Animal models for partial heart transplantation

• Published in: Pediatric transplantation Vol. 28; no. 4; pp. e14788 - n/a
• Main Authors: Yerger, Julia, Hill, Morgan A., Fitzgerald, David C., Rajab, Taufiek K.
• Format: Journal Article
• Language: English
• Published: Denmark Wiley Subscription Services, Inc 01.06.2024
• Subjects: Allografts; animal model; Animal models; Animals; Disease Models, Animal; Graft rejection; Graft Rejection - immunology; Heart surgery; Heart transplantation; Heart Transplantation - methods; Heart transplants; heart valve; Humans; Immunosuppression; Ischemia; Models, Animal; Papio; partial heart transplantation; pediatric cardiac surgery; Primates; Rats; Rodentia; Rodents; Swine; Transplantation, Heterologous; Transplantation, Heterotopic; Xenografts; pediatric cardiac surgery; partial heart transplantation; animal model; heart valve
• ISSN: 1397-3142; 1399-3046
• DOI: 10.1111/petr.14788

Background Partial heart transplantation delivers growing heart valve implants by transplanting the part of the heart containing the necessary heart valve only. In contrast to heart transplantation, partial heart transplantation spares the native ventricles. This has important implications for partial heart transplant biology, including the allowable ischemia time, optimal graft preservation, primary graft dysfunction, immune rejection, and optimal immunosuppression. Aims Exploration of partial heart transplant biology will depend on suitable animal models. Here we review our experience with partial heart transplantation in rodents, piglets, and non‐human primates. Materials & Methods This review is based on our experience with partial heart transplantation using over 100 rodents, over 50 piglets and one baboon. Results Suitable animal models for partial heart transplantation include rodent heterotopic partial heart transplantation, piglet orthotopic partial heart transplantation, and non‐human primate partial heart xenotransplantation. Discussion Rodent models are relatively cheap and offer extensive availability of research tools. However, rodent open‐heart surgery is technically not feasible. This limits rodents to heterotopic partial heart transplant models. Piglets are comparable in size to children. This allows for open‐heart surgery using clinical grade equipment for orthoptic partial heart transplantation. Piglets also grow rapidly, which is useful for studying partial heart transplant growth. Finally, nonhuman primates are immunologically most closely related to humans. Therefore, nonhuman primates are most suitable for studying partial heart transplant immunobiology and xenotransplantation. Conclusions Animal research is a privilege that is contingent on utilitarian ethics and the 3R principles of replacement, reduction and refinement. This privilege allows the research community to seek fundamental knowledge about partial heart transplantation, and to apply this knowledge to enhance the health of children who require partial heart transplants.