Evidence map›Paper›PMID 37277736›Full record

ArticleBMC infectious diseases2023

Assessment of Anti-SARS-CoV-2 antibody levels among university students vaccinated with different COVID-19 primary and booster doses - fall 2021, Wisconsin.

Peter M DeJonge, Anastasia S Lambrou, Hannah E Segaloff, Allen Bateman, Alana Sterkel, Carol Griggs, Jake Baggott, Patrick Kelly, Natalie Thornburg, Monica Epperson and 15 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

25 authors at 5 institutions in 1 country.

Peter M DeJongeEpidemic Intelligence Service, CDC, Atlanta, Georgia, 30329, USA. peter.dejonge@dhs.wisconsin.gov.
Anastasia S LambrouEpidemic Intelligence Service, CDC, Atlanta, Georgia, 30329, USA.
Hannah E SegaloffEpidemic Intelligence Service, CDC, Atlanta, Georgia, 30329, USA.
Allen BatemanWisconsin State Laboratory of Hygiene, Madison, Wisconsin, 53703, USA.
Alana SterkelWisconsin State Laboratory of Hygiene, Madison, Wisconsin, 53703, USA.
Carol GriggsUniversity Health Services, University of Wisconsin - Madison, Madison, Wisconsin, 53703, USA.
Jake BaggottUniversity Health Services, University of Wisconsin - Madison, Madison, Wisconsin, 53703, USA.
Patrick KellyUniversity Health Services, University of Wisconsin - Madison, Madison, Wisconsin, 53703, USA.
Natalie ThornburgCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Monica EppersonCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Rodel Desamu-ThorpeCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Glen AbediCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Christopher H HsuCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Jasmine Y NakayamaEpidemic Intelligence Service, CDC, Atlanta, Georgia, 30329, USA.
Jasmine RuffinCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Darlene Turner-HarperCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Almea MatanockCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Olivia AlmendaresCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Melissa WhaleyCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Ayan ChakrabartiCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Kyle DeGruyCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Michele DalyCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Ryan WestergaardWisconsin Department of Health Services, Division of Public Health, Madison, Wisconsin, 53703, USA.
Jacqueline E TateCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
Hannah L KirkingCDC COVID-19 Response Team, Atlanta, Georgia, 30329, USA.
CDC Foundation · USEpidemic Intelligence Service · USUniversity of Wisconsin Health · USWisconsin Department of Health Services · USUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUniversity students commonly received COVID-19 vaccinations before returning to U.S. campuses in the Fall of 2021. Given likely immunologic variation among students based on differences in type of primary series and/or booster dose vaccine received, we conducted serologic investigations in September and December 2021 on a large university campus in Wisconsin to assess anti-SARS-CoV-2 antibody levels.

methodsWe collected blood samples, demographic information, and COVID-19 illness and vaccination history from a convenience sample of students. Sera were analyzed for both anti-spike (anti-S) and anti-nucleocapsid (anti-N) antibody levels using World Health Organization standardized binding antibody units per milliliter (BAU/mL). Levels were compared across categorical primary COVID-19 vaccine series received and binary COVID-19 mRNA booster status. The association between anti-S levels and time since most recent vaccination dose was estimated by mixed-effects linear regression.

resultsIn total, 356 students participated, of whom 219 (61.5%) had received a primary vaccine series of Pfizer-BioNTech or Moderna mRNA vaccines and 85 (23.9%) had received vaccines from Sinovac or Sinopharm. Median anti-S levels were significantly higher for mRNA primary vaccine series recipients (2.90 and 2.86 log [BAU/mL], respectively), compared with those who received Sinopharm or Sinovac vaccines (1.63 and 1.95 log [BAU/mL], respectively). Sinopharm and Sinovac vaccine recipients were associated with a significantly faster anti-S decline over time, compared with mRNA vaccine recipients (P <.001). By December, 48/172 (27.9%) participants reported receiving an mRNA COVID-19 vaccine booster, which reduced the anti-S antibody discrepancies between primary series vaccine types.

conclusionsOur work supports the benefit of heterologous boosting against COVID-19. COVID-19 mRNA vaccine booster doses were associated with increases in anti-SARS-CoV-2 antibody levels; following an mRNA booster dose, students with both mRNA and non-mRNA primary series receipt were associated with comparable levels of anti-S IgG.

Indexed as

COVID-19COVID-19 VaccinesAntibodies, ViralHumansImmunization, SecondaryRNA, MessengerUniversitiesWisconsinAntibodies, ViralCOVID-19 VaccinesRNA, MessengerCOVID-19 vaccinesHeterologous boostersMeso scale discoverySARS-CoV-2 serology

Identifiers

PMID37277736
PMCPMC10240450
OpenAlexW4379469946

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.