Article
作者: Frigola, Gerard ; Santos, Claudio ; Navarro, Irene ; Menéndez, Pablo ; Guijarro, Francesca ; Pérez-Amill, Lorena ; Minguela, Alfredo ; Peña, Sergio ; Casanovas-Albertí, Berta ; Colomer, Dolors ; González-Navarro, E Azucena ; Delgado, Julio ; Esteve, Jordi ; Uribe-Herranz, Mireia ; Klein-González, Nela ; Guerreiro, Manuel ; Altuna, Ane ; Rovira, Montse ; Martínez, Antonio ; Juan, Manel ; Bataller, Àlex ; Tirado, Néstor ; Velasco-Hernandez, Talía ; Sánchez-Martínez, Diego ; Val-Casals, Maria ; Armand-Ugón, Mercedes ; Montesinos, Pau ; Martín-Herreros, Beatriz ; Urbano-Ispizua, Álvaro ; Álamo, José R
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).