Cryopreserved hematopoietic stem/progenitor cells stability program-development, current status and recommendations: A brief report from the AABB-ISCT joint working group cellular therapy product stability project team.


Journal

Cytotherapy
ISSN: 1477-2566
Titre abrégé: Cytotherapy
Pays: England
ID NLM: 100895309

Informations de publication

Date de publication:
05 2022
Historique:
pubmed: 26 3 2022
medline: 27 4 2022
entrez: 25 3 2022
Statut: ppublish

Résumé

The AABB-ISCT Joint Working Group Stability Project Team (SPT) was assigned to roadmap a path toward standardization of cryopreserved hematopoietic stem/progenitor cell (HSPC) stability programs. HSPC stability encompasses a broad scope of conditions including non-frozen ("fresh") and cryopreserved cell products, and varying methods for storage, thaw, and administration. This report assessed current practices and focused solely on cryopreserved HSPC cell therapy products to establish preliminary recommendations for a stability program roadmap. A survey was prepared by the SPT and distributed to ISCT and AABB members. Survey results were summarized and recommendations were outlined based on the responses from the survey. This report highlights current practices for cryopreserved HSPC stability programs, including additional considerations and recommendations. Eighty-two (82) centers worldwide participated in the survey. Survey results indicate variability across programs. HSPC stability depends on multiple factors within the processing facility (e.g., cryopreservation techniques, reagents used, and storage temperature) and independent variables (e.g., donor-related factors and starting material variability). While retention of hematopoietic engraftment potential is the primary goal for cryopreserved HSPC stability, engraftment results should not be used as the sole metric for stability programs. Based on the survey results, the SPT provides recommendations for consideration. The SPT recommendations for best practices are not intended to replace existing standards. The survey results emphasize the need for the community to optimize best practices and consider initiating collaborative projects to improve the standardization of cryopreserved HSPC stability programs for cell therapy products.

Sections du résumé

BACKGROUND
The AABB-ISCT Joint Working Group Stability Project Team (SPT) was assigned to roadmap a path toward standardization of cryopreserved hematopoietic stem/progenitor cell (HSPC) stability programs. HSPC stability encompasses a broad scope of conditions including non-frozen ("fresh") and cryopreserved cell products, and varying methods for storage, thaw, and administration. This report assessed current practices and focused solely on cryopreserved HSPC cell therapy products to establish preliminary recommendations for a stability program roadmap.
METHODS
A survey was prepared by the SPT and distributed to ISCT and AABB members. Survey results were summarized and recommendations were outlined based on the responses from the survey. This report highlights current practices for cryopreserved HSPC stability programs, including additional considerations and recommendations.
RESULTS AND DISCUSSION
Eighty-two (82) centers worldwide participated in the survey. Survey results indicate variability across programs. HSPC stability depends on multiple factors within the processing facility (e.g., cryopreservation techniques, reagents used, and storage temperature) and independent variables (e.g., donor-related factors and starting material variability). While retention of hematopoietic engraftment potential is the primary goal for cryopreserved HSPC stability, engraftment results should not be used as the sole metric for stability programs. Based on the survey results, the SPT provides recommendations for consideration.
CONCLUSIONS
The SPT recommendations for best practices are not intended to replace existing standards. The survey results emphasize the need for the community to optimize best practices and consider initiating collaborative projects to improve the standardization of cryopreserved HSPC stability programs for cell therapy products.

Identifiants

pubmed: 35331646
pii: S1465-3249(22)00070-6
doi: 10.1016/j.jcyt.2022.03.001
pii:
doi:

Substances chimiques

Antigens, CD34 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

473-481

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Conflicts of interest This is a joint cooperation between the two organizations, ISCT and AABB, who have agreed to share the output of this work and to co-publish in both Transfusion (https://www.aabb.org/news-resources/news/transfusion-journal) and Cytotherapy (https://www.isct-cytotherapy.org/). This manuscript has not been published or is not under consideration by another journal. The authors of this manuscript have read and understood this journal's polices, and believe that the studies presented here do not violate any of these. The authors have disclosed no conflicts of interest.

Auteurs

Ronit Reich-Slotky (R)

John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey, USA.

Ljiljana V Vasovic (LV)

Weill Cornell Medicine, New York-Presbyterian Hospital, New York, New York, USA.

Kevin J Land (KJ)

Vitalant Biotherapies, Phoenix, Arizona, USA; University of Texas Health Science Center San Antonio, Department of Pathology Transfusion Medicine, San Antonio, Texas, USA.

Mike Halpenny (M)

Canadian Blood Services, Ottawa, Ontario, Canada.

Joan Woeltz (J)

Blood & Marrow Transplantation and Cellular Therapy Stanford Health Care, Stanford, California, USA.

Aby J Mathew (AJ)

BioLife Solutions, Inc. Bothell, Washington, USA.

Diane Fournier (D)

Héma-Québec, Montreal, Quebec, Canada.

Brenda Alder (B)

Northside Hospital, Blood and Marrow Transplant Program, Cell Therapy Lab, Atlanta, Georgia, USA.

Karl Stasko (K)

Dana-Farber Cancer Institute Cell Manipulation Core Facility, Boston, Massachusetts, USA.

Nadim Mahmud (N)

Division of Hematology/Oncology, Department of Medicine, University of Illinois College of Medicine, Chicago, Illinois, USA. Electronic address: nadim@uic.edu.

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