Evidence map›Paper›PMID 36949041›Full record

ArticleNature communications2023

Correlates of protection and viral load trajectories in omicron breakthrough infections in triple vaccinated healthcare workers.

Ulrika Marking, Sebastian Havervall, Nina Greilert Norin, Oscar Bladh, Wanda Christ, Max Gordon, Henry Ng, Kim Blom, Mia Phillipson, Sara Mangsbo and 7 more

Open access · goldFull text read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

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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

17 authors at 5 institutions in 1 country.

Ulrika Marking *Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.
Sebastian Havervall *Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.
Nina Greilert NorinDepartment of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.
Oscar BladhDepartment of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.
Wanda ChristCenter for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-3886-5248
Max GordonDepartment of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.ORCID 0000-0002-8080-5815
Henry NgDepartment of Medical Cell Biology and SciLifeLab, Uppsala University, Uppsala, Sweden.
Kim BlomDepartment of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.
Mia PhillipsonDepartment of Medical Cell Biology and SciLifeLab, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-2387-0266
Sara MangsboDepartment of Pharmacy and SciLifeLab, Uppsala University, Uppsala, Sweden.
Jessica J AlmDepartment of Microbiology, Tumor and Cell Biology & National Pandemic Center, Karolinska Institutet, Solna, Sweden.
Anna Smed-SörensenDivision of Immunology and Allergy, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Peter NilssonDepartment of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.ORCID 0000-0002-4657-8532
Sophia HoberDepartment of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.
Mikael ÅbergDepartment of Medical Sciences, Clinical Chemistry and SciLifeLab, Uppsala University, Uppsala, Sweden.
Jonas KlingströmCenter for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-9076-1441
Charlotte ThålinDepartment of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden. charlotte.thalin@ki.se.
Karolinska Institutet · SEUppsala University · SEScience for Life Laboratory · SEKarolinska University Hospital · SELinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccination offers protection against severe COVID-19 caused by SARS-CoV-2 omicron but is less effective against infection. Characteristics such as serum antibody titer correlation to protection, viral abundance and clearance of omicron infection in vaccinated individuals are scarce. We present a 4-week twice-weekly SARS-CoV-2 qPCR screening in 368 triple vaccinated healthcare workers. Spike-specific IgG levels, neutralization titers and mucosal spike-specific IgA-levels were determined at study start and qPCR-positive participants were sampled repeatedly for two weeks. 81 (cumulative incidence 22%) BA.1, BA.1.1 and BA.2 infections were detected. High serum antibody titers are shown to be protective against infection (p < 0.01), linked to reduced viral load (p < 0.01) and time to viral clearance (p < 0.05). Pre-omicron SARS-CoV-2 infection is independently associated to increased protection against omicron, largely mediated by mucosal spike specific IgA responses (nested models lr test p = 0.02 and 0.008). Only 10% of infected participants remain asymptomatic through the course of their infection. We demonstrate that high levels of vaccine-induced spike-specific WT antibodies are linked to increased protection against infection and to reduced viral load if infected, and suggest that the additional protection offered by pre-omicron SARS-CoV-2 infection largely is mediated by mucosal spike-specific IgA.

Indexed as

Breakthrough InfectionsCOVID-19Antibodies, NeutralizingAntibodies, ViralHealth PersonnelHumansImmunoglobulin ASARS-CoV-2Viral LoadAntibodies, NeutralizingAntibodies, ViralImmunoglobulin A

Identifiers

PMID36949041
PMCPMC10031702
OpenAlexW4360600555

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read61
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.