Evidence map›Paper›PMID 34523986›Full record

ArticleMicrobiology spectrum2021

A Multiplex Noninvasive Salivary Antibody Assay for SARS-CoV-2 Infection and Its Application in a Population-Based Survey by Mail.

Andrey I Egorov, Shannon M Griffin, Miyu Fuzawa, Jason Kobylanski, Rachel Grindstaff, William Padgett, Steven Simmons, Daniel R Hallinger, Jennifer N Styles, Lindsay Wickersham and 3 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Andrey I EgorovU.S. Environmental Protection Agencygrid.418698.a, Chapel Hill, North Carolina, USA.ORCID 0000-0003-2870-124X
Shannon M GriffinU.S. Environmental Protection Agencygrid.418698.a, Cincinnati, Ohio, USA.
Miyu FuzawaU.S. Environmental Protection Agencygrid.418698.a, Chapel Hill, North Carolina, USA.
Jason KobylanskiU.S. Environmental Protection Agencygrid.418698.a, Chapel Hill, North Carolina, USA.
Rachel GrindstaffU.S. Environmental Protection Agencygrid.418698.a, Research Triangle Park, North Carolina, USA.
William PadgettU.S. Environmental Protection Agencygrid.418698.a, Research Triangle Park, North Carolina, USA.
Steven SimmonsU.S. Environmental Protection Agencygrid.418698.a, Research Triangle Park, North Carolina, USA.
Daniel R HallingerU.S. Environmental Protection Agencygrid.418698.a, Research Triangle Park, North Carolina, USA.
Jennifer N StylesU.S. Environmental Protection Agencygrid.418698.a, Chapel Hill, North Carolina, USA.
Lindsay WickershamU.S. Environmental Protection Agencygrid.418698.a, Research Triangle Park, North Carolina, USA.
Elizabeth SamsU.S. Environmental Protection Agencygrid.418698.a, Chapel Hill, North Carolina, USA.
Edward HudgensU.S. Environmental Protection Agencygrid.418698.a, Chapel Hill, North Carolina, USA.
Timothy J WadeU.S. Environmental Protection Agencygrid.418698.a, Chapel Hill, North Carolina, USA.
Environmental Protection Agency · USUniversity of North Carolina at Chapel Hill · US

Funding

Environmental Protection Agency (EPA) Intramural funding
6 · The paper itself

Abstract

Noninvasive salivary antibody immunoassays can enable low-cost epidemiological surveillance of infections. This study involved developing and validating a multiplex suspension immunoassay on the Luminex platform to measure immunoglobulin G (IgG) responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleocapsid and spike (S) proteins, and the spike protein's S1 and S2 subunits and receptor binding domain. Multiple versions of these recombinant proteins acquired from commercial and noncommercial sources were evaluated. Assay development and validation utilized saliva and serum samples from coronavirus disease 2019 (COVID-19) cases procured from commercial sources and negative controls from a prepandemic survey. Saliva was also collected in a demonstration survey by mail involving adult individuals in the United States who were diagnosed with SARS-CoV-2 infection 15 to 80 days prior to sample collection. The survey had an 83% valid sample return rate (192 samples from 38 states). Most COVID-19 cases (93%) reported mildly symptomatic or asymptomatic infections. The final salivary assay based on the best-performing spike and nucleocapsid proteins had a sensitivity of 87.1% (95% bootstrap confidence interval, 82.1 to 91.7%) and specificity of 98.5% (95.0 to 100%) using 227 and 285 saliva samples, respectively. The same assay had 95.9% (92.8 to 98.9%) sensitivity and 100% (98.4 to 100%) specificity in serum (174 and 285 serum samples, respectively). Salivary and serum antibody responses to spike and nucleocapsid proteins were strongly correlated in 22 paired samples (

Indexed as

AdolescentAdultAgedAntibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19COVID-19 Serological TestingFemaleHumansImmunoglobulin GMaleMiddle AgedPhosphoproteinsPostal ServiceSalivaSARS-CoV-2Antibodies, ViralCoronavirus Nucleocapsid ProteinsImmunoglobulin Gnucleocapsid phosphoprotein, SARS-CoV-2PhosphoproteinsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19immunoassayspopulation surveysalivaSARS-CoV-2

Identifiers

PMID34523986
PMCPMC8557941
OpenAlexW3199865002

What OpenQuestion holds

Textmetadata
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.