TY - JOUR
T1 - Is the time right for transplanting immature testicular tissue or cells to restore male fertility? Expert perspectives on clinical implementation of autotransplantation of cryopreserved testicular tissue or cells for fertility restoration
AU - Safrai, Myriam
AU - Goossens, Ellen
AU - Mitchell, Rod T.
AU - Orwig, Kyle E.
AU - Mulder, Callista L.
AU - van Pelt, Ans M.M.
AU - Gook, Debra A.
AU - Feraille, Aurélie
AU - Delgouffe, Emily
AU - Ginsberg, Jill P.
AU - Stukenborg, Jan Bernd
AU - Duffin, Kathleen
AU - Jahnukainen, Kirsi
AU - Andersen, Claus Yding
AU - van de Wetering, Marianne D.
AU - Rimmer, Michael P.
AU - Barraud-Lange, Virginie
AU - Neuhaus, Nina
AU - Lane, Sheila
AU - Sadri-Ardekani, Hooman
AU - Rives, Nathalie
AU - Wyns, Christine
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025
Y1 - 2025
N2 - Transplantations of cryopreserved immature testicular tissue (ITT) or spermatogonial stem cells (SSCs) represent promising approaches to restore fertility in patients with testicular tissue or cell suspension cryopreserved for fertility preservation. With over 3000 testicular samples cryopreserved globally, clinically viable and standardized protocols restoring fertility using cryopreserved testicular tissue/cells are urgently needed. Decades of research demonstrate the feasibility of immature testicular tissue transplantation (ITTT) or spermatogonial stem cell transplantation (SSCT) in animal models, including non-human primates. However, significant challenges remain in translating these options to human clinical practice. Critical factors include rigorous patient selection, robust pre-transplant evaluations to mitigate risks of malignant cell reintroduction, and the optimization of transplantation timing to support spermatogenesis. Developing comprehensive follow-up protocols and international data-sharing frameworks is essential to optimize outcomes. While offering the potential for genetic parenthood and enhanced quality of life for cancer survivors, these techniques require further refinement to ensure safety, efficacy, and realistic expectations. This paper outlines the framework for advancing the clinical translation of autotransplantation of testicular tissue/cells through collaboration and innovation.
AB - Transplantations of cryopreserved immature testicular tissue (ITT) or spermatogonial stem cells (SSCs) represent promising approaches to restore fertility in patients with testicular tissue or cell suspension cryopreserved for fertility preservation. With over 3000 testicular samples cryopreserved globally, clinically viable and standardized protocols restoring fertility using cryopreserved testicular tissue/cells are urgently needed. Decades of research demonstrate the feasibility of immature testicular tissue transplantation (ITTT) or spermatogonial stem cell transplantation (SSCT) in animal models, including non-human primates. However, significant challenges remain in translating these options to human clinical practice. Critical factors include rigorous patient selection, robust pre-transplant evaluations to mitigate risks of malignant cell reintroduction, and the optimization of transplantation timing to support spermatogenesis. Developing comprehensive follow-up protocols and international data-sharing frameworks is essential to optimize outcomes. While offering the potential for genetic parenthood and enhanced quality of life for cancer survivors, these techniques require further refinement to ensure safety, efficacy, and realistic expectations. This paper outlines the framework for advancing the clinical translation of autotransplantation of testicular tissue/cells through collaboration and innovation.
KW - Fertility preservation
KW - Immature testicular tissue
KW - Pre-pubertal boys
KW - Spermatogonial stem cell transplantation
KW - Testicular tissue cryopreservation
KW - Testicular tissue transplantation
U2 - 10.1016/j.bpobgyn.2025.102638
DO - 10.1016/j.bpobgyn.2025.102638
M3 - Review
C2 - 40695104
AN - SCOPUS:105011050196
SN - 1521-6934
VL - 102
JO - Best Practice and Research: Clinical Obstetrics and Gynaecology
JF - Best Practice and Research: Clinical Obstetrics and Gynaecology
M1 - 102638
ER -