Evidence map›Paper›PMID 36255426›Full record

ArticleJAMA2022

Association of mRNA Vaccination With Clinical and Virologic Features of COVID-19 Among US Essential and Frontline Workers.

HEROES-RECOVER Network, Mark G Thompson, Sarang K Yoon, Allison L Naleway, Jennifer Meece, Thomas P Fabrizio, Alberto J Caban-Martinez, Jefferey L Burgess, Manjusha Gaglani, Lauren E W Olsho and 39 more

Open access · greenAbstract read
In one paragraph

Article in JAMA, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.5field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Kinetics of SARS-CoV-2 Shedding in Nursing Home Residents and Staff.Journal of the American Geriatrics Society · 2025
    Article
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Article
  12. Does the COVID-19 Vaccination Reduce the Risk to Transmit SARS-CoV-2 to Others?Advances in experimental medicine and biology · 2024
    Review
  13. Observational
  14. Observational
  15. Observational
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

49 authors at 9 institutions in 1 country.

HEROES-RECOVER Network
Mark G ThompsonCenters for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
Sarang K YoonRocky Mountain Center for Occupational and Environmental Health, Department of Family and Preventive Medicine, University of Utah Health, Salt Lake City, Utah.
Allison L NalewayKaiser Permanente Northwest Center for Health Research, Portland, Oregon.
Jennifer MeeceMarshfield Clinic Research Institute, Marshfield, Wisconsin.
Thomas P FabrizioSt Jude Children's Research Hospital, Memphis, Tennessee.
Alberto J Caban-MartinezLeonard M. Miller School of Medicine, University of Miami, Miami, Florida.
Jefferey L BurgessMel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona.
Manjusha GaglaniBaylor Scott and White Health, Temple, Texas.
Lauren E W OlshoAbt Associates Inc, Rockville, Maryland.
Allen BatemanWisconsin State Laboratory of Hygiene, Madison.
Jessica LundgrenSt Luke's Regional Health Care System, Duluth, Minnesota.
Lauren GrantCenters for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
Andrew L PhillipsRocky Mountain Center for Occupational and Environmental Health, Department of Family and Preventive Medicine, University of Utah Health, Salt Lake City, Utah.
Holly C GroomKaiser Permanente Northwest Center for Health Research, Portland, Oregon.
Elisha StefanskiMarshfield Clinic Research Institute, Marshfield, Wisconsin.
Natasha Schaefer SolleLeonard M. Miller School of Medicine, University of Miami, Miami, Florida.
Katherine EllingsonMel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona.
Karen LutrickCollege of Medicine - Tucson, University of Arizona, Tucson.
Kayan DunniganBaylor Scott and White Health, Temple, Texas.
Meredith G WesleyAbt Associates Inc, Rockville, Maryland.
Kyley GuentherWisconsin State Laboratory of Hygiene, Madison.
Angela HuntSt Luke's Regional Health Care System, Duluth, Minnesota.
Josephine MakCenters for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
Kurt T HegmannRocky Mountain Center for Occupational and Environmental Health, Department of Family and Preventive Medicine, University of Utah Health, Salt Lake City, Utah.
Jennifer L KuntzKaiser Permanente Northwest Center for Health Research, Portland, Oregon.
Adam BissonnetteMarshfield Clinic Research Institute, Marshfield, Wisconsin.
James HollisterMel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona.
Spencer RoseBaylor Scott and White Health, Temple, Texas.
Tyler C MorrillAbt Associates Inc, Rockville, Maryland.
Karley RespetSt Luke's Regional Health Care System, Duluth, Minnesota.
Ashley L FowlkesCenters for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
Matthew S ThieseRocky Mountain Center for Occupational and Environmental Health, Department of Family and Preventive Medicine, University of Utah Health, Salt Lake City, Utah.
Patrick RiversCollege of Medicine - Tucson, University of Arizona, Tucson.
Meghan K HerringAbt Associates Inc, Rockville, Maryland.
Marilyn J OdeanWhiteside Institute for Clinical Research, St Luke's, Duluth, Minnesota.
Young M YooCenters for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
Matthew BrunnerRocky Mountain Center for Occupational and Environmental Health, Department of Family and Preventive Medicine, University of Utah Health, Salt Lake City, Utah.
Edward J BedrickMel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona.
Deanna E FlearyAbt Associates Inc, Rockville, Maryland.
John T JonesCenters for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
Jenna PraggastisRocky Mountain Center for Occupational and Environmental Health, Department of Family and Preventive Medicine, University of Utah Health, Salt Lake City, Utah.
James RomineMel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona.
Monica DickersonCenters for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
Sana M KhanMel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona.
Julie Mayo LamberteCenters for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
Shawn BeitelMel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona.
Richard J WebbySt Jude Children's Research Hospital, Memphis, Tennessee.
Harmony L TynerSt Luke's Regional Health Care System, Duluth, Minnesota.
Centers for Disease Control and Prevention · USUniversity of Arizona · USAbt Global (United States) · USSaint Luke's Health System · USSt. Jude Children's Research Hospital · USUniversity of Utah · USKaiser Permanente Center for Health Research · USTemple College · USUniversity of Miami · US

Funding

Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
University of Arizona's Initiative for Maximizing Student Development (IMSD)T32GM139779 · NIGMS · UNIVERSITY OF ARIZONA · PI FRANS E TAX · 2022 to 2026
$2.9M
NCATS NIH HHS UL1 TR002538NIGMS NIH HHS T32 GM139779
6 · The paper itself

Abstract

Importance: Data on the epidemiology of mild to moderately severe COVID-19 are needed to inform public health guidance. Objective: To evaluate associations between 2 or 3 doses of mRNA COVID-19 vaccine and attenuation of symptoms and viral RNA load across SARS-CoV-2 viral lineages. Design, Setting, and Participants: A prospective cohort study of essential and frontline workers in Arizona, Florida, Minnesota, Oregon, Texas, and Utah with COVID-19 infection confirmed by reverse transcriptase-polymerase chain reaction testing and lineage classified by whole genome sequencing of specimens self-collected weekly and at COVID-19 illness symptom onset. This analysis was conducted among 1199 participants with SARS-CoV-2 from December 14, 2020, to April 19, 2022, with follow-up until May 9, 2022, reported. Exposures: SARS-CoV-2 lineage (origin strain, Delta variant, Omicron variant) and COVID-19 vaccination status. Main Outcomes and Measures: Clinical outcomes included presence of symptoms, specific symptoms (including fever or chills), illness duration, and medical care seeking. Virologic outcomes included viral load by quantitative reverse transcriptase-polymerase chain reaction testing along with viral viability. Results: Among 1199 participants with COVID-19 infection (714 [59.5%] women; median age, 41 years), 14.0% were infected with the origin strain, 24.0% with the Delta variant, and 62.0% with the Omicron variant. Participants vaccinated with the second vaccine dose 14 to 149 days before Delta infection were significantly less likely to be symptomatic compared with unvaccinated participants (21/27 [77.8%] vs 74/77 [96.1%]; OR, 0.13 [95% CI, 0-0.6]) and, when symptomatic, those vaccinated with the third dose 7 to 149 days before infection were significantly less likely to report fever or chills (5/13 [38.5%] vs 62/73 [84.9%]; OR, 0.07 [95% CI, 0.0-0.3]) and reported significantly fewer days of symptoms (10.2 vs 16.4; difference, -6.1 [95% CI, -11.8 to -0.4] days). Among those with Omicron infection, the risk of symptomatic infection did not differ significantly for the 2-dose vaccination status vs unvaccinated status and was significantly higher for the 3-dose recipients vs those who were unvaccinated (327/370 [88.4%] vs 85/107 [79.4%]; OR, 2.0 [95% CI, 1.1-3.5]). Among symptomatic Omicron infections, those vaccinated with the third dose 7 to 149 days before infection compared with those who were unvaccinated were significantly less likely to report fever or chills (160/311 [51.5%] vs 64/81 [79.0%]; OR, 0.25 [95% CI, 0.1-0.5]) or seek medical care (45/308 [14.6%] vs 20/81 [24.7%]; OR, 0.45 [95% CI, 0.2-0.9]). Participants with Delta and Omicron infections who received the second dose 14 to 149 days before infection had a significantly lower mean viral load compared with unvaccinated participants (3 vs 4.1 log10 copies/μL; difference, -1.0 [95% CI, -1.7 to -0.2] for Delta and 2.8 vs 3.5 log10 copies/μL, difference, -1.0 [95% CI, -1.7 to -0.3] for Omicron). Conclusions and Relevance: In a cohort of US essential and frontline workers with SARS-CoV-2 infections, recent vaccination with 2 or 3 mRNA vaccine doses less than 150 days before infection with Delta or Omicron variants, compared with being unvaccinated, was associated with attenuated symptoms, duration of illness, medical care seeking, or viral load for some comparisons, although the precision and statistical significance of specific estimates varied.

Indexed as

COVID-19COVID-19 VaccinesVaccinationViral LoadAdultAsymptomatic InfectionsFemaleHumansMalemRNA VaccinesPatient Acceptance of Health CareProspective StudiesRNA-Directed DNA PolymeraseRNA, ViralSARS-CoV-2Time FactorsCOVID-19 VaccinesmRNA VaccinesRNA-Directed DNA PolymeraseRNA, Viral

Identifiers

PMID36255426
PMCPMC9579910
OpenAlexW4306729513

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.