Research Report

Enhancing Immunotolerance in Genetically Modified Pigs for Xenotransplantation: Mechanisms and Outcomes  

Tao Zhang
Hangzhou Mono Biotechnology Co., Ltd, Hangzhou, 310000, Zhejiang, China
Author    Correspondence author
International Journal of Molecular Zoology, 2024, Vol. 14, No. 2   doi: 10.5376/ijmz.2024.14.0009
Received: 16 Jan., 2024    Accepted: 25 Feb., 2024    Published: 10 Mar., 2024
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This is an open access article published under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Preferred citation for this article:

Zhang T., 2024, Enhancing immunotolerance in genetically modified pigs for xenotransplantation: mechanisms and outcomes, International Journal of Molecular Zoology, 14(2): 72-83 (doi: 10.5376/ijmz.2024.14.0009)

Abstract

The shortage of human organs for transplantation has driven significant interest in xenotransplantation, particularly using genetically modified pigs. This study explores the mechanisms and outcomes of enhancing immunotolerance in genetically modified pigs for xenotransplantation. Recent advancements in genetic engineering, such as the deletion of xenoantigens and the expression of human complement and coagulation regulatory proteins, have shown promise in reducing immune rejection and prolonging graft survival. Studies have demonstrated that genetically engineered pig hearts and kidneys can survive for extended periods in non-human primates, with some grafts functioning beyond one year. These findings suggest that targeted genetic modifications, combined with specific immunosuppressive regimens, can significantly improve the viability of pig organs for clinical xenotransplantation. However, challenges remain, including the need for further optimization of genetic modifications and immunosuppressive protocols to prevent chronic rejection and ensure long-term graft function.

Keywords
Genetically modified pigs; Xenotransplantation; Immunotolerance; Organ transplantation; Genetic engineering
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