Evidence map›Paper›PMID 40770072›Full record

ArticleLeukemia2025

A novel chimeric antigen receptor T-cell therapy targeting CD84 for the treatment of acute myeloid and T-cell lymphoblastic leukemias.

Lorena Pérez-Amill, Mercedes Armand-Ugón, Maria Val-Casals, Beatriz Martín-Herreros, José R Álamo, Sergio Peña, Gerard Frigola, Ane Altuna, Claudio Santos, Francesca Guijarro and 20 more

Abstract read
In one paragraph

Article in Leukemia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
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

30 authors.

Lorena Pérez-AmillInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Mercedes Armand-UgónInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0002-4069-9915
Maria Val-CasalsInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0003-2481-3295
Beatriz Martín-HerrerosHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.ORCID 0000-0001-7286-9555
José R ÁlamoHematopathology Section, Pathology Department, CDB, Hospital Clínic of Barcelona, Barcelona, Spain.
Sergio PeñaInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0009-0008-1619-3990
Gerard FrigolaHematopathology Section, Pathology Department, CDB, Hospital Clínic of Barcelona, Barcelona, Spain.ORCID 0000-0001-6794-6456
Ane AltunaInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0001-8350-1609
Claudio SantosGyala Therapeutics S.L., Barcelona, Spain.
Francesca GuijarroInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0001-6376-0929
Alfredo MinguelaImmunology Service, Clinic University Hospital Virgen de la Arrixaca (HCUVA) and Biomedical Research Institute of Murcia Pascual Parrilla (IMIB-PP), Murcia, Spain.
Àlex BatallerDepartment of Hematology, Hospital Clínic of Barcelona, Barcelona, Spain.ORCID 0000-0002-6085-2745
Berta Casanovas-AlbertíInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0001-5728-2932
Mireia Uribe-HerranzInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0002-2618-1116
Irene NavarroHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Manuel GuerreiroHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.ORCID 0000-0001-5978-2578
Diego Sánchez-MartínezJosep Carreras Leukemia Research Institute (JCLRI), School of Medicine, University of Barcelona, Barcelona, Spain.
Néstor TiradoJosep Carreras Leukemia Research Institute (JCLRI), School of Medicine, University of Barcelona, Barcelona, Spain.
Talía Velasco-HernandezSchool of Medicine, University of Barcelona, Barcelona, Spain.ORCID 0000-0003-2183-7443
Pablo MenéndezSchool of Medicine, University of Barcelona, Barcelona, Spain.
Antonio MartínezHematopathology Section, Pathology Department, CDB, Hospital Clínic of Barcelona, Barcelona, Spain.
Montse RoviraInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Dolors ColomerInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0001-7486-8484
E Azucena González-NavarroInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Jordi EsteveInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0002-8056-648X
Álvaro Urbano-IspizuaInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Pau MontesinosHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.ORCID 0000-0002-3275-5593
Julio DelgadoInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0002-5157-4376
Manel JuanInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. mjuan@clinic.cat.ORCID 0000-0002-3064-1648
Nela Klein-GonzálezInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. Klein@recerca.clinic.cat.ORCID 0000-0002-4593-6457

Funding

"la Caixa" Foundation (Caixa Foundation) CP042702/LCF/PR/GN18/50310007
6 · The paper itself

Abstract

Despite the remarkable clinical successes of chimeric antigen receptor (CAR) T-cell therapies in treating B-cell malignancies and multiple myeloma, similar outcomes have not been achieved in other indications. For patients with relapsed or refractory (R/R) acute myeloid leukemia (AML) or T-cell acute lymphoblastic leukemia (T-ALL), treatment options are limited, yet CART-cell therapies offer significant potential to address this unmet need. Here, we introduce a first-in-class CART-cell therapy targeting CD84, a novel antigen, for the treatment of R/R AML and T-ALL. CD84 is highly expressed on leukemic blasts, with limited expression on hematopoietic stem progenitor cells (HSPC), and is largely absent in healthy human tissues. Our second-generation CARTs targeting CD84 (CART84) demonstrate potent cytotoxicity against AML and T-ALL cells both in vitro and in vivo in patient-derived xenograft (PDX) models. Furthermore, CART84 eliminated primary leukemic blasts while exhibiting low cytotoxicity against CD34+ HSPC in vitro and in humanized mouse models in vivo, suggesting a low risk of myelotoxicity. These results support CD84 as a promising target for AML and T-ALL and provide the foundation for our upcoming first-in-human phase I/II clinical trial using CD84-directed CAR T cell therapy for patients with R/R AML and T-ALL (EudraCT 2024-519966-31-00).

Indexed as

Antigens, CDImmunotherapy, AdoptiveLeukemia, Myeloid, AcutePrecursor T-Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenAnimalsHumansMiceMice, Inbred NODMice, SCIDXenograft Model Antitumor AssaysAntigens, CDReceptors, Chimeric Antigen

Identifiers

PMID40770072
PMCPMC12463657

What OpenQuestion holds

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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.