Evidence map›Paper›PMID 25814029›Full record

ArticleLeukemia2015

Oncolytic reovirus enhances rituximab-mediated antibody-dependent cellular cytotoxicity against chronic lymphocytic leukaemia.

C Parrish, G B Scott, G Migneco, K J Scott, L P Steele, E Ilett, E J West, K Hall, P J Selby, D Buchanan and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. The combination therapy of oncolytic virotherapy.Frontiers in pharmacology · 2024
    Review
  7. Comprehensive Single-Cell Immune Profiling Defines the Patient Multiple Myeloma Microenvironment Following Oncolytic Virus Therapy in a Phase Ib Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
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  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Potentiating Oncolytic Virus-Induced Immune-Mediated Tumor Cell Killing Using Histone Deacetylase Inhibition.Molecular therapy : the journal of the American Society of Gene Therapy · 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

16 authors at 4 institutions in 2 countries.

C ParrishSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
G B ScottSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
G MignecoSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
K J ScottSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
L P SteeleSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
E IlettSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
E J WestSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
K HallSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
P J SelbySection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
D BuchananSt James's University Hospital, Leeds, UK.
A VargheseSt James's University Hospital, Leeds, UK.
M S CraggAntibody and Vaccine Group, Cancer Sciences Unit, Southampton University, General Hospital, Southampton, UK.
M CoffeyOncolytics Biotech Inc., Calgary, AB, Canada.
P HillmenExperimental Haematology, LICAP, University of Leeds, Leeds, UK.
A A MelcherSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
F Errington-MaisSection of Oncology and Clinical Research, Leeds Institute of Cancer and Pathology (LICAP), University of Leeds, St James's University Hospital, Leeds, UK.
St James's University Hospital · GBUniversity of Leeds · GBOncolytics Biotech (Canada) · CASouthampton General Hospital · GB

Funding

Cancer Research UK A13244Cancer Research UK L374RADepartment of Health RP-PG-0707-10101Yorkshire Cancer Research L374RA
6 · The paper itself

Abstract

The naturally occurring oncolytic virus (OV), reovirus, replicates in cancer cells causing direct cytotoxicity, and can activate innate and adaptive immune responses to facilitate tumour clearance. Reovirus is safe, well tolerated and currently in clinical testing for the treatment of multiple myeloma, in combination with dexamethasone/carfilzomib. Activation of natural killer (NK) cells has been observed after systemic delivery of reovirus to cancer patients; however, the ability of OV to potentiate NK cell-mediated antibody-dependent cellular cytotoxicity (ADCC) is unexplored. This study elucidates the potential of oncolytic reovirus for the treatment of chronic lymphocytic leukaemia (CLL), both as a direct cytotoxic agent and as an immunomodulator. We demonstrate that reovirus: (i) is directly cytotoxic against CLL, which requires replication-competent virus; (ii) phenotypically and functionally activates patient NK cells via a monocyte-derived interferon-α (IFNα)-dependent mechanism; and (iii) enhances ADCC-mediated killing of CLL in combination with anti-CD20 antibodies. Our data provide strong preclinical evidence to support the use of reovirus in combination with anti-CD20 immunotherapy for the treatment of CLL.

Indexed as

AgedAged, 80 and overAntibody-Dependent Cell CytotoxicityAntineoplastic AgentsCell Line, TumorCytopathogenic Effect, ViralFemaleHumansImmunity, InnateImmunologic FactorsImmunophenotypingImmunotherapyKiller Cells, NaturalLeukemia, Lymphocytic, Chronic, B-CellLymphocyte ActivationMaleAntineoplastic AgentsImmunologic FactorsRituximab

Identifiers

PMID25814029
PMCPMC4490165
OpenAlexW1985361166

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.