Evidence map›Paper›PMID 33976880›Full record

ArticleClinical & translational immunology2021

Mutated GM-CSF-based CAR-T cells targeting CD116/CD131 complexes exhibit enhanced anti-tumor effects against acute myeloid leukaemia.

Aiko Hasegawa, Shoji Saito, Shogo Narimatsu, Shigeru Nakano, Mika Nagai, Hideki Ohnota, Yoichi Inada, Hirokazu Morokawa, Ikumi Nakashima, Daisuke Morita and 6 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. CAR-T cell therapy for treatment of acute myeloid leukemia, advances and outcomes.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  6. Review
  7. Recent advances of CAR-T cells in acute myeloid leukemia.Therapeutic advances in hematology · 2025
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Therapeutic Advances in Immunotherapies for Hematological Malignancies.International journal of molecular sciences · 2022
    Review
  14. Review
  15. Frontiers in immunology · 2022
    Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. 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

16 authors at 3 institutions in 1 country.

Aiko HasegawaDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.
Shoji SaitoDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.ORCID https://orcid.org/0000-0003-3866-3582
Shogo NarimatsuDepartment of Drug Discovery Science Shinshu University Matsumoto Japan.
Shigeru NakanoDepartment of Drug Discovery Science Shinshu University Matsumoto Japan.
Mika NagaiDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.
Hideki OhnotaDepartment of Drug Discovery Science Shinshu University Matsumoto Japan.
Yoichi InadaDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.
Hirokazu MorokawaDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.
Ikumi NakashimaDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.
Daisuke MoritaDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.
Yuichiro IdeDepartment of Laboratory Medicine Shinshu University Hospital Matsumoto Japan.ORCID https://orcid.org/0000-0002-3117-974X
Kazuyuki MatsudaDepartment of Health and Medical Sciences Graduate School of Medicine Shinshu University Matsumoto Japan.ORCID https://orcid.org/0000-0002-4056-7242
Haruko TashiroDepartment of Hematology/Oncology Teikyo University School of Medicine Itabashi Japan.ORCID https://orcid.org/0000-0002-9038-1710
Shigeki YagyuCenter for Advanced Research of Gene and Cell Therapy Shinshu University Matsumoto Japan.ORCID https://orcid.org/0000-0003-4256-9783
Miyuki TanakaDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.ORCID https://orcid.org/0000-0001-9317-6694
Yozo NakazawaDepartment of Pediatrics Shinshu University School of Medicine Matsumoto Japan.ORCID https://orcid.org/0000-0003-0793-815X
Shinshu University · JPShinshu University Hospital · JPTeikyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAs the prognosis of relapsed/refractory (R/R) acute myeloid leukaemia (AML) remains poor, novel treatment strategies are urgently needed. Clinical trials have shown that chimeric antigen receptor (CAR)-T cells for AML are more challenging than those targeting CD19 in B-cell malignancies. We recently developed

methodsTo further improve the efficacy of the original GMR CAR-T cells, we have developed novel GMR CAR vectors incorporating a mutated GM-CSF for the antigen-binding domain and G4S spacer. All GMR CAR-T cells were generated using a

resultsNearly 80% of the AML cells predominant in myelomonocytic leukaemia were found to express CD116. GMR CAR-T cells exhibited potent cytotoxic activities against CD116

conclusionsGMR CAR-T cell therapy represents a promising strategy for CD116

Indexed as

AMLCD116GM‐CSFGM‐CSF receptorGMRlow affinity

Identifiers

PMID33976880
PMCPMC8102137
OpenAlexW3160048324

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.