Stable SARS-CoV-2 antibody levels and functionality in serum and COVID-19 convalescent plasma after long-term storage.

IF 1.6 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-08-01 Epub Date: 2025-06-09 DOI:10.1111/vox.70059
Sandra Laner-Plamberger, Anita Siller, Wanda Lauth, Jan Marco Kern, Lenka Baskova, Nina Held, Orkan Kartal, Harald Schennach, Eva Rohde, Christoph Grabmer
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引用次数: 0

Abstract

Background and objectives: The coronavirus disease 2019 (COVID-19) pandemic necessitated various therapeutic approaches, including convalescent plasma (CP) administration. The administration timing of COVID-19 CP (CCP), antibody specificity and quantity were identified as crucial factors for therapeutic success. Currently, antibody durability and storage time are still under debate. The aim of this study was to evaluate the stability and in vitro functionality of severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) antibodies in human plasma and serum after long-term storage, to provide a framework for generally applicable rules regarding the long-term storage of CCP.

Materials and methods: Serum and plasma samples of CCP donations were investigated at the time of donation and after 2 and 3 years' storage at less than -30°C using (electro)chemiluminescence immunoassays and enzyme-linked immunosorbent assays, with the plasma undergoing multiple freezing and thawing.

Results: Our data reveal robust levels of SARS-CoV-2 antibodies after long-term storage. Furthermore, our findings also indicate that multiple freezing and thawing cycles do not affect the antibody levels or their neutralizing capability.

Conclusion: As antibody stability and in vitro functionality are maintained over extended periods, even after repeated freezing and thawing, our findings support long-term storage of CCP, particularly benefiting vulnerable populations such as immunocompromised individuals. By now, donors have likely encountered various SARS-CoV-2 variants and vaccine-acquired antibodies. This antibody mix present in CCP is suggested to protect even against new variants. Our data indicate that current regulations for the storage of CCP can be extended and that CCPs could be used for therapeutic purposes after long-term storage without significant loss of antibody quantity.

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长期储存后血清和COVID-19恢复期血浆中稳定的SARS-CoV-2抗体水平和功能
背景与目的:2019冠状病毒病(COVID-19)大流行需要多种治疗方法,包括恢复期血浆(CP)给药。结果表明,给药时机、抗体特异性和剂量是影响治疗成功的关键因素。目前,抗体的耐久性和储存时间仍在争论中。本研究旨在评价严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)抗体在人血浆和血清中长期储存后的稳定性和体外功能,为CCP长期储存的一般适用规则提供框架。材料和方法:采用(电)化学发光免疫法和酶联免疫吸附法对CCP捐献时和-30℃以下保存2年和3年的血清和血浆进行检测,血浆进行多次冷冻和解冻。结果:我们的数据显示,在长期储存后,SARS-CoV-2抗体水平稳定。此外,我们的研究结果还表明,多次冷冻和解冻循环不会影响抗体水平或它们的中和能力。结论:即使在反复冷冻和解冻后,抗体的稳定性和体外功能也能在较长时间内保持,我们的研究结果支持CCP的长期储存,特别是对免疫功能低下的弱势群体。到目前为止,捐赠者可能已经遇到了各种SARS-CoV-2变体和疫苗获得性抗体。这种抗体混合存在于CCP中,被认为甚至可以防止新的变异。我们的数据表明,CCP的现行储存法规可以延长,并且CCP可以在长期储存后用于治疗目的,而不会显著损失抗体数量。
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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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