Evidence map›Paper›PMID 35895418›Full record

ArticleThe American journal of tropical medicine and hygiene2022

Performance of SARS-CoV-2 Antigens in a Multiplex Bead Assay for Integrated Serological Surveillance of Neglected Tropical and Other Diseases.

Sarah Gwyn, Ado Abubakar, Oluwaseun Akinmulero, Eric Bergeron, Ugboaja Nkechi Blessing, Jasmine Chaitram, Melissa M Coughlin, Ayuba B Dawurung, Felicia Nwatu Dickson, Mudiaga Esiekpe and 13 more

Abstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

23 authors.

Sarah GwynDivision of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia.
Ado AbubakarInstitute of Human Virology, Abuja, Nigeria.
Oluwaseun AkinmuleroInstitute of Human Virology, Abuja, Nigeria.
Eric BergeronDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
Ugboaja Nkechi BlessingInstitute of Human Virology, Abuja, Nigeria.
Jasmine ChaitramDivision of Laboratory Systems, Centers for Disease Control and Prevention, Atlanta, Georgia.
Melissa M CoughlinDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Ayuba B DawurungInstitute of Human Virology, Abuja, Nigeria.
Felicia Nwatu DicksonInstitute of Human Virology, Abuja, Nigeria.
Mudiaga EsiekpeInstitute of Human Virology, Abuja, Nigeria.
Erasogie EvbuomwanNigeria Centre for Disease Control, Abuja, Nigeria.
Stacie M GrebyDivision of Global HIV and TB, Centers for Disease Control and Prevention, Abuja, Nigeria.
Nnaemeka C IriemenamDivision of Global HIV and TB, Centers for Disease Control and Prevention, Abuja, Nigeria.
Markus H KainulainenDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
Thomas Andrew NaanpoenInstitute of Human Virology, Abuja, Nigeria.
Loveth NapoloenInstitute of Human Virology, Abuja, Nigeria.
Ifeanyichukwu OdohInstitute of Human Virology, Abuja, Nigeria.
McPaul OkoyeDivision of Global HIV and TB, Centers for Disease Control and Prevention, Abuja, Nigeria.
Temitope OlaleyeInstitute of Human Virology, Abuja, Nigeria.
Amy J SchuhDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
S Michele OwenNational Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention, Atlanta, Georgia.
Awala SamuelInstitute of Human Virology, Abuja, Nigeria.
Diana L MartinDivision of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serosurveillance can provide estimates of population-level exposure to infectious pathogens and has been used extensively during the COVID-19 pandemic. Simultaneous, serological testing for multiple pathogens can be done using bead-based immunoassays to add value to disease-specific serosurveys. We conducted a validation of four SARS-CoV-2 antigens-full-length spike protein, two receptor binding domain proteins, and the nucleocapsid protein-on our existing multiplex bead assay (MBA) for enteric diseases, malaria, and vaccine preventable diseases. After determining the optimal conditions for coupling the antigens to microsphere beads, the sensitivity and specificity of the assay were determined on two instruments (Luminex-200 and MAGPIX) when testing singly (monoplex) versus combined (multiplex). Sensitivity was assessed using plasma from 87 real-time reverse transcription polymerase chain reaction (rRT-PCR) positive persons collected in March-May of 2020 and ranged from 94.3% to 96.6% for the different testing conditions. Specificity was assessed using 98 plasma specimens collected prior to December 2019 and plasma from 19 rRT-PCR negative persons and ranged from 97.4% to 100%. The positive percent agreement was 93.8% to 97.9% using 48 specimens collected > 21 days post-symptom onset, while the negative percent agreement was ≥ 99% for all antigens. Test performance was similar using monoplex or multiplex testing. Integrating SARS-CoV-2 serology with other diseases of public health interest could add significant value to public health programs that have suffered severe programmatic setbacks during the COVID-19 pandemic.

Indexed as

COVID-19SARS-CoV-2HumansImmunoassayPandemicsSensitivity and Specificity

Identifiers

PMID35895418
PMCPMC9393470

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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.