Evidence map›Paper›PMID 32704169›Full record

ArticleNature biotechnology2020

A SARS-CoV-2 surrogate virus neutralization test based on antibody-mediated blockage of ACE2-spike protein-protein interaction.

Chee Wah Tan, Wan Ni Chia, Xijian Qin, Pei Liu, Mark I-C Chen, Charles Tiu, Zhiliang Hu, Vivian Chih-Wei Chen, Barnaby E Young, Wan Rong Sia and 6 more

3 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in Nature biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 830 papers.

0numbers the graph read from it
0cells of the map it votes in
830citing 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.

NCT04961385 completednot on this mapstarted 2021, after this paper: background citation

Immunogenicity of the ChAdox1 n CoV-19 Vaccine Against SARS-CoV-2 With 12-dose Vials: an Interim Analysis

TypeobservationalSponsorBangkok Metropolitan Administration Medical College and Vajira HospitalRan2021 to 2021Enrolled60ConditionsCovid19, Vaccine, ImmunogenicityArmsImmunogenicity after first dose of participants who received first dose of ChAdox-1 n COV-19 vaccine
NCT05205746 phase2completednot on this mapstarted 2021, after this paper: background citation

Phase II Study to Evaluate Immunogenicity and Safety in Subjects With Evidence of Prior Immunity to SARS-CoV-2 of a Single Intramuscular or Intranasal Dose of the Live Recombinant Newcastle Disease Virus Based AVX/COVID-12 Vaccine

TypeinterventionalSponsorLaboratorio Avi-Mex, S.A. de C.V.Ran2021 to 2023Enrolled158ConditionsSARS CoV 2 InfectionArmsRecombinant NDV Vectored Vaccine for SARS-CoV-2, Placebo
NCT05710783 phase2 / phase3completednot on this mapstarted 2022, after this paper: background citation

Phase II/III Parallel, Double-blind, Non-inferiority Study With Active Control, to Evaluate the Immunogenicity and Safety of a Booster Immunization Scheme With a Single Intramuscular Dose of the Recombinant Vaccine Against SARS-CoV-2

TypeinterventionalSponsorLaboratorio Avi-Mex, S.A. de C.V.Ran2022 to 2023Enrolled4,065ConditionsSARS-CoV-2 InfectionArmsAVX-COVID/12, ChAdOx-1-S[recombinant]
3 · Its place in the literature

Who cites it

830 citing papers in PubMed.

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  18. Observational
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  20. Construction of a localized immune nicheActa pharmaceutica Sinica. B · 2026
    Article

770 more citing papers are in PubMed but not listed here.

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.

Chee Wah Tan *Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
Wan Ni Chia *Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
Xijian QinGenScript Biotech, Nanjing, China.
Pei LiuGenScript Biotech, Nanjing, China.
Mark I-C ChenNational Centre for Infectious Diseases, Singapore, Singapore.
Charles TiuProgramme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
Zhiliang HuNanjing Infectious Disease Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.
Vivian Chih-Wei ChenProgramme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.ORCID http://orcid.org/0000-0001-8757-0644
Barnaby E YoungNational Centre for Infectious Diseases, Singapore, Singapore.ORCID http://orcid.org/0000-0003-1010-2230
Wan Rong SiaProgramme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.ORCID http://orcid.org/0000-0003-2694-4192
Yee-Joo TanDepartment of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, Singapore, Singapore.
Randy FooProgramme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
Yongxiang YiNanjing Infectious Disease Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.
David C LyeNational Centre for Infectious Diseases, Singapore, Singapore.
Danielle E AndersonProgramme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore. Danielle.anderson@duke-nus.edu.sg.ORCID http://orcid.org/0000-0003-4791-5024
Lin-Fa WangProgramme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore. linfa.wang@duke-nus.edu.sg.ORCID http://orcid.org/0000-0003-2752-0535

Funding

MOH | National Medical Research Council (NMRC) COVID19RF-003MOH | National Medical Research Council (NMRC) STPRG-FY19-001
6 · The paper itself

Abstract

A robust serological test to detect neutralizing antibodies to SARS-CoV-2 is urgently needed to determine not only the infection rate, herd immunity and predicted humoral protection, but also vaccine efficacy during clinical trials and after large-scale vaccination. The current gold standard is the conventional virus neutralization test requiring live pathogen and a biosafety level 3 laboratory. Here, we report a SARS-CoV-2 surrogate virus neutralization test that detects total immunodominant neutralizing antibodies targeting the viral spike (S) protein receptor-binding domain in an isotype- and species-independent manner. Our simple and rapid test is based on antibody-mediated blockage of the interaction between the angiotensin-converting enzyme 2 (ACE2) receptor protein and the receptor-binding domain. The test, which has been validated with two cohorts of patients with COVID-19 in two different countries, achieves 99.93% specificity and 95-100% sensitivity, and differentiates antibody responses to several human coronaviruses. The surrogate virus neutralization test does not require biosafety level 3 containment, making it broadly accessible to the wider community for both research and clinical applications.

Indexed as

Angiotensin-Converting Enzyme 2AntibodiesBetacoronavirusCoronavirus InfectionsCOVID-19HumansNeutralization TestsPandemicsPeptidyl-Dipeptidase APneumonia, ViralProtein Interaction Domains and MotifsSARS-CoV-2Spike Glycoprotein, CoronavirusACE2 protein, humanAngiotensin-Converting Enzyme 2AntibodiesPeptidyl-Dipeptidase ASpike Glycoprotein, Coronavirus

Identifiers

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.