Evidence map›Paper›PMID 33664294›Full record

ArticleScientific reports2021

A novel highly quantitative and reproducible assay for the detection of anti-SARS-CoV-2 IgG and IgM antibodies.

Kenta Noda, Kouki Matsuda, Shigehiro Yagishita, Kenji Maeda, Yutaro Akiyama, Junko Terada-Hirashima, Hiromichi Matsushita, Satoshi Iwata, Kazuto Yamashita, Yusuke Atarashi and 6 more

Abstract readEvaluation Study
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

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  18. Neutralising activity and antibody titre in 10 patients with breakthrough infections of the SARS-CoV-2 Omicron variant in Japan.Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy · 2022
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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

16 authors.

Kenta NodaCentral Research Laboratories, Sysmex Corporation, Kobe, Hyogo, Japan.
Kouki MatsudaDepartment of Refractory Viral Infections, National Center for Global Health and Medicine (NCGM) Research Institute, Tokyo, Japan.
Shigehiro YagishitaDivision of Molecular Pharmacology, National Cancer Center Research Institute, Tokyo, Japan.
Kenji MaedaDepartment of Refractory Viral Infections, National Center for Global Health and Medicine (NCGM) Research Institute, Tokyo, Japan. kmaeda@ri.ncgm.go.jp.
Yutaro AkiyamaDisease Control and Prevention Center (DCC), NCGM, Tokyo, Japan.
Junko Terada-HirashimaCenter for Clinical Science, NCGM, Tokyo, Japan.
Hiromichi MatsushitaDepartment of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.
Satoshi IwataDepartment of Infectious Diseases, National Cancer Center Hospital, Tokyo, Japan.
Kazuto YamashitaCentral Research Laboratories, Sysmex Corporation, Kobe, Hyogo, Japan.
Yusuke AtarashiCentral Research Laboratories, Sysmex Corporation, Kobe, Hyogo, Japan.
Shunsuke WatanabeCentral Research Laboratories, Sysmex Corporation, Kobe, Hyogo, Japan.
Nobuyuki IdeBio-Diagnostic Reagent Technology Center, Sysmex Corporation, Kobe, Hyogo, Japan.
Tomokazu YoshidaCentral Research Laboratories, Sysmex Corporation, Kobe, Hyogo, Japan. Yoshida.Tomokazu@sysmex.co.jp.
Norio OhmagariDisease Control and Prevention Center (DCC), NCGM, Tokyo, Japan.
Hiroaki MitsuyaDepartment of Refractory Viral Infections, National Center for Global Health and Medicine (NCGM) Research Institute, Tokyo, Japan.
Akinobu HamadaDivision of Molecular Pharmacology, National Cancer Center Research Institute, Tokyo, Japan. akhamad@ncc.go.jp.

Funding

Development of therapeutics for SARS-CoV-2 infectionZIABC012018 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MITSUYA, HIROAKI · 2020 to 2025
$2.6M
Japan Agency for Medical Research and Development JP20fk0108160
6 · The paper itself

Abstract

The quantitative range and reproducibility of current serological tests for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) are not optimized. Herein, we developed a diagnostic test that detects SARS-CoV-2 IgG and IgM with high quantitativeness and reproducibility and low interference. The system was based on the high-sensitivity chemiluminescence enzyme immunoassay (HISCL) platform and detects IgG and IgM specific to SARS-CoV-2 spike and nucleocapsid proteins. Quantification accuracy and reproducibility were evaluated using serially diluted samples from 60 SARS-CoV-2-infected patients. Assay performance was evaluated using serum samples from the SARS-CoV-2-infected patients and 500 SARS-CoV-2-negative serum samples collected before the emergence of SARS-CoV-2. The system showed high quantification accuracy (range, 10

Indexed as

AdolescentAdultAgedAged, 80 and overChildCOVID-19 TestingFemaleHumansImmunoenzyme TechniquesImmunoglobulin GImmunoglobulin MLuminescent MeasurementsMaleMiddle AgedROC CurveSARS-CoV-2Immunoglobulin GImmunoglobulin M

Identifiers

PMID33664294
PMCPMC7933429

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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.