Evidence map›Paper›PMID 21246583›Full record

ArticleHepatology (Baltimore, Md.)2011

Effect of immune pressure on hepatitis C virus evolution: insights from a single-source outbreak.

Shahzma Merani, Danijela Petrovic, Ian James, Abha Chopra, Don Cooper, Elizabeth Freitas, Andri Rauch, Julia di Iulio, Mina John, Michaela Lucas and 6 more

Abstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Frontiers in microbiology · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. CD8Frontiers in immunology · 2022
    Article
  10. Review
  11. Adaptive Immune Response against Hepatitis C Virus.International journal of molecular sciences · 2020
    Review
  12. Article
  13. Article
  14. Differential escape of HCV from CD8Journal of viral hepatitis · 2019
    Article
  15. Evidence of CD4Scientific reports · 2018
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Viral hepatitis: HCV compartmentalization in HCC: driver, passenger or both?Nature reviews. Gastroenterology & hepatology · 2016
    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

16 authors.

Shahzma MeraniCentre for Forensic Science, University of Western Australia, Western Australia, Australia.
Danijela Petrovic
Ian James
Abha Chopra
Don Cooper
Elizabeth Freitas
Andri Rauch
Julia di Iulio
Mina John
Michaela Lucas
Karen Fitzmaurice
Susan McKiernan
Suzanne Norris
Dermot Kelleher
Paul Klenerman
Silvana Gaudieri

Funding

Virology CoreU19AI082630 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG, GEORG Michael LAUER · 2009 to 2026
$48.1M
NIAID NIH HHS 1U19AI082630-01NIAID NIH HHS U19 AI082630Wellcome Trust 091663
6 · The paper itself

Abstract

unlabelledThe host's immune response to hepatitis C virus (HCV) can result in the selection of characteristic mutations (adaptations) that enable the virus to escape this response. The ability of the virus to mutate at these sites is dependent on the incoming virus, the fitness cost incurred by the mutation, and the benefit to the virus in escaping the response. Studies examining viral adaptation in chronic HCV infection have shown that these characteristic immune escape mutations can be observed at the population level as human leukocyte antigen (HLA)-specific viral polymorphisms. We examined 63 individuals with chronic HCV infection who were infected from a single HCV genotype 1b source. Our aim was to determine the extent to which the host's immune pressure affects HCV diversity and the ways in which the sequence of the incoming virus, including preexisting escape mutations, can influence subsequent mutations in recipients and infection outcomes.

conclusionHCV sequences from these individuals revealed 29 significant associations between specific HLA types within the new hosts and variations within their viruses, which likely represent new viral adaptations. These associations did not overlap with previously reported adaptations for genotypes 1a and 3a and possibly reflected a combination of constraint due to the incoming virus and genetic distance between the strains. However, these sites accounted for only a portion of the sites in which viral diversity was observed in the new hosts. Furthermore, preexisting viral adaptations in the incoming (source) virus likely influenced the outcomes in the new hosts.

Indexed as

Disease OutbreaksAdaptation, PhysiologicalEpitopesFemaleHepacivirusHepatitis C, ChronicHumansMolecular Sequence DataMutationPolymorphism, Single NucleotideRetrospective StudiesEpitopes

Identifiers

PMID21246583
PMCPMC3044208

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.