Evidence map›Paper›PMID 35363818›Full record

ArticlePloS one2022

Validation of xMAP SARS-CoV-2 Multi-Antigen IgG assay in Nigeria.

Nnaemeka C Iriemenam, Fehintola A Ige, Stacie M Greby, Augustine Mpamugo, Ado G Abubakar, Ayuba B Dawurung, Mudiaga K Esiekpe, Andrew N Thomas, Mary U Okoli, Samuel S Awala and 21 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 6 institutions in 3 countries.

Nnaemeka C IriemenamDivision of Global HIV and TB, Center for Global Health, Centers for Disease Control and Prevention, Abuja, Nigeria.ORCID 0000-0003-2187-8894
Fehintola A IgeMicrobiology Department, Center for Human Virology and Genomics, Nigerian Institute of Medical Research, Yaba, Lagos, Nigeria.
Stacie M GrebyDivision of Global HIV and TB, Center for Global Health, Centers for Disease Control and Prevention, Abuja, Nigeria.
Augustine MpamugoUniversity of Maryland, Baltimore, Abuja, Nigeria.
Ado G AbubakarInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Ayuba B DawurungInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Mudiaga K EsiekpeInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Andrew N ThomasInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Mary U OkoliNational Reference Laboratory, Nigeria Centre for Disease Control Abuja, Abuja, Nigeria.
Samuel S AwalaInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Blessing N UgboajaInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Chimaoge C AchugbuNational Reference Laboratory, Nigeria Centre for Disease Control Abuja, Abuja, Nigeria.
Ifeanyichukwu OdohInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Felicia D NwatuInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Temitope OlaleyeInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Loveth AkayiInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Oluwaseun O AkinmuleroInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Joseph DattijoInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Edewede OnokevbagbeUniversity of Maryland, Baltimore, Abuja, Nigeria.
Olumide OkunoyeDivision of Global HIV and TB, Center for Global Health, Centers for Disease Control and Prevention, Abuja, Nigeria.
Nwando MbaNational Reference Laboratory, Nigeria Centre for Disease Control Abuja, Abuja, Nigeria.
Ndidi P AgalaInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Mabel UwanduMicrobiology Department, Center for Human Virology and Genomics, Nigerian Institute of Medical Research, Yaba, Lagos, Nigeria.
Maureen AniedobeMicrobiology Department, Center for Human Virology and Genomics, Nigerian Institute of Medical Research, Yaba, Lagos, Nigeria.
Kristen A StaffordUniversity of Maryland School of Medicine, Baltimore, MD, United States of America.ORCID 0000-0001-5620-6436
Alash'le AbimikuInternational Research Center of Excellence, Institute of Human Virology, Abuja, Nigeria.
Yohhei HamadaInstitute for Global Health, University College London, London, United Kingdom.
Mahesh SwaminathanDivision of Global HIV and TB, Center for Global Health, Centers for Disease Control and Prevention, Abuja, Nigeria.
McPaul I OkoyeDivision of Global HIV and TB, Center for Global Health, Centers for Disease Control and Prevention, Abuja, Nigeria.
Laura C SteinhardtMalaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Rosemary AuduMicrobiology Department, Center for Human Virology and Genomics, Nigerian Institute of Medical Research, Yaba, Lagos, Nigeria.ORCID 0000-0002-0330-5219
Institute of Human Virology · NGNigeria Centre for Disease Control · NGNigerian Institute of Medical Research · NGUniversity of Maryland, Baltimore · USCenters for Disease Control and Prevention · USUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThere is a need for reliable serological assays to determine accurate estimates of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) seroprevalence. Most single target antigen assays have shown some limitations in Africa. To assess the performance of a multi-antigen assay, we evaluated a commercially available SARS-CoV-2 Multi-Antigen IgG assay for human coronavirus disease 2019 (COVID-19) in Nigeria.

methodsValidation of the xMAP SARS-CoV-2 Multi-Antigen IgG assay was carried out using well-characterized SARS-CoV-2 reverse transcription polymerase chain reactive positive (97) and pre-COVID-19 pandemic (86) plasma panels. Cross-reactivity was assessed using pre-COVID-19 pandemic plasma specimens (213) from the 2018 Nigeria HIV/AIDS Indicator and Impact Survey (NAIIS).

resultsThe overall sensitivity of the xMAP SARS-CoV-2 Multi-Antigen IgG assay was 75.3% [95% CI: 65.8%- 82.8%] and specificity was 99.0% [95% CI: 96.8%- 99.7%]. The sensitivity estimate increased to 83.3% [95% CI: 70.4%- 91.3%] for specimens >14 days post-confirmation of diagnosis. However, using the NAIIS pre-pandemic specimens, the false positivity rate was 1.4% (3/213).

conclusionsOur results showed overall lower sensitivity and a comparable specificity with the manufacturer's validation. There appears to be less cross-reactivity with NAIIS pre-pandemic COVID-19 specimens using the xMAP SARS-CoV-2 Multi-Antigen IgG assay. In-country SARS-CoV-2 serology assay validation can help guide the best choice of assays in Africa.

Indexed as

COVID-19PandemicsAntibodies, ViralHumansImmunoglobulin GNigeriaSARS-CoV-2Sensitivity and SpecificitySeroepidemiologic StudiesAntibodies, ViralImmunoglobulin G

Identifiers

PMID35363818
PMCPMC8974966
OpenAlexW4220892888

What OpenQuestion holds

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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.