Evidence map›Paper›PMID 39023111›Full record

ArticleJournal of medical virology2024

Specific long-term changes in anti-SARS-CoV-2 IgG modifications and antibody functions in mRNA, adenovector, and protein subunit vaccines.

Sebastian Reinig, Chin Kuo, Chia-Chun Wu, Sheng-Yu Huang, Jau-Song Yu, Shin-Ru Shih

Abstract read
In one paragraph

Article in Journal of medical virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Sebastian ReinigResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.
Chin KuoResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.
Chia-Chun WuMolecular Medicine Research Center, Chang Gung University, Taoyuan, Taiwan.
Sheng-Yu HuangResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.
Jau-Song YuMolecular Medicine Research Center, Chang Gung University, Taoyuan, Taiwan.
Shin-Ru ShihResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.

Funding

University of Washington Arboviral Research Network (UWARN)U01AI151698 · NIAID · UNIVERSITY OF WASHINGTON · PI Michael Gale, PETER MACGARR RABINOWITZ · 2020 to 2026
$13.3M
Chang Gung Memorial Hospital CLRPD1J0015Chang Gung Memorial Hospital CORPD1K0011-12Higher Education Sprout Project by the Ministry of Education (MOE)Ministry of Education (MOE) EMRPD1N0071Ministry of Science and Technology (MOST) MOST 109-2327-B-182-002Ministry of Science and Technology (MOST) MOST 111-2634-F-182-001Ministry of Science and Technology, TaiwanNIAID NIH HHS U01 AI151698NIH HHS U01 AI151698Research Center for Emerging Viral Infections from The Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education (MOE)United World Antiviral Research Network
6 · The paper itself

Abstract

Various vaccine platforms were developed and deployed against the COVID-19 disease. The Fc-mediated functions of IgG antibodies are essential in the adaptive immune response elicited by vaccines. However, the long-term changes of protein subunit vaccines and their combinations with messenger RNA (mRNA) vaccines are unknown. A total of 272 serum and plasma samples were collected from individuals who received first to third doses of the protein subunit Medigen, the mRNA (BNT, Moderna), or the adenovector AstraZeneca vaccines. The IgG subclass level was measured using enzyme-linked immunosorbent assay, and Fc-N glycosylation was measured using liquid chromatography coupled to tandem mass spectrometry. Antibody-dependent-cellular-phagocytosis (ADCP) and complement deposition (ADCD) of anti-spike (S) IgG antibodies were measured by flow cytometry. IgG1 and 3 reached the highest anti-S IgG subclass level. IgG1, 2, and 4 subclass levels significantly increased in mRNA- and Medigen-vaccinated individuals. Fc-glycosylation was stable, except in female BNT vaccinees, who showed increased bisection and decreased galactosylation. Female BNT vaccinees had a higher anti-S IgG titer than that of males. ADCP declined in all groups. ADCD was significantly lower in AstraZeneca-vaccinated individuals. Each vaccine produced specific long-term changes in Fc structure and function. This finding is critical when selecting a vaccine platform or combination to achieve the desired immune response.

Indexed as

Antibodies, ViralCOVID-19COVID-19 VaccinesImmunoglobulin GmRNA VaccinesSARS-CoV-2Vaccines, SubunitAdultAgedFemaleGlycosylationHumansMaleMiddle AgedProtein Subunit VaccinesRNA, MessengerAntibodies, ViralCOVID-19 VaccinesImmunoglobulin GmRNA VaccinesProtein Subunit VaccinesRNA, MessengerSpike Glycoprotein, CoronavirusVaccines, Subunitadenovector vaccineantibody functionsanti‐SARS‐CoV‐2 IgGCOVID‐19 diseasemRNA vaccineprotein subunit vaccine

Identifiers

PMID39023111
PMCPMC13152800

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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.