Evidence map›Paper›PMID 38012415›Full record

ArticleNature immunology2024

Dual targeting of cancer metabolome and stress antigens affects transcriptomic heterogeneity and efficacy of engineered T cells.

Patricia Hernández-López, Eline van Diest, Peter Brazda, Sabine Heijhuurs, Angelo Meringa, Lauren Hoorens van Heyningen, Caterina Riillo, Caroline Schwenzel, Marina Zintchenko, Inez Johanna and 16 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. γδ T cells and cancer.The Journal of clinical investigation · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Autologous profiling reveals inter-patient heterogeneity in Vδ2Journal for immunotherapy of cancer · 2025
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. A GD (Gamma-Delta) type of cancel culture.Immuno-oncology technology · 2024
    Review
  19. Review
  20. 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

26 authors at 6 institutions in 4 countries.

Patricia Hernández-López *Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Eline van Diest *Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Peter BrazdaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-0215-1692
Sabine HeijhuursCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Angelo MeringaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Lauren Hoorens van HeyningenCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-6025-3398
Caterina RiilloCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Caroline SchwenzelFaculty of Biology, University of Freiburg, Freiburg, Germany.
Marina ZintchenkoFaculty of Biology, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0001-9717-0732
Inez JohannaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Mara J T NicolasenCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Astrid ClevenCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Thomas A KluiverPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0003-2224-480X
Rosemary MillenOncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW), Utrecht, the Netherlands.
Jiali ZhengCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Froso KaraiskakiCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Trudy StraetemansCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Hans CleversPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-3077-5582
Remco de BreeDepartment of Head and Neck Surgical Oncology, University Medical Center Utrecht, Utrecht, the Netherlands.
Hendrik G StunnenbergPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-0066-1576
Weng Chuan PengPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0001-5467-5458
Jeanine RoodhartDepartment of Medical Oncology, University Medical Center Utrecht, Utrecht, the Netherlands.
Susana MinguetFaculty of Biology, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0001-8211-5538
Zsolt SebestyénCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Dennis X BeringerCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-5986-1134
Jürgen KuballCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands. j.h.e.kuball@umcutrecht.nl.ORCID http://orcid.org/0000-0002-3914-7806
Utrecht University · NLPrincess Máxima Center · NLUniversity of Freiburg · DEUniversity Medical Center Utrecht · NLRoche (Switzerland) · CHRoyal Netherlands Academy of Arts and Sciences · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Few cancers can be targeted efficiently by engineered T cell strategies. Here, we show that γδ T cell antigen receptor (γδ TCR)-mediated cancer metabolome targeting can be combined with targeting of cancer-associated stress antigens (such as NKG2D ligands or CD277) through the addition of chimeric co-receptors. This strategy overcomes suboptimal γ9δ2 TCR engagement of αβ T cells engineered to express a defined γδ TCR (TEGs) and improves serial killing, proliferation and persistence of TEGs. In vivo, the NKG2D-CD28

Indexed as

NeoplasmsT-LymphocytesGene Expression ProfilingHumansNK Cell Lectin-Like Receptor Subfamily KReceptors, Antigen, T-Cell, gamma-deltaNK Cell Lectin-Like Receptor Subfamily KReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID38012415
OpenAlexW4389045721

What OpenQuestion holds

Textmetadata
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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.