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Key quality parameter comparison of mesenchymal stem cell product cryopreserved in different cryopreservation solutions for clinical applications.

作者信息

Tan Yuan, Salkhordeh Mahmoud, Murray Aidan B P, Souza-Moreira Luciana, Stewart Duncan J, Mei Shirley H J

机构信息

Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.

出版信息

Front Bioeng Biotechnol. 2024 Aug 1;12:1412811. doi: 10.3389/fbioe.2024.1412811. eCollection 2024.


DOI:10.3389/fbioe.2024.1412811
PMID:39148941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11324487/
Abstract

INTRODUCTION: Cryopreservation is a critical process of cell products for achieving a commercial viability through wide scale adoption. By preserving cells in a lower temperature, cryopreservation enables a product to be off-the-shelf and ready for infusion. An optimized cryopreservation strategy can maintain the viability, phenotype, and potency of thawed mesenchymal stromal/stem cells (MSCs) while being regulatory compliant. We compared three clinical-ready formulations with one research cryopreservation solutions and evaluated key quality parameters of post thawed MSCs. METHOD AND RESULT: MSCs were cryopreserved at 3, 6, and 9 million cells/mL (M/mL) in four different cryopreservation solutions: NutriFreez (10% dimethyl sulfoxide [DMSO]), Plasmalyte A (PLA)/5% human albumin (HA)/10% DMSO (PHD10), CryoStor CS5 (5% DMSO), and CryoStor CS10 (10% DMSO). To establish post thaw viability, cells were evaluated with no dilution of DMSO (from 3 M/mL), 1:1 dilution (from 6 M/mL), or 1:2 dilution (from 9 M/mL) with PLA/5% HA, to achieve uniform concentration at 3 M/mL. Cell viability was measured at 0-, 2-, 4-, and 6-h post thaw with Trypan blue exclusion and Annexin V/PI staining. Dilution (1:2) of final cell products from 9M/mL resulted in an improvement of cell viability over 6 h but showed a trend of decreased recovery. MSCs cryopreserved in solutions with 10% DMSO displayed comparable viabilities and recoveries up to 6 h after thawing, whereas a decreasing trend was noted in cell viability and recovery with CS5. Cells from all groups exhibited surface marker characteristics of MSCs. We further evaluated cell proliferation after 6-day recovery in culture. While cells cryopreserved in NutriFreez and PHD10 presented similar cell growth post thaw, MSCs cryopreserved in CS5 and CS10 at 3 M/mL and 6M/mL showed 10-fold less proliferative capacity. No significant differences were observed between MSCs cryopreserved in NutriFreez and PHD10 in their potency to inhibit T cell proliferation and improve monocytic phagocytosis. CONCLUSION: MSCs can be cryopreserved up to 9 M/mL without losing notable viability and recovery, while exhibiting comparable post thaw potency with NutriFreez and PHD10. These results highlight the importance of key parameter testing for selecting the optimal cryopreservation solution for MSC-based therapy.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/ee526b7eed45/fbioe-12-1412811-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/11d56afe7223/fbioe-12-1412811-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/afed8caa4c5b/fbioe-12-1412811-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/ec030cffcbfa/fbioe-12-1412811-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/04b14ebead12/fbioe-12-1412811-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/113cd7d8b04e/fbioe-12-1412811-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/ee526b7eed45/fbioe-12-1412811-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/11d56afe7223/fbioe-12-1412811-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/afed8caa4c5b/fbioe-12-1412811-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/ec030cffcbfa/fbioe-12-1412811-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/04b14ebead12/fbioe-12-1412811-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/113cd7d8b04e/fbioe-12-1412811-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/178d/11324487/ee526b7eed45/fbioe-12-1412811-g006.jpg

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Key quality parameter comparison of mesenchymal stem cell product cryopreserved in different cryopreservation solutions for clinical applications.

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引用本文的文献

[1]
Dimethyl sulfoxide in cryopreserved mesenchymal stromal cell therapy products: is there a safety risk to patients?

J Transl Med. 2025-8-18

本文引用的文献

[1]
Mesenchymal stem cells induce dynamic immunomodulation of airway and systemic immune cells but do not improve survival for mice with H1N1 virus-induced acute lung injury.

Front Bioeng Biotechnol. 2023-6-8

[2]
Strategies in developing dimethyl sulfoxide (DMSO)-free cryopreservation protocols for biotherapeutics.

Front Immunol. 2022-10-5

[3]
Cryostorage of Mesenchymal Stem Cells and Biomedical Cell-Based Products.

Cells. 2022-8-29

[4]
Impact of Cryopreservation and Freeze-Thawing on Therapeutic Properties of Mesenchymal Stromal/Stem Cells and Other Common Cellular Therapeutics.

Curr Stem Cell Rep. 2022

[5]
Poly(I:C) enhances mesenchymal stem cell control of myeloid cells from COVID-19 patients.

iScience. 2022-5-20

[6]
Axicabtagene ciloleucel as first-line therapy in high-risk large B-cell lymphoma: the phase 2 ZUMA-12 trial.

Nat Med. 2022-4

[7]
Effects of storage media, supplements and cryopreservation methods on quality of stem cells.

World J Stem Cells. 2021-9-26

[8]
KTE-X19 for relapsed or refractory adult B-cell acute lymphoblastic leukaemia: phase 2 results of the single-arm, open-label, multicentre ZUMA-3 study.

Lancet. 2021-8-7

[9]
Mesenchymal stromal cells reduce evidence of lung injury in patients with ARDS.

JCI Insight. 2021-6-22

[10]
Thawed cryopreserved synovial mesenchymal stem cells show comparable effects to cultured cells in the inhibition of osteoarthritis progression in rats.

Sci Rep. 2021-5-6

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