Evidence map›Paper›PMID 25469725›Full record

Trial reportClinical and experimental immunology2015

Controlled infection with a therapeutic virus defines the activation kinetics of human natural killer cells in vivo.

Y M El-Sherbiny, T D Holmes, L F Wetherill, E V I Black, E B Wilson, S L Phillips, G B Scott, R A Adair, R Dave, K J Scott and 5 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Clinical and experimental immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

24 citing papers in PubMed, 43 citations in OpenAlex.

  1. Oncolytic viruses: advanced strategies in cancer therapy.Signal transduction and targeted therapy · 2026
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  18. Pembrolizumab in Combination with the Oncolytic Virus Pelareorep and Chemotherapy in Patients with Advanced Pancreatic Adenocarcinoma: A Phase Ib Study.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
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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

15 authors at 4 institutions in 4 countries.

Y M El-SherbinyLeeds Institute of Cancer and Pathology, University of Leeds School of Medicine, St James's University Hospital, Leeds, UK; Affiliated with the Clinical Pathology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
T D Holmes
L F Wetherill
E V I Black
E B Wilson
S L Phillips
G B Scott
R A Adair
R Dave
K J Scott
R S M Morgan
M Coffey
G J Toogood
A A Melcher
G P Cook
University of Leeds · GBSt James's University Hospital · GBNIHR Leeds Musculoskeletal Biomedical Research Unit · GBOncolytics Biotech (Canada) · CA

Funding

Cancer Research UK
6 · The paper itself

Abstract

Human natural killer (NK) cells play an important role in anti-viral immunity. However, studying their activation kinetics during infection is highly problematic. A clinical trial of a therapeutic virus provided an opportunity to study human NK cell activation in vivo in a controlled manner. Ten colorectal cancer patients with liver metastases received between one and five doses of oncolytic reovirus prior to surgical resection of their tumour. NK cell surface expression of the interferon-inducible molecules CD69 and tetherin peaked 24-48 h post-infection, coincident with a peak of interferon-induced gene expression. The interferon response and NK cell activation were transient, declining by 96 h post-infection. Furthermore, neither NK cell activation nor the interferon response were sustained in patients undergoing multiple rounds of virus treatment. These results show that reovirus modulates human NK cell activity in vivo and suggest that this may contribute to any therapeutic effect of this oncolytic virus. Detection of a single, transient peak of activation, despite multiple treatment rounds, has implications for the design of reovirus-based therapy. Furthermore, our results suggest the existence of a post-infection refractory period when the interferon response and NK cell activation are blunted. This refractory period has been observed previously in animal models and may underlie the enhanced susceptibility to secondary infections that is seen following viral infection.

Indexed as

Immunity, CellularNeoplasmsOncolytic VirotherapyAgedAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensFemaleHumansInterferonsKiller Cells, NaturalLectins, C-TypeMaleMiddle AgedOncolytic VirusesReoviridaeAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensInterferonsLectins, C-Typehuman infectioninnate immunityinterferon responsenatural killer cellsviral infection

Identifiers

PMID25469725
PMCPMC4367098
OpenAlexW2106443586

What Socratic 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 Socratic graph.