红细胞压积、储存时间和受体性别对小鼠输血后红细胞恢复的影响。

IF 1.6 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-09-01 Epub Date: 2025-07-31 DOI:10.1111/vox.70074
Shwatina Jagnarine, Daniel Guobadia, Tayler A Van Denakker, Emmalene Kyritsis, Tiffany A Thomas, Krystalyn E Hudson
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引用次数: 0

摘要

背景和目的:在冷藏过程中,红细胞(rbc)经历渐进性生化和结构变化,即贮藏损伤,影响其功能和输血后恢复(PTR)。虽然抗凝剂和添加剂溶液有助于减轻这些影响,但它们也会影响单位红细胞压积。红细胞压积对PTR的影响尚不清楚。本研究探讨红细胞压积的储存、储存时间和受体性别对PTR的影响。材料和方法:利用表达荧光蛋白的转基因红细胞小鼠,制备白细胞诱导红细胞单位,并在60%或75%红细胞压积下保存1、6或11天。输血前,将新鲜采集的红细胞加入储存单位,以方便PTR计算。然后将红细胞单位输注到雌性或雄性受体小鼠中,并在多个时间点评估PTR。结果:PTR随储存时间延长而降低。红细胞压积对储存6天的红细胞PTR无显著影响。然而,储存11天后,较高的红细胞压积与降低的PTR相关。此外,无论单位红细胞压积如何,女性受体的PTR明显低于男性受体。结论:红细胞压积和受体性别影响长期保存红细胞的PTR。这些发现强调了在优化红细胞储存和输血策略时需要考虑这两个因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of haematocrit, storage duration and recipient sex on post-transfusion recovery of red blood cells in a murine model.

Background and objectives: During cold storage, red blood cells (RBCs) undergo progressive biochemical and structural changes, known as the storage lesion, which affects their function and post-transfusion recovery (PTR). While anticoagulants and additive solutions help mitigate these effects, they also influence unit haematocrit. The impact of haematocrit on PTR remains unclear. This study investigates how storage of haematocrit, storage duration and recipient sex influence PTR.

Materials and methods: Using transgenic mice with RBCs expressing fluorescent proteins, leukoreduced RBC units were prepared and stored at 60% or 75% haematocrit for 1, 6 or 11 days. Before transfusion, freshly collected RBCs were added to stored units to facilitate PTR calculations. RBC units were then transfused into female or male recipient mice and PTR was evaluated at multiple time points.

Results: PTR decreased with storage duration. Haematocrit had no significant effect on PTR for RBC units stored up to 6 days. However, after 11 days of storage, a higher haematocrit was associated with reduced PTR. Additionally, female recipients exhibited significantly lower PTR than male recipients, regardless of unit haematocrit.

Conclusion: Haematocrit and recipient sex influence PTR for RBC units stored for a long time. These findings highlight the need to consider both factors when optimizing RBC storage and transfusion strategies.

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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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