Evidence map›Paper›PMID 34452043›Full record

ArticleVaccines2021

mRNA Vaccines Enhance Neutralizing Immunity against SARS-CoV-2 Variants in Convalescent and ChAdOx1-Primed Subjects.

Dorit Fabricius, Carolin Ludwig, Judith Scholz, Immanuel Rode, Chrysanthi Tsamadou, Eva-Maria Jacobsen, Martina Winkelmann, Aline Grempels, Ramin Lotfi, Aleš Janda and 5 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  16. Review
  17. Heterologous gam-COVID-vac (sputnik V)/mRNA-1273 (moderna) vaccination induces a stronger humoral response than homologous sputnik V in a real-world data analysis.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2022
    Article
  18. Article
  19. The durability of natural infection and vaccine-induced immunity against future infection by SARS-CoV-2.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  20. Review
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

15 authors at 1 institution in 1 country.

Dorit FabriciusDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Carolin LudwigDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.ORCID 0000-0001-8820-8479
Judith ScholzDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Immanuel RodeDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Chrysanthi TsamadouDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Eva-Maria JacobsenDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Martina WinkelmannDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Aline GrempelsDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Ramin LotfiDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Aleš JandaDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.ORCID 0000-0001-5604-8378
Sixten KörperDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Guido AdlerDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Klaus-Michael DebatinDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Hubert SchrezenmeierDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Bernd JahrsdörferDivision of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.ORCID 0000-0002-8334-5244
Immungenetics (Germany) · DE

Funding

German Federal Ministry of Health N/AGerman Red Cross Blood Transfusion Service Baden-Württemberg - Hessen N/AMinistry for Science, Research and Arts of Baden-Württemberg, Germany N/A
6 · The paper itself

Abstract

To identify the most efficient methods of immunological protection against SARS-CoV-2, including the currently most widespread variants of concern (VOCs)-B.1.1.7, B.1.351 and P.1-a simultaneous side-by-side-comparison of available vaccination regimes is required. In this observational cohort study, we compared immunological responses in 144 individuals vaccinated with the mRNA vaccines BNT162b2 or mRNA-1273 and the vector vaccine ChAdOx1-nCoV-19, either alone, in combination, or in the context of COVID-19-convalescence. Unvaccinated COVID-19-convalescent subjects served as a reference. We found that cellular and serological immune responses, including neutralizing capacity against VOCs, were significantly stronger with mRNA vaccines as compared with COVID-19-convalescent individuals or vaccinated individuals receiving the vector vaccine ChAdOx1-nCoV-19. Booster immunizations with mRNA vaccines triggered strong and broadly neutralizing antibody and IFN-γ responses in 100% of vaccinated individuals investigated. This effect was particularly strong in COVID-19-convalescent and ChAdOx1-nCoV-19-primed individuals, who were characterized by comparably moderate cellular and neutralizing antibody responses before mRNA vaccine booster. Heterologous vaccination regimes and convalescent booster regimes using mRNA vaccines may allow enhanced protection against SARS-CoV-2, including current VOCs. Furthermore, such regimes may facilitate rapid (re-)qualification of convalescent plasma donors with high titers of broadly neutralizing antibodies.

Indexed as

heterologous vaccination regimes using mRNA vaccines may allow enhanced protection against SARS-CoV-2, including current VOCsRNA vaccines may facilitate rapid (re-) qualification of convalescent plasma donors with high titers of broadly neutralizing antibodies

Identifiers

PMID34452043
PMCPMC8402682
OpenAlexW3195549443

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.