Evidence map›Paper›PMID 35879361›Full record

ArticleNature biotechnology2023

Uncovering the mode of action of engineered T cells in patient cancer organoids.

Johanna F Dekkers, Maria Alieva, Astrid Cleven, Farid Keramati, Amber K L Wezenaar, Esmée J van Vliet, Jens Puschhof, Peter Brazda, Inez Johanna, Angelo D Meringa and 28 more

Open access · hybridAbstract read
In one paragraph

Article in Nature biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 1 pooled it
19.0field-weighted citation impact, top 1% 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

125 citing papers in PubMed, 1 synthesis or guideline pooled it, 202 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Leveraging Microphysiological Systems to Facilitate Neutrophil-Based Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Organoid technology in cancer research.Molecular biomedicine · 2026
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Tumor-targeted IL2 promotes specific CD8Journal of experimental & clinical cancer research : CR · 2026
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

38 authors at 6 institutions in 3 countries.

Johanna F Dekkers *Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.
Maria Alieva *Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Astrid ClevenCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Farid KeramatiPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Amber K L WezenaarPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Esmée J van VlietPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-9301-1598
Jens PuschhofHubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.
Peter BrazdaPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-0215-1692
Inez JohannaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Angelo D MeringaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Heggert G RebelPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Maj-Britt BuchholzPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Mario Barrera RománPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-5919-2962
Amber L ZeemanPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Sam de BlankPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0003-2191-5675
Domenico FasciCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Maarten H GeurtsHubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.
Annelisa M CornelPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Else DriehuisHubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.
Rosemary MillenHubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.
Trudy StraetemansCenter 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.
Tineke Aarts-RiemensCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Hendrikus C R AriesePrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-1796-1292
Hannah R JohnsonPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Ravian L van IneveldPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Froso KaraiskakiCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Oded KopperHubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.
Yotam E Bar-EphraimHubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.
Kai KretzschmarHubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-4745-6684
Alexander M M EggermontPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Stefan NierkensPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Ellen J WehrensPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Henk G StunnenbergPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-0066-1576
Hans CleversHubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-3077-5582
Jürgen KuballCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-3914-7806
Zsolt SebestyenCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0001-6184-7676
Anne C RiosPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands. a.c.rios@prinsesmaximacentrum.nl.ORCID http://orcid.org/0000-0002-9082-8068
Oncode Institute · NLUtrecht University · NLRoyal Netherlands Academy of Arts and Sciences · NLPrincess Máxima Center · NLRoche (Switzerland) · CHUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extending the success of cellular immunotherapies against blood cancers to the realm of solid tumors will require improved in vitro models that reveal therapeutic modes of action at the molecular level. Here we describe a system, called BEHAV3D, developed to study the dynamic interactions of immune cells and patient cancer organoids by means of imaging and transcriptomics. We apply BEHAV3D to live-track >150,000 engineered T cells cultured with patient-derived, solid-tumor organoids, identifying a 'super engager' behavioral cluster comprising T cells with potent serial killing capacity. Among other T cell concepts we also study cancer metabolome-sensing engineered T cells (TEGs) and detect behavior-specific gene signatures that include a group of 27 genes with no previously described T cell function that are expressed by super engager killer TEGs. We further show that type I interferon can prime resistant organoids for TEG-mediated killing. BEHAV3D is a promising tool for the characterization of behavioral-phenotypic heterogeneity of cellular immunotherapies and may support the optimization of personalized solid-tumor-targeting cell therapies.

Indexed as

NeoplasmsT-LymphocytesHumansImmunotherapyOrganoids

Identifiers

PMID35879361
PMCPMC9849137
OpenAlexW4287510231

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.