4.8 Review

Current Topics of Relevance to the Xenotransplantation of Free Pig Islets

Journal

FRONTIERS IN IMMUNOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.854883

Keywords

immunosuppression; islets; nonhuman primate; pig; genetically-engineered; type 1 diabetes; islet transplantation; xenotransplantation

Categories

Funding

  1. Shenzhen Foundation of Science and Technology [GJHZ20200731095207021]
  2. National Key R&D Program of China [2017YFC1103704]
  3. Special Funds for the Construction of High Level Hospitals in Guangdong Province

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Pig islet xenotransplantation shows promise as a treatment for type 1 diabetes. The optimal age of the pig donors and the immunological barrier are still being studied. Isolation of adult islets using GMP grade collagenase is effective, but neonatal islets have cost advantages. Genetic modification in pigs may prevent rejection, but its efficacy in islet transplantation needs further research.
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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