Evidence map›Paper›PMID 35795665›Full record

Observational studyFrontiers in immunology2022

BNT162b2 Booster Vaccination Elicits Cross-Reactive Immunity Against SARS-CoV-2 Variants B.1.1.529 and B.1.617.2 in Convalescents of All Ages.

Bernd Jahrsdörfer, Matthias Proffen, Judith Scholz, Janina Hägele, Carolin Ludwig, Christiane Vieweg, Aline Grempels, Dorit Fabricius, Ramin Lotfi, Sixten Körper and 2 more

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
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

12 authors.

Bernd JahrsdörferDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Matthias ProffenDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Judith ScholzDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Janina HägeleDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Carolin LudwigDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Christiane ViewegDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Aline GrempelsDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Dorit FabriciusDepartment of Pediatrics and Adolescent Medicine, Ulm University Medical Center, Ulm, Germany.
Ramin LotfiDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Sixten KörperDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.
Guido AdlerMedical Faculty, Ulm University, Ulm, Germany.
Hubert SchrezenmeierDepartment of Transfusion Medicine, Ulm University, Ulm, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this prospective observational cohort study we analyzed cellular and serological immune response parameters against SARS-CoV-2 and current variants of concern (VOC) in 147 COVID-19-convalescent and 39 COVID-19-naïve individuals before and after BNT162b2 booster vaccination. No significant differences regarding immunological response parameters were observed between younger and older individuals. Booster vaccination induced full recovery of both cellular and serological response parameters including IFN-γ secretion and anti-spike antibody titers with strong neutralization capacities against wild type SARS-COV-2 and Delta. Surprisingly, even serological neutralization capacity against Omicron was detectable one month after second vaccination and four months before it had been first observed in South Africa. As a result, more than 90% of convalescent individuals exhibited detectable and 75% strong Omicron neutralization capacity after booster vaccination, compared with 72% and 46% of COVID-19-naïve individuals. Our results support the notion that broad and cross-reactive immune memory against SARS-CoV-2 including currently known VOCs can be established by booster vaccination with spike-based mRNA vaccines like BNT162b2, particularly in COVID-19-convalescent individuals of all ages. Nevertheless, especially in COVID-19-naïve individuals future variants escaping the memory immune response may require vaccine approaches such as

Indexed as

COVID-19Viral VaccinesBNT162 VaccineHumansProspective StudiesSARS-CoV-2VaccinationVaccines, InactivatedBNT162 VaccineVaccines, InactivatedViral VaccinesB.1.1.529B.1.617.2BNT162b2COVID-19deltamRNA vaccineneutralization capacityomicron

Identifiers

PMID35795665
PMCPMC9250979

What OpenQuestion holds

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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.