Evidence map›Paper›PMID 30996103›Full record

ArticleJournal of virology2019

Oral Vaccination with Replication-Competent Adenovirus in Mice Reveals Dissemination of the Viral Vaccine beyond the Gastrointestinal Tract.

Emeline Goffin, Justine Javaux, Eric Destexhe, Carla D Pretto, Katherine R Spindler, Bénédicte Machiels, Laurent Gillet

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  5. Review
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  7. Article
  8. Article
  9. COVID-19: should oral vaccination strategies be given more consideration?Therapeutic advances in vaccines and immunotherapy · 2020
    Article
  10. 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

7 authors at 3 institutions in 2 countries.

Emeline GoffinLaboratory of Immunology and Vaccinology, Department of Infectious Diseases Faculty of Veterinary Medicine, FARAH, University of Liège, Liège, Belgium.
Justine JavauxLaboratory of Immunology and Vaccinology, Department of Infectious Diseases Faculty of Veterinary Medicine, FARAH, University of Liège, Liège, Belgium.
Eric DestexheGSK, Rixensart, Belgium.
Carla D PrettoDepartment of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.
Katherine R SpindlerDepartment of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0002-9829-6051
Bénédicte MachielsLaboratory of Immunology and Vaccinology, Department of Infectious Diseases Faculty of Veterinary Medicine, FARAH, University of Liège, Liège, Belgium.
Laurent GilletLaboratory of Immunology and Vaccinology, Department of Infectious Diseases Faculty of Veterinary Medicine, FARAH, University of Liège, Liège, Belgium L.Gillet@uliege.be.ORCID 0000-0002-1047-2525
University of Liège · BEUniversity of Michigan · USGlaxoSmithKline (Belgium) · BE

Funding

Viral interaction with host eIF2alpha kinasesR01AI133935 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SPINDLER, KATHERINE R. · 2018 to 2022
$3.0M
Mechanisms of blood-brain barrier disruption by an encephalitic virusR01AI091721 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SPINDLER, KATHERINE R. · 2011 to 2015
$2.5M
NIAID NIH HHS R01 AI091721NIAID NIH HHS R01 AI133935
6 · The paper itself

Abstract

Since the 1970s, replication-competent human adenoviruses 4 and 7 have been used as oral vaccines to protect U.S. soldiers against the severe respiratory diseases caused by these viruses. These vaccines are thought to establish a digestive tract infection conferring protection against respiratory challenge through antibodies. The success of these vaccines makes replication-competent adenoviruses attractive candidates for use as oral vaccine vectors. However, the inability of human adenoviruses to replicate efficiently in laboratory animals has hampered the study of such vectors. Here, we used mouse adenovirus type 1 (MAV-1) in mice to study oral replication-competent adenovirus-based vaccines. We show that MAV-1 oral administration provides protection that recapitulates the protection against homologous respiratory challenge observed with adenovirus 4 and 7 vaccines. Moreover, live oral MAV-1 vaccine better protected against a respiratory challenge than inactivated vaccines. This protection was linked not only with the presence of MAV-1-specific antibodies but also with a better recruitment of effector CD8 T cells. However, unexpectedly, we found that such oral replication-competent vaccine systemically spread all over the body. Our results therefore support the use of MAV-1 to study replication-competent oral adenovirus-based vaccines but also highlight the fact that those vaccines can disseminate widely in the body.

Indexed as

Administration, OralVaccinationAdenoviridaeAdenoviridae InfectionsAdenoviruses, HumanAdenovirus VaccinesAnimalsAntibodies, ViralDisease Models, AnimalFemaleGastrointestinal TractHumansImmunizationLungMiceMice, Inbred BALB CAdenovirus VaccinesAntibodies, ViralVaccines, AttenuatedVaccines, Syntheticadenovirusmouse modeloral vaccination

Identifiers

PMID30996103
PMCPMC6580940
OpenAlexW2939499355

What OpenQuestion holds

Textmetadata
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.