Abstract |
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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Authors | Lisha Mou, Guanghan Shi, David K C Cooper, Ying Lu, Jiao Chen, Shufang Zhu, Jing Deng, Yuanyuan Huang, Yong Ni, Yongqiang Zhan, Zhiming Cai, Zuhui Pu |
Journal | Frontiers in immunology
(Front Immunol)
Vol. 13
Pg. 854883
( 2022)
ISSN: 1664-3224 [Electronic] Switzerland |
PMID | 35432379
(Publication Type: Journal Article, Review, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2022 Mou, Shi, Cooper, Lu, Chen, Zhu, Deng, Huang, Ni, Zhan, Cai and Pu. |
Chemical References |
- CD40 Antigens
- Immunosuppressive Agents
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Topics |
- Animals
- CD40 Antigens
- Diabetes Mellitus, Type 1
(therapy)
- Humans
- Immunosuppressive Agents
- Islets of Langerhans Transplantation
- Transplantation, Heterologous
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