Evidence map›Paper›PMID 39426662›Full record

ReviewCancer letters2024

Functional diversity and regulation of IL-9-producing T cells in cancer immunotherapy.

Muhammad Kalim, Rui Jing, Wei Guo, Hui Xing, Yong Lu

Abstract readReview
In one paragraph

Review in Cancer letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. 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

5 authors.

Muhammad KalimHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX, 77030, USA.
Rui JingHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX, 77030, USA.
Wei GuoHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX, 77030, USA.
Hui XingHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX, 77030, USA.
Yong LuHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX, 77030, USA. Electronic address: ylu2@houstonmethodist.org.

Funding

Induction of autosis to overcome resistance in adoptive cell therapy for solid tumorsR01CA278911 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Yong Lu · 2023 to 2026
$2.3M
The Unique Roles of Tumor-Specific Th9 Cells for Solid Tumor EradicationR01CA258477 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2021 to 2025
$1.9M
Eradication of Escaped Variant Tumor Cells for Cancer ImmunotherapyR01CA248111 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2021 to 2025
$1.9M
P38 MAPK is a molecular switch that controls the acquired resistance in adoptive cell therapyR37CA251318 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2020 to 2024
$1.8M
Decoupling acute toxicities and antitumor efficacy in adoptive cell therapyR01CA288403 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Yong Lu · 2024 to 2026
$1.8M
NCI NIH HHS R01 CA248111NCI NIH HHS R01 CA258477NCI NIH HHS R01 CA278911NCI NIH HHS R01 CA288403NCI NIH HHS R37 CA251318
6 · The paper itself

Abstract

IL-9-producing T cells (T9) regulate immunological responses that affect various cellular biological processes, though their precise function remains fully understood. Previous studies have linked T9 cells to conditions such as allergic disorders, parasitic infection clearance, and various types of cancers. While the functional heterogeneity of IL-9 and T9 cells in cancer development has been documented, these cells present promising therapeutic opportunities for treating solid tumors. This review highlights the roles of IL-9 and T9 cells in cancer progression and treatment responses, focusing on potential discrepancies in IL-9/IL-9R signaling between murine tumors and cancer patients. Additionally, we discuss the regulation of tumor-specific Th9/Tc9 cell differentiation, the therapeutic potential of these cells, and current strategies to enhance their anti-tumor activities.

Indexed as

ImmunotherapyInterleukin-9NeoplasmsAnimalsCell DifferentiationHumansMiceSignal TransductionIL9 protein, humanInterleukin-9CAR-TIL-9ImmunotherapyTc9Th9

Identifiers

PMID39426662
PMCPMC11675864

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Registered trials

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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.