Evidence map›Paper›PMID 26289050›Full record

ArticleBMC medicine2015

The role of a hepatitis C virus vaccine: modelling the benefits alongside direct-acting antiviral treatments.

Nick Scott, Emma McBryde, Peter Vickerman, Natasha K Martin, Jack Stone, Heidi Drummer, Margaret Hellard

Abstract read
In one paragraph

Article in BMC medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

  1. Article
  2. Article
  3. Controlled Human Infection Model for Hepatitis C Virus Vaccine Development: Trial Design Considerations.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  4. [Development approaches for vaccines against hepatitis C virus infections].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2022
    Review
  5. Review
  6. Review
  7. Review
  8. Ethical and Practical Issues Associated With the Possibility of Using Controlled Human Infection Trials in Developing a Hepatitis C Virus Vaccine.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Challenges and Promise of a Hepatitis C Virus Vaccine.Cold Spring Harbor perspectives in medicine · 2020
    Review
  15. Article
  16. Review
  17. Withaferin A Improves Nonalcoholic Steatohepatitis in Mice.The Journal of pharmacology and experimental therapeutics · 2019
    Article
  18. Article
  19. Article
  20. Spontaneous Clearance of Chronic HCV: The Key Ending Left in the Dark.Open access Macedonian journal of medical sciences · 2019
    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

7 authors.

Nick ScottCentre for Population Health, Burnet Institute, 85 Commercial Rd, Melbourne, VIC, 3004, Australia. nick.scott@burnet.edu.au.
Emma McBrydeCentre for Population Health, Burnet Institute, 85 Commercial Rd, Melbourne, VIC, 3004, Australia. Emma.McBryde@mh.org.au.
Peter VickermanSchool of Social and Community Medicine, University of Bristol, Bristol, UK. Peter.Vickerman@bristol.ac.uk.
Natasha K MartinSchool of Social and Community Medicine, University of Bristol, Bristol, UK. Natasha.Martin@bristol.ac.uk.
Jack StoneSchool of Social and Community Medicine, University of Bristol, Bristol, UK. Jack.Stone@bristol.ac.uk.
Heidi DrummerCentre for Biomedical Research, Burnet Institute, 85 Commercial Rd, Melbourne, VIC, 3004, Australia. hdrummer@burnet.edu.au.
Margaret HellardCentre for Population Health, Burnet Institute, 85 Commercial Rd, Melbourne, VIC, 3004, Australia. Hellard@burnet.edu.au.

Funding

Modeling Structural HIV Determinants in Substance Users and related populationsR01DA037773 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MARTIN, NATASHA, STRATHDEE, STEFFANIE A. · 2015 to 2017
$1.4M
Department of Health PDF-2011-04-049Medical Research Council G0701627NIDA NIH HHS R01 DA037773NIDA NIH HHS R01 DA037773-01A1NKM
6 · The paper itself

Abstract

backgroundHepatitis C virus (HCV) elimination is being seriously considered globally. Current elimination models require a combination of highly effective HCV treatment and harm reduction, but high treatment costs make such strategies prohibitively expensive. Vaccines should play a key role in elimination but their best use alongside treatments is unclear. For three vaccines with different efficacies we used a mathematical model to estimate the additional reduction in HCV prevalence when vaccinating after treatment; and to identify in which settings vaccines could most effectively reduce the number of treatments required to achieve fixed reductions in HCV prevalence among people who inject drugs (PWID).

methodsA deterministic model of HCV transmission among PWID was calibrated for settings with 25, 50 and 75% chronic HCV prevalence among PWID, stratified by high-risk or low-risk PWID. For vaccines with 30, 60 or 90% efficacies, different rates of treatment and vaccination were introduced. We compared prevalence reductions achieved by vaccinating after treatment to prevent reinfection and vaccinating independently of treatment history in the community; and by allocating treatments and vaccinations to specific risk groups and proportionally across risk groups.

resultsVaccinating after treatment was minimally different to vaccinating independently of treatment history, and allocating treatments and vaccinations to specific risk groups was minimally different to allocating them proportionally across risk groups. Vaccines with 30 or 60% efficacy provided greater additional prevalence reduction per vaccination in a setting with 75% chronic HCV prevalence among PWID than a 90% efficacious vaccine in settings with 25 or 50% chronic HCV prevalence among PWID.

conclusionsVaccinating after treatment is an effective and practical method of administration. In settings with high chronic HCV prevalence among PWID, even modest coverage with a low-efficacy vaccine could provide significant additional prevalence reduction beyond treatment alone, and would likely reduce the cost of achieving prevalence reduction targets.

Indexed as

Health Care CostsHepatitis C, ChronicSubstance Abuse, IntravenousVaccinationViral Hepatitis VaccinesAntiviral AgentsHepacivirusHumansModels, TheoreticalPrevalenceAntiviral AgentsViral Hepatitis Vaccines

Identifiers

PMID26289050
PMCPMC4546023

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.