Evidence map›Paper›PMID 29619416›Full record

ArticleHepatology communications2018

Early and late changes in natural killer cells in response to ledipasvir/sofosbuvir treatment.

Lucy Golden-Mason, Rachel H McMahan, Michael S Kriss, Alexandra L Kilgore, Linling Cheng, Rachael J Dran, Amanda Wieland, Hugo R Rosen

Open access · goldAbstract read
In one paragraph

Article in Hepatology communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Chronic HCV infection promotes cytotoxicity in antigen-specific CD8Frontiers in virology (Lausanne, Switzerland) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Control of HCV Infection by Natural Killer Cells and Macrophages.Cold Spring Harbor perspectives in medicine · 2020
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. 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

8 authors at 2 institutions in 1 country.

Lucy Golden-MasonDivision of Gastroenterology and Hepatology University of Colorado Denver Aurora CO.
Rachel H McMahanDivision of Gastroenterology and Hepatology University of Colorado Denver Aurora CO.
Michael S KrissDivision of Gastroenterology and Hepatology University of Colorado Denver Aurora CO.
Alexandra L KilgoreDepartment of Pediatrics, School of Medicine University of Colorado Denver Aurora CO.
Linling ChengDivision of Gastroenterology and Hepatology University of Colorado Denver Aurora CO.
Rachael J DranDivision of Gastroenterology and Hepatology University of Colorado Denver Aurora CO.
Amanda WielandDivision of Gastroenterology and Hepatology University of Colorado Denver Aurora CO.
Hugo R RosenDivision of Gastroenterology and Hepatology University of Colorado Denver Aurora CO.
University of Colorado Denver · USDenver VA Medical Center · US

Funding

Institutional Training Grant in Pediatric GastroenterologyT32DK067009 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI RONALD J. SOKOL, Edwin Fulco de Zoeten · 2005 to 2026
$7.1M
Mechanisms of hepatic innate immune activation by HCVR01AI127463 · NIAID · UNIVERSITY OF WASHINGTON · PI GALE, MICHAEL, ROSEN, HUGO RAMON · 2017 to 2021
$2.8M
Human Group 2 Innate Lympohocyte Cell (ILC2) populations contribute to Hepatic FibrosisR01DK106491 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI GOLDEN, LUCY MARY · 2015 to 2019
$1.8M
RESUBMISSION -R01 AI120622 –Restoration of Immunity and Function with DAA Treatment in HCV infectionR01AI120622 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ROSEN, HUGO RAMON · 2017 to 2020
$1.6M
NIAID NIH HHS R01 AI120622NIAID NIH HHS R01 AI127463NIDDK NIH HHS R01 DK106491NIDDK NIH HHS T32 DK067009
6 · The paper itself

Abstract

Chronic hepatitis C virus (HCV) infection is characterized by dysregulated natural killer (NK) cell responses. NKs play a critical role in achieving sustained responses to interferon (IFN)-α-based therapy. Rapid sustained HCV-RNA clearance is now achieved with direct-acting antivirals (DAAs). Studies of patients receiving first-wave DAAs suggest NK functional restoration. Here, we investigate the effect of mainstream DAA treatment on NKs. We collected a prospective cohort of male HCV genotype 1-infected patients treated with ledipasvir/sofosbuvir (n = 22). Peripheral blood was obtained at treatment start, week 2 (W2), W4, W8, and W12 of treatment and 12 weeks posttreatment. Flow cytometry was used to characterize NK responses to therapy. Mean baseline viral load was 1.75 million IU/mL. All subjects rapidly cleared virus and remained HCV RNA-negative posttreatment. No change was seen in total NK levels; however, the frequency of immature NKs (clusters of differentiation [CD]56

Identifiers

PMID29619416
PMCPMC5880201
OpenAlexW2789888893

What OpenQuestion holds

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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.