Evidence map›Paper›PMID 36932031›Full record

ArticleVaccine2023

Estimated COVID-19 vaccine effectiveness against seroconversion from SARS-CoV-2 Infection, March-October, 2021.

Ian D Plumb, Lida M Fette, Ashley H Tjaden, Leora Feldstein, Sharon Saydah, Amina Ahmed, Ruth Link-Gelles, Thomas F Wierzba, Andrea A Berry, DeAnna Friedman-Klabanoff and 8 more

Abstract read
In one paragraph

Article in Vaccine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 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

18 authors.

Ian D PlumbCenters for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA. Electronic address: iplumb@cdc.gov.
Lida M FetteBiostatistics Center, Milken Institute School of Public Health, The George Washington University, 6110 Executive Blvd., Suite 750, Rockville, MD 20852, USA.
Ashley H TjadenBiostatistics Center, Milken Institute School of Public Health, The George Washington University, 6110 Executive Blvd., Suite 750, Rockville, MD 20852, USA.
Leora FeldsteinCenters for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA.
Sharon SaydahCenters for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA.
Amina AhmedAtrium Health Levine Children's Hospital, 1000 Blythe Blvd, Charlotte, NC 28203, USA.
Ruth Link-GellesCenters for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA.
Thomas F WierzbaDepartment of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Andrea A BerryCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, 685 W. Baltimore Street, Room 480, Baltimore, MD 21201, USA.
DeAnna Friedman-KlabanoffCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, 685 W. Baltimore Street, Room 480, Baltimore, MD 21201, USA.
Moira P LarsenMedstar Health Research Institute, 6525 Belcrest Road, Suite 700, Hyattsville, MD 20782, USA.
Michael S RunyonDepartment of Emergency Medicine, Atrium Health Carolinas Medical Center, 1000 Blythe Blvd, Charlotte, NC 28203, USA.
Lori M WardUniversity of Mississippi Medical Center, 2500 N State St, Jackson, MS 39216, USA.
Roberto P SantosUniversity of Mississippi Medical Center, 2500 N State St, Jackson, MS 39216, USA.
Johnathan WardVysnova Partners, 8400 Corporate Drive Suite 130, Landover, MD 20785, USA.
William S WeintraubMedstar Health Research Institute, 6525 Belcrest Road, Suite 700, Hyattsville, MD 20782, USA.
Sharon EdelsteinBiostatistics Center, Milken Institute School of Public Health, The George Washington University, 6110 Executive Blvd., Suite 750, Rockville, MD 20852, USA.
Diane UschnerBiostatistics Center, Milken Institute School of Public Health, The George Washington University, 6110 Executive Blvd., Suite 750, Rockville, MD 20852, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMonitoring the effectiveness of COVID-19 vaccines against SARS-CoV-2 infections remains important to inform public health responses. Estimation of vaccine effectiveness (VE) against serological evidence of SARS-CoV-2 infection might provide an alternative measure of the benefit of vaccination against infection.

methodsWe estimated mRNA COVID-19 vaccine effectiveness (VE) against development of SARS-CoV-2 anti-nucleocapsid antibodies in March-October 2021, during which the Delta variant became predominant. Participants were enrolled from four participating healthcare systems in the United States, and completed electronic surveys that included vaccination history. Dried blood spot specimens collected on a monthly basis were analyzed for anti-spike antibodies, and, if positive, anti-nucleocapsid antibodies. We used detection of new anti-nucleocapsid antibodies to indicate SARS-CoV-2 infection, and estimated VE by comparing 154 case-participants with new detection of anti-nucleocapsid antibodies to 1,540 seronegative control-participants matched by calendar period. Using conditional logistic regression, we estimated VE ≥ 14 days after the 2nd dose of an mRNA vaccine compared with no receipt of a COVID-19 vaccine dose, adjusting for age group, healthcare worker occupation, urban/suburban/rural residence, healthcare system region, and reported contact with a person testing positive for SARS-CoV-2.

resultsAmong individuals who completed a primary series, estimated VE against seroconversion from SARS-CoV-2 infection was 88.8% (95% confidence interval [CI], 79.6%-93.9%) after any mRNA vaccine, 87.8% (95% CI, 75.9%-93.8%) after BioNTech vaccine and 91.7% (95% CI, 75.7%-97.2%) after Moderna vaccine. VE was estimated to be lower ≥ 3 months after dose 2 compared with < 3 months after dose 2, and among participants who were older or had underlying health conditions, although confidence intervals overlapped between subgroups.

conclusionsVE estimates generated using infection-induced antibodies were consistent with published estimates from clinical trials and observational studies that used virologic tests to confirm infection during the same period. Our findings support recommendations for eligible adults to remain up to date with COVID-19 vaccination.

Indexed as

COVID-19COVID-19 VaccinesAdultHumansSARS-CoV-2SeroconversionVaccine EfficacyCOVID-19 VaccinesAdultsCOVID-19COVID-19 vaccinesSARS-CoV-2SerologyVaccine effectiveness

Identifiers

PMID36932031
PMCPMC9995303

What OpenQuestion holds

Textmetadata
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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.