The impact of the cryopreservation period on the CD34+ cell viability of cryopreserved cord blood units.

IF 1.6 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2026-05-08 DOI:10.1111/vox.70281
Hye Ryun Lee, Eun Youn Roh, Namhee Kim, Hyunwoong Park, Jong Hyun Yoon, Sue Shin
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Abstract

Background and objectives: Cord blood (CB) is an important source for haematopoietic stem cell transplantation because of its long-term cryopreservation. However, concerns remain regarding the potential decline in CB quality with prolonged cryopreservation. This study aimed to evaluate the post-thaw viability of CD45+ and CD34+ cells in CB units and to investigate how their viabilities change over prolonged cryopreservation.

Materials and methods: We enrolled 726 CB units that underwent pre-transplantation examination from May 2006 through June 2023. Post-thaw viabilities of CD45+ and CD34+ cells were analysed in relation to cryopreservation period and across 4-year cryopreservation groups.

Results: The mean post-thaw viabilities were 60.5% for CD45+ cells and 91.2% for CD34+ cells. CD45+ cell viability showed a positive correlation with the cryopreservation period (r = 0.304, p < 0.001); however, no consistent trend was observed among the cryopreservation period groups. In contrast, CD34+ cell viability showed a significant negative correlation with the cryopreservation period (r = - 0.306, p <0.001) and decreased, with units cryopreserved for 1-4 years and 5-8 years having significantly higher viabilities than those cryopreserved for 9-12 years and 13-16 years.

Conclusion: Our findings demonstrate that the post-thaw viabilities of CD45+ and CD34+ cells in cryopreserved CB units exceed internationally accepted standards, with CD34+ cell viability showing a tendency to decline with prolonged cryopreservation. These results underscore the importance of securing an adequate CD34+ cell dose at the time of cryopreservation to maintain the long-term quality and clinical utility of CB units.

低温保存时间对脐带血单位CD34+细胞活力的影响。
背景与目的:脐带血因其长期低温保存而成为造血干细胞移植的重要来源。然而,人们仍然担心长时间冷冻保存可能会导致CB质量下降。本研究旨在评估CD45+和CD34+细胞在CB单元中解冻后的生存能力,并研究它们在长时间冷冻保存过程中的生存能力变化。材料和方法:从2006年5月到2023年6月,我们招募了726个CB单位进行移植前检查。分析CD45+和CD34+细胞的解冻后存活率与低温保存时间和4年低温保存组的关系。结果:CD45+细胞解冻后存活率为60.5%,CD34+细胞解冻后存活率为91.2%。结论:CD45+和CD34+细胞冻融后存活率均超过国际标准,且CD34+细胞存活率随冻融时间延长呈下降趋势。这些结果强调了在冷冻保存时确保足够的CD34+细胞剂量以保持CB单位的长期质量和临床效用的重要性。
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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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