Evidence map›Paper›PMID 35054099›Full record

ArticleJournal of clinical medicine2022

ELISA-Based Analysis Reveals an Anti-SARS-CoV-2 Protein Immune Response Profile Associated with Disease Severity.

Charline Herrscher, Sébastien Eymieux, Christophe Gaborit, Hélène Blasco, Julien Marlet, Karl Stefic, Philippe Roingeard, Leslie Grammatico-Guillon, Christophe Hourioux

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 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
0.6field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  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

9 authors at 2 institutions in 1 country.

Charline HerrscherInserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.
Sébastien EymieuxInserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.ORCID 0000-0002-4738-510X
Christophe GaboritEpidémiologie des Données Cliniques en Centre-Val de Loire (EpiDcliC), Centre Hospitalier Universitaire de Tours, 37000 Tours, France.
Hélène BlascoService de Biochimie et Biologie Moléculaire, CHRU de Tours, 37000 Tours, France.
Julien MarletInserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.ORCID 0000-0002-8645-8703
Karl SteficInserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.ORCID 0000-0002-9686-9194
Philippe RoingeardInserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.
Leslie Grammatico-GuillonInserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.ORCID 0000-0001-7934-8912
Christophe HouriouxInserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.
Université de Tours · FRCentre Hospitalier Universitaire de Tours · FR

Funding

Agence Nationale de la Recherche ANR-20-COVI-0011-01Centre Val de Loire 2020 00140687
6 · The paper itself

Abstract

Since the start of the COVID-19 pandemic, many studies have investigated the humoral response to SARS-CoV-2 during infection. Studies with native viral proteins constitute a first-line approach to assessing the overall immune response, but small peptides are an accurate and valuable tool for the fine characterization of B-cell epitopes, despite the restriction of this approach to the determination of linear epitopes. In this study, we used ELISA and peptides covering a selection of structural and non-structural SARS-CoV-2 proteins to identify key epitopes eliciting a strong immune response that could serve as a biological signature of disease characteristics, such as severity, in particular. We used 213 plasma samples from a cohort of patients well-characterized clinically and biologically and followed for COVID-19 infection. We found that patients developing severe disease had higher titers of antibodies mapping to multiple specific epitopes than patients with mild to moderate disease. These data are potentially important as they could be used for immunological profiling to improve our knowledge of the quantitative and qualitative characteristics of the humoral response in relation to patient outcome.

Indexed as

COVID-19disease severitySARS-CoV-2 antibodiesSARS-CoV-2 linear epitopes

Identifiers

PMID35054099
PMCPMC8781066
OpenAlexW4206637928

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.