A prevascularized subcutaneous device-less site for islet and cellular transplantation
Abstract
Transplantation of donor-derived islets into the liver is a successful cellular replacement therapy for individuals with diabetes. However, the hepatic vasculature is not an optimal transplant site for several reasons, including graft attrition and the inability to retrieve or image the islets. Here we describe islet transplantation into a prevascularized, subcutaneous site created by temporary placement of a medically approved vascular access catheter. In mice with streptozotocin (STZ)-induced diabetes, transplantation of ∼500 syngeneic islets into the resulting 'device-less' space reversed diabetes in 91% of mice and maintained normoglycemia for >100 days. The approach was also effective in mice with pre-existing diabetes, in another mouse strain that mounts a more vigorous inflammatory response, and across an allogeneic barrier. These results demonstrate that transient priming of a subcutaneous site supports diabetes-reversing islet transplantation in mouse models without the need for a permanent cell-encapsulation device.
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Several alternative transplantation sites to the liver have been proposed in humans, including the subcutaneous space, intramuscular space, and omentum.
“In humans, several alternative transplantation sites to the liver have been proposed144, including the subcutaneous space145, intramuscular space146, and the omentum147,148.”
From Developments in stem cell-derived islet replacement therapy for treating type 1 diabetes (2023) · cites this paper as [145]
Implanting a device into the subcutaneous space one month prior to cell transplantation pre-vascularized the graft site and avoided the several week lag time for vascularization.
“For example, implanting a device into the subcutaneous space one month prior to cell transplantation pre-vascularized the graft site and avoided the several week lag time that it takes for vascularization to occur.145,151”
From Developments in stem cell-derived islet replacement therapy for treating type 1 diabetes (2023) · cites this paper as [145]
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References 38 · Cited by 381
- Authors
- Pepper, A. R., Gala-Lopez, B., Pawlick, R., Merani, S., Kin, T., & Shapiro, A. M. J.
- Affiliations
- University of Alberta (CA)
- Corresponding author
- Shapiro, A M James
- Venue
- Nature Biotechnology
- Published
- 2015-04-20
- Volume
- 33
- Issue
- 5
- Pages
- 518-523
- ISSN
- 0733-222X (ISSN-L)
- 1087-0156
- 1546-1696
- OpenAlex
- W1973424799
- Cited by
- 381
- References
- 38
- Citations by year
- 2026: 22 · 2025: 23 · 2024: 45 · 2023: 37 · 2022: 27 · 2021: 35 · 2020: 35 · 2019: 43 · 2018: 35 · 2017: 39 · 2016: 31 · 2015: 9
- FWCI
- 38.26
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Biotechnology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Keywords
- islet transplantation, subcutaneous transplantation, prevascularization, vascular access catheters, diabetes reversal, streptozotocin-induced diabetes, allogeneic islets
- MeSH terms
- Animals, Blood Glucose, Diabetes Mellitus, Experimental, Graft Survival, Humans, Liver, Neovascularization, Pathologic, Islets of Langerhans Transplantation, Mice, Translational Research, Biomedical, Cell- and Tissue-Based Therapy
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