Evidence map›Paper›PMID 18305577›Full record

ArticleGene therapy2008

Loading of oncolytic vesicular stomatitis virus onto antigen-specific T cells enhances the efficacy of adoptive T-cell therapy of tumors.

J Qiao, H Wang, T Kottke, R M Diaz, C Willmon, A Hudacek, J Thompson, K Parato, J Bell, J Naik and 5 more

Abstract read
In one paragraph

Article in Gene therapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Oncolytic Viruses and the Immune System: The Dynamic Duo.Molecular therapy. Methods & clinical development · 2020
    Review
  12. Review
  13. Article
  14. Oncolytic viruses: overcoming translational challenges.The Journal of clinical investigation · 2019
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

15 authors.

J QiaoMolecular Medicine Program, Mayo Clinic College of Medicine, Rochester, MN 55902, USA.
H Wang
T Kottke
R M Diaz
C Willmon
A Hudacek
J Thompson
K Parato
J Bell
J Naik
J Chester
P Selby
K Harrington
A Melcher
R G Vile

Funding

T Cell Based Carriers for In Vivo Gene Therapy of CancerR01CA107082 · NCI · MAYO CLINIC ROCHESTER · PI VILE, RICHARD G. · 2005 to 2014
$2.5M
NCI NIH HHS CA RO1107082-02NCI NIH HHS R01 CA107082
6 · The paper itself

Abstract

Although adoptive T-cell therapy has shown clinical success, efficacy is limited by low levels of T-cell trafficking to, and survival in, the immunosuppressive environment of an established tumor. Oncolytic virotherapy has recently emerged as a promising approach to induce both direct tumor cell killing and local proinflammatory environments within tumors. However, inefficient systemic delivery of oncolytic viruses remains a barrier to use of these agents against metastatic disease that is not directly accessible to the end of a needle. Here we show that the ability of antigen-specific T cells to circulate freely, and to localize to tumors, can be exploited to achieve the systemic delivery of replication-competent, oncolytic vesicular stomatitis virus (VSV). Thus, VSV loaded onto OT-I T cells, specific for the SIINFEKL epitope of the ovalbumin antigen, was efficiently delivered to established B16ova tumors in the lungs of fully immune-competent C57Bl/6 mice leading to significant increases in therapy compared to the use of virus, or T cells, alone. Although OT-I T-cell-mediated delivery of VSV led to viral replication within tumors and direct viral oncolysis, therapy was also dependent upon an intact host immune system. Moreover, VSV loading onto the T cells increased both T-cell activation in vitro and T-cell trafficking in vivo. The combination of adoptive T-cell transfer of antigen-specific T cells, along with oncolytic virotherapy, can, therefore, increase the therapeutic utility of both approaches through multiple mechanisms and should be of direct translational value.

Indexed as

Adoptive TransferAnimalsAntigens, NeoplasmCell MovementCombined Modality TherapyGenetic TherapyLung NeoplasmsLymphocyte ActivationLymphocytes, Tumor-InfiltratingMelanoma, ExperimentalMiceMice, Inbred C57BLMice, NudeNeoplasm MetastasisNeoplasmsNeoplasm TransplantationAntigens, Neoplasm

Identifiers

PMID18305577
PMCPMC3046771

What OpenQuestion holds

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Registered trials

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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.