PTPEPTIDE THERAPIES
Peptide Therapies/November 8, 2025/2 min read

Pilot Study: Functional Survival of Human Stem Cell-Derived Islets Microencapsulated With Alginate Incorporating CXCL12 in Non-Human Primates Without Systemic Immunosuppression.

Glucose-responsive insulin-secreting stem cell-derived islet-like cells (SC-islets) are a promising source for beta cell replacement to treat type 1 diabetes (T1D).

PubMed indexed literature

Evidence label explains the kind of source behind this article (for example peer-reviewed literature vs community video). It is not medical advice.

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Key takeaways

  • Glucose-responsive insulin-secreting stem cell-derived islet-like cells (SC-islets) are a promising source for beta cell replacement to treat type 1 diabetes (T1D).
  • However, immune rejection and limited function of SC-islets post-transplantation are key barriers to this treatment.
  • We previously reported glycemic control and prolonged function of SC-islets microencapsulated in alginate that incorporates the pro-survival and immunomodulatory chemokine CXCL12 in immunocompetent diabetic mice without systemic immune suppression.

What the research looked at

Glucose-responsive insulin-secreting stem cell-derived islet-like cells (SC-islets) are a promising source for beta cell replacement to treat type 1 diabetes (T1D).

However, immune rejection and limited function of SC-islets post-transplantation are key barriers to this treatment.

We previously reported glycemic control and prolonged function of SC-islets microencapsulated in alginate that incorporates the pro-survival and immunomodulatory chemokine CXCL12 in immunocompetent diabetic mice without systemic immune suppression.

Here, in a pilot study, we translated this SC-islet microencapsulation approach in nonhuman primates (NHPs) via transplantation of a therapeutic dose of SC-islets microencapsulated in alginate incorporating CXCL12 into the greater omental sac of a healthy and a diabetic NHP.

We demonstrate that treatment did not cause metabolic dysfunction over a 6-month period in the NHPs.

What it reported

The healthy NHP maintained stable C-peptide and blood glucose levels, while the diabetic NHP had detectable serum C-peptide through 13 weeks post-transplant and a significant reduction in exogenous insulin requirements compared with a corresponding diabetic NHP recipient in the absence of immunosuppressive treatment.

Serum biochemistry as well as hematological and immunological parameters of the NHPs remained normal throughout the post-transplantation period.

At termination, the retrieved microencapsulated SC-islets were predominantly free floating without pericapsular fibrotic overgrowth and were glucose-responsive, expressing all major endocrine cell markers, albeit a significant decrease in viability compared with pre-transplant levels.

Overall, these findings demonstrate feasibility, safety, and function of microencapsulated SC-islets in two NHPs in this small pilot study an…

What it means for the Type 1 community

This is pubmed indexed literature and is shared for information, not as medical advice. One study is a data point, not a verdict, so read it alongside the broader body of evidence and your own care team's guidance.

Evidence label

Source: Xenotransplantation. Evidence type: PubMed indexed literature. Type1Cure is an information and intelligence hub, not a medical advice service. This article summarizes published research and does not provide diagnosis, treatment, or personal medical guidance. Always talk to your own care team before changing anything about your Type 1 diabetes management.

Type1Cure is an information and intelligence hub, not a medical advice service. This article summarizes published research and does not provide diagnosis, treatment, or personal medical guidance. Always talk to your own care team before changing anything about your Type 1 diabetes management.

More evidence-labeled coverage across the Type1Cure library.