Evidence map›Paper›PMID 38580329›Full record

ArticleJournal for immunotherapy of cancer2024

Combining CRISPR-Cas9 and TCR exchange to generate a safe and efficient cord blood-derived T cell product for pediatric relapsed AML.

Vania Lo Presti, Angelo Meringa, Ester Dunnebach, Alice van Velzen, Aida Valera Moreira, Ronald W Stam, Rishi S Kotecha, Anja Krippner-Heidenreich, Olaf T Heidenreich, Maud Plantinga and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Strategic innovations: Tackling challenges of immunotherapy in acute myeloid leukemia.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
    Article
  4. 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

15 authors at 3 institutions in 4 countries.

Vania Lo PrestiPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Angelo MeringaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Ester DunnebachPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Alice van VelzenPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-8768-215X
Aida Valera MoreiraPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Ronald W StamPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Rishi S KotechaDepartment of Clinical Haematology, Oncology, Blood and Marrow Transplantation, Perth Children's Hospital, Perth, Western Australia, Australia.
Anja Krippner-HeidenreichPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Olaf T HeidenreichPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Maud PlantingaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Annelisa CornelPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Zsolt SebestyenCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Jurgen KuballCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Niek P van Til *Center for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
S Nierkens *Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands S.Nierkens-2@prinsesmaximacentrum.nl.
University Medical Center Utrecht · NLPrincess Máxima Center · NLThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHematopoietic cell transplantation (HCT) is an effective treatment for pediatric patients with high-risk, refractory, or relapsed acute myeloid leukemia (AML). However, a large proportion of transplanted patients eventually die due to relapse. To improve overall survival, we propose a combined strategy based on cord blood (CB)-HCT with the application of AML-specific T cell receptor (TCR)-engineered T cell therapy derived from the same CB graft.

methodsWe produced CB-CD8

resultsThe gene editing and transduction procedures achieved high efficiency, with up to 95% of cells lacking eTCR and over 70% of T cells expressing rWT1-TCR. WT1-TCR-engineered T cells lacking the expression of their eTCR (eTCR

conclusionsIn summary, we show the feasibility of developing a potent CB-derived CD8

Indexed as

Antineoplastic AgentsLeukemia, Myeloid, AcuteCD8-Positive T-LymphocytesCell Line, TumorChildCRISPR-Cas SystemsFetal BloodHumansReceptors, Antigen, T-CellRecurrenceAntineoplastic AgentsReceptors, Antigen, T-CellCD8-Positive T-LymphocytesCell EngineeringHematologic NeoplasmsPediatricsT cell Receptor - TCR

Identifiers

PMID38580329
PMCPMC11002379
OpenAlexW4393973986

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.