Evidence map›Paper›PMID 35113647›Full record

ArticleScience immunology2022

Divergent SARS-CoV-2 Omicron-reactive T and B cell responses in COVID-19 vaccine recipients.

Corine H GeurtsvanKessel, Daryl Geers, Katharina S Schmitz, Anna Z Mykytyn, Mart M Lamers, Susanne Bogers, Sandra Scherbeijn, Lennert Gommers, Roos S G Sablerolles, Nella N Nieuwkoop and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Science immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 286 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
286citing papers in PubMed, 1 pooled it
43.1field-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

286 citing papers in PubMed, 1 synthesis or guideline pooled it, 436 citations in OpenAlex.

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226 more citing papers are in PubMed but not listed here.

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

24 authors at 2 institutions in 2 countries.

Corine H GeurtsvanKesselDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-7678-314X
Daryl GeersDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-3432-0761
Katharina S SchmitzDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-8537-0646
Anna Z MykytynDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0001-7188-6871
Mart M LamersDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-1431-4022
Susanne BogersDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-8212-2946
Sandra ScherbeijnDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.
Lennert GommersDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-4542-0303
Roos S G SablerollesDepartment of Hospital Pharmacy, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-6647-6584
Nella N NieuwkoopDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.
Laurine C RijsbergenDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0001-8328-2899
Laura L A van DijkDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0001-5716-2738
Janet de WildeDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.
Kimberley AlblasDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0001-7815-3806
Tim I BreugemDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.
Bart J A RijndersDepartment of Medical Microbiology and Infectious Diseases, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0003-3343-9610
Herbert de JagerDepartment of Occupational Health Services, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0001-7516-6054
Daniela WeiskopfCenter for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, CA 92037, USA.ORCID 0000-0003-2968-7371
P Hugo M van der KuyDepartment of Hospital Pharmacy, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-7128-8801
Alessandro SetteCenter for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, CA 92037, USA.ORCID 0000-0001-7013-2250
Marion P G KoopmansDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-5204-2312
Alba GrifoniCenter for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, CA 92037, USA.ORCID 0000-0002-2209-5966
Bart L HaagmansDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0001-6221-2015
Rory D de VriesDepartment of Viroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0003-2817-0127
Erasmus MC · NLLa Jolla Institute for Immunology · US

Funding

NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00016 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEBBY, RICHARD · 2021 to 2025
$91.4M
NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00014 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GARCIA-SASTRE, ADOLFO · 2021 to 2025
$62.6M
NIAID NIH HHS 75N93021C00014NIAID NIH HHS 75N93021C00016
6 · The paper itself

Abstract

The severe acute respiratory distress syndrome coronavirus 2 (SARS-CoV-2) Omicron variant is spreading rapidly, even in vaccinated individuals, raising concerns about immune escape. Here, we studied neutralizing antibodies and T cell responses targeting SARS-CoV-2 D614G [wild type (WT)] and the Beta, Delta, and Omicron variants of concern in a cohort of 60 health care workers after immunization with ChAdOx-1 S, Ad26.COV2.S, mRNA-1273, or BNT162b2. High binding antibody levels against WT SARS-CoV-2 spike (S) were detected 28 days after vaccination with both mRNA vaccines (mRNA-1273 or BNT162b2), which substantially decreased after 6 months. In contrast, antibody levels were lower after Ad26.COV2.S vaccination but did not wane. Neutralization assays showed consistent cross-neutralization of the Beta and Delta variants, but neutralization of Omicron was significantly lower or absent. BNT162b2 booster vaccination after either two mRNA-1273 immunizations or Ad26.COV2 priming partially restored neutralization of the Omicron variant, but responses were still up to 17-fold decreased compared with WT. SARS-CoV-2-specific T cells were detected up to 6 months after all vaccination regimens, with more consistent detection of specific CD4

Indexed as

COVID-19SARS-CoV-2Ad26COVS1BNT162 VaccineCD8-Positive T-LymphocytesCOVID-19 VaccinesHumansAd26COVS1BNT162 VaccineCOVID-19 Vaccines

Identifiers

PMID35113647
PMCPMC8939771
OpenAlexW4210708247

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.