Evidence map›Paper›PMID 27490575›Full record

ArticleVaccines2016

Highly-Immunogenic Virally-Vectored T-cell Vaccines Cannot Overcome Subversion of the T-cell Response by HCV during Chronic Infection.

Leo Swadling, John Halliday, Christabel Kelly, Anthony Brown, Stefania Capone, M Azim Ansari, David Bonsall, Rachel Richardson, Felicity Hartnell, Jane Collier and 11 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Safety and immunogenicity of ChAd63-KH vaccine in post-kala-azar dermal leishmaniasis patients in Sudan.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Trial
  4. Trial
  5. Article
  6. Article
  7. Review
  8. Article
  9. NK cells limit therapeutic vaccine-induced CD8Science translational medicine · 2022
    Article
  10. Review
  11. Viral hepatitis update: Progress and perspectives.World journal of gastroenterology · 2021
    Review
  12. Review
  13. Article
  14. Lymphocyte Landscape after ChronicInternational journal of molecular sciences · 2020
    Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Progress toward approval of an HCV vaccine.Canadian liver journal · 2018
    Review
  20. 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

21 authors at 4 institutions in 3 countries.

Leo SwadlingNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. leo.swadling@ndm.ox.ac.uk.
John HallidayNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. johnshalliday@gmail.com.
Christabel KellyNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. christabel_k@hotmail.com.
Anthony BrownNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. anthony.brown@ndm.ox.ac.uk.
Stefania CaponeReithera Srl (former Okairos Srl), Viale Città d'Europa, 679, Rome 00144, Italy. Stefania.Capone@reithera.com.
M Azim AnsariNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. ansari.azim@gmail.com.
David BonsallNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. david.bonsall@ndm.ox.ac.uk.
Rachel RichardsonNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. r.richardson@ucl.ac.uk.
Felicity HartnellNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. felicity.hartnell@worc.ox.ac.uk.
Jane CollierOxford NIHR BRC, and Translational Gastroenterology Unit, Oxford OX3 9DU, UK. jane.collier@msd.ox.ac.uk.
Virginia AmmendolaReithera Srl (former Okairos Srl), Viale Città d'Europa, 679, Rome 00144, Italy. Virginia.Ammendola@reithera.com.
Mariarosaria Del SorboReithera Srl (former Okairos Srl), Viale Città d'Europa, 679, Rome 00144, Italy. Virginia.Ammendola@reithera.com.
Annette Von DelftNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. annette.vondelft@chch.ox.ac.uk.
Cinzia TraboniReithera Srl (former Okairos Srl), Viale Città d'Europa, 679, Rome 00144, Italy. Cinzia.Traboni@reithera.com.
Adrian V S HillNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. adrian.hill@ndm.ox.ac.uk.
Stefano CollocaReithera Srl (former Okairos Srl), Viale Città d'Europa, 679, Rome 00144, Italy. Stefano.Colloca@reithera.com.
Alfredo NicosiaReithera Srl (former Okairos Srl), Viale Città d'Europa, 679, Rome 00144, Italy. alfredo.nicosia@reithera.com.
Riccardo CorteseKeires AG, Bäumleingasse 18, Basel CH 4051, Switzerland. Riccardo.Cortese@reithera.com.
Paul KlenermanNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. paul.klenerman@ndm.ox.ac.uk.
Antonella FolgoriReithera Srl (former Okairos Srl), Viale Città d'Europa, 679, Rome 00144, Italy. Antonella.Folgori@reithera.com.
Eleanor BarnesNuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK. ellie.barnes@ndm.ox.ac.uk.
University of Oxford · GBCeinge Biotecnologie Avanzate (Italy) · ITOxford BioMedica (United Kingdom) · GBThe Royal Melbourne Hospital · AU

Funding

Virology CoreU19AI082630 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG, GEORG Michael LAUER · 2009 to 2026
$48.1M
Medical Research Council G0701694Medical Research Council MR/K010239/1NIAID NIH HHS U19 AI082630Wellcome Trust 091663Wellcome Trust 109965/Z/15/Z
6 · The paper itself

Abstract

An effective therapeutic vaccine for the treatment of chronic hepatitis C virus (HCV) infection, as an adjunct to newly developed directly-acting antivirals (DAA), or for the prevention of reinfection, would significantly reduce the global burden of disease associated with chronic HCV infection. A recombinant chimpanzee adenoviral (ChAd3) vector and a modified vaccinia Ankara (MVA), encoding the non-structural proteins of HCV (NSmut), used in a heterologous prime/boost regimen induced multi-specific, high-magnitude, durable HCV-specific CD4+ and CD8+ T-cell responses in healthy volunteers, and was more immunogenic than a heterologous Ad regimen. We now assess the immunogenicity of this vaccine regimen in HCV infected patients (including patients with a low viral load suppressed with interferon/ribavirin therapy), determine T-cell cross-reactivity to endogenous virus, and compare immunogenicity with that observed previously in both healthy volunteers and in HCV infected patients vaccinated with the heterologous Ad regimen. Vaccination of HCV infected patients with ChAd3-NSmut/MVA-NSmut was well tolerated. Vaccine-induced HCV-specific T-cell responses were detected in 8/12 patients; however, CD4+ T-cell responses were rarely detected, and the overall magnitude of HCV-specific T-cell responses was markedly reduced when compared to vaccinated healthy volunteers. Furthermore, HCV-specific cells had a distinct partially-functional phenotype (lower expression of activation markers, granzyme B, and TNFα production, weaker in vitro proliferation, and higher Tim3 expression, with comparable Tbet and Eomes expression) compared to healthy volunteers. Robust anti-vector T-cells and antibodies were induced, showing that there is no global defect in immunity. The level of viremia at the time of vaccination did not correlate with the magnitude of the vaccine-induced T-cell response. Full-length, next-generation sequencing of the circulating virus demonstrated that T-cells were only induced by vaccination when there was a sequence mismatch between the autologous virus and the vaccine immunogen. However, these T-cells were not cross-reactive with the endogenous viral variant epitopes. Conversely, when there was complete homology between the immunogen and circulating virus at a given epitope T-cells were not induced. T-cell induction following vaccination had no significant impact on HCV viral load. In vitro T-cell culture experiments identified the presence of T-cells at baseline that could be expanded by vaccination; thus, HCV-specific T-cells may have been expanded from pre-existing low-level memory T-cell populations that had been exposed to HCV antigens during natural infection, explaining the partial T-cell dysfunction. In conclusion, vaccination with ChAd3-NSmut and MVA-NSmut prime/boost, a potent vaccine regimen previously optimized in healthy volunteers was unable to reconstitute HCV-specific T-cell immunity in HCV infected patients. This highlights the major challenge of overcoming T-cell exhaustion in the context of persistent antigen exposure.

Indexed as

adenovirusexhaustionHCVimmunotherapymodified vaccinia AnkaraT-cellstherapeutic vaccination

Identifiers

PMID27490575
PMCPMC5041021
OpenAlexW2499392493

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.