由于处理延迟而导致的脐带血移植物效力降低可以通过补充海藻糖来预防。

IF 1.8 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-03-25 DOI:10.1111/vox.70012
Suria Jahan, Harinad B Maganti, Jaina Patel, Roya Pasha, Emily Doxtator, Javed K Manesia, Nicolas Pineault
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引用次数: 0

摘要

背景和目的:最大限度地发挥脐带血(CB)单位(CBU)的效力是所有脐带血银行的目标。CB移植中移植细胞剂量低是导致移植缓慢的几个原因之一。处理延迟也可能起作用,因为CBU可以在室温(RT)下储存长达48小时,然后进行冷冻保存。我们假设,由于造血干细胞(hsc)和祖细胞的丢失,在RT下的长时间储存降低了CBU的效力和植入活性。材料和方法:将CBU分成两半,一半在收集后不久处理,另一半在室温保存40 h后处理。解冻后比较其活力和效力,并在异种移植中检测其移植活性。进行了生物信息学分析识别途径调制通过长期存储在RT.Results:长期存储在RT CB细胞的生存能力和效力降低移植基于体外和体内试验。转录组学分析显示,CBU释放的旁分泌因子诱导CD34+细胞中基因表达程序的一些变化。其中包括衰老基因CDKN1B的激活以及细胞周期和自噬基因的下调。添加海藻糖的CBU可以防止细胞活力和效力的丧失。后者与自噬的恢复和衰老基因CDKN1B的抑制有关。结论:这些结果强调了快速加工CBU的重要性,并支持进一步研究海藻糖作为天然补充剂在储存期间保护CBU的效力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduction in cord blood graft potency due to processing delay can be prevented by trehalose supplementation.

Background and objectives: Maximizing the potency of cord blood (CB) units (CBU) is a goal of all CB banks. Low transplant cell dose in CB transplantation is one of several contributors to the slower engraftment. Processing delays could also be at play because CBU can be stored at room temperature (RT) for up to 48 h before cryopreservation. We hypothesized that prolonged storage at RT reduces the potency and engraftment activities of CBU due to the loss of haematopoietic stem cells (HSCs) and progenitor cells.

Materials and methods: CBU were split in half, with one half processed shortly after collection and the other half after 40 h of storage at RT. Viabilities and potencies were compared post thaw, and engraftment activity was tested in xenotransplants. Bioinformatic analysis was carried out to identify pathways modulated by prolonged storage at RT.

Results: Prolonged storage at RT reduced the viability of CB cells and potency of grafts based on in vitro and in vivo assays. Transcriptomic analyses revealed that paracrine factors released in CBU induce several changes in gene expression programmes in CD34+ cells. These included the activation of the senescence gene CDKN1B and down-regulation of cell cycle and autophagy genes. Supplementation of CBU with trehalose prevented the loss in cell viability and potency. The latter was associated with the restoration of autophagy and suppression of the senescence gene CDKN1B.

Conclusion: These results stress the importance of rapid processing of CBU and support further investigations on trehalose as a natural supplement to protect CBU' potency during storage.

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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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