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Cover Illustration. An abstract illustration of the uterus, the female hormone cycle, and an embryo. Illustration by Edina Sehic.
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Edina Sehic: The future of an artificial uterus

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Transplants rely on donors while recipients face lifelong immunosuppressive treatment. Edina Sehic is exploring an alternative that addresses both issues: crafting an artificial uterus from a patient鈥檚 own cells.

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Edina Sehic.

EDINA SEHIC
Dissertation defense: 19 January 2024 (click for more info)
Doctoral thesis:
Research area: Obstetrics and Gynecology

Sahlgrenska Academy, The Institute of Clinical 91探花s

What is the backstory behind your research?
鈥淢any women struggle with infertility due to uterine dysfunction, arising from post-surgical damage, congenital absence, or cancer-related removal. These conditions often lead to infertility treatable solely through uterus transplantation. However, this procedure carries significant risks and side effects,鈥 says Edina Sehic.

Utilizing the patient鈥檚 cells

Under Professor Mats Br盲nnstr枚m鈥檚 guidance, Gothenburg became the pioneer in uterus transplants in 2012. Edina Sehic, a pharmacist and molecular biologist, is currently a PhD student in Br盲nnstr枚m鈥檚 group at the Sahlgrenska University Hospital.

鈥淥ur research aims to create a patient-specific artificial uterus made from the individual鈥檚 own cells. This approach sidesteps the risks tied to immunosuppressive treatment and eliminates the need for a donor. We are also exploring an option where patient-specific uterine biomaterial could replace a damaged segment rather than requiring a complete uterus transplant.鈥

Assessed on larger animal models

Could you summarize the primary focus of your PhD project?
鈥淢y thesis centers on creating biomaterials for repairing a damaged uterus, by scaling our previous findings into larger animal models. The uterine material, previously assessed and transplanted into rats, has now undergone evaluation in sheep,鈥 explains Edina Sehic.

鈥淚 have also further developed protocols for producing our material using tissue from cows and baboons, to ensure the protocols鈥 readiness for human applications soon. Evaluating materials across various animal species helps assess production safety and efficacy.鈥

Figure 14. Illustration of the biomaterial production. The uterus is decellularized, and a patch is cut out. Mesenchymal stem cells are injected into the scaffold, which is incubated for 14 days to let the cells attach and colonize before transplantation.

鈥淐onstructing a complete uterus鈥

What are the key outcomes of your research?
鈥淲e have successfully translated our prior studies from rat models to larger animal models. This is crucial for effectively producing biomaterials for future clinical applications. Additionally, our research has deepened our understanding of the immune system鈥檚 response to our material and its implications.鈥

What patient benefit will this research result in?
鈥淚n the future, our research will not only assist women with damaged uteruses in achieving pregnancy. Our findings also provide insights into the body鈥檚 regenerative processes, and how we can design tools and materials to create patient-adapted grafts,鈥 says Edina Sehic, adding:

鈥淥nce we achieve our interim goal of producing a section of the uterus and accumulate sufficient knowledge, the next step is to construct a complete uterus. Such advancement could replace the need for a donor in a uterus transplant, minimizing risks for patients and reducing dependency on organ availability.鈥

Text: Jakob Lundberg

Figure 4, page 8. Illustration of (A) uterus transplantation, (B) whole organ decellularization and recellularization followed by uterus transplantation, and (C) partial patch repair of uterine defects.