Evidence map›Paper›PMID 24025748›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

Sindbis viral vectors transiently deliver tumor-associated antigens to lymph nodes and elicit diversified antitumor CD8+ T-cell immunity.

Tomer Granot, Yoshihide Yamanashi, Daniel Meruelo

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

35 citing papers in PubMed, 50 citations in OpenAlex.

  1. Arboviruses in Cancer therapy: pros and cons.Journal of neurovirology · 2026
    Review
  2. Article
  3. Article
  4. VSVNature communications · 2024
    Article
  5. Article
  6. Review
  7. Review
  8. Purification Process for a Secreted Protein Produced in Insect Cells.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Alphaviruses in Cancer Therapy.Frontiers in molecular biosciences · 2022
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  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

3 authors.

Tomer GranotDepartment of Pathology, NYU School of Medicine, NYU Cancer Institute, NYU Gene Therapy Center, New York, New York, USA.
Yoshihide YamanashiDepartment of Pathology, NYU School of Medicine, NYU Cancer Institute, NYU Gene Therapy Center, New York, New York, USA.
Daniel MerueloDepartment of Pathology, NYU School of Medicine, NYU Cancer Institute, NYU Gene Therapy Center, New York, New York, USA.

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Sindbis Vectors For Advanced Pancreatic Cancer TherapyR01CA100687 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MERUELO, DANIEL · 2004 to 2008
$1.5M
NCI NIH HHS CA100687NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA100687
6 · The paper itself

Abstract

Tumors are theoretically capable of eliciting an antitumor immune response, but are often poorly immunogenic. Oncolytic viruses (OVs) have recently emerged as a promising strategy for the immunogenic delivery of tumor-associated antigens (TAAs) to cancer patients. However, safe and effective OV/TAA therapies have not yet been established. We have previously demonstrated that vectors based on Sindbis virus (SV) can inhibit tumor growth and activate the innate immune system in mice. Here, we demonstrate that SV vectors carrying a TAA generate a dramatically enhanced therapeutic effect in mice bearing subcutaneous, intraperitoneal, and lung cancers. Notably, SV/TAA efficacy was not dependent on tumor cell targeting, but was characterized by the transient expression of TAAs in lymph nodes draining the injection site. Early T-cell activation at this site was followed by a robust influx of NKG2D expressing antigen-specific cytotoxic CD8+ T cells into the tumor site, subsequently leading to the generation of long-lasting memory T cells which conferred protection against rechallenge with TAA-positive as well as TAA-negative tumor cells. By combining in vivo imaging, flow cytometry, cytotoxicity/cytokine assays, and tetramer analysis, we investigated the relationship between these events and propose a model for CD8+ T-cell activation during SV/TAA therapy.

Indexed as

AnimalsAntigens, NeoplasmCD8-Positive T-LymphocytesCricetinaeCytotoxicity, ImmunologicDisease Models, AnimalEpitopes, T-LymphocyteFemaleGene ExpressionGenes, ReporterGenetic VectorsGene Transfer TechniquesImmunologic MemoryLymph NodesLymphocyte ActivationMiceAntigens, NeoplasmEpitopes, T-Lymphocyte

Identifiers

PMID24025748
PMCPMC3978799
OpenAlexW2077364584

What OpenQuestion 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 OpenQuestion graph.