Evidence map›Paper›PMID 16920215›Full record

ArticleVirus research2006

Members of adenovirus species B utilize CD80 and CD86 as cellular attachment receptors.

Joshua J Short, Chenthamarakshan Vasu, Mark J Holterman, David T Curiel, Alexander Pereboev

Open access · greenAbstract read
In one paragraph

Article in Virus research, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

41 citing papers in PubMed, 96 citations in OpenAlex.

  1. Article
  2. Article
  3. Construction and application of adenoviral vectors.Molecular therapy. Nucleic acids · 2023
    Review
  4. Review
  5. Article
  6. Article
  7. Cryptic association of B7-2 molecules and its implication for clustering.Protein science : a publication of the Protein Society · 2021
    Article
  8. Viral Respiratory Pathogens and Lung Injury.Clinical microbiology reviews · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Oncolytic viruses for cancer immunotherapy.Journal of hematology & oncology · 2020
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Joshua J ShortDivision of Human Gene Therapy, Departments of Medicine, Obstetrics and Gynecology, Pathology, and Surgery, and the Gene Therapy Center, University of Alabama at Birmingham, Birmingham, AL 35294-2172, USA.
Chenthamarakshan Vasu
Mark J Holterman
David T Curiel
Alexander Pereboev
University of Alabama at Birmingham · USUniversity of Illinois Chicago · US

Funding

Targeted immunotherapy programP50CA083591 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PARTRIDGE, EDWARD E · 1999 to 2005
$9.6M
Enhanced CRAd for Pancreatic CancerR01CA094084 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2002 to 2013
$2.7M
REPLICATIVE ADENOVIRUSES WITH ENHANCED INFECTIVITYR01CA083821 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURIEL, DAVID TERRY · 2000 to 2008
$1.9M
Canine model for evaluating CRAD efficacyR01CA093796 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SIEGAL, GENE P · 2002 to 2005
$1.1M
NCI NIH HHS P50 CA083591NCI NIH HHS P50 CA83591NCI NIH HHS R01 CA083821NCI NIH HHS R01 CA093796NCI NIH HHS R01 CA094084NCI NIH HHS R01 CA83821NCI NIH HHS R01 CA93796NCI NIH HHS R01 CA94084
6 · The paper itself

Abstract

Alternate serotypes of adenovirus (Ad), including Ads of species B, are being explored to circumvent the disadvantages of Ad serotype 5 gene delivery vectors. Whereas the majority of human Ads utilize the Coxsackievirus and adenovirus receptor (CAR), none of the Ad species B use CAR. Ad species B is further divided into two subspecies, B1 and B2, and utilizes at least two classes of receptors: common Ad species B receptors and B2 specific receptors. CD46 has been implicated as a B2-specific receptor. Ad serotype 3 (Ad3), a member of B1, utilizes CD80 and CD86 as cellular attachment receptors. The receptor-interacting Ad fiber-knob domain is highly homologous among species B Ads. We hypothesized that other members of Ad species B may utilize CD80 and CD86 as cellular attachment receptors. All tested species B members showed specific binding to cells expressing CD80 and CD86, and the Ad fiber-knob domain from both B1 and B2 Ad efficiently blocked CD80- and CD86-mediated infection of Ad3 vectors. Members of both B1 and B2 demonstrated CD80- and CD86-specific infection of CHO cells expressing CD80 and CD86. Therefore, all of the members of Ad species B utilize CD80 and CD86 for infection of cells.

Indexed as

Virus AttachmentAdenoviridaeAnimalsB7-1 AntigenB7-2 AntigenCHO CellsCricetinaeCricetulusReceptors, VirusB7-1 AntigenB7-2 AntigenReceptors, Virus

Identifiers

PMID16920215
PMCPMC2203219
OpenAlexW2085862839

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.