Evidence map›Paper›PMID 38974469›Full record

ArticleiScience2024

Evolution of protective SARS-CoV-2-specific B and T cell responses upon vaccination and Omicron breakthrough infection.

Mohamed I M Ahmed, Sebastian Einhauser, Clemens Peiter, Antonia Senninger, Olga Baranov, Tabea M Eser, Manuel Huth, Laura Olbrich, Noemi Castelletti, Raquel Rubio-Acero and 11 more

Abstract read
In one paragraph

Article in iScience, 2024. 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. Article
  2. Article
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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

21 authors.

Mohamed I M AhmedDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Sebastian EinhauserInstitute for Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Clemens PeiterFaculty of Mathematics and Natural Sciences, University of Bonn, 53113 Bonn, Germany.
Antonia SenningerInstitute for Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Olga BaranovDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Tabea M EserDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Manuel HuthFaculty of Mathematics and Natural Sciences, University of Bonn, 53113 Bonn, Germany.
Laura OlbrichDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Noemi CastellettiDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Raquel Rubio-AceroDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
George CarnellLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Jonathan HeeneyLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Inge KroidlDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Kathrin HeldDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Andreas WieserDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Christian JankeDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Michael HoelscherDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
Jan HasenauerFaculty of Mathematics and Natural Sciences, University of Bonn, 53113 Bonn, Germany.
Ralf WagnerInstitute for Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Christof GeldmacherDivision of Infectious Diseases and Tropical Medicine, University Hospital, LMU Munich, 80799 Munich, Germany.
KoCo19/ORCHESTRA working group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron breakthrough infection (BTI) induced better protection than triple vaccination. To address the underlying immunological mechanisms, we studied antibody and T cell response dynamics during vaccination and after BTI. Each vaccination significantly increased peak neutralization titers with simultaneous increases in circulating spike-specific T cell frequencies. Neutralization titers significantly associated with a reduced hazard rate for SARS-CoV-2 infection. Yet, 97% of triple vaccinees became SARS-CoV-2 infected. BTI further boosted neutralization magnitude and breadth, broadened virus-specific T cell responses to non-vaccine-encoded antigens, and protected with an efficiency of 88% from further infections by December 2022. This effect was then assessed by utilizing mathematical modeling, which accounted for time-dependent infection risk, the antibody, and T cell concentration at any time point after BTI. Our findings suggest that cross-variant protective hybrid immunity induced by vaccination and BTI was an important contributor to the reduced virus transmission observed in Bavaria in late 2022 and thereafter.

Indexed as

immunologymicrobiologyvirology

Identifiers

PMID38974469
PMCPMC11225850

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.