Evidence map›Paper›PMID 16461009›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2006

Evaluation of adenovirus vectors containing serotype 35 fibers for vaccination.

Nelson DiPaolo, Shaoheng Ni, Anuj Gaggar, Robert Strauss, Sebastian Tuve, Zong Yi Li, Daniel Stone, Dmitry Shayakhmetov, Nancy Kiviat, Papa Touré and 3 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  7. Review
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  9. Review
  10. Transient removal of CD46 is safe and increases B-cell depletion by rituximab in CD46 transgenic mice and macaques.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Article
  11. Article
  12. Adenovirus-triggered innate signalling pathways.European journal of microbiology & immunology · 2011
    Review
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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

13 authors at 4 institutions in 3 countries.

Nelson DiPaoloDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195, USA.
Shaoheng Ni
Anuj Gaggar
Robert Strauss
Sebastian Tuve
Zong Yi Li
Daniel Stone
Dmitry Shayakhmetov
Nancy Kiviat
Papa Touré
Salif Sow
Branka Horvat
André Lieber
University of Washington Medical Center · USCheikh Anta Diop University · SNUniversity of Washington · USInserm · FR

Funding

Evaluation of Vectors based on group B adenovirusesR01CA144057 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2010 to 2014
$2.5M
ONCOLYTIC ADENOVIRUSES FOR CERVICAL CANCER GENE THERAPYR01CA080192 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 1999 to 2009
$2.0M
Evaluation of vectors based on group B adenovirusesR01HL078836 · NHLBI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2005 to 2009
$1.4M
NCI NIH HHS CA080192NCI NIH HHS R01 CA080192NCI NIH HHS R01 CA144057NHLBI NIH HHS HL-00-008NHLBI NIH HHS R01 HL078836PHS HHS HLA078836
6 · The paper itself

Abstract

In contrast to commonly used serotype 5-based adenovirus (Ad) vectors, Ad's containing fibers derived from B-group serotype 35 (Ad5/35) efficiently transduce human DCs ex vivo and appear to target antigen-presenting cells after intravenous injection into baboons. Based on this, Ad5/35 vectors could be valuable tools for immunotherapy and vaccination. On the other hand, a number of studies indicate that signaling through the B-group Ad receptor, CD46, can cause tolerance or immunosuppression. Since mice do not express CD46 in a human-like pattern, we studied the in vivo properties of Ad5/35 in transgenic mice that express CD46 in a pattern and at a level similar to those of humans. Hypersensitivity assays and analyses of frequencies of regulatory T cells and T cell responses did not indicate that Ad5/35 injection exerts detrimental effects on the host's immune system. An Ad5/35 vector expressing a model antigen was able to trigger a strong T cell response against the test antigen after intramuscular injection. Overall, compared to Ad5 vectors, Ad5/35 vectors had a better safety profile, reflected by lower serum levels of proinflammatory cytokines.

Indexed as

VaccinationViral VaccinesAdenoviridaeAnimalsBreast NeoplasmsDendritic CellsEscherichia coliFemaleFluorescent Antibody TechniqueGene ExpressionGenetic VectorsGenome, ViralGreen Fluorescent ProteinsHumansImmunity, InnateLeukocytes, MononuclearGreen Fluorescent ProteinsMembrane Cofactor ProteinViral Vaccines

Identifiers

PMID16461009
PMCPMC1424671
OpenAlexW1984723811

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.