Evidence map›Paper›PMID 27920023›Full record

ArticleCancer immunology research2017

IL4 from T Follicular Helper Cells Downregulates Antitumor Immunity.

Hidekazu Shirota, Dennis M Klinman, Shuku-Ei Ito, Hiroyasu Ito, Masato Kubo, Chikashi Ishioka

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.1field-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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  8. International journal of molecular sciences · 2022
    Article
  9. The past, present, and future of immunotherapy for bladder tumors.Medical oncology (Northwood, London, England) · 2022
    Review
  10. Article
  11. Article
  12. Review
  13. Involvement of IL-4, IL-13 and Their Receptors in Pancreatic Cancer.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
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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

6 authors at 4 institutions in 2 countries.

Hidekazu ShirotaDepartment of Clinical Oncology, Tohoku University Hospital, Sendai, Japan. hidekazu.shirota.e1@tohoku.ac.jp.
Dennis M KlinmanCancer and Inflammation Program, National Cancer Institute, Frederick, Maryland.
Shuku-Ei ItoDepartment of Clinical Oncology, Tohoku University Hospital, Sendai, Japan.
Hiroyasu ItoDepartment of Informative Clinical Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Masato KuboDivision of Molecular Pathology, Research Institute for Biological Science, Tokyo University of Science, Chiba, Japan.
Chikashi IshiokaDepartment of Clinical Oncology, Tohoku University Hospital, Sendai, Japan.
Tohoku University Hospital · JPFrederick National Laboratory for Cancer Research · USGifu University · JPTokyo University of Science · JP

Funding

Mechanism of action and therapeutic utility of stimulatory CpG oligonucleotidesZIABC010852 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KLINMAN, DENNIS · 2009 to 2019
$11.3M
Mechanism of action and therapeutic utility of immunostimulatory CpG oligonucleoZ01BC010852 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KLINMAN, DENNIS · 2007 to 2008
$1.9M
Intramural NIH HHS Z01 BC010852
6 · The paper itself

Abstract

Immune cells constitute a large fraction of the tumor microenvironment and modulate tumor progression. Clinical data indicate that chronic inflammation is present at tumor sites and that IL4 in particular is upregulated. Here, we demonstrate that T follicular helper (Tfh) cells arise in tumor-draining lymph nodes where they produce an abundance of IL4. Deletion of IL4-expressing Tfh cells improves antitumor immunity, delays tumor growth, and reduces the generation of immunosuppressive myeloid cells in the lymph nodes. These findings suggest that IL4 from Tfh cells affects antitumor immunity and constitutes an attractive therapeutic target to reduce immunosuppression in the tumor microenvironment, and thus enhance the efficacy of cancer immunotherapy. Cancer Immunol Res; 5(1); 61-71. ©2016 AACR.

Indexed as

ImmunityAnimalsCytokinesDisease Models, AnimalGene ExpressionGerminal CenterInterleukin-4Lymph NodesMiceMice, KnockoutNeoplasmsT-Lymphocytes, Helper-InducerTumor MicroenvironmentCytokinesInterleukin-4

Identifiers

PMID27920023
PMCPMC6385600
OpenAlexW2560784009

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.