Session Time: 6:00pm-7:00pm
Presentation Time: 6:00pm-7:00pm
Location: Hall D1
Background: Penis transplantation has been successfully employed in the recent past and represents an exciting avenue for restoration of male urogenitalia and function by using “like-with-like” tissue. This animal model is designed to fill a critical void as only little is known on the immunology of these unique tissue grafts. Methods: In 8-week old BN & Lewis rats the penis was dissected to design a penile graft based on the internal pudendal artery and dorsal penile vein including the skin of the prepuce. A non-suture cuff technique was employed to perform end-to-end anastomosis of the graft vessels to the recipient inferior epigastric vessels. Syngeneic and allogeneic transplants were performed. Native and graft penile tissue were obtained at various time points for histologic analysis. Results: Graft design yields suitable caliber and length of graft vessels at the radix of the penis. Anastomosis of the dorsal penile vein and the distal internal pudendal artery at the bifurcation into dorsal and deep penile arteries ensures optimal perfusion of the entire superficial and deep graft tissues. The non-suture cuff technique allows for successful microvascular anastomosis by a single surgeon in an average of 2.5 hours. Long-term graft survival (>45 days) was observed in syngeneic transplants (N=3). To date, allogeneic transplant combinations from BN to Lewis rats have been performed and tissues have been harvested for analysis at various time points (i.e. POD 3, 5, 7, 9, 11, 14, 16; N=2-3). Clinical allograft rejection can be monitored easily due to the heterotopic inset location at the dorsal aspect of the thigh and graft rejection follows a 4 stage clinical progression indicating comparability to other skin containing VCAs. Graft rejection, however appears to be minimally delayed compared to hind limb allografts. Conclusion: We have been able to establish a robust and reproducible murine model to study the unique immunobiology of urogenital tissue in the context of reconstructive transplantation. The design of the graft ensures optimal vascular perfusion of superficial and deep penile tissues. Heterotopic inset further allows for visual monitoring of graft viability, while the native penis serves an optimal control. The graft design includes the dorsal penile nerve and may thus be a platform for studies on erectile tissues and function.
CITATION INFORMATION: Furtmüller G, Fidder S, Simons B, Oh B, Kern B, Lough D, Chicco M, Brayton C, Lee W, Cooney D, Redett R, Brandacher G. A Novel Microsurgical Penis Transplant Model to Study Distinct Immunologic Features of Urogenital Tissues. Am J Transplant. 2017;17 (suppl 3).
To cite this abstract in AMA style:Furtmüller G, Fidder S, Simons B, Oh B, Kern B, Lough D, Chicco M, Brayton C, Lee W, Cooney D, Redett R, Brandacher G. A Novel Microsurgical Penis Transplant Model to Study Distinct Immunologic Features of Urogenital Tissues. [abstract]. Am J Transplant. 2017; 17 (suppl 3). https://atcmeetingabstracts.com/abstract/a-novel-microsurgical-penis-transplant-model-to-study-distinct-immunologic-features-of-urogenital-tissues/. Accessed December 12, 2018.
« Back to 2017 American Transplant Congress