Evidence map›Paper›PMID 24374965›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

Clinical assessment of a novel recombinant simian adenovirus ChAdOx1 as a vectored vaccine expressing conserved Influenza A antigens.

Richard D Antrobus, Lynda Coughlan, Tamara K Berthoud, Matthew D Dicks, Adrian Vs Hill, Teresa Lambe, Sarah C Gilbert

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed, 2 pooled it
8.6field-weighted citation impact, top 2% 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

137 citing papers in PubMed, 2 syntheses or guidelines pooled it, 197 citations in OpenAlex.

  1. Pooled it
  2. Viral vector-based influenza vaccines.Human vaccines & immunotherapeutics · 2016
    Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Review
  8. Article
  9. Review
  10. Developing the next-generation of adenoviral vector vaccines.Human vaccines & immunotherapeutics · 2025
    Review
  11. Review
  12. Article
  13. Article
  14. Frontiers in cellular and infection microbiology · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

77 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Richard D AntrobusThe Jenner Institute, University of Oxford, Oxford, UK.
Lynda CoughlanThe Jenner Institute, University of Oxford, Oxford, UK.
Tamara K BerthoudThe Jenner Institute, University of Oxford, Oxford, UK.
Matthew D DicksThe Jenner Institute, University of Oxford, Oxford, UK.
Adrian Vs HillThe Jenner Institute, University of Oxford, Oxford, UK.
Teresa LambeThe Jenner Institute, University of Oxford, Oxford, UK. Electronic address: teresa.lambe@ndm.ox.ac.uk.
Sarah C GilbertThe Jenner Institute, University of Oxford, Oxford, UK. Electronic address: sarah.gilbert@ndm.ox.ac.uk.
University of Oxford · GBJenner Institute · GB

Funding

Medical Research Council G0802507Wellcome Trust 090532Wellcome Trust 095540
6 · The paper itself

Abstract

Adenoviruses are potent vectors for inducing and boosting cellular immunity to encoded recombinant antigens. However, the widespread seroprevalence of neutralizing antibodies to common human adenovirus serotypes limits their use. Simian adenoviruses do not suffer from the same drawbacks. We have constructed a replication-deficient chimpanzee adenovirus-vectored vaccine expressing the conserved influenza antigens, nucleoprotein (NP), and matrix protein 1 (M1). Here, we report safety and T-cell immunogenicity following vaccination with this novel recombinant simian adenovirus, ChAdOx1 NP+M1, in a first in human dose-escalation study using a 3+3 study design, followed by boosting with modified vaccinia virus Ankara expressing the same antigens in some volunteers. We demonstrate ChAdOx1 NP+M1 to be safe and immunogenic. ChAdOx1 is a promising vaccine vector that could be used to deliver vaccine antigens where strong cellular immune responses are required for protection.

Indexed as

Adenoviruses, SimianAdolescentAdultAnimalsAntigens, ViralDose-Response Relationship, ImmunologicGenetic VectorsHEK293 CellsHumansInfluenza A virusInfluenza VaccinesMiddle AgedNucleocapsid ProteinsPan troglodytesRecombinant ProteinsRNA-Binding ProteinsAntigens, ViralInfluenza VaccinesM1 protein, Influenza A virusNP protein, Influenza A virusNucleocapsid ProteinsRecombinant ProteinsRNA-Binding ProteinsViral Core ProteinsViral Matrix Proteins

Identifiers

PMID24374965
PMCPMC3944330
OpenAlexW1970569268

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.