Evidence map›Paper›PMID 23248259›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Vaccine injection site matters: qualitative and quantitative defects in CD8 T cells primed as a function of proximity to the tumor in a murine glioma model.

John R Ohlfest, Brian M Andersen, Adam J Litterman, Junzhe Xia, Christopher A Pennell, Lauryn E Swier, Andres M Salazar, Michael R Olin

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
2.8field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 2 syntheses or guidelines pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. The recent advances in vaccine adjuvants.Frontiers in immunology · 2025
    Review
  6. Progress towards Adjuvant Development: Focus on Antiviral Therapy.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. IFN-γ- and IL-17-producing CD8Journal for immunotherapy of cancer · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Exploration of Pattern Recognition Receptor Agonists as Candidate Adjuvants.Frontiers in cellular and infection microbiology · 2021
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  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

8 authors at 2 institutions in 1 country.

John R OhlfestDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Brian M Andersen
Adam J Litterman
Junzhe Xia
Christopher A Pennell
Lauryn E Swier
Andres M Salazar
Michael R Olin
University of Minnesota · USOncovir (United States) · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008244 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SHIMIZU, YOJI · 1988 to 2024
$13.6M
TRAINING GRANT IN MICROBIOLOGY/CANCER RESEARCHT32CA009138 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Scott M. Dehm · 1985 to 2026
$11.3M
Oxygen as a master immunologic switchR01CA154345 · NCI · UNIVERSITY OF MINNESOTA · PI PENNELL, CHRISTOPHER A · 2011 to 2015
$1.5M
Discovery and Validation of Tumor Immunoevasion MechanismsR01CA160782 · NCI · UNIVERSITY OF MINNESOTA · PI LARGAESPADA, DAVID ANDREW · 2011 to 2014
$963k
NCI NIH HHS L30 CA142371NCI NIH HHS R01 CA154345NCI NIH HHS R01 CA160782NCI NIH HHS T32 CA009138NIGMS NIH HHS T32 GM008244
6 · The paper itself

Abstract

Malignant gliomas are lethal brain tumors for which novel therapies are urgently needed. In animal models, vaccination with tumor-associated Ags efficiently primes T cells to clear gliomas. In clinical trials, cancer vaccines have been less effective at priming T cells and extending survival. Generalized immune suppression in the tumor draining lymph nodes has been documented in multiple cancers. However, a systematic analysis of how vaccination at various distances from the tumor (closest to farthest) has not been reported. We investigated how the injection site chosen for vaccination dictates CD8 T cell priming and survival in an OVA-transfected murine glioma model. Glioma-bearing mice were vaccinated with Poly:ICLC plus OVA protein in the neck, hind leg, or foreleg for drainage into the cervical, inguinal, or axillary lymph nodes, respectively. OVA-specific CD8 T cell number, TCR affinity, effector function, and infiltration into the brain decreased as the vaccination site approached the tumor. These effects were dependent on the presence of the tumor, because injection site did not appreciably affect CD8 T cell priming in tumor-free mice. Our data suggest the site of vaccination can greatly impact the effectiveness of cancer vaccines. Considering that previous and ongoing clinical trials have used a variety of injection sites, vaccination site is potentially a critical aspect of study design that is being overlooked.

Indexed as

AnimalsBrain NeoplasmsCancer VaccinesCD8-Positive T-LymphocytesDisease Models, AnimalFemaleGliomaMiceReceptors, Antigen, T-CellCancer VaccinesReceptors, Antigen, T-Cell

Identifiers

PMID23248259
PMCPMC3538956
OpenAlexW2131861973

What OpenQuestion holds

Textmetadata
LicenceTDM
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.