Evidence map›Paper›PMID 34575700›Full record

ArticleJournal of personalized medicine2021

αβ-T Cells Engineered to Express γδ-T Cell Receptors Can Kill Neuroblastoma Organoids Independent of MHC-I Expression.

Josephine G M Strijker, Ronja Pscheid, Esther Drent, Jessica J F van der Hoek, Bianca Koopmans, Kimberley Ober, Sander R van Hooff, Waleed M Kholosy, Annelisa M Cornel, Chris Coomans and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Blocking MIF secretion enhances CAR T-cell efficacy against neuroblastoma.European journal of cancer (Oxford, England : 1990) · 2025
    Article
  5. The therapeutic role of γδT cells in TNBC.Frontiers in immunology · 2024
    Review
  6. Review
  7. Review
  8. Article
  9. 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

14 authors at 3 institutions in 1 country.

Josephine G M StrijkerPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Ronja PscheidGadeta B.V., 3584 CM Utrecht, The Netherlands.ORCID 0000-0001-7184-8453
Esther DrentGadeta B.V., 3584 CM Utrecht, The Netherlands.
Jessica J F van der HoekPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Bianca KoopmansPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Kimberley OberPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Sander R van HooffPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.ORCID 0000-0002-0402-5681
Waleed M KholosyPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.ORCID 0000-0002-7910-6419
Annelisa M CornelPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.ORCID 0000-0001-8349-121X
Chris CoomansGadeta B.V., 3584 CM Utrecht, The Netherlands.
Andrea BissoGadeta B.V., 3584 CM Utrecht, The Netherlands.
Marleen M van LoenenGadeta B.V., 3584 CM Utrecht, The Netherlands.
Jan J MolenaarPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Judith WienkePrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Princess Máxima Center · NLGadeta (Netherlands) · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently ~50% of patients with a diagnosis of high-risk neuroblastoma will not survive due to relapsing or refractory disease. Recent innovations in immunotherapy for solid tumors are highly promising, but the low MHC-I expression of neuroblastoma represents a major challenge for T cell-mediated immunotherapy. Here, we propose a novel T cell-based immunotherapy approach for neuroblastoma, based on the use of TEG002, αβ-T cells engineered to express a defined γδ-T cell receptor, which can recognize and kill target cells independent of MHC-I. In a co-culture killing assay, we showed that 3 out of 6 neuroblastoma organoids could activate TEG002 as measured by IFNγ production. Transcriptional profiling showed this effect correlates with an increased activity of processes involved in interferon signaling and extracellular matrix organization. Analysis of the dynamics of organoid killing by TEG002 over time confirmed that organoids which induced TEG002 activation were efficiently killed independent of their MHC-I expression. Of note, efficacy of TEG002 treatment was superior to donor-matched untransduced αβ-T cells or endogenous γδ-T cells. Our data suggest that TEG002 may be a promising novel treatment option for a subset of neuroblastoma patients.

Indexed as

immunotherapyMHC-IneuroblastomaTEG002γδ-T cells

Identifiers

PMID34575700
PMCPMC8471928
OpenAlexW3200324116

What OpenQuestion holds

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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.