Evidence map›Paper›PMID 38132272›Full record

ArticleDiagnostics (Basel, Switzerland)2023

Performance Evaluation of Three Antibody Binding Assays, a Neutralizing Antibody Assay, and an Interferon-Gamma Release Assay for SARS-CoV-2 According to Vaccine Type in Vaccinated Group.

Minjeong Nam, Jae Hyun Cha, Sang-Wook Kim, Sun Bean Kim, Ki-Byung Lee, You-Seung Chung, Seung Gyu Yun, Myung-Hyun Nam, Chang Kyu Lee, Yunjung Cho

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2023. 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
0.2field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  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 at 1 institution in 1 country.

Minjeong NamDepartment of Laboratory Medicine, Korea University College of Medicine, Seoul 02841, Republic of Korea.ORCID 0000-0003-3542-3487
Jae Hyun ChaDepartment of Laboratory Medicine, Korea University Anam Hospital, Seoul 02841, Republic of Korea.
Sang-Wook KimDepartment of Laboratory Medicine, Korea University Anam Hospital, Seoul 02841, Republic of Korea.
Sun Bean KimDivision of Infectious Diseases, Department of Internal Medicine, Korea University College of Medicine, Korea University Anam Hospital, Seoul 02841, Republic of Korea.
Ki-Byung LeeDivision of Infectious Diseases, Department of Internal Medicine, Korea University College of Medicine, Korea University Anam Hospital, Seoul 02841, Republic of Korea.
You-Seung ChungDivision of Infectious Diseases, Department of Internal Medicine, Korea University College of Medicine, Korea University Anam Hospital, Seoul 02841, Republic of Korea.
Seung Gyu YunDepartment of Laboratory Medicine, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Myung-Hyun NamDepartment of Laboratory Medicine, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Chang Kyu LeeDepartment of Laboratory Medicine, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Yunjung ChoDepartment of Laboratory Medicine, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Korea University · KR

Funding

Abbott KoreaBeckman CoulterRoche Diagnostics
6 · The paper itself

Abstract

We evaluated the performance of SARS-CoV-2 assays in the vaccinated group using receptor-binding domain antibody assays (RBD Ab assay), neutralizing antibody assay (nAb assay), and interferon-gamma release assay (IGR assay). We also compared the performance of the SARS-CoV-2 assays based on vaccine type in a large population. We collected 1851 samples from vaccinated individuals with vector, mix-and-match (MM), and mRNA vaccines. The performance of the RBD Ab assays was assessed by SARS-CoV-2 IgG II Quant (Abbott Laboratories, Sligo, Ireland), SARS-CoV-2 IgG (Beckman Coulter, CA, USA), and anti-SARS-CoV-2 S (Roche Diagnostics GmbH, Mannheim, Germany). The nAb assay was assessed by cPass SARS-CoV-2 neutralization antibody detection kits (GenScript, NJ, USA). The IGR assay was assessed by QuantiFERON (Qiagen, Venlo, The Netherlands). Median values of the RBD Ab assays and nAb assay sequentially increased after the first and second vaccinations. RBD Ab assays and nAb assay showed very strong correlations. The median values of the RBD Ab, nAb, and IGR were higher in the mRNA vaccine group than in the vector and MM vaccine groups. The agreement and correlation among the RBD Ab assays, nAb assay, and IGR assay were higher in the mRNA vaccine group than in the vector and MM vaccine groups. We compared the performance of the RBD Ab assay, nAb assay, and IGR assay based on the vaccine types using the RBD Ab, nAb, and IGR assays. This study provides a better understanding of the assessment of humoral and cellular immune responses after vaccination.

Indexed as

antibody binding assayIGRAmix-and-match vaccinemRNA vaccineneutralizing assaySARS-CoV-2vaccinevector vaccine

Identifiers

PMID38132272
PMCPMC10742828
OpenAlexW4389892368

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.