Evidence map›Paper›PMID 20817880›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

IRAK-M removal counteracts dendritic cell vaccine deficits in migration and longevity.

Meghan E Turnis, Xiao-Tong Song, Adham Bear, Aaron E Foster, Stephen Gottschalk, Malcolm K Brenner, Si-Yi Chen, Cliona M Rooney

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Inhibiting METTL3 in macrophages alleviates colitis by enhancing M2 polarization via upregulating IRAKM.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
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  9. Critical Role of IRAK-M in Regulating Antigen-Induced Airway Inflammation.American journal of respiratory cell and molecular biology · 2017
    Article
  10. Article
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  12. Cell Signaling Pathways That Regulate Antigen Presentation.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Review
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  20. Role of IL-1 receptor-associated kinase-M (IRAK-M) in priming of immune and inflammatory responses by nitrogen bisphosphonates.Proceedings of the National Academy of Sciences of the United States of America · 2011
    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 3 institutions in 2 countries.

Meghan E TurnisCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Xiao-Tong Song
Adham Bear
Aaron E Foster
Stephen Gottschalk
Malcolm K Brenner
Si-Yi Chen
Cliona M Rooney
Gene Therapy Laboratory · FRUniversity of Houston · USBaylor Genetics · US

Funding

Tissue ResourceP50CA126752 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Leonid S Metelitsa · 2007 to 2026
$51.4M
Training In Cell and Gene TherapyT32HL092332 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, Bruno Di Stefano · 2008 to 2026
$6.9M
Overcoming Immune Suppression to Enhance Tumor Vaccine EfficacyR01CA090427 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHEN, SI-YI · 2002 to 2013
$3.1M
Conference on Wnt and Beta Catenin SignalingR13CA094234 · NCI · KEYSTONE SYMPOSIA · PI MOON, RANDALL TODD · 2002 to 2002
$8k
NCI NIH HHS P01 CA94234-01A1NCI NIH HHS P50 CA126752NCI NIH HHS R01 CA090427NHLBI NIH HHS T32 HL092332NHLBI NIH HHS T32 HL 092332-06
6 · The paper itself

Abstract

To function optimally as vaccines, dendritic cells (DCs) must actively migrate to lymphoid organs and maintain a viable, mature state for sufficient time to effectively present their Ag to cognate T cells. Unfortunately, mature DCs rapidly lose viability and function after injection, and only a minority leaves the vaccine site and migrates to lymph nodes. We show that all of these functions can be enhanced in DCs by removal of IL-1R-associated kinase M (IRAK-M). We found that IRAK-M is induced in DCs by TLR ligation and that its absence from these cells leads to increased activation of the p38-MAPK and NF-κB pathways, which, in turn, improves DC migration to lymph nodes, increases their longevity, and augments their secretion of Th1-skewing cytokines and chemokines. These biological effects have immunological consequences. IRAK-M(-/-) DCs increase the proliferation and activation of Ag-specific T cells, and a single vaccination with Ag-pulsed, LPS-matured IRAK-M(-/-) DCs eliminates established tumors and prolongs the survival of EG7 or B16.f10 tumor-bearing mice, without discernible induction of autoimmune disease. Thus, manipulation of IRAK-M levels can increase the potency of DC vaccines by enhancing their Ag-presenting function, migration, and longevity.

Indexed as

AnimalsAntigen PresentationBlotting, WesternCancer VaccinesCell ProliferationCell SeparationCell SurvivalChemotaxis, LeukocyteDendritic CellsEnzyme-Linked Immunosorbent AssayFlow CytometryInterleukin-1 Receptor-Associated KinasesMiceMice, Inbred BALB CMice, Inbred C57BLCancer VaccinesInterleukin-1 Receptor-Associated KinasesIRAK3 protein, human

Identifiers

PMID20817880
PMCPMC3153346
OpenAlexW2147361618

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.