Evidence map›Paper›PMID 23354626›Full record

ArticleCancer immunology, immunotherapy : CII2013

Modulation of p38 MAPK signaling enhances dendritic cell activation of human CD4+ Th17 responses to ovarian tumor antigen.

Martin J Cannon, Hannah E Goyne, Pamela J B Stone, Laura J Macdonald, Lindsey E James, Everardo Cobos, Maurizio Chiriva-Internati

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06144632 (Safety and Effectiveness Evaluation of the THERMOCOOL SMARTTOUCH SF Catheter With the TRUPULSE Generator for Treatment of Drug Refractory Symptomatic Paroxysmal Atrial Fibrillation), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 19% 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.

NCT06144632 nacompletednot on this mapstarted 2023, after this paper: background citation

Safety and Effectiveness Evaluation of the THERMOCOOL SMARTTOUCH SF Catheter With the TRUPULSE Generator for Treatment of Drug Refractory Symptomatic Paroxysmal Atrial Fibrillation (PAF)

TypeinterventionalSponsorBiosense Webster, Inc.Ran2023 to 2025Enrolled237ConditionsDrug Refractory Paroxysmal Atrial FibrillationArmsTHERMOCOOL STSF Bi- Directional Navigation Catheter, TRUPULSE Generator
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Tumor-infiltrating CD8Drug discovery today · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. 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

7 authors at 3 institutions in 1 country.

Martin J CannonDepartment of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. CannonMartin@uams.edu
Hannah E Goyne
Pamela J B Stone
Laura J Macdonald
Lindsey E James
Everardo Cobos
Maurizio Chiriva-Internati
University of Arkansas for Medical Sciences · USTexas Tech University · USTexas Tech University Health Sciences Center · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR029884 · NCRR · UNIV OF ARKANSAS FOR MED SCIS · PI LOWERY, CURTIS L · 2009 to 2011
$11.4M
Novel target antigens for ovarian cancer immunotherapyR01CA098927 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI CANNON, MARTIN J. · 2004 to 2007
$1.0M
NCI NIH HHS R01 CA098927NCRR NIH HHS UL1 RR029884
6 · The paper itself

Abstract

The recent finding that Th17 infiltration of ovarian tumors positively predicts patient outcomes suggests that Th17 responses play a protective role in ovarian tumor immunity. This observation has led to the question of whether Th17 cells could be induced or expanded to therapeutic advantage by tumor vaccination. In this study, we show that treatment of ovarian tumor antigen-loaded, cytokine-matured human dendritic cells (DC) with a combination of IL-15 and a p38 MAP kinase inhibitor offers potent synergy in antagonism of CD4(+) Treg induction and redirection toward CD4(+) Th17 responses that correlate with strong CD8(+) cytotoxic T lymphocyte (CTL) activation. Ovarian tumor antigen-specific CD4(+) T cells secrete high levels of IL-17 and show reduced expression of CTLA-4, PD-1, and Foxp3 following activation with IL-15/p38 inhibitor-treated DC. We further show that modulation of p38 MAPK signaling in DC is associated with reduced expression of B7-H1 (PD-L1), loss of indoleamine 2,3-dioxygenase activity, and increased phosphorylation of ERK 1/2 MAPK. These observations may allow the development of innovative DC vaccination strategies to boost Th17 immunity in ovarian cancer patients.

Indexed as

Signal TransductionAntigens, NeoplasmDendritic CellsEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryHumansIndoleamine-Pyrrole 2,3,-DioxygenaseLymphocytesOvarian Neoplasmsp38 Mitogen-Activated Protein KinasesPhenotypeTh17 CellsT-Lymphocytes, CytotoxicAntigens, NeoplasmIndoleamine-Pyrrole 2,3,-Dioxygenasep38 Mitogen-Activated Protein Kinases

Identifiers

PMID23354626
PMCPMC3915291
OpenAlexW2036767300

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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.