Evidence map›Paper›PMID 32462078›Full record

ArticleMolecular therapy oncolytics2020

Rapidly Switchable Universal CAR-T Cells for Treatment of CD123-Positive Leukemia.

Simon Loff, Josephine Dietrich, Jan-Erik Meyer, Julia Riewaldt, Johannes Spehr, Malte von Bonin, Cordula Gründer, Mridula Swayampakula, Kristin Franke, Anja Feldmann and 4 more

Abstract read
In one paragraph

Article in Molecular therapy oncolytics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

74 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  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. Trial
  4. Review
  5. Pediatric AML CAR T cell therapy.Molecular therapy. Oncology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. CAR-T cell therapy for cancer: current challenges and future directions.Signal transduction and targeted therapy · 2025
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Significant Advancements and Evolutions in Chimeric Antigen Receptor Design.International journal of molecular sciences · 2024
    Review

14 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

14 authors.

Simon LoffGEMoaB Monoclonals GmbH, 01307 Dresden, Germany.
Josephine DietrichCellex Patient Treatment GmbH, 01307 Dresden, Germany.
Jan-Erik MeyerCellex Patient Treatment GmbH, 01307 Dresden, Germany.
Julia RiewaldtCellex Patient Treatment GmbH, 01307 Dresden, Germany.
Johannes SpehrCellex Patient Treatment GmbH, 01307 Dresden, Germany.
Malte von BoninMedical Clinic and Policlinic I, University Hospital "Carl Gustav Carus," TU Dresden, 01307 Dresden, Germany.
Cordula GründerGEMoaB Monoclonals GmbH, 01307 Dresden, Germany.
Mridula SwayampakulaGEMoaB Monoclonals GmbH, 01307 Dresden, Germany.
Kristin FrankeGEMoaB Monoclonals GmbH, 01307 Dresden, Germany.
Anja FeldmannHelmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, 01328 Dresden, Germany.
Michael BachmannUniversity Cancer Center "Carl Gustav Carus," TU Dresden, Tumor Immunology, 01307 Dresden, Germany.
Gerhard EhningerGEMoaB Monoclonals GmbH, 01307 Dresden, Germany.
Armin EhningerGEMoaB Monoclonals GmbH, 01307 Dresden, Germany.
Marc CartellieriGEMoaB Monoclonals GmbH, 01307 Dresden, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T cells (CAR-T) targeting CD19 or B cell maturation antigen (BCMA) are highly effective against B cell malignancies. However, application of CAR-T to less differentially expressed targets remains a challenge due to lack of tumor-specific antigens and CAR-T controllability. CD123, a highly promising leukemia target, is expressed not only by leukemic and leukemia-initiating cells, but also by myeloid, hematopoietic progenitor, and certain endothelial cells. Thus, CAR-T lacking fine-tuned control mechanisms pose a high toxicity risk. To extend the CAR-T target landscape and widen the therapeutic window, we adapted our rapidly switchable universal CAR-T platform (UniCAR) to target CD123. UniCAR-T efficiently eradicated CD123

Indexed as

adoptive cell therapyALLAMLCAR-TCD123immunotherapyUniCAR

Identifiers

PMID32462078
PMCPMC7240059

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.