Evidence map›Paper›PMID 16554842›Full record

ArticleGene therapy2006

Efficient immunization of rhesus macaques with an HCV candidate vaccine by heterologous priming-boosting with novel adenoviral vectors based on different serotypes.

E Fattori, I Zampaglione, M Arcuri, A Meola, B B Ercole, A Cirillo, A Folgori, A Bett, M Cappelletti, E Sporeno and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 47 citations in OpenAlex.

  1. Viral hepatitis update: Progress and perspectives.World journal of gastroenterology · 2021
    Review
  2. Article
  3. Challenges and Promise of a Hepatitis C Virus Vaccine.Cold Spring Harbor perspectives in medicine · 2020
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Will there be a vaccine to prevent HCV infection?Seminars in liver disease · 2014
    Review
  10. Article
  11. Genetic vaccine for respiratory syncytial virus provides protection without disease potentiation.Molecular therapy : the journal of the American Society of Gene Therapy · 2014
    Article
  12. Article
  13. Ever closer to a prophylactic vaccine for HCV.Expert opinion on biological therapy · 2013
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. New insights on adenovirus as vaccine vectors.Molecular therapy : the journal of the American Society of Gene Therapy · 2009
    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

13 authors at 3 institutions in 2 countries.

E FattoriDepartment of Molecular and Cellular Biololgy, Istituto di Ricerche di Biologia Molecolare P Angeletti, Pomezia, Rome, Italy. elena_fattori@merck.com
I Zampaglione
M Arcuri
A Meola
B B Ercole
A Cirillo
A Folgori
A Bett
M Cappelletti
E Sporeno
R Cortese
A Nicosia
S Colloca
Istituto di Genetica Molecolare · ITInstitute of Molecular Biology and Pathology · ITUnited States Military Academy · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient vaccination against viral agents requires a strong T-cell-mediated immune response to clear viral-infected cells. Optimal vaccination can be achieved by administration of recombinant viral vectors encoding phatogen antigens. Adenoviral vectors have attracted considerable attention as potential viral vectors for genetic vaccination owing to their favorable safety profile and potent transduction efficiency following intramuscular injection. However, the neutralizing antibody response against adenoviral capsid proteins following adenoviral vectors injection limits the success of vaccination protocols based on multiple administrations of the same adenoviral serotype. In this work, we describe efficient immunization of rhesus macaques, the preferred model for preclinical assessment, with an HCV candidate vaccine by heterologous priming-boosting with adenoviral vectors based on different serotypes. The induced responses are broad and show significant cross-strain reactivity. Boosting can be delayed for over 2 years after priming, indicating that there is long-term maintenance of resting memory cells.

Indexed as

AdenoviridaeAnimalsAntibodies, ViralGenetic EngineeringGenetic TherapyGenetic VectorsGenotypeHepacivirusHepatitis CHumansImmunization ScheduleImmunization, SecondaryInterferon-gammaMacaca mulattaMiceMice, Inbred C57BLAntibodies, ViralInterferon-gammaViral Hepatitis Vaccines

Identifiers

PMID16554842
OpenAlexW2014690236

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.