Evidence map›Paper›PMID 24293627›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

CD8+ T cell-independent tumor regression induced by Fc-OX40L and therapeutic vaccination in a mouse model of glioma.

Katherine A Murphy, Jami R Erickson, Charles S Johnson, Charles E Seiler, Jessica Bedi, Peisheng Hu, G Elizabeth Pluhar, Alan L Epstein, John R Ohlfest

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. TREM2 mediates MHCII-associated CD4bioRxiv : the preprint server for biology · 2023
    Article
  3. Article
  4. Blocking antibody-mediated phosphatidylserine enhances cancer immunotherapy.Journal of cancer research and clinical oncology · 2021
    Review
  5. Review
  6. Anti-PD-1 Induces M1 Polarization in the Glioma Microenvironment and Exerts Therapeutic Efficacy in the Absence of CD8 Cytotoxic T Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. 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

9 authors at 2 institutions in 1 country.

Katherine A MurphyDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455;
Jami R Erickson
Charles S Johnson
Charles E Seiler
Jessica Bedi
Peisheng Hu
G Elizabeth Pluhar
Alan L Epstein
John R Ohlfest
University of Minnesota · USUniversity of Southern California · US

Funding

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 R01 CA154345NCI NIH HHS R01CA154345NCI NIH HHS R01 CA160782
6 · The paper itself

Abstract

Despite the growing number of preclinical and clinical trials focused on immunotherapy for the treatment of malignant gliomas, the prognosis for this disease remains grim. Although some promising advances have been made, the immune response stimulated as a result of immunotherapeutic protocols has been inefficient at complete tumor elimination, primarily due to our lack of understanding of the necessary effector functions of the immune system. We previously demonstrated that a tumor lysate vaccine/Fc-OX40L therapy is capable of inducing enhanced survival and tumor elimination in the GL261 mouse glioma model. The following experiments were performed to determine the mechanism(s) of action of this therapy that elicits a potent antitumor immune response. The evidence subsequently outlined indicates a CD8(+) T cell-independent and CD4(+) T cell-, NK cell-, and B cell-dependent means of prolonged survival. CD8(+) T cell-independent tumor clearance is surprising considering the current focus of many cancer immunotherapy protocols. These results provide evidence for CD8(+) T cell-independent means of antitumor response and should lead to additional examination of the potential manipulation of this mechanism for future treatment strategies.

Indexed as

AnimalsAntibodiesB-LymphocytesBrain NeoplasmsCancer VaccinesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDisease Models, AnimalGliomaHumansImmunotherapyKiller Cells, NaturalLymphocyte DepletionLymphocytes, Tumor-InfiltratingMiceReceptors, FcAntibodiesCancer VaccinesReceptors, FcRecombinant Proteins

Identifiers

PMID24293627
PMCPMC4068509
OpenAlexW2141013666

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.