Evidence map›Paper›PMID 27518241›Full record

ArticleBlood cancer journal2016

Switching CAR T cells on and off: a novel modular platform for retargeting of T cells to AML blasts.

M Cartellieri, A Feldmann, S Koristka, C Arndt, S Loff, A Ehninger, M von Bonin, E P Bejestani, G Ehninger, M P Bachmann

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04014881 (Single-center, Open-label, Single-arm Clinical Study of Efficacy and Safety of Anti-CD123 CAR-T Therapy in Patients With Refractory/Relapsed CD123+ Acute Myeloid Leukemia.), which is not on this map. Cited by 171 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed, 2 pooled it
10.7field-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.

NCT04014881 phase1unknown statusnot on this mapstarted 2019, after this paper: background citation

Single-center, Open-label, Single-arm Clinical Study of Efficacy and Safety of Anti-CD123 CAR-T Therapy in Patients With Refractory/Relapsed CD123+ Acute Myeloid Leukemia.

TypeinterventionalSponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and TechnologyRan2019 to 2022Enrolled50ConditionsCD123+ Acute Myeloid LeukemiaArmsThird-generation anti-CD123 CAR-T cells
3 · Its place in the literature

Who cites it

171 citing papers in PubMed, 2 syntheses or guidelines pooled it, 246 citations in OpenAlex.

  1. Mapping the clinical landscape of multifunctional CAR T cells: Targets, trends, and synergies.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Pooled it
  2. Modular (universal) CAR-T platformsFrontiers in immunology · 2024
    Pooled it
  3. Article
  4. Article
  5. Engineering the next generation of cellular therapies for solid tumors: multi-specific armored CARs and TME reprogramming strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. The Current Landscape of Modular CAR T Cells.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. CAR-T cell therapy for cancer: current challenges and future directions.Signal transduction and targeted therapy · 2025
    Review
  20. Review

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

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

10 authors at 3 institutions in 1 country.

M CartellieriUniversity Cancer Center (UCC), Carl Gustav Carus University Hospital TU-Dresden, Tumorimmunology, Dresden, Germany.
A FeldmannUniversity Cancer Center (UCC), Carl Gustav Carus University Hospital TU-Dresden, Tumorimmunology, Dresden, Germany.
S KoristkaUniversity Cancer Center (UCC), Carl Gustav Carus University Hospital TU-Dresden, Tumorimmunology, Dresden, Germany.
C ArndtUniversity Cancer Center (UCC), Carl Gustav Carus University Hospital TU-Dresden, Tumorimmunology, Dresden, Germany.
S LoffUniversity Cancer Center (UCC), Carl Gustav Carus University Hospital TU-Dresden, Tumorimmunology, Dresden, Germany.
A EhningerGEMoaB Monoclonals GmbH, Dresden, Germany.
M von BoninUniversity Hospital Carl Gustav Carus, Medical Clinic and Policlinic I, Dresden, Germany.
E P BejestaniUniversity Hospital Carl Gustav Carus, Medical Clinic and Policlinic I, Dresden, Germany.
G EhningerUniversity Hospital Carl Gustav Carus, Medical Clinic and Policlinic I, Dresden, Germany.
M P BachmannUniversity Cancer Center (UCC), Carl Gustav Carus University Hospital TU-Dresden, Tumorimmunology, Dresden, Germany.
University Hospital Carl Gustav Carus · DEHelmholtz-Zentrum Dresden-Rossendorf · DETU Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The adoptive transfer of CD19-specific chimeric antigen receptor engineered T cells (CAR T cells) resulted in encouraging clinical trials in indolent B-cell malignancies. However, they also show the limitations of this fascinating technology: CAR T cells can lead to even life-threatening off-tumor, on-target side effects if CAR T cells crossreact with healthy tissues. Here, we describe a novel modular universal CAR platform technology termed UniCAR that reduces the risk of on-target side effects by a rapid and reversible control of CAR T-cell reactivity. The UniCAR system consists of two components: (1) a CAR for an inert manipulation of T cells and (2) specific targeting modules (TMs) for redirecting UniCAR T cells in an individualized time- and target-dependent manner. UniCAR T cells can be armed against different tumor targets simply by replacement of the respective TM for (1) targeting more than one antigen simultaneously or subsequently to enhance efficacy and (2) reducing the risk for development of antigen-loss tumor variants under treatment. Here we provide 'proof of concept' for retargeting of UniCAR T cells to CD33- and/or CD123-positive acute myeloid leukemia blasts in vitro and in vivo.

Indexed as

Gene Expression RegulationAnimalsAntigens, NeoplasmCytokinesCytotoxicity, ImmunologicDisease Models, AnimalGenetic VectorsHumansImmunotherapy, AdoptiveInterleukin-3 Receptor alpha SubunitLentivirusLeukemia, Myeloid, AcuteMiceMice, KnockoutReceptors, Antigen, T-CellSialic Acid Binding Ig-like Lectin 3Antigens, NeoplasmCD19-specific chimeric antigen receptorCD33 protein, humanCytokinesInterleukin-3 Receptor alpha SubunitReceptors, Antigen, T-CellSialic Acid Binding Ig-like Lectin 3

Identifiers

PMID27518241
PMCPMC5022178
OpenAlexW2508697147

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.