Evidence map›Paper›PMID 35509410›Full record

ArticleHealth science reports2022

The serological diversity of serum IgG/IgA/IgM against SARS-CoV-2 nucleoprotein, spike, and receptor-binding domain and neutralizing antibodies in patients with COVID-19 in Japan.

Yudai Kaneko, Akira Sugiyama, Toshiya Tanaka, Kazushige Fukui, Akashi Taguchi, Kenji Tatsuno, Aya Nakayama, Kazumasa Koga, Yoshiro Kishi, Wang Daming and 9 more

Open access · goldAbstract read
In one paragraph

Article in Health science reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Antibody response to third and fourth BNT162b2 mRNA booster vaccinations in healthcare workers in Tokyo, Japan.Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy · 2023
    Article
  5. Article
  6. Dynamics of CD4Infection and drug resistance · 2023
    Article
  7. Article
  8. Article
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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

19 authors at 6 institutions in 2 countries.

Yudai KanekoResearch Center for Advanced Science and Technology (RCAST) The University of Tokyo Tokyo Japan.ORCID 0000-0003-0967-782X
Akira SugiyamaResearch Center for Advanced Science and Technology (RCAST) The University of Tokyo Tokyo Japan.
Toshiya TanakaResearch Center for Advanced Science and Technology (RCAST) The University of Tokyo Tokyo Japan.
Kazushige FukuiIsotope Science Center The University of Tokyo Tokyo Japan.
Akashi TaguchiResearch Center for Advanced Science and Technology (RCAST) The University of Tokyo Tokyo Japan.
Kenji TatsunoResearch Center for Advanced Science and Technology (RCAST) The University of Tokyo Tokyo Japan.
Aya NakayamaIsotope Science Center The University of Tokyo Tokyo Japan.
Kazumasa KogaDepartment of Neurology Nissan Tamagawa Hospital Tokyo Japan.
Yoshiro KishiMedical & Biological Laboratories Co. Ltd Tokyo Japan.
Wang DamingSuzhou Institute of Biomedical Engineering and Technology Chinese Academy of Sciences Suzhou China.
Chungen QianDepartment of Biomedical Engineering, The Key Laboratory for Biomedical Photonics of MOE at Wuhan National Laboratory for Optoelectronics-Hubei Bioinformatics & Molecular Imaging Key Laboratory, Systems Biology Theme College of Life Science and Technology, Huazhong University of Science and Technology Hubei China.
Fuzhen XiaReagent R&D Center Shenzhen YHLO Biotech Co. Ltd Guangdong China.
Fan HeReagent R&D Center Shenzhen YHLO Biotech Co. Ltd Guangdong China.
Liang ZhengReagent R&D Center Shenzhen YHLO Biotech Co. Ltd Guangdong China.
Yi YuReagent R&D Center Shenzhen YHLO Biotech Co. Ltd Guangdong China.
Youichiro WadaResearch Center for Advanced Science and Technology (RCAST) The University of Tokyo Tokyo Japan.
Yoshiaki WadaDepartment of Neurology Nissan Tamagawa Hospital Tokyo Japan.
Tatsuhiko KodamaResearch Center for Advanced Science and Technology (RCAST) The University of Tokyo Tokyo Japan.
Takeshi KawamuraResearch Center for Advanced Science and Technology (RCAST) The University of Tokyo Tokyo Japan.ORCID 0000-0003-1613-6968
Tokyo University of Science · JPThe University of Tokyo · JPChinese Academy of Sciences · CNMedical & Biological Laboratories (Japan) · JPNissan Tamagawa Hospital · JPWuhan National Laboratory for Optoelectronics · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: We compared the temporal changes of immunoglobulin M (IgM), IgG, and IgA antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleoprotein (N), spike 1 subunit (S1), and receptor-binding domain (RBD), and neutralizing antibodies (NAbs) against SARS-CoV-2 in patients with coronavirus disease 2019 (COVID-19) to understand the humoral immunity in COVID-19 patients for developing drugs and vaccines for COVID-19. Methods: A total of five confirmed COVID-19 cases in Nissan Tamagawa Hospital in early August 2020 were recruited in this study. Using a fully automated chemiluminescence immunoassay analyzer, we measured the levels of IgG, IgA, and IgM against SARS-CoV-2 N, S1, and RBD and NAbs against SARS-CoV-2 in COVID-19 patients' sera acquired multiple times in individuals from 0 to 76 days after symptom onset. Results: IgG levels against SARS-CoV-2 structural proteins increased over time in all cases but IgM and IgA levels against SARS-CoV-2 showed different increasing trends among individuals in the early stage. In particular, we observed IgA increasing before IgG and IgM in some cases. The NAb levels were more than cut-off value in 4/5 COVID-19 patients some of whose antibodies against RBD did not exceed the cut-off value in the early stage. Furthermore, NAb levels against SARS-CoV-2 increased and kept above cut-off value more than around 70 days after symptom onset in all cases. Conclusion: Our findings indicate COVID-19 patients should be examined for IgG, IgA, and IgM against SARS-CoV-2 structural proteins and NAbs against SARS-CoV-2 to analyze the diversity of patients' immune mechanisms.

Indexed as

antibodyCOVID‐19neutralizing antibodypatientSARS‐CoV‐2

Identifiers

PMID35509410
PMCPMC9059222
OpenAlexW4226382841

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.