Evidence map›Paper›PMID 35398602›Full record

ArticleJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2022

SARS-CoV-2 infections in mRNA vaccinated individuals are biased for viruses encoding spike E484K and associated with reduced infectious virus loads that correlate with respiratory antiviral IgG levels.

Heba H Mostafa, Chun Huai Luo, C Paul Morris, Maggie Li, Nicholas J Swanson, Adannaya Amadi, Nicholas Gallagher, Andrew Pekosz

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 15 citations in OpenAlex.

  1. Mechanisms of sex differences in acute and long COVID sequelae in mice.bioRxiv : the preprint server for biology · 2025
    Article
  2. Review
  3. Article
  4. Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  5. Article
  6. Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization.medRxiv : the preprint server for health sciences · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. In vivo kinetics of SARS-CoV-2 infection and its relationship with a person's infectiousness.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Article
  15. SARS-CoV-2 Variants: Mutations and Effective Changes.Biotechnology and bioprocess engineering : BBE · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Heba H MostafaJohns Hopkins School of Medicine, Department of Pathology, Division of Medical Microbiology, 600 N. Wolfe St, Meyer B-121F, Baltimore, MD, 21287 USA. Electronic address: hmostaf2@jhmi.edu.
Chun Huai LuoJohns Hopkins School of Medicine, Department of Pathology, Division of Medical Microbiology, 600 N. Wolfe St, Meyer B-121F, Baltimore, MD, 21287 USA.
C Paul MorrisJohns Hopkins School of Medicine, Department of Pathology, Division of Medical Microbiology, 600 N. Wolfe St, Meyer B-121F, Baltimore, MD, 21287 USA; National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, MD, USA.
Maggie LiW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Nicholas J SwansonW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Adannaya AmadiJohns Hopkins School of Medicine, Department of Pathology, Division of Medical Microbiology, 600 N. Wolfe St, Meyer B-121F, Baltimore, MD, 21287 USA.
Nicholas GallagherJohns Hopkins School of Medicine, Department of Pathology, Division of Medical Microbiology, 600 N. Wolfe St, Meyer B-121F, Baltimore, MD, 21287 USA.
Andrew PekoszW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA; Department of Emergency Medicine, Johns Hopkins School of Medicine, 615 North Wolfe Street, rm W2116, Baltimore, MD, 21205-2103 USA. Electronic address: apekosz1@jhu.edu.
Johns Hopkins University · US

Funding

The Center for Advancing Point of Care in Heart, Lung, Blood and Sleep DiseasesU54HL143541 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Nathaniel Scott Hafer · 2018 to 2026
$141.0M
LC: HIV Prevention Trials Network - Laboratory Support for the SARS-CoV-2 Seroprevalence Study (CoVPN 5002)UM1AI068613 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SUSAN H ESHLEMAN, Mark A Marzinke · 2011 to 2026
$100.2M
Juntos (Together): A community led approach to enhance to Covid-19 testing among vulnerable LatinosR01DA045556 · NIDA · JOHNS HOPKINS UNIVERSITY · PI LUCAS, GREGORY M, PAGE, KATHLEEN R · 2017 to 2022
$6.8M
NHLBI NIH HHS U54 HL143541NIAID NIH HHS HHSN272201400007CNIAID NIH HHS UM1 AI068613NIDA NIH HHS R01 DA045556
6 · The paper itself

Abstract

introductionCOVID-19 large scale immunization in the US has been associated with breakthrough positive molecular testing. In this study, we investigated whether a positive test is associated with a high anti-viral IgG, specific viral variant, recovery of infectious virus, or symptomatic infection during an early phase after vaccination rollout.

methodsWe identified 133 SARS-CoV-2 positive patients who had received two doses of either Pfizer-BioNTech (BNT162b2) or Moderna (mRNA-1273) vaccines, the 2nd of which was received between January and April of 2021. The positive samples were collected between January and May of 2021. Samples were sequenced to characterize the whole genome and Spike protein changes and cycle thresholds that reflect viral loads were determined using a single molecular assay. Respiratory SARS-CoV-2 IgG antibodies were examined using ELISA and specimens were grown on cell culture to assess the recovery of infectious virus as compared to a control unvaccinated cohort.

resultsOf 133 specimens, 24 failed sequencing and yielded a negative or very low viral load on the repeat PCR. Of 109 specimens that were used for further genome analysis, 68 (62.4%) were from symptomatic infections, 11 (10.1%) were admitted for COVID-19, and 2 (1.8%) required ICU admission with no associated mortality. The predominant virus variant was the Alpha (B.1.1.7), however a significant association between lineage B.1.526 and amino acid change S: E484K with positives after vaccination was noted. A significant reduction of the recovery of infectious virus on cell culture was accompanied by an increase in localized IgG levels in respiratory samples of vaccinated individuals.

conclusionsVaccination reduces the recovery of infectious virus in breakthrough infections caused primarily by the Alpha variant accompanied by an increase in upper respiratory tract IgG levels.

Indexed as

COVID-19Antibodies, ViralAntiviral AgentsBNT162 VaccineCOVID-19 VaccinesHumansImmunoglobulin GRespiratory SystemRNA, MessengerSARS-CoV-2VaccinationAntibodies, ViralAntiviral AgentsBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GRNA, MessengerCell cultureCOVID-19SARS-CoV-2Vaccination

Identifiers

PMID35398602
PMCPMC8979609
OpenAlexW4225765401

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.