Evidence map›Paper›PMID 36679857›Full record

ArticleVaccines2022

Full-Lung Prophylaxis against SARS-CoV-2 by One-Shot or Booster Intranasal Lentiviral Vaccination in Syrian Golden Hamsters.

Benjamin Vesin, Pierre Authié, Catherine Blanc, Ingrid Fert, Amandine Noirat, Fabien Le Chevalier, Yu Wei, Min-Wen Ku, Kirill Nemirov, François Anna and 7 more

Abstract read
In one paragraph

Article in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  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

17 authors.

Benjamin VesinTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Pierre AuthiéTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Catherine BlancTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Ingrid FertTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.ORCID 0000-0003-1389-1159
Amandine NoiratTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.ORCID 0000-0002-7724-7461
Fabien Le ChevalierTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Yu WeiTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Min-Wen KuTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Kirill NemirovTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
François AnnaTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
David HardyHistopathology Platform, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.ORCID 0000-0001-5874-4377
Cyril PlanchaisLaboratory of Humoral Immunology, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Hugo MouquetLaboratory of Humoral Immunology, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.ORCID 0000-0002-4230-610X
Françoise GuinetLymphocytes and Immunity Unit, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Pierre CharneauTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.
Laleh MajlessiTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.ORCID 0000-0001-8648-4058
Maryline BourgineTheraVectys Joint Lab, Institut Pasteur, Université Paris Cité, F-75015 Paris, France.ORCID 0000-0002-8850-8073

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Following the breakthrough of numerous severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants in recent months and the incomplete efficiency of the currently available vaccines, development of more effective vaccines is desirable. Non-integrative, non-cytopathic and non-inflammatory lentiviral vectors elicit sterilizing prophylaxis against SARS-CoV-2 in preclinical animal models and are particularly suitable for mucosal vaccination, which is acknowledged as the most effective in reducing viral transmission. Here, we demonstrate that a single intranasal administration of a vaccinal lentiviral vector encoding a stabilized form of the original SARS-CoV-2 Spike glycoprotein induces full-lung protection of respiratory tracts and strongly reduces pulmonary inflammation in the susceptible Syrian golden hamster model against the prototype SARS-CoV-2. In addition, we show that a lentiviral vector encoding stabilized Spike of SARS-CoV-2 Beta variant (LV::S

Indexed as

cross-neutralizationintranasal vaccinationlentiviral vectorslung inflammationmucosal immunitySARS-CoV-2 variants

Identifiers

PMID36679857
PMCPMC9865670

What OpenQuestion holds

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Registered trials

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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.