Evidence map›Paper›PMID 37266444›Full record

ArticleFrontiers in immunology2023

Analysis and comparison of SARS-CoV-2 variant antibodies and neutralizing activity for 6 months after a booster mRNA vaccine in a healthcare worker population.

Sina Hosseinian, Rafael de Assis, Ghali Khalil, Madeleine K Luu, Aarti Jain, Peter Horvath, Rie Nakajima, Anton M Palma, Anthony Hoang, Eisa Razzak and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 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
1.4field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 1 country.

Sina HosseinianSchool of Medicine, University of California Irvine, Irvine, CA, United States.
Rafael de AssisDepartment of Physiology and Biophysics, University of California Irvine, Irvine, CA, United States.
Ghali KhalilSchool of Medicine, University of California Irvine, Irvine, CA, United States.
Madeleine K LuuSchool of Biological Sciences, University of California Irvine, Irvine, CA, United States.
Aarti JainDepartment of Physiology and Biophysics, University of California Irvine, Irvine, CA, United States.
Peter HorvathInstitute for Clinical and Translational Science, University of California Irvine, Irvine, CA, United States.
Rie NakajimaDepartment of Physiology and Biophysics, University of California Irvine, Irvine, CA, United States.
Anton M PalmaInstitute for Clinical and Translational Science, University of California Irvine, Irvine, CA, United States.
Anthony HoangSchool of Biological Sciences, University of California Irvine, Irvine, CA, United States.
Eisa RazzakSchool of Biological Sciences, University of California Irvine, Irvine, CA, United States.
Nicholas GarciaSchool of Medicine, University of California Irvine, Irvine, CA, United States.
Joshua AlgerInstitute for Clinical and Translational Science, University of California Irvine, Irvine, CA, United States.
Mina KalantariInnovative Health Diagnostics, Irvine, CA, United States.
Emily K SilzelDepartment of Physiology and Biophysics, University of California Irvine, Irvine, CA, United States.
Algis JasinskasDepartment of Physiology and Biophysics, University of California Irvine, Irvine, CA, United States.
Frank ZaldivarDepartment of Physiology and Biophysics, University of California Irvine, Irvine, CA, United States.
Sebastian D SchublDepartment of Surgery, School of Medicine, University of California Irvine, Irvine, CA, United States.
Philip L FelgnerDepartment of Physiology and Biophysics, University of California Irvine, Irvine, CA, United States.
Saahir KhanDepartment of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.
University of California, Irvine · USInnovative Clinical Research · USUniversity of Southern California · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
University of California Health Participation in the National COVID Cohort Collaborative (N3C)UL1TR001414 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M, VILAIN, ERIC J. · 2015 to 2023
$35.1M
Institutional Career Development CoreKL2TR001416 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAIOZZO, VINCENT JAMES, DEMETRIOU, MICHAEL · 2015 to 2023
$5.6M
Summer Mentoring and Research Training (SMART)T35DK128788 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI GUPTA, KALPNA, RHEE, CONNIE MEEYOUNG · 2021 to 2025
$375k
NCATS NIH HHS KL2 TR001416NCATS NIH HHS UL1 TR001414NCI NIH HHS P30 CA062203NIDDK NIH HHS T35 DK128788
6 · The paper itself

Abstract

Introduction: In the context of recurrent surges of SARS-CoV-2 infections, a detailed characterization of antibody persistence over a 6-month period following vaccine booster dose is necessary to crafting effective public health policies on repeat vaccination. Methods: To characterize the SARS-CoV-2 antibody profile of a healthcare worker population over a 6-month period following mRNA vaccination and booster dose. 323 healthcare workers at an academic medical center in Orange County, California who had completed primary vaccination and booster dose against SARS-CoV-2 were recruited for the study. A total of 690 blood specimens over a 6-month period were collected Results: The primary outcome of this study was the average SARS-CoV-2 antibody level as measured using a novel coronavirus antigen microarray. Additional outcomes measured include levels of antibodies specific to SARS-CoV-2 variants including Delta, Omicron BA.1, and BA.2. We also measured SARS-CoV-2 neutralization capacity for a subset of the population to confirm correlation with antibody levels. Although antibodies against SARS-CoV-2 wane throughout the 6-month period following a booster dose, antibody levels remain higher than pre-boost levels. However, a booster dose of vaccine based on the original Wuhan strain generates approximately 3-fold lower antibody reactivity against Omicron variants BA.1 and BA.2 as compared to the vaccine strain. Despite waning antibody levels, neutralization activity against the vaccine strain is maintained throughout the 6-month period. Discussion: In the context of recurrent surges of SARS-CoV-2 infections, our data indicate that breakthrough infections are likely driven by novel variants with different antibody specificity and not by time since last dose of vaccination, indicating that development of vaccinations specific to these novel variants is necessary to prevent future surges of SARS-CoV-2 infections.

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralHealth PersonnelHumansmRNA VaccinesAntibodies, ViralmRNA Vaccineshealthcare worker (HCW)mRNASARS-CoV-2serologyvaccine

Identifiers

PMID37266444
PMCPMC10229859
OpenAlexW4376875567

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.