Costimulation blockade in pig artery patch xenotransplantation - a simple model to monitor the adaptive immune response in nonhuman primates |
| |
| Authors: | Mohamed B Ezzelarab Burcin Ekser Gabriel Echeverri Hidetaka Hara Corin Ezzelarab Cassandra Long Pietro Bajona Bertha Garcia Noriko Murase David Ayares David K C Cooper |
| |
| Affiliation: | Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, PA, USA Department of Surgery, Transplantation and Advanced Technologies, Vascular Surgery and Organ Transplant Unit, University Hospital of Catania, Catania, Italy Transplant Unit, Fundacion Valle del Lili, Cali, Colombia Department of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, PA, USA Department of Pathology, University of Western Ontario, London, ON, Canada Revivicor, Blacksburg, VA, USA. |
| |
| Abstract: | Ezzelarab MB, Ekser B, Echeverri G, Hara H, Ezzelarab C, Long C, Bajona P, Garcia B, Murase N, Ayares D, Cooper DKC. Costimulation blockade in pig artery patch xenotransplantation – a simple model to monitor the adaptive immune response in nonhuman primates. Xenotransplantation 2012; 19: 221–232. © 2012 John Wiley & Sons A/S. Abstract: Background: CD154 blockade‐based immunosuppression successfully prevents both humoral and cellular adaptive immune responses in baboons receiving α1,3‐galactosyltransferase gene‐knockout (GTKO) pig organs. Using a GTKO pig artery transplantation model in baboons, we evaluated the efficacy of CD28/B7 costimulatory pathway blockade in comparison with CD154 blockade. Methods: Baboons received artery patch grafts from GTKO pigs, with no (Group1), anti‐CD154mAb‐based (Group2), or CTLA4‐Ig‐based (Group3) immunosuppressive therapy. Anti‐pig IgM and IgG antibody and cellular responses were monitored. Xenografts were immunohistologically evaluated for antibody and complement deposition, and cellular infiltration. Results: Group1 baboons developed increased IgM and IgG antibody and cellular responses against GTKO antigens. In Group2, anti‐CD154mAb alone prevented the development of both IgM and IgG antibody and cellular responses,but not cellular infiltration of the graft. In the single baboon that received anti‐thymocyte globulin (ATG) + mycophenolate mofetil (MMF) + anti‐CD154mAb, cellular infiltration of the graft was not seen. In Group3, CTLA4‐Ig with ATG + MMF inhibited the cellular proliferative response to pig antigens but did not prevent the IgG response or cellular infiltration. Conclusions: (i) Artery patch transplantation is a simple model to monitor the adaptive immune response to xenografts; (ii) anti‐CD154mAb prevents sensitization but not cellular infiltration (but, without anticoagulation, may result in early thrombosis of a pig xenograft); (iii) although in only one baboon, the addition of ATG and MMF prevents cellular infiltration and (iv) replacement of anti‐CD154mAb by CTLA4‐Ig (at the doses used), even in combination with ATG and MMF, prevents the cellular proliferative response to GTKO pig antigens but is insufficient to prevent the development of anti‐pig antibodies. |
| |
| Keywords: | α1,3‐galactosyltransferase gene‐knockout anti‐CD154 monoclonal antibody artery patch costimulation blockade CTLA4‐Ig pig xenotransplantation |
| 本文献已被 PubMed 等数据库收录！ |
|
