Evidence map›Paper›PMID 25460506›Full record

ArticleOncotarget2015

An HSV-2 based oncolytic virus can function as an attractant to guide migration of adoptively transferred T cells to tumor sites.

Xinping Fu, Armando Rivera, Lihua Tao, Xiaoliu Zhang

Abstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Review
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  5. Article
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  14. Review
  15. Prospects for combined use of oncolytic viruses and CAR T-cells.Journal for immunotherapy of cancer · 2017
    Review
  16. Article
  17. Article
  18. Review
  19. Oncolytic viruses-immunotherapeutics on the rise.Journal of molecular medicine (Berlin, Germany) · 2016
    Review
  20. Review
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

4 authors.

Xinping FuDepartment of Biology and Biochemistry and Center for Nuclear Receptors and Cell Signaling, University of Houston, Texas, USA.
Armando RiveraDepartment of Biology and Biochemistry and Center for Nuclear Receptors and Cell Signaling, University of Houston, Texas, USA.
Lihua TaoDepartment of Biology and Biochemistry and Center for Nuclear Receptors and Cell Signaling, University of Houston, Texas, USA.
Xiaoliu ZhangDepartment of Biology and Biochemistry, University of Houston, Houston, Texas, USA.

Funding

Development of an HSV-2 based oncolytic virusR01CA132792 · NCI · UNIVERSITY OF HOUSTON · PI ZHANG, SHAUN XIAOLIU · 2009 to 2013
$1.6M
NCI NIH HHS R01 CA132792NCI NIH HHS R01CA132792
6 · The paper itself

Abstract

Adoptive T-cell therapy has shown promises for cancer treatment. However, for treating solid tumors, there is a need for improving the ability of the adoptively transferred T cells to home to tumor sites. We explored the possibility of using an oncolytic virus derived from HSV-2, which can actively pull T effector cells to the site of infection, as a local attractant for migration of adoptively transferred T cells. Our data show that intratumoral administration of this virus can indeed attract active migration of the adoptively transferred T cells to the treated tumor. Moreover, once attracted to the tumor site by the virus, T cells persisted in there significantly longer than in mock-treated tumor. Chemokine profiling identified significant elevation of CXCL9 and CXCL10, as well as several other chemokines belonging to the inflammatory chemokine family in the virus-treated tumors. These chemokines initially guided the T-cell migration to and then maintained their persistence in the tumor site, leading to a significantly enhanced therapeutic effect. Our data suggests that this virotherapy may be combined with adoptive T-cell therapy to potentiate its therapeutic effect against solid tumors that are otherwise difficult to manage with the treatment alone.

Indexed as

AnimalsCell LineCell Line, TumorCell MovementChemokinesChlorocebus aethiopsCombined Modality TherapyHerpesvirus 2, HumanHumansImmunotherapy, AdoptiveInterleukin Receptor Common gamma SubunitMice, Inbred C57BLMice, Inbred NODMice, KnockoutMice, SCIDMice, TransgenicChemokinesIl2rg protein, mouseInterleukin Receptor Common gamma SubunitReceptors, Chemokine

Identifiers

PMID25460506
PMCPMC4359264

What OpenQuestion holds

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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.