Cell therapy for type 1 diabetes: Tracing historical progress and exploring emerging technologies
Type 1 diabetes remains an incurable autoimmune disease, and despite advances in insulin-delivery systems, many patients still face severe hypoglycemia, glucose variability, and psychological burden. Beta-cell replacement offers a transformative alternative, with allogeneic islet transplantation providing durable protection and improved quality of life, yet limited by donor availability and the need for immunosuppression. Stem cell-derived islet-like clusters are now reaching clinical milestones, showing promising insulin independence and glycemic control, while encapsulation, autologous induced pluripotent stem cells (iPSC)-derived therapies, and gene-edited "hypo-immune" cells aim to overcome immune barriers. Porcine islet xenotransplantation is also being revisited, although regulatory and immunological hurdles remain. Key challenges persist in cell delivery, engraftment, and long-term function. As cell therapy transitions from experimental proof-of-concept to clinical reality, success will require scalable manufacturing, safe and effective delivery, regulatory alignment, and patient-centered approaches to ensure broad and meaningful impact.
Authors
- Sandrine Lablanche (ORCID: https://orcid.org/0000-0001-7044-8474)
- Quentin Perrier (ORCID: https://orcid.org/0000-0002-7445-7922)
- Pierre‐Yves Benhamou (ORCID: https://orcid.org/0000-0003-4378-0468)
Institutions
- Inserm (FR)
- Grenoble Institute of Neurosciences (FR)
- Université Grenoble Alpes (FR)
Publication Details
- Journal
- Cell Transplantation
- Published
- 2025-10-01
- DOI
- https://doi.org/10.1177/09636897251394787
- Primary Topic
- Pancreatic function and diabetes
- Type
- article
- Field-Weighted Citation Impact
- 0.00