Evidence map›Paper›PMID 34183681›Full record

Observational studyNature communications2021

COVID-19 mRNA vaccine induced antibody responses against three SARS-CoV-2 variants.

Pinja Jalkanen, Pekka Kolehmainen, Hanni K Häkkinen, Moona Huttunen, Paula A Tähtinen, Rickard Lundberg, Sari Maljanen, Arttu Reinholm, Sisko Tauriainen, Sari H Pakkanen and 17 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 190 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
190citing papers in PubMed, 3 pooled it
18.2field-weighted citation impact, top 1% 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

190 citing papers in PubMed, 3 syntheses or guidelines pooled it, 296 citations in OpenAlex.

  1. Long-Term Consequences of Asymptomatic SARS-CoV-2 Infection: A Systematic Review and Meta-Analysis.International journal of environmental research and public health · 2023
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130 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 3 institutions in 1 country.

Pinja JalkanenInstitute of Biomedicine, University of Turku, Turku, Finland. pinja.r.jalkanen@utu.fi.ORCID 0000-0001-7218-4732
Pekka KolehmainenInstitute of Biomedicine, University of Turku, Turku, Finland.ORCID 0000-0001-5997-8167
Hanni K HäkkinenDepartment of Infectious Diseases, Meilahti Vaccination Research Center, MeVac, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Moona HuttunenInstitute of Biomedicine, University of Turku, Turku, Finland.ORCID 0000-0002-4745-0477
Paula A TähtinenDepartment of Paediatrics and Adolescent Medicine, Turku University Hospital and University of Turku, Turku, Finland.
Rickard LundbergInstitute of Biomedicine, University of Turku, Turku, Finland.
Sari MaljanenInstitute of Biomedicine, University of Turku, Turku, Finland.
Arttu ReinholmInstitute of Biomedicine, University of Turku, Turku, Finland.
Sisko TauriainenInstitute of Biomedicine, University of Turku, Turku, Finland.ORCID 0000-0003-3423-5409
Sari H PakkanenDepartment of Infectious Diseases, Meilahti Vaccination Research Center, MeVac, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Iris LevonenDepartment of Infectious Diseases, Meilahti Vaccination Research Center, MeVac, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Arttu NousiainenDepartment of Infectious Diseases, Meilahti Vaccination Research Center, MeVac, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Taru MillerDepartment of Infectious Diseases, Meilahti Vaccination Research Center, MeVac, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Hanna VälimaaDepartment of Infectious Diseases, Meilahti Vaccination Research Center, MeVac, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Lauri IvaskaDepartment of Paediatrics and Adolescent Medicine, Turku University Hospital and University of Turku, Turku, Finland.ORCID 0000-0001-8935-5032
Arja PasternackDepartment of Physiology, University of Helsinki, Helsinki, Finland.
Rauno NavesDepartment of Physiology, University of Helsinki, Helsinki, Finland.
Olli RitvosDepartment of Physiology, University of Helsinki, Helsinki, Finland.
Pamela ÖsterlundFinnish Institute for Health and Welfare, Helsinki, Finland.ORCID 0000-0002-2229-6661
Suvi KuivanenDepartment of Virology, University of Helsinki, Helsinki, Finland.
Teemu SmuraDepartment of Virology, University of Helsinki, Helsinki, Finland.
Jussi HepojokiDepartment of Virology, University of Helsinki, Helsinki, Finland.ORCID 0000-0001-5699-214X
Olli VapalahtiDepartment of Virology, University of Helsinki, Helsinki, Finland.
Johanna LempainenInstitute of Biomedicine, University of Turku, Turku, Finland.
Laura KakkolaInstitute of Biomedicine, University of Turku, Turku, Finland.
Anu KanteleDepartment of Infectious Diseases, Meilahti Vaccination Research Center, MeVac, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Ilkka JulkunenInstitute of Biomedicine, University of Turku, Turku, Finland. ilkka.julkunen@utu.fi.ORCID 0000-0003-0165-2564
University of Helsinki · FIUniversity of Turku · FIFinnish Institute for Health and Welfare · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As SARS-CoV-2 has been circulating for over a year, dozens of vaccine candidates are under development or in clinical use. The BNT162b2 mRNA COVID-19 vaccine induces spike protein-specific neutralizing antibodies associated with protective immunity. The emergence of the B.1.1.7 and B.1.351 variants has raised concerns of reduced vaccine efficacy and increased re-infection rates. Here we show, that after the second dose, the sera of BNT162b2-vaccinated health care workers (n = 180) effectively neutralize the SARS-CoV-2 variant with the D614G substitution and the B.1.1.7 variant, whereas the neutralization of the B.1.351 variant is five-fold reduced. Despite the reduction, 92% of the seronegative vaccinees have a neutralization titre of >20 for the B.1.351 variant indicating some protection. The vaccinees' neutralization titres exceeded those of recovered non-hospitalized COVID-19 patients. Our work provides evidence that the second dose of the BNT162b2 vaccine induces cross-neutralization of at least some of the circulating SARS-CoV-2 variants.

Indexed as

Immunogenicity, VaccineAdultAgedAged, 80 and overAntibodies, ViralBNT162 VaccineBroadly Neutralizing AntibodiesCOVID-19COVID-19 VaccinesCross ProtectionFemaleFinlandHumansImmunization, SecondaryMaleMass VaccinationAntibodies, ViralBNT162 VaccineBroadly Neutralizing AntibodiesCOVID-19 Vaccines

Identifiers

PMID34183681
PMCPMC8239026
OpenAlexW3174829503

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.