Evidence map›Paper›PMID 35851055›Full record

ArticleNature communications2022

Immune responses in Omicron SARS-CoV-2 breakthrough infection in vaccinated adults.

Hassen Kared, Asia-Sophia Wolf, Amin Alirezaylavasani, Anthony Ravussin, Guri Solum, Trung The Tran, Fridtjof Lund-Johansen, John Torgils Vaage, Lise Sofie Nissen-Meyer, Unni C Nygaard and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

51 citing papers in PubMed, 71 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 3 institutions in 1 country.

Hassen KaredKG Jebsen Centre for B cell malignancy, Institute of Clinical medicine, University of Oslo, Oslo, Norway. hassen.kared@medisin.uio.no.ORCID 0000-0002-8220-997X
Asia-Sophia WolfDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.ORCID 0000-0003-1982-9487
Amin AlirezaylavasaniKG Jebsen Centre for B cell malignancy, Institute of Clinical medicine, University of Oslo, Oslo, Norway.
Anthony RavussinDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.
Guri SolumDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.
Trung The TranDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
Fridtjof Lund-JohansenDepartment of Immunology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-2445-1258
John Torgils VaageDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
Lise Sofie Nissen-MeyerDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
Unni C NygaardDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.ORCID 0000-0002-2955-9970
Olav HungnesDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.
Anna H RobertsonDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.
Lisbeth Meyer NæssDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.
Lill TrogstadDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.
Per MagnusCenter for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway.
Ludvig A Munthe *KG Jebsen Centre for B cell malignancy, Institute of Clinical medicine, University of Oslo, Oslo, Norway. l.a.munthe@medisin.uio.no.ORCID 0000-0002-0344-3654
Siri Mjaaland *Division of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.
Norwegian Institute of Public Health · NOOslo University Hospital · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SARS-CoV-2 Omicron variant has more than 15 mutations in the receptor binding domain of the Spike protein enabling increased transmissibility and viral escape from antibodies in vaccinated individuals. It is unclear how vaccine immunity protects against Omicron infection. Here we show that vaccinated participants at a super-spreader event have robust recall response of humoral and pre-existing cellular immunity induced by the vaccines, and an emergent de novo T cell response to non-Spike antigens. Individuals with Omicron SARS-CoV-2 breakthrough infections have significantly increased activated SARS-CoV-2 wild type Spike-specific cytotoxic T cells, activated follicular helper (T

Indexed as

COVID-19Viral VaccinesAdultAntibodies, ViralHumansImmunitySARS-CoV-2Spike Glycoprotein, CoronavirusViral Envelope ProteinsAntibodies, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Envelope ProteinsViral Vaccines

Identifiers

PMID35851055
PMCPMC9293966
OpenAlexW4285727519

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.