Hye Ryun Lee, Eun Youn Roh, Namhee Kim, Hyunwoong Park, Jong Hyun Yoon, Sue Shin
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引用次数: 0
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.
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.