Evidence map›Paper›PMID 31947966›Full record

ArticleCancers2020

In the Absence of a TCR Signal IL-2/IL-12/18-Stimulated γδ T Cells Demonstrate Potent Anti-Tumoral Function Through Direct Killing and Senescence Induction in Cancer Cells.

Karin Schilbach, Christian Welker, Naomi Krickeberg, Carlotta Kaißer, Sabine Schleicher, Hisayoshi Hashimoto

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  9. Article
  10. IL-23 Promotes γδT Cell Activity in Dry Eye Disease Progression.Investigative ophthalmology & visual science · 2025
    Article
  11. Article
  12. Article
  13. Controversial role of γδ T cells in colorectal cancer.American journal of cancer research · 2024
    Review
  14. Article
  15. Review
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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 1 institution in 1 country.

Karin SchilbachDepartment of Pediatric Hematology and Oncology, University Children's Hospital Tuebingen, Hoppe-Seyler Street 1, 72076 Tübingen, Germany.ORCID 0000-0001-8041-055X
Christian WelkerDepartment of Pediatric Hematology and Oncology, University Children's Hospital Tuebingen, Hoppe-Seyler Street 1, 72076 Tübingen, Germany.
Naomi KrickebergDepartment of Pediatric Hematology and Oncology, University Children's Hospital Tuebingen, Hoppe-Seyler Street 1, 72076 Tübingen, Germany.
Carlotta KaißerDepartment of Pediatric Hematology and Oncology, University Children's Hospital Tuebingen, Hoppe-Seyler Street 1, 72076 Tübingen, Germany.
Sabine SchleicherDepartment of Pediatric Hematology and Oncology, University Children's Hospital Tuebingen, Hoppe-Seyler Street 1, 72076 Tübingen, Germany.
Hisayoshi HashimotoDepartment of Pediatric Hematology and Oncology, University Children's Hospital Tuebingen, Hoppe-Seyler Street 1, 72076 Tübingen, Germany.
University Children's Hospital Tübingen · DE

Funding

Jürgen Manchot Foundation CWJürgen Manchot Foundation KSStefan Morsch Foundation HH
6 · The paper itself

Abstract

Abundant IFN-γ secretion, potent cytotoxicity, and major histocompatibility complex-independent targeting of a large spectrum of tumors make γδ T cells attractive candidates for cancer immunotherapy. Upon tumor recognition through the T-cell receptor (TCR), NK-receptors, or NKG2D, γδ T cells generate the pro-inflammatory cytokines TNF-α and IFN-γ, or granzymes and perforin that mediate cellular apoptosis. Despite these favorable potentials, most clinical trials testing the adoptive transfer of pharmacologically TCR-targeted and expanded γδ T cells resulted in a limited response. Recently, the TCR-independent activation of γδ T cells was identified. However, the modulation of γδ T cell's effector functions solely by cytokines remains to be elucidated. In the present study, we systematically analyzed the impact of IL-2, IL-12, and IL-18 in parallel with TCR stimulation on proliferation, cytokine production, and anti-tumor activity of γδ T cells. Our results demonstrate that IL-12 and IL-18, when combined, constitute the most potent stimulus to enhance anti-tumor activity and induce proliferation and IFN-γ production by γδ T cells in the absence of TCR signaling. Intriguingly, stimulation with IL-12 and IL-18 without TCR stimulus induces a comparable degree of anti-tumor activity in γδ T cells to TCR crosslinking by killing tumor cells and driving cancer cells into senescence. These findings approve the use of IL-12/IL-18-stimulated γδ T cells for adoptive cell therapy to boost anti-tumor activity by γδ T cells.

Indexed as

IL-12IL-18senescenceTCR bypass stimulationγδ T cells

Identifiers

PMID31947966
PMCPMC7017313
OpenAlexW2998727329

What OpenQuestion holds

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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.