Evidence map›Paper›PMID 37795087›Full record

ArticleFrontiers in immunology2023

Optimization of universal allogeneic CAR-T cells combining CRISPR and transposon-based technologies for treatment of acute myeloid leukemia.

Cristina Calviño, Candela Ceballos, Ana Alfonso, Patricia Jauregui, Maria E Calleja-Cervantes, Patxi San Martin-Uriz, Paula Rodriguez-Marquez, Angel Martin-Mallo, Elena Iglesias, Gloria Abizanda and 13 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

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  11. Generation and GMP scale-up of human CAR-T cells using non-viralMolecular therapy. Methods & clinical development · 2025
    Article
  12. Review
  13. Current Non-Viral-Based Strategies to Manufacture CAR-T Cells.International journal of molecular sciences · 2024
    Review
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  15. [The impact of immune cells selection on the therapeutic efficacy of CAR-T cell therapy].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2024
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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

23 authors at 3 institutions in 1 country.

Cristina CalviñoHematology and Cell Therapy Department, Clinica Universidad de Navarra, IdiSNA, Pamplona, Spain.
Candela CeballosHematology Department, Hospital Universitario de Navarra, IdiSNA, Pamplona, Spain.
Ana AlfonsoHematology and Cell Therapy Department, Clinica Universidad de Navarra, IdiSNA, Pamplona, Spain.
Patricia JaureguiHematology and Cell Therapy Department, Clinica Universidad de Navarra, IdiSNA, Pamplona, Spain.
Maria E Calleja-CervantesHemato-Oncology Program, Cima Universidad de Navarra, IdiSNA, Pamplona, Spain.
Patxi San Martin-UrizHemato-Oncology Program, Cima Universidad de Navarra, IdiSNA, Pamplona, Spain.
Paula Rodriguez-MarquezCentro de Investigacion Biomedica en Red de Cancer (CIBERONC), Madrid, Spain.
Angel Martin-MalloHemato-Oncology Program, Cima Universidad de Navarra, IdiSNA, Pamplona, Spain.
Elena IglesiasHemato-Oncology Program, Cima Universidad de Navarra, IdiSNA, Pamplona, Spain.
Gloria AbizandaHemato-Oncology Program, Cima Universidad de Navarra, IdiSNA, Pamplona, Spain.
Saray Rodriguez-DiazHemato-Oncology Program, Cima Universidad de Navarra, IdiSNA, Pamplona, Spain.
Rebeca Martinez-TurrillasCentro de Investigacion Biomedica en Red de Cancer (CIBERONC), Madrid, Spain.
Jorge IllarramendiHematology Department, Hospital Universitario de Navarra, IdiSNA, Pamplona, Spain.
Maria C ViguriaHematology Department, Hospital Universitario de Navarra, IdiSNA, Pamplona, Spain.
Margarita RedondoHematology Department, Hospital Universitario de Navarra, IdiSNA, Pamplona, Spain.
Jose RifonHematology and Cell Therapy Department, Clinica Universidad de Navarra, IdiSNA, Pamplona, Spain.
Sara VillarHematology and Cell Therapy Department, Clinica Universidad de Navarra, IdiSNA, Pamplona, Spain.
Juan J LasarteImmunology and Immunotherapy Program, Cima Universidad de Navarra, IdiSNA, Pamplona, Spain.
Susana InogesHematology and Cell Therapy Department, Clinica Universidad de Navarra, IdiSNA, Pamplona, Spain.
Ascension Lopez-Diaz de CerioHematology and Cell Therapy Department, Clinica Universidad de Navarra, IdiSNA, Pamplona, Spain.
Mikel HernaezCentro de Investigacion Biomedica en Red de Cancer (CIBERONC), Madrid, Spain.
Felipe ProsperHematology and Cell Therapy Department, Clinica Universidad de Navarra, IdiSNA, Pamplona, Spain.
Juan R Rodriguez-MadozCentro de Investigacion Biomedica en Red de Cancer (CIBERONC), Madrid, Spain.
Universidad de Navarra · ESClinica Universidad de Navarra · ESCentro de Investigación Biomédica en Red de Cáncer · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the potential of CAR-T therapies for hematological malignancies, their efficacy in patients with relapse and refractory Acute Myeloid Leukemia has been limited. The aim of our study has been to develop and manufacture a CAR-T cell product that addresses some of the current limitations. We initially compared the phenotype of T cells from AML patients and healthy young and elderly controls. This analysis showed that T cells from AML patients displayed a predominantly effector phenotype, with increased expression of activation (CD69 and HLA-DR) and exhaustion markers (PD1 and LAG3), in contrast to the enriched memory phenotype observed in healthy donors. This differentiated and more exhausted phenotype was also observed, and corroborated by transcriptomic analyses, in CAR-T cells from AML patients engineered with an optimized CAR construct targeting CD33, resulting in a decreased

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteAgedAnimalsDisease Models, AnimalHumansImmunotherapy, AdoptiveReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-Cellallogeneic CAR-TAMLCRISPRtranscriptomics (RNA sequencing)transposon

Identifiers

PMID37795087
PMCPMC10546312
OpenAlexW4386893932

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.