Evidence map›Paper›PMID 36146537›Full record

ArticleVaccines2022

Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses.

Alexa J Roeder, Megan A Koehler, Paniz Jasbi, Davis McKechnie, John Vanderhoof, Baylee A Edwards, Maria J Gonzalez-Moa, Alim Seit-Nebi, Sergei A Svarovsky, Douglas F Lake

Abstract read
In one paragraph

Article in Vaccines, 2022. 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.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
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

10 authors.

Alexa J RoederSchool of Life Sciences, Arizona State University, Tempe, AZ 85281, USA.ORCID 0000-0002-3975-3179
Megan A KoehlerSchool of Life Sciences, Arizona State University, Tempe, AZ 85281, USA.ORCID 0000-0003-3921-237X
Paniz JasbiCollege of Health Solutions, Arizona State University, Phoenix, AZ 85004, USA.ORCID 0000-0002-2129-3098
Davis McKechnieSchool of Life Sciences, Arizona State University, Tempe, AZ 85281, USA.
John VanderhoofSchool of Life Sciences, Arizona State University, Tempe, AZ 85281, USA.
Baylee A EdwardsSchool of Life Sciences, Arizona State University, Tempe, AZ 85281, USA.
Maria J Gonzalez-MoaSapphire/AXIM Biotechnologies, San Diego, CA 92121, USA.
Alim Seit-NebiSapphire/AXIM Biotechnologies, San Diego, CA 92121, USA.ORCID 0000-0003-4371-3206
Sergei A SvarovskySapphire/AXIM Biotechnologies, San Diego, CA 92121, USA.
Douglas F LakeSchool of Life Sciences, Arizona State University, Tempe, AZ 85281, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 mRNA vaccines protect against severe disease and hospitalization. Neutralizing antibodies (NAbs) are a first-line defense mechanism, but protective NAb responses are variable. Currently, NAb testing is not widely available. This study employed a lateral flow assay for monitoring NAb levels postvaccination and natural infection, using a finger-stick drop of blood. We report longitudinal NAb data from BNT162b2 (Pfizer) and mRNA-1273 (Moderna) recipients after second and third doses. Results demonstrate a third dose of mRNA vaccine elicits higher and more durable NAb titers than the second dose, independent of manufacturer, sex, and age. Our analyses also revealed that vaccinated individuals could be categorized as strong, moderate, and poorly neutralizing responders. After the second dose, 34% of subjects were classified as strong responders, compared to 79% after the third dose. The final months of this study coincided with the emergence of the SARS-CoV-2 Omicron variant and symptomatic breakthrough infections within our study population. Lastly, we show that NAb levels sufficient for protection from symptomatic infection with early SARS-CoV-2 variants were not protective against Omicron infection and disease. This work highlights the need for accessible vaccine response monitoring for use in healthcare, such that individuals, particularly those in vulnerable populations, can make informed vaccination decisions.

Indexed as

lateral flow assaymRNA vaccinesneutralizing antibodySARS-CoV-2

Identifiers

PMID36146537
PMCPMC9504054

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.