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Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine via Mixed Chimerism

BACKGROUND: Vascularized composite allografts (VCAs) allow reconstruction of devastating injuries and amputations, yet require lifelong immunosuppression that is associated with significant morbidity. Induction of immune tolerance of VCAs would permit widespread use of these procedures. VCAs are acq...

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Autores principales: Lellouch, Alexandre G., Andrews, Alec R., Saviane, Gaelle, Ng, Zhi Yang, Schol, Ilse M., Goutard, Marion, Gama, Amon-Ra, Rosales, Ivy A., Colvin, Robert B., Lantieri, Laurent A., Randolph, Mark A., Benichou, Gilles, Cetrulo, Curtis L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9128064/
https://www.ncbi.nlm.nih.gov/pubmed/35619720
http://dx.doi.org/10.3389/fimmu.2022.829406
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author Lellouch, Alexandre G.
Andrews, Alec R.
Saviane, Gaelle
Ng, Zhi Yang
Schol, Ilse M.
Goutard, Marion
Gama, Amon-Ra
Rosales, Ivy A.
Colvin, Robert B.
Lantieri, Laurent A.
Randolph, Mark A.
Benichou, Gilles
Cetrulo, Curtis L.
author_facet Lellouch, Alexandre G.
Andrews, Alec R.
Saviane, Gaelle
Ng, Zhi Yang
Schol, Ilse M.
Goutard, Marion
Gama, Amon-Ra
Rosales, Ivy A.
Colvin, Robert B.
Lantieri, Laurent A.
Randolph, Mark A.
Benichou, Gilles
Cetrulo, Curtis L.
author_sort Lellouch, Alexandre G.
collection PubMed
description BACKGROUND: Vascularized composite allografts (VCAs) allow reconstruction of devastating injuries and amputations, yet require lifelong immunosuppression that is associated with significant morbidity. Induction of immune tolerance of VCAs would permit widespread use of these procedures. VCAs are acquired from deceased donors most likely to be fully-MHC-mismatched (in contrast to living-related renal transplant donor-recipient pairs matched at one MHC haplotype). After achieving VCA tolerance in a swine model equivalent to clinical living-related renal transplants (single-haplotype MHC mismatches: e.g., “mother-daughter”/haploidentical), we tested our protocol in MHC class I, class II, and fully-MHC-mismatched pairs. Although class II mismatched swine demonstrated similar results as the haploidentical scenario (stable mixed chimerism and tolerance), our protocol failed to prevent rejection of class I and full mismatch VCAs. Here, we describe a new adapted conditioning protocol that successfully achieved tolerance across MHC class-I-mismatch barriers in swine. METHODS: Swine were treated with non-myeloablative total body and thymic irradiation two days prior to infusion of bone marrow cells from an MHC class I-mismatched donor. They also received a short-term treatment with CTLA4-Ig (Belatacept(®)) and anti-IL6R mAb (Tociluzimab(®)) and were transplanted with an osteomyocutaneous VCA from the same donor. RESULTS: Stable mixed chimerism and tolerance of MHC class-I-mismatched VCAs was achieved in 3 recipients. Allograft tolerance was associated with a sustained lack of anti-donor T cell response and a concomitant expansion of double negative CD4(-)CD8(-) T cells producing IL-10. CONCLUSIONS: This study demonstrates the first successful mixed chimerism-induced VCA tolerance in a large animal model across a MHC class-I-mismatch. Future studies aimed at fully-mismatched donor-recipient pairs are under investigation with this protocol.
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spelling pubmed-91280642022-05-25 Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine via Mixed Chimerism Lellouch, Alexandre G. Andrews, Alec R. Saviane, Gaelle Ng, Zhi Yang Schol, Ilse M. Goutard, Marion Gama, Amon-Ra Rosales, Ivy A. Colvin, Robert B. Lantieri, Laurent A. Randolph, Mark A. Benichou, Gilles Cetrulo, Curtis L. Front Immunol Immunology BACKGROUND: Vascularized composite allografts (VCAs) allow reconstruction of devastating injuries and amputations, yet require lifelong immunosuppression that is associated with significant morbidity. Induction of immune tolerance of VCAs would permit widespread use of these procedures. VCAs are acquired from deceased donors most likely to be fully-MHC-mismatched (in contrast to living-related renal transplant donor-recipient pairs matched at one MHC haplotype). After achieving VCA tolerance in a swine model equivalent to clinical living-related renal transplants (single-haplotype MHC mismatches: e.g., “mother-daughter”/haploidentical), we tested our protocol in MHC class I, class II, and fully-MHC-mismatched pairs. Although class II mismatched swine demonstrated similar results as the haploidentical scenario (stable mixed chimerism and tolerance), our protocol failed to prevent rejection of class I and full mismatch VCAs. Here, we describe a new adapted conditioning protocol that successfully achieved tolerance across MHC class-I-mismatch barriers in swine. METHODS: Swine were treated with non-myeloablative total body and thymic irradiation two days prior to infusion of bone marrow cells from an MHC class I-mismatched donor. They also received a short-term treatment with CTLA4-Ig (Belatacept(®)) and anti-IL6R mAb (Tociluzimab(®)) and were transplanted with an osteomyocutaneous VCA from the same donor. RESULTS: Stable mixed chimerism and tolerance of MHC class-I-mismatched VCAs was achieved in 3 recipients. Allograft tolerance was associated with a sustained lack of anti-donor T cell response and a concomitant expansion of double negative CD4(-)CD8(-) T cells producing IL-10. CONCLUSIONS: This study demonstrates the first successful mixed chimerism-induced VCA tolerance in a large animal model across a MHC class-I-mismatch. Future studies aimed at fully-mismatched donor-recipient pairs are under investigation with this protocol. Frontiers Media S.A. 2022-05-10 /pmc/articles/PMC9128064/ /pubmed/35619720 http://dx.doi.org/10.3389/fimmu.2022.829406 Text en Copyright © 2022 Lellouch, Andrews, Saviane, Ng, Schol, Goutard, Gama, Rosales, Colvin, Lantieri, Randolph, Benichou and Cetrulo https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Lellouch, Alexandre G.
Andrews, Alec R.
Saviane, Gaelle
Ng, Zhi Yang
Schol, Ilse M.
Goutard, Marion
Gama, Amon-Ra
Rosales, Ivy A.
Colvin, Robert B.
Lantieri, Laurent A.
Randolph, Mark A.
Benichou, Gilles
Cetrulo, Curtis L.
Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine via Mixed Chimerism
title Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine via Mixed Chimerism
title_full Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine via Mixed Chimerism
title_fullStr Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine via Mixed Chimerism
title_full_unstemmed Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine via Mixed Chimerism
title_short Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine via Mixed Chimerism
title_sort tolerance of a vascularized composite allograft achieved in mhc class-i-mismatch swine via mixed chimerism
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9128064/
https://www.ncbi.nlm.nih.gov/pubmed/35619720
http://dx.doi.org/10.3389/fimmu.2022.829406
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