Evidence map›Paper›PMID 26679149›Full record

ArticlePloS one2015

Adenovirus Specific Pre-Immunity Induced by Natural Route of Infection Does Not Impair Transduction by Adenoviral Vaccine Vectors in Mice.

Bruna de Andrade Pereira, Leoneide E Maduro Bouillet, Natalia A Dorigo, Cornel Fraefel, Oscar Bruna-Romero

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-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.

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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Viral vector-based therapeutic HPV vaccines.Clinical and experimental medicine · 2024
    Review
  4. 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

5 authors at 2 institutions in 2 countries.

Bruna de Andrade PereiraDepartment of Microbiology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Leoneide E Maduro BouilletDepartment of Microbiology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Natalia A DorigoDepartment of Microbiology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Cornel FraefelInstitute of Virology, University of Zürich, Zürich, Switzerland.
Oscar Bruna-RomeroDepartment of Microbiology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Universidade Federal de Minas Gerais · BRUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant human adenovirus serotype 5 (HAd5V) vectors are gold standards of T-cell immunogenicity as they efficiently induce also humoral responses to exogenous antigens, in particular when used in prime-boost protocols. Some investigators have shown that pre-existing immunity to adenoviruses interferes with transduction by adenoviral vectors, but the actual extent of this interference is not known since it has been mostly studied in mice using unnatural routes of infection and virus doses. Here we studied the effects of HAd5V-specific immune responses induced by intranasal infection on the transduction efficiency of recombinant adenovirus vectors. Of interest, when HAd5V immunity was induced in mice by the natural respiratory route, the pre-existing immunity against HAd5V did not significantly interfere with the B and T-cell immune responses against the transgene products induced after a prime/boost inoculation protocol with a recombinant HAd5V-vector, as measured by ELISA and in vivo cytotoxic T-cell assays, respectively. We also correlated the levels of HAd5V-specific neutralizing antibodies (Ad5NAbs) induced in mice with the levels of Ad5NAb titers found in humans. The data indicate that approximately 60% of the human serum samples tested displayed Ad5NAb levels that could be overcome with a prime-boost vaccination protocol. These results suggest that recombinant HAd5V vectors are potentially useful for prime-boost vaccination strategies, at least when pre-existing immunity against HAd5V is at low or medium levels.

Indexed as

Adenovirus Infections, HumanAdenovirus VaccinesAnimalsAntibodies, NeutralizingAntibodies, ViralB-LymphocytesCells, CulturedFemaleHumansMiceMice, Inbred BALB CT-LymphocytesVaccines, SyntheticAdenovirus VaccinesAntibodies, NeutralizingAntibodies, ViralVaccines, Synthetic

Identifiers

PMID26679149
PMCPMC4682971
OpenAlexW2218117846

What OpenQuestion holds

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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.