Evidence map›Paper›PMID 23064366›Full record

ArticleThe Journal of clinical investigation2012

Th9 cells promote antitumor immune responses in vivo.

Yong Lu, Sungyoul Hong, Haiyan Li, Jungsun Park, Bangxing Hong, Lijuan Wang, Yuhuan Zheng, Zhiqiang Liu, Jingda Xu, Jin He and 3 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 204 papers.

0numbers the graph read from it
0cells of the map it votes in
204citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

204 citing papers in PubMed, 343 citations in OpenAlex.

  1. Trial
  2. FOXP1 Knockdown Reprograms Th9 CAR-T Cells to Overcome Antigen Escape.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  16. GITRL enhances cytotoxicity and persistence of CAR-T cells in cancer therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  17. Go to the scene: TJournal for immunotherapy of cancer · 2025
    Article
  18. Review
  19. Review
  20. Review

144 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Yong LuDepartment of Lymphoma and Myeloma, Division of Cancer Medicine, and Center for Cancer Immunology Research, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Sungyoul Hong
Haiyan Li
Jungsun Park
Bangxing Hong
Lijuan Wang
Yuhuan Zheng
Zhiqiang Liu
Jingda Xu
Jin He
Jing Yang
Jianfei Qian
Qing Yi
The University of Texas MD Anderson Cancer Center · USLymphoma Research Foundation · USMelanoma Institute Australia · AU

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
P4 -TARGETING MULTIPLE MYELOMA BY COMBINING CDK INHIBITORS AND BCL-2 ANTAGONISTSP50CA142509 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2010 to 2014
$11.1M
Targeting Plasmacytoid Dendritic Cells to Treat Human MyelomaR01CA163881 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2012 to 2016
$2.0M
C-reactive protein promotes myeloma cell-mediated bone destructionR01CA138398 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2010 to 2014
$1.6M
Targeting surface b2M for myeloma and bone therapyR01CA138402 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2009 to 2013
$1.3M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA142509NCI NIH HHS P50CA142509NCI NIH HHS R01 CA138398NCI NIH HHS R01CA138398NCI NIH HHS R01 CA138402NCI NIH HHS R01CA138402NCI NIH HHS R01 CA163881NCI NIH HHS R01CA163881
6 · The paper itself

Abstract

Th9 cells are a subset of CD4+ Th cells that produce the pleiotropic cytokine IL-9. IL-9/Th9 can function as both positive and negative regulators of immune response, but the role of IL-9/Th9 in tumor immunity is unknown. We examined the role of IL-9/Th9 in a model of pulmonary melanoma in mice. Lack of IL-9 enhanced tumor growth, while tumor-specific Th9 cell treatment promoted stronger antitumor responses in both prophylactic and therapeutic models. Th9 cells also elicited strong host antitumor CD8+ CTL responses by promoting Ccl20/Ccr6-dependent recruitment of DCs to the tumor tissues. Subsequent tumor antigen delivery to the draining LN resulted in CD8+ T cell priming. In agreement with this model, Ccr6 deficiency abrogated the Th9 cell-mediated antitumor response. Our data suggest a distinct role for tumor-specific Th9 cells in provoking CD8+ CTL-mediated antitumor immunity and indicate that Th9 cell-based cancer immunotherapy may be a promising therapeutic approach.

Indexed as

Immunity, CellularAnimalsAntigen PresentationCD8-Positive T-LymphocytesCell Line, TumorChemokine CCL20Dendritic CellsImmunotherapyInterleukin-9Lung NeoplasmsMelanomaMiceMice, KnockoutReceptors, CCR6T-Lymphocytes, Helper-InducerCCL20 protein, mouseCCR6 protein, mouseChemokine CCL20Interleukin-9Receptors, CCR6

Identifiers

PMID23064366
PMCPMC3484462
OpenAlexW2066906123

What OpenQuestion holds

Textmetadata
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.