Evidence map›Paper›PMID 27119100›Full record

ArticleMolecular therapy oncolytics2015

Oncolytic HSV virotherapy in murine sarcomas differentially triggers an antitumor T-cell response in the absence of virus permissivity.

Jennifer L Leddon, Chun-Yu Chen, Mark A Currier, Pin-Yi Wang, Francesca A Jung, Nicholas L Denton, Kevin M Cripe, Kellie B Haworth, Michael A Arnold, Amy C Gross and 7 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

34 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
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  4. VSVNature communications · 2024
    Article
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  11. Immune Activity and Response Differences of Oncolytic Viral Therapy in Recurrent Glioblastoma: Gene Expression Analyses of a Phase IB Study.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
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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

17 authors at 4 institutions in 1 country.

Jennifer L LeddonCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA; Medical Scientist Training Program, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA; Immunobiology Graduate Training Program, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.
Chun-Yu ChenCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University , Columbus, Ohio, USA.
Mark A CurrierCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University , Columbus, Ohio, USA.
Pin-Yi WangCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University , Columbus, Ohio, USA.
Francesca A JungCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University , Columbus, Ohio, USA.
Nicholas L DentonCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University , Columbus, Ohio, USA.
Kevin M CripeCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University , Columbus, Ohio, USA.
Kellie B HaworthCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA; Division of Hematology/Oncology/Blood and Marrow Transplantation, Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA.
Michael A ArnoldDepartment of Pathology and Laboratory Medicine, Nationwide Children's Hospital, The Ohio State University , Columbus, Ohio, USA.
Amy C GrossDivision of Pulmonary, Allergy, Critical Care & Sleep Medicine, The Ohio State University , Columbus, Ohio, USA.
Timothy D EubankDivision of Pulmonary, Allergy, Critical Care & Sleep Medicine, The Ohio State University , Columbus, Ohio, USA.
William F GoinsDepartment of Microbiology and Molecular Genetics, University of Pittsburgh, School of Medicine , Pittsburgh, Pennsylvania, USA.
Joseph C GloriosoDepartment of Microbiology and Molecular Genetics, University of Pittsburgh, School of Medicine , Pittsburgh, Pennsylvania, USA.
Justus B CohenDepartment of Microbiology and Molecular Genetics, University of Pittsburgh, School of Medicine , Pittsburgh, Pennsylvania, USA.
Paola GrandiDepartment of Microbiology and Molecular Genetics, University of Pittsburgh, School of Medicine , Pittsburgh, Pennsylvania, USA.
David A HildemanDivision of Cellular and Molecular Immunology, Cincinnati Children's Hospital Medical Center, University of Cincinnati , Cincinnati, Ohio, USA.
Timothy P CripeCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA; Division of Hematology/Oncology/Blood and Marrow Transplantation, Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA.
Nationwide Children's Hospital · USThe Ohio State University · USUniversity of Pittsburgh · USCincinnati Children's Hospital Medical Center · US

Funding

The Tumor Microenvironmental Barrier to Effective Viral OncolysisP01CA163205 · NCI · OHIO STATE UNIVERSITY · PI MICHAEL A CALIGIURI · 2013 to 2026
$26.0M
NCI NIH HHS P01 CA163205
6 · The paper itself

Abstract

Multiple studies have indicated that in addition to direct oncolysis, virotherapy promotes an antitumor cytotoxic T cell response important for efficacy. To study this phenomenon further, we tested three syngeneic murine sarcoma models that displayed varied degrees of permissiveness to oncolytic herpes simplex virus replication and cytotoxicity in vitro, with the most permissive being comparable to some human sarcoma tumor lines. The in vivo antitumor effect ranged from no or modest response to complete tumor regression and protection from tumor rechallenge. The in vitro permissiveness to viral oncolysis was not predictive of the in vivo antitumor effect, as all three tumors showed intact interferon signaling and minimal permissiveness to virus in vivo. Tumor shrinkage was T-cell mediated with a tumor-specific antigen response required for maximal antitumor activity. Further analysis of the innate and adaptive immune microenvironment revealed potential correlates of susceptibility and resistance, including favorable and unfavorable cytokine profiles, differential composition of intratumoral myeloid cells, and baseline differences in tumor cell immunogenicity and tumor-infiltrating T-cell subsets. It is likely that a more complete understanding of the interplay between the immunologic immune microenvironment and virus infection will be necessary to fully leverage the antitumor effects of this therapeutic platform.

Identifiers

PMID27119100
PMCPMC4782947
OpenAlexW2324106738

What OpenQuestion holds

Textmetadata
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.