Evidence map›Paper›PMID 16699033›Full record

ArticleJournal of virology2006

Epitopes expressed in different adenovirus capsid proteins induce different levels of epitope-specific immunity.

Anja Krause, Ju H Joh, Neil R Hackett, Peter W Roelvink, Joseph T Bruder, Thomas J Wickham, Imre Kovesdi, Ronald G Crystal, Stefan Worgall

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

40 citing papers in PubMed, 70 citations in OpenAlex.

  1. Developing the next-generation of adenoviral vector vaccines.Human vaccines & immunotherapeutics · 2025
    Review
  2. Article
  3. Review
  4. Role of Adenoviruses in Cancer Therapy.Frontiers in oncology · 2022
    Review
  5. Article
  6. Review
  7. Immunoinformatic construction of an adenovirus-based modular vaccine platform and its application in the design of a SARS-CoV-2 vaccine.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2020
    Article
  8. Review
  9. Article
  10. Future Prospects for the Development of Cost-Effective Adenovirus Vaccines.International journal of molecular sciences · 2017
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. The March Toward Malaria Vaccines.American journal of preventive medicine · 2015
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  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

9 authors at 2 institutions in 1 country.

Anja KrauseDepartment of Genetic Medicine, Weill Medical College of Cornell University, 515 East 71st Street, New York, NY 10021, USA.
Ju H Joh
Neil R Hackett
Peter W Roelvink
Joseph T Bruder
Thomas J Wickham
Imre Kovesdi
Ronald G Crystal
Stefan Worgall
GenVec · USCornell University · US

Funding

WEILL CORNELL PROGRAM OF EXCELLENCE IN GENE THERAPYU01HL066952 · NHLBI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI CRYSTAL, RONALD G · 2000 to 2005
$15.9M
NHLBI NIH HHS U01 HL066952NHLBI NIH HHS U01 HL 66952
6 · The paper itself

Abstract

On the basis of the concept that the capsid proteins of adenovirus (Ad) gene transfer vectors can be genetically manipulated to enhance the immunogenicity of Ad-based vaccines, the present study compared the antiantigen immunogenicity of Ad vectors with a common epitope of the hemagglutinin (HA) protein of the influenza A virus incorporated into the outer Ad capsid protein hexon, penton base, fiber knob, or protein IX. Incorporation of the same epitope into the different capsid proteins provided insights into the correlation between epitope position and antiepitope immunity. Following immunization of three different strains of mice (C57BL/6, BALB/c, and CBA) with either an equal number of Ad particles (resulting in a different total HA copy number) or different Ad particle numbers (to achieve the same HA copy number), the highest primary (immunoglobulin M [IgM]) and secondary (IgG) anti-HA humoral and cellular CD4 gamma interferon and interleukin-4 responses against HA were always achieved with the Ad vector carrying the HA epitope in fiber knob. These observations suggest that the immune response against an epitope inserted into Ad capsid proteins is not necessarily dependent on the capsid protein number and imply that the choice of incorporation site in Ad capsid proteins in their use as vaccines needs to be compared in vivo.

Indexed as

AdenoviridaeAdenoviridae InfectionsAnimalsCapsid ProteinsEpitopesGenetic VectorsMiceMice, Inbred C57BLViral VaccinesCapsid ProteinsEpitopesViral Vaccines

Identifiers

PMID16699033
PMCPMC1472137
OpenAlexW2139130466

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.