Related Experiment Video
Updated: Dec 22, 2025

Quantification of Circulating Pig-Specific DNA in the Blood of a Xenotransplantation Model
Published on: September 22, 2020
Regulatory changes in China on xenotransplantation and related products
Yuping Liu1, Lixia Qin2, Rongsheng Tong3
1Center for Health Management, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu, China.
Background:
Given the persistence and the worldwide shortage of organs from both the deceased and living donors for clinical transplantation, pig organs or tissues hold immense promises for the patients on the waiting list, and xenotransplantation is deemed as one of the solutions to the organ shortage crisis. Indeed, the emerging gene editing technologies, such as CRISPR/Cas9, have led to tremendous progress in the generation of genetically modified pigs to overcome many barriers associated.
Method:
We presented a description of the xenotransplantation regulations in China and the related products.
Result:
Several groups in China have successfully generated transgenic pigs with the elimination of immune rejection or coagulation-related genes, and both pre-clinical and clinical studies have been reported. However, the pre-clinical evaluation and clinical application of porcine xenotransplantation raises ethical and regulatory considerations. Herein, in this review, we will summarize and discuss the progress in xenotransplantation in China and xenotransplantation-related products from the regulatory perspective.
Conclusion:
There has been remarkable progress in both the genetically modified pigs and pre-clinical studies in China, and China will be the first country to successfully fulfill the xenotransplantation from pig organ to human in the near future.
Related Concept Videos
Drug Products: Biologics, Biosimilars and Interchangeables
Transgenic Organisms
FDA Approved Drugs: Changes to Approved Drugs
CRISPR

