Evidence map›Paper›PMID 36101832›Full record

ArticleiScience2022

Recent infection with HCoV-OC43 may be associated with protection against SARS-CoV-2 infection.

A H Ayesha Lavell, Jonne J Sikkens, Arthur W D Edridge, Karlijn van der Straten, Ferdyansyah Sechan, Melissa Oomen, David T P Buis, Michiel Schinkel, Judith A Burger, Meliawati Poniman and 9 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 24 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

19 authors at 5 institutions in 2 countries.

A H Ayesha LavellAmsterdam UMC Location Vrije Universiteit Amsterdam, Department of Internal Medicine, De Boelelaan 1117, 1081 HV, Amsterdam, the Netherlands.
Jonne J SikkensAmsterdam UMC Location Vrije Universiteit Amsterdam, Department of Internal Medicine, De Boelelaan 1117, 1081 HV, Amsterdam, the Netherlands.
Arthur W D EdridgeAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Karlijn van der StratenAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Ferdyansyah SechanAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Melissa OomenAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
David T P BuisAmsterdam UMC Location Vrije Universiteit Amsterdam, Department of Internal Medicine, De Boelelaan 1117, 1081 HV, Amsterdam, the Netherlands.
Michiel SchinkelAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Judith A BurgerAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Meliawati PonimanAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Jacqueline van RijswijkAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Menno D de JongAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Godelieve J de BreeAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Edgar J G PetersAmsterdam UMC Location Vrije Universiteit Amsterdam, Department of Internal Medicine, De Boelelaan 1117, 1081 HV, Amsterdam, the Netherlands.
Yvo M SmuldersAmsterdam UMC Location Vrije Universiteit Amsterdam, Department of Internal Medicine, De Boelelaan 1117, 1081 HV, Amsterdam, the Netherlands.
Rogier W SandersAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Marit J van GilsAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Lia van der HoekAmsterdam Institute for Infection and Immunity, Amsterdam, the Netherlands.
Marije K BomersAmsterdam UMC Location Vrije Universiteit Amsterdam, Department of Internal Medicine, De Boelelaan 1117, 1081 HV, Amsterdam, the Netherlands.
Amsterdam University Medical Centers · NLUniversity of Amsterdam · NLVrije Universiteit Amsterdam · NLAcademic Medical Center · NLCornell University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies against seasonal human coronaviruses (HCoVs) are known to cross-react with SARS-CoV-2, but data on cross-protective effects of prior HCoV infections are conflicting. In a prospective cohort of healthcare workers (HCWs), we studied the association between seasonal HCoV (OC43, HKU1, 229E and NL63) nucleocapsid protein IgG and SARS-CoV-2 infection during the first pandemic wave in the Netherlands (March 2020 - June 2020), by 4-weekly serum sampling. HCW with HCoV-OC43 antibody levels in the highest quartile, were less likely to become SARS-CoV-2 seropositive when compared with those with lower levels (6/32, 18.8%, versus 42/97, 43.3%, respectively: p = 0.019; HR 0.37, 95% CI 0.16-0.88). We found no significant association with HCoV-OC43 spike protein IgG, or with antibodies against other HCoVs. Our results indicate that the high levels of HCoV-OC43-nucleocapsid antibodies, as an indicator of a recent infection, are associated with protection against SARS-CoV-2 infection; this supports and informs efforts to develop pancoronavirus vaccines.

Indexed as

ImmunologyMolecular physiologyVirology

Identifiers

PMID36101832
PMCPMC9458542
OpenAlexW4295206851

What OpenQuestion holds

Textmetadata
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.