Evidence map›Paper›PMID 35632683›Full record

ArticleViruses2022

Changes in Anti-SARS-CoV-2 IgG Subclasses over Time and in Association with Disease Severity.

Zoia R Korobova, Elena V Zueva, Natalia A Arsentieva, Oleg K Batsunov, Natalia E Liubimova, Irina V Khamitova, Raisa N Kuznetsova, Artem A Rubinstein, Tikhon V Savin, Oksana V Stanevich and 3 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.3field-weighted citation impact, top 6% of its field
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

22 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  7. B Cell Dynamics and Transitional B Cells in Long COVID.Current issues in molecular biology · 2025
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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

13 authors at 2 institutions in 1 country.

Zoia R KorobovaSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.ORCID 0000-0003-0535-5014
Elena V ZuevaSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.
Natalia A ArsentievaSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.
Oleg K BatsunovSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.
Natalia E LiubimovaSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.
Irina V KhamitovaSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.
Raisa N KuznetsovaSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.ORCID 0000-0003-4932-6733
Artem A RubinsteinDepartment of Immunology, Department of Infectious Diseases, Intensive Care Unit, Pavlov First State Medical University of St. Petersburg, 6-8 Ulitsa L'va Tolstovo, 197022 St. Petersburg, Russia.ORCID 0000-0002-8493-5211
Tikhon V SavinSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.ORCID 0000-0003-4550-4870
Oksana V StanevichDepartment of Immunology, Department of Infectious Diseases, Intensive Care Unit, Pavlov First State Medical University of St. Petersburg, 6-8 Ulitsa L'va Tolstovo, 197022 St. Petersburg, Russia.
Alexandr N KulikovDepartment of Immunology, Department of Infectious Diseases, Intensive Care Unit, Pavlov First State Medical University of St. Petersburg, 6-8 Ulitsa L'va Tolstovo, 197022 St. Petersburg, Russia.
Dmitry E PevtsovDepartment of Immunology, Department of Infectious Diseases, Intensive Care Unit, Pavlov First State Medical University of St. Petersburg, 6-8 Ulitsa L'va Tolstovo, 197022 St. Petersburg, Russia.
Areg A TotolianSaint Petersburg Pasteur Institute, 14 Ulitsa Mira, 197101 St. Petersburg, Russia.ORCID 0000-0003-4571-8799
First Pavlov State Medical University of St. Petersburg · RUSaint Petersburg Pasteur Institute · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgG is the most prominent marker of post-COVID-19 immunity. Not only does this subtype mark the late stages of infection, but it also stays in the body for a timespan of at least 6 months. However, different IgG subclasses have different properties, and their roles in specific anti-COVID-19 responses have yet to be determined. We assessed the concentrations of IgG1, IgG2, IgG3, and IgG4 against different SARS-CoV-2 antigens (N protein, S protein RBD) using a specifically designed method and samples from 348 COVID-19 patients. We noted a statistically significant association between severity of COVID-19 infection and IgG concentrations (both total and subclasses). When assessing anti-N protein and anti-RBD IgG subclasses, we noted the importance of IgG3 as a subclass. Since it is often associated with early antiviral response, we presumed that the IgG3 subclass is the first high-affinity IgG antibody to be produced during COVID-19 infection.

Indexed as

COVID-19Antibodies, ViralHumansImmunoglobulin GSARS-CoV-2Severity of Illness IndexAntibodies, ViralImmunoglobulin GCOVID-19IgGIgG subclassesseverity

Identifiers

PMID35632683
PMCPMC9143443
OpenAlexW4225371391

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.