bioRxivCell BiologyPreprint
Clinical grade cryopreservation unlocks transplant ready human pancreatic and stem cell derived islets for diabetes therapy
Joseph Sushil RaoiD, Zongqi Guo, Zenith KhashimiD, Kyle R KnofczynskiiD, Diane K. Tobolt, Sharath Belame Shivakumar, Parthasarathy RangarajaniD, Adam HermaniD, Muhamad Abdulla, Anna TraniD, Benjamin J. Fisher, Tiana Salomon, Sean Lewis-BrinkmaniD, Magie Steinhoff, Appakalai N. BalamuruganiD, Michael L. EtheridgeiD, Bernhard J. HeringiD, Sabarinathan RamachandraniD, Quinn P. PetersoniD, John C. BischofiD, Erik B. FingeriD
Abstract
Pancreatic islet transplantation can restore endogenous insulin production and offers a potential cure for diabetes, but its clinical impact has been limited by the inability to preserve large numbers of functional islets for timely use. Cryopreservation could provide an on-demand supply, yet conventional methods cause ice formation, cell injury, and loss of insulin secretion. We developed CryoMesh, a vitrification platform that combines a low-toxicity cryoprotectant with a thermally conductive, biocompatible mesh to enable ultra-rapid cooling and rewarming for ice-free cryopreservation. This approach supports long-term, clinical-scale preservation of both human pancreatic and stem cell-derived islets while maintaining viability, architecture, mitochondrial integrity, and glucose-responsive insulin secretion. Human islets preserved for up to one year restored normoglycemia in diabetic mice, with complete recovery of function and no increase in immunogenicity or loss of potency. The combination of high viability, recovery, and functional preservation at clinical scale has not been achieved previously. By decoupling islet isolation and manufacture from transplantation, CryoMesh enables extended quality, potency, and safety testing, cost-effective batch production, and global banking and distribution. These capabilities remove a major barrier to curative cell therapy for diabetes and establish a generalizable strategy for preserving complex multicellular therapeutics. One Sentence SummaryA clinical scale vitrification platform enables long-term banking of human pancreatic and stem cell-derived islets for transplantation.
- organism: human
- research focus: drug response / drug discovery
- research focus: cell type annotation
- research focus: clustering
- research focus: cell-cell communication
- approach: experimental assay
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Bridging scale-up to transplantation: pluripotent stem cell-derived pancreatic islet encapsulation in emulsion-generated high concentration alginate beads
Arianna Castro Rojas, J. Brassard, … Corinne A. Hoesli·CytotherapyPeer-reviewed·Apr 30, 2026
- Adipose-derived stromal cells preserve pancreatic islet function in a transplantable 3D bioprinted scaffold
S. Abadpour, E. M. Niemi, … H. Scholz·bioRxiv·May 30, 2022
- Generation and long-term expansion of human pancreatic islet organoids in vitro
Wenqian Song, Chunye Liu, … Yi Arial Zeng·bioRxiv·Apr 20, 2026
- Inhibition of eIF5A hypusination improves pancreatic islet transplantation outcomes by promoting ischemia tolerance
Hajar Ouahmi, Filippo Massa, … Didier F. Pisani·bioRxiv·Nov 24, 2025
- Scalable 3D Bioprinting of Human Islets in a Pancreatic Decellularized Extracellular Matrix-Enriched Bioink for Beta-Cell Replacement Therapy
Wonwoo Jeong, Quentin Perrier, … Amish Asthana·Acta BiomaterialiaPeer-reviewed·Aug 8, 2026
- Fusion of blood vessel organoids with human pancreatic islets improves insulin response over time.
E. Tubbs, M. Mehanovic, … X. Gidrol·bioRxiv·Jan 15, 2024