Evidence map›Paper›PMID 24907384›Full record

ArticleThe Journal of infectious diseases2014

Interferon γ-induced protein 10 kinetics in treatment-naive versus treatment-experienced patients receiving interferon-free therapy for hepatitis C virus infection: implications for the innate immune response.

Jennifer C Lin, François Habersetzer, Maribel Rodriguez-Torres, Nezam Afdhal, Eric J Lawitz, Matthew S Paulson, Yanni Zhu, Gangadharan Mani Subramanian, John G McHutchison, Mark Sulkowski and 2 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Trial
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  4. Trial
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Editorial Commentary: Another Call to Cure Hepatitis B.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2015
    Article
  12. Article
  13. Modelling hepatitis C therapy--predicting effects of treatment.Nature reviews. Gastroenterology & hepatology · 2015
    Review
  14. 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

12 authors.

Jennifer C LinUniversity of California-San Diego, La Jolla.
François HabersetzerPôle Hépato-digestif, Hôpitaux Universitaires de Strasbourg Inserm 1110 Université de Strasbourg, Strasbourg, France.
Maribel Rodriguez-TorresFundacion de Investigacion de Diego, San Juan, Puerto Rico.
Nezam AfdhalBeth Israel Deaconess Medical Center, Boston, Massachusetts.
Eric J LawitzAlamo Medical Research, San Antonio, Texas.
Matthew S PaulsonGilead Sciences, Foster City, California.
Yanni ZhuGilead Sciences, Foster City, California.
Gangadharan Mani SubramanianGilead Sciences, Foster City, California.
John G McHutchisonGilead Sciences, Foster City, California.
Mark SulkowskiJohns Hopkins University School of Medicine, Baltimore, Maryland.
David L WylesUniversity of California-San Diego, La Jolla.
Robert T SchooleyUniversity of California-San Diego, La Jolla.

Funding

RESEARCH IN INFECTIOUS DISEASEST32AI007036 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NIZET, VICTOR · 1985 to 2025
$9.2M
NIAID NIH HHS 2T32AI007036NIAID NIH HHS T32 AI007036PHS HHS R01A1076558
6 · The paper itself

Abstract

We measured interferon γ-induced protein 10 (IP-10) levels in 428 patients at baseline, week 1, and week 2 of all-oral treatment for hepatitis C virus (HCV) infection. An increased baseline IP-10 level was associated with a T allele in the IL28B gene, an increased alanine aminotransferase level in treatment-naive but not experienced patients, and an increased body mass index. At week 1, the mean decline in plasma IP-10 levels was the same in treatment-naive and treatment-experienced patients (-49%), whereas during week 2 the mean decline in IP-10 levels in treatment-naive patients (-14%) was significantly larger than in treatment-experienced patients (-2%; P = .0176). IP-10 thus may be a surrogate marker of the rate of intracellular viral replication complex decay.

Indexed as

Immunity, InnateAdultAgedAntiviral AgentsChemokine CXCL10FemaleHepacivirusHepatitis C, ChronicHumansMaleMiddle AgedPlasmaAntiviral AgentsChemokine CXCL10CXCL10 protein, humandirect-acting antiviral therapyhepatitis Cinnate immunityIP-10

Identifiers

PMID24907384
PMCPMC4296177

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.