Evidence map›Paper›PMID 40490397›Full record

ArticleVox sanguinis2025

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

Sandra Laner-Plamberger, Anita Siller, Wanda Lauth, Jan Marco Kern, Lenka Baskova, Nina Held, Orkan Kartal, Harald Schennach, Eva Rohde, Christoph Grabmer

Abstract read
In one paragraph

Article in Vox sanguinis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sandra Laner-PlambergerDepartment of Transfusion Medicine, University Hospital of Salzburg (SALK), Paracelsus Medical University (PMU) Salzburg, Salzburg, Austria.ORCID https://orcid.org/0000-0002-1416-6023
Anita SillerCentral Institute for Blood Transfusion and Immunology, University Hospital Innsbruck, Tirol Kliniken GmbH, Innsbruck, Austria.ORCID https://orcid.org/0009-0003-7860-7144
Wanda LauthTeam Biostatistics and Big Medical Data, IDA Lab Salzburg, PMU Salzburg, Salzburg, Austria.ORCID https://orcid.org/0009-0002-5774-0846
Jan Marco KernDepartment of Clinical Microbiology and Hygiene, University Hospital of Salzburg, PMU Salzburg, Salzburg, Austria.ORCID https://orcid.org/0009-0000-9126-4543
Lenka BaskovaDepartment of Clinical Microbiology and Hygiene, University Hospital of Salzburg, PMU Salzburg, Salzburg, Austria.
Nina HeldDepartment of Transfusion Medicine, University Hospital of Salzburg (SALK), Paracelsus Medical University (PMU) Salzburg, Salzburg, Austria.
Orkan KartalDepartment of Transfusion Medicine, University Hospital of Salzburg (SALK), Paracelsus Medical University (PMU) Salzburg, Salzburg, Austria.
Harald SchennachCentral Institute for Blood Transfusion and Immunology, University Hospital Innsbruck, Tirol Kliniken GmbH, Innsbruck, Austria.
Eva RohdeDepartment of Transfusion Medicine, University Hospital of Salzburg (SALK), Paracelsus Medical University (PMU) Salzburg, Salzburg, Austria.ORCID https://orcid.org/0000-0001-8692-886X
Christoph GrabmerDepartment of Transfusion Medicine, University Hospital of Salzburg (SALK), Paracelsus Medical University (PMU) Salzburg, Salzburg, Austria.

Funding

Bundesland Salzburg 20102-F1901166-KZPBundesland Salzburg 20204-WISS/225/197-2019
6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe 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

methodsSerum 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.

resultsOur 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.

conclusionAs 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.

Indexed as

Antibodies, ViralCOVID-19SARS-CoV-2Antibodies, NeutralizingCOVID-19 SerotherapyHumansImmunization, PassiveTime FactorsAntibodies, NeutralizingAntibodies, ViralantibodiesCOVID‐19 convalescent plasmalong‐term storageplasmapheresisSARS‐CoV‐2

Identifiers

PMID40490397
PMCPMC12390367

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.