Evidence map›Paper›PMID 32235616›Full record

ReviewCells2020

Vγ9Vδ2 T Cells: Can We Re-Purpose a Potent Anti-Infection Mechanism for Cancer Therapy?

Klaus-Peter Künkele, Daniela Wesch, Hans-Heinrich Oberg, Martin Aichinger, Verena Supper, Christoph Baumann

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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  7. Article
  8. Article
  9. Review
  10. Directing the migration of serum-free,Frontiers in immunology · 2024
    Article
  11. Article
  12. BTN3A: A Promising Immune Checkpoint for Cancer Prognosis and Treatment.International journal of molecular sciences · 2022
    Review
  13. Article
  14. Article
  15. Tumor-infiltrating lymphocytes in the immunotherapy era.Cellular & molecular immunology · 2021
    Review
  16. Article
  17. Article
  18. Review
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 2 institutions in 2 countries.

Klaus-Peter KünkeleBoehringer Ingelheim RCV GmbH & Co KG, 1121 Vienna, Austria.
Daniela WeschInstitute of Immunology, University Hospital Schleswig-Holstein, Christian-Albrechts University of Kiel, 24105 Kiel, Germany.
Hans-Heinrich ObergInstitute of Immunology, University Hospital Schleswig-Holstein, Christian-Albrechts University of Kiel, 24105 Kiel, Germany.
Martin AichingerBoehringer Ingelheim RCV GmbH & Co KG, 1121 Vienna, Austria.
Verena SupperBoehringer Ingelheim RCV GmbH & Co KG, 1121 Vienna, Austria.ORCID 0000-0003-2831-600X
Christoph BaumannBoehringer Ingelheim RCV GmbH & Co KG, 1121 Vienna, Austria.
Boehringer Ingelheim (Austria) · ATChristian-Albrechts-Universität zu Kiel · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer therapies based on in vivo stimulation, or on adoptive T cell transfer of Vγ9Vδ2 T cells, have been tested in the past decades but have failed to provide consistent clinical efficacy. New, promising concepts such as γδ Chimeric Antigen Receptor (CAR) -T cells and γδ T-cell engagers are currently under preclinical evaluation. Since the impact of factors, such as the relatively low abundance of γδ T cells within tumor tissue is still under investigation, it remains to be shown whether these effector T cells can provide significant efficacy against solid tumors. Here, we highlight key learnings from the natural role of Vγ9Vδ2 T cells in the elimination of host cells bearing intracellular bacterial agents and we translate these into the setting of tumor therapy. We discuss the availability and relevance of preclinical models as well as currently available tools and knowledge from a drug development perspective. Finally, we compare advantages and disadvantages of existing therapeutic concepts and propose a role for Vγ9Vδ2 T cells in immune-oncology next to Cluster of Differentiation (CD) 3 activating therapies.

Indexed as

AnimalsCell PlasticityHumansInfectionsNeoplasmsReceptors, Antigen, T-Cell, gamma-deltaReceptors, Pattern RecognitionT-LymphocytesReceptors, Antigen, T-Cell, gamma-deltaReceptors, Pattern RecognitionBTN3Acancerdrug developmentgamma delta T cellsimmuno-oncologyinfectionphoshorylated antigensVγ9Vδ2 T cells

Identifiers

PMID32235616
PMCPMC7226769
OpenAlexW3013649389

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.