissues: presence and distribution of the epitope before and after cell removal from xenogeneic heart valves [J]
  publication-title: Acta Biomater.
  doi: 10.1016/j.actbio.2010.11.030
– volume: 30
  start-page: 619
  issue: 5
  year: 2021
  ident: 10.1016/j.mtbio.2022.100505_bib36
  article-title: Human immune reactivity of GGTA1/CMAH/A3GALT2 triple knockout Yucatan miniature pigs [J]
  publication-title: Transgenic Res.
  doi: 10.1007/s11248-021-00271-w
– volume: 21
  start-page: 231
  issue: 2
  year: 2015
  ident: 10.1016/j.mtbio.2022.100505_bib2
  article-title: Avoiding detrimental human immune response against Mammalian extracellular matrix implants [J]
  publication-title: Tissue Eng. B Rev.
  doi: 10.1089/ten.teb.2014.0392
– volume: 144
  start-page: 130
  year: 2017
  ident: 10.1016/j.mtbio.2022.100505_bib22
  article-title: Collagenase treatment enhances proteomic coverage of low-abundance proteins in decellularized matrix bioscaffolds [J]
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2017.08.012
– volume: 162
  start-page: 573
  issue: 2
  year: 1985
  ident: 10.1016/j.mtbio.2022.100505_bib5
  article-title: Human natural anti-alpha-galactosyl IgG. II. The specific recognition of alpha (1----3)-linked galactose residues [J]
  publication-title: J. Exp. Med.
  doi: 10.1084/jem.162.2.573
– start-page: 137
  year: 2019
  ident: 10.1016/j.mtbio.2022.100505_bib30
– volume: 20
  start-page: 109
  issue: 2
  year: 2008
  ident: 10.1016/j.mtbio.2022.100505_bib34
  article-title: Immune response to biologic scaffold materials [J]
  publication-title: Semin. Immunol.
  doi: 10.1016/j.smim.2007.11.003
– volume: 97
  start-page: 311
  issue: 3
  year: 2011
  ident: 10.1016/j.mtbio.2022.100505_bib26
  article-title: Short duration gluteraldehyde cross linking of decellularized bovine pericardium improves biological response [J]
  publication-title: J. Biomed. Mater. Res.
  doi: 10.1002/jbm.a.33061
– volume: 92
  start-page: 1
  year: 2016
  ident: 10.1016/j.mtbio.2022.100505_bib17
  article-title: In vivo xenogeneic scaffold fate is determined by residual antigenicity and extracellular matrix preservation [J]
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2016.03.024
– volume: 25
  start-page: 281
  issue: 2
  year: 2021
  ident: 10.1016/j.mtbio.2022.100505_bib29
  article-title: Development and evaluation of alpha-galactosyl antigen-deficient rabbit model [J]
  publication-title: Chin. J. Tissue Eng. Res.
– volume: 23
  start-page: 54
  issue: 1
  year: 2022
  ident: 10.1016/j.mtbio.2022.100505_bib18
  article-title: alpha-Gal antigen-deficient rabbits with GGTA1 gene disruption via CRISPR/Cas9 [J]
  publication-title: BMC Genom Data
  doi: 10.1186/s12863-022-01068-4
– volume: 268
  year: 2021
  ident: 10.1016/j.mtbio.2022.100505_bib23
  article-title: Extracellular matrix scaffold crosslinked with vancomycin for multifunctional antibacterial bone infection therapy
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2020.120603
– volume: 9
  issue: 1
  year: 2012
  ident: 10.1016/j.mtbio.2022.100505_bib16
  article-title: Rabbit as an animal model for experimental research [J]
  publication-title: Dent. Res. J.
  doi: 10.4103/1735-3327.92960
– volume: 29
  start-page: 3514
  issue: 26
  year: 2008
  ident: 10.1016/j.mtbio.2022.100505_bib15
  article-title: Immunoproteomic identification of bovine pericardium xenoantigens [J]
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2008.05.006
– volume: 32
  start-page: 6692
  issue: 28
  year: 2011
  ident: 10.1016/j.mtbio.2022.100505_bib32
  article-title: Immune responses to implants–a review of the implications for the design of immunomodulatory biomaterials [J]
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2011.05.078
– volume: 65
  start-page: 1129
  issue: 8
  year: 1998
  ident: 10.1016/j.mtbio.2022.100505_bib21
  article-title: A sensitive assay for measuring alpha-Gal epitope expression on cells by a monoclonal anti-Gal antibody [J]
  publication-title: Transplantation
  doi: 10.1097/00007890-199804270-00020
– volume: 7
  start-page: 427
  issue: 4
  year: 2020
  ident: 10.1016/j.mtbio.2022.100505_bib10
  article-title: Immune risk assessment of residual alphaGal in xenogeneic decellularized cornea using GTKO mice [J]
  publication-title: Regen Biomater
  doi: 10.1093/rb/rbaa020
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Snippet Wild type (WT) animals cannot be used to objectively assess the immunogenicity of animal tissue-derived biomaterials when used as recipients due to difference...
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SubjectTerms anti-Gal antibody
Full Length
Graft material-specific antibody
GTKO rabbit
Immunogenicity evaluation
In situ implantation
Xenograft
α-Gal
Title GTKO rabbit: A novel animal model for preclinical assessment of decellularized xenogeneic grafts via in situ implantation
URI https://dx.doi.org/10.1016/j.mtbio.2022.100505
https://www.proquest.com/docview/2747277744
https://pubmed.ncbi.nlm.nih.gov/PMC9719100
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Volume 18
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