Aggregates in cold-stored platelet units have diverse phenotypes and are removed by pre-transfusion filters.

IF 1.6 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-09-10 DOI:10.1111/vox.70114
Kathleen Kelly, Crystal Stanley, Micaela Jones, Jeff Finlon, David Buesing, Maria Rahman, Michelle Poffel, Deanna Janosko, Susanne Marschner
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引用次数: 0

Abstract

Background and objectives: The US Food and Drug Administration guidance for cold-stored platelets (CSPs) permits storage of apheresis platelets at 1-6°C for ≤14 days. During a pilot programme, CSPs were evaluated in a large US blood centre over a 10-month period (September 2023 to July 2024) to better understand the formation of aggregates under routine use.

Materials and methods: Platelets collected in 100% plasma were moved into cold storage within 4 h of collection and shipped to local hospitals. Hospitals returned any units with aggregates to the blood centre. Units were visually inspected and tested for platelet concentration, pH, metabolism and activation parameters. At expiration (Day 14), units were passed through a transfusion filter (170-260 μm) and assessed post-filtration and after 24 h.

Results: Aggregation rates were high initially but decreased to 9% of released CSPs by study conclusion. Fifty-five aggregated units were returned. The majority of units (42%) had a small, flaky phenotype, which did not change over storage. Platelet counts significantly decreased with a 50% drop by expiry. Lactadherin and P-selectin increased, CD63 and CD41/61 complex decreased and there was slower metabolism. Filtration removed all aggregates, except for one unit with small aggregates being observed 24 h post-filtration. Platelet recovery after filtration was 94% ± 26%. Seven repeat donors donated 6 units with no aggregates and 17 units with aggregates, with variable aggregate phenotypes between donations.

Conclusion: This study demonstrates that aggregate phenotypes in CSPs are highly variable and removed effectively by filtration; they appear to arise more from external handling conditions than from any intrinsic product property.

聚集在冷藏血小板单位有不同的表型,并通过输血前过滤器去除。
背景和目的:美国食品和药物管理局关于冷藏血小板(CSPs)的指南允许在1-6°C下储存单采血小板≤14天。在一个试点项目中,美国一家大型血液中心对csp进行了为期10个月的评估(2023年9月至2024年7月),以更好地了解常规使用下聚集体的形成。材料和方法:100%血浆收集的血小板在收集后4小时内移入冷库,并运往当地医院。医院将任何有血块的单位退回血液中心。目视检查并检测血小板浓度、pH、代谢和活化参数。呼气时(第14天),单位通过输血过滤器(170-260 μm),并在过滤后和24 h后进行评估。结果:最初的聚集率很高,但根据研究结论,释放的csp的聚集率降至9%。总共归还了55个单位。大多数单位(42%)具有小而片状的表型,在储存过程中不会发生变化。血小板计数显著下降,到期时下降50%。乳酸粘附素和p -选择素升高,CD63和CD41/61复合物降低,代谢减慢。过滤除去了所有的聚集体,除了过滤24小时后观察到的一个小聚集体。滤过后血小板回收率为94%±26%。7名重复献血者捐赠6个无聚集体单位和17个有聚集体单位,捐赠之间的聚集体表型不同。结论:本研究表明,csp的聚集表型是高度可变的,可以通过过滤有效地去除;它们似乎更多地是由外部处理条件引起的,而不是由任何内在的产物性质引起的。
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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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