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Current Topics of Relevance to the Xenotransplantation of Free Pig Islets

Pig islet xenotransplantation is a potential treatment for patients with type 1 diabetes. Current efforts are focused on identifying the optimal pig islet source and overcoming the immunological barrier. The optimal age of the pig donors remains controversial since both adult and neonatal pig islets...

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Autores principales: Mou, Lisha, Shi, Guanghan, Cooper, David K.C., Lu, Ying, Chen, Jiao, Zhu, Shufang, Deng, Jing, Huang, Yuanyuan, Ni, Yong, Zhan, Yongqiang, Cai, Zhiming, Pu, Zuhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010617/
https://www.ncbi.nlm.nih.gov/pubmed/35432379
http://dx.doi.org/10.3389/fimmu.2022.854883
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author Mou, Lisha
Shi, Guanghan
Cooper, David K.C.
Lu, Ying
Chen, Jiao
Zhu, Shufang
Deng, Jing
Huang, Yuanyuan
Ni, Yong
Zhan, Yongqiang
Cai, Zhiming
Pu, Zuhui
author_facet Mou, Lisha
Shi, Guanghan
Cooper, David K.C.
Lu, Ying
Chen, Jiao
Zhu, Shufang
Deng, Jing
Huang, Yuanyuan
Ni, Yong
Zhan, Yongqiang
Cai, Zhiming
Pu, Zuhui
author_sort Mou, Lisha
collection PubMed
description Pig islet xenotransplantation is a potential treatment for patients with type 1 diabetes. Current efforts are focused on identifying the optimal pig islet source and overcoming the immunological barrier. The optimal age of the pig donors remains controversial since both adult and neonatal pig islets have advantages. Isolation of adult islets using GMP grade collagenase has significantly improved the quantity and quality of adult islets, but neonatal islets can be isolated at a much lower cost. Certain culture media and coculture with mesenchymal stromal cells facilitate neonatal islet maturation and function. Genetic modification in pigs affords a promising strategy to prevent rejection. Deletion of expression of the three known carbohydrate xenoantigens (Gal, Neu5Gc, Sda) will certainly be beneficial in pig organ transplantation in humans, but this is not yet proven in islet transplantation, though the challenge of the ‘4th xenoantigen’ may prove problematic in nonhuman primate models. Blockade of the CD40/CD154 costimulation pathway leads to long-term islet graft survival (of up to 965 days). Anti-CD40mAbs have already been applied in phase II clinical trials of islet allotransplantation. Fc region-modified anti-CD154mAbs successfully prevent the thrombotic complications reported previously. In this review, we discuss (I) the optimal age of the islet-source pig, (ii) progress in genetic modification of pigs, (iii) the immunosuppressive regimen for pig islet xenotransplantation, and (iv) the reduction in the instant blood-mediated inflammatory reaction.
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spelling pubmed-90106172022-04-16 Current Topics of Relevance to the Xenotransplantation of Free Pig Islets Mou, Lisha Shi, Guanghan Cooper, David K.C. Lu, Ying Chen, Jiao Zhu, Shufang Deng, Jing Huang, Yuanyuan Ni, Yong Zhan, Yongqiang Cai, Zhiming Pu, Zuhui Front Immunol Immunology Pig islet xenotransplantation is a potential treatment for patients with type 1 diabetes. Current efforts are focused on identifying the optimal pig islet source and overcoming the immunological barrier. The optimal age of the pig donors remains controversial since both adult and neonatal pig islets have advantages. Isolation of adult islets using GMP grade collagenase has significantly improved the quantity and quality of adult islets, but neonatal islets can be isolated at a much lower cost. Certain culture media and coculture with mesenchymal stromal cells facilitate neonatal islet maturation and function. Genetic modification in pigs affords a promising strategy to prevent rejection. Deletion of expression of the three known carbohydrate xenoantigens (Gal, Neu5Gc, Sda) will certainly be beneficial in pig organ transplantation in humans, but this is not yet proven in islet transplantation, though the challenge of the ‘4th xenoantigen’ may prove problematic in nonhuman primate models. Blockade of the CD40/CD154 costimulation pathway leads to long-term islet graft survival (of up to 965 days). Anti-CD40mAbs have already been applied in phase II clinical trials of islet allotransplantation. Fc region-modified anti-CD154mAbs successfully prevent the thrombotic complications reported previously. In this review, we discuss (I) the optimal age of the islet-source pig, (ii) progress in genetic modification of pigs, (iii) the immunosuppressive regimen for pig islet xenotransplantation, and (iv) the reduction in the instant blood-mediated inflammatory reaction. Frontiers Media S.A. 2022-04-01 /pmc/articles/PMC9010617/ /pubmed/35432379 http://dx.doi.org/10.3389/fimmu.2022.854883 Text en Copyright © 2022 Mou, Shi, Cooper, Lu, Chen, Zhu, Deng, Huang, Ni, Zhan, Cai and Pu 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
Mou, Lisha
Shi, Guanghan
Cooper, David K.C.
Lu, Ying
Chen, Jiao
Zhu, Shufang
Deng, Jing
Huang, Yuanyuan
Ni, Yong
Zhan, Yongqiang
Cai, Zhiming
Pu, Zuhui
Current Topics of Relevance to the Xenotransplantation of Free Pig Islets
title Current Topics of Relevance to the Xenotransplantation of Free Pig Islets
title_full Current Topics of Relevance to the Xenotransplantation of Free Pig Islets
title_fullStr Current Topics of Relevance to the Xenotransplantation of Free Pig Islets
title_full_unstemmed Current Topics of Relevance to the Xenotransplantation of Free Pig Islets
title_short Current Topics of Relevance to the Xenotransplantation of Free Pig Islets
title_sort current topics of relevance to the xenotransplantation of free pig islets
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010617/
https://www.ncbi.nlm.nih.gov/pubmed/35432379
http://dx.doi.org/10.3389/fimmu.2022.854883
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