Evidence map›Paper›PMID 37063916›Full record

ArticleFrontiers in immunology2023

Breakthrough infections due to SARS-CoV-2 Delta variant: relation to humoral and cellular vaccine responses.

Matthieu Buscot, Marion Cremoni, Daisy Graça, Vesna Brglez, Johan Courjon, Jonathan Allouche, Maxime Teisseyre, Laurent Boyer, Jérôme Barrière, Emmanuel Chamorey and 2 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 31% 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.

NCT04355351 nacompletednot on this map

Study of Immune Response During SARS-CoV-2 Infection

TypeinterventionalSponsorCentre Hospitalier Universitaire de NiceRan2020 to 2022Enrolled303ConditionsNew Coronavirus Disease (COVID-19), Infection With SARS-CoV-2Armsblood sampling, additional blood tubes
NCT04429594 narecruitingnot on this map

Study of the Incidence of SARS-CoV-2 Infection in the Alpes-Maritimes Department by Analysis of the Specific Humoral and Cellular Response During Deconfinement

TypeinterventionalSponsorCentre Hospitalier Universitaire de NiceRan2020 to 2026Enrolled1,000ConditionsCoronavirus InfectionsArmsblood sampling
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

12 authors at 5 institutions in 1 country.

Matthieu BuscotInfectious Diseases Department, Nice University Hospital, Nice, France.
Marion CremoniImmunology Laboratory, Archet 1 Hospital, Nice University Hospital, Nice, France.
Daisy GraçaImmunology Laboratory, Archet 1 Hospital, Nice University Hospital, Nice, France.
Vesna BrglezImmunology Laboratory, Archet 1 Hospital, Nice University Hospital, Nice, France.
Johan CourjonInfectious Diseases Department, Nice University Hospital, Nice, France.
Jonathan AlloucheClinical Research Unit Côte d'Azur (UR2CA), Côte d'Azur University, Nice, France.
Maxime TeisseyreClinical Research Unit Côte d'Azur (UR2CA), Côte d'Azur University, Nice, France.
Laurent BoyerMediterranean Center for Molecular Medicine (C3M), Côte d'Azur University, Nice, France.
Jérôme BarrièreDepartment of Oncology, Clinique St Jean, Cagnes sur Mer, France.
Emmanuel ChamoreyDepartment of Biostatistics, Centre Antoine Lacassagne, Nice, France.
Michel CarlesInfectious Diseases Department, Nice University Hospital, Nice, France.
Barbara Seitz-PolskiImmunology Laboratory, Archet 1 Hospital, Nice University Hospital, Nice, France.
Observatoire de la Côte d’Azur · FRCentre Hospitalier Universitaire de Nice · FRCentre Méditerranéen de Médecine Moléculaire · FRCentre Antoine Lacassagne · FRClinique Saint Jean Languedoc · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: COVID-19 vaccines are expected to provide effective protection. However, emerging strains can cause breakthrough infection in vaccinated individuals. The immune response of vaccinated individuals who have experienced breakthrough infection is still poorly understood. Methods: Here, we studied the humoral and cellular immune responses of fully vaccinated individuals who subsequently experienced breakthrough infection due to the Delta variant of SARS-CoV-2 and correlated them with the severity of the disease. Results: In this study, an effective humoral response alone was not sufficient to induce effective immune protection against severe breakthrough infection, which also required effective cell-mediated immunity to SARS-CoV-2. Patients who did not require oxygen had significantly higher specific (p=0.021) and nonspecific (p=0.004) cellular responses to SARS-CoV-2 at the onset of infection than those who progressed to a severe form. Discussion: Knowing both humoral and cellular immune response could allow to adapt preventive strategy, by better selecting patients who would benefit from additional vaccine boosters. Trial registration numbers: https://clinicaltrials.gov, identifier NCT04355351; https://clinicaltrials.gov, identifier NCT04429594.

Indexed as

COVID-19VaccinesBreakthrough InfectionsCOVID-19 VaccinesHumansSARS-CoV-2COVID-19 VaccinesVaccinesbreakthrough infectionscellular responseCOVID-19humoral responsevaccination

Identifiers

PMID37063916
PMCPMC10101330
OpenAlexW4361268261

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.