Institut Català de la Salut
[López A, Charbonnier D, Vela P, Díez B, Río P, Sánchez R] Biomedical Innovation Unit, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), Madrid, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain. Instituto de Investigaciones Sanitarias, Fundación Jiménez Díaz, Madrid, Spain. [Balmaña J] Vall d’Hebron Insititute of Oncology (VHIO), Barcelona, Spain. Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain
Vall d'Hebron Barcelona Hospital Campus
2025-12-19T08:31:35Z
2025-12-19T08:31:35Z
2025-12-18
CAR-T cells; EGFR; ErbB receptors
Células CAR-T; EGFR; Receptores ErbB
Cèl·lules CAR-T; EGFR; Receptors ErbB
Fanconi anemia (FA) is a DNA repair syndrome characterized by bone marrow failure and cancer predisposition, including acute myeloid leukemia and solid tumors such as head and neck squamous cell carcinoma (HNSCC). Due to the exacerbated toxicity of radio-chemotherapy in FA patients with HNSCC, there is an urgent need of safer and more efficient antitumoral therapies for these patients, such as those based on chimeric antigen receptor (CAR)-T cells. Here, we show that HNSCC cell lines from both the general population and patients with FA express ErbB family members, which can be recognized by the T1E panErbB ligand. The generation of a lentiviral vector encoding for a second-generation T1E-CAR allowed us to generate panErbB CAR-T cells from healthy donors (HDs) and patients with FA. Despite the molecular and cellular defects characteristic of FA cells, a similar efficacy of CAR-T generation was observed, regardless of the donor origin. In all cases, panErbB CAR-T cells exerted potent cytotoxicity against all HNSCC cell lines tested in vitro. In addition, intratumoral administration of these CAR-T cells in HNSCC xenografts markedly reduced tumor growth. These preclinical results suggest that panErbB CAR-T cells would represent a safe, non-genotoxic therapy for HNSCC, with particular applicability for patients with FA.
This work was supported by grants from “Red Española de Terapias Avanzadas RICORS/TERAV (RD21/0017/0027)”, “RICORS/TERAVplus (RD24/0014/0023)” from Instituto de Salud Carlos III (ISCIII), and by grants from the Spanish Government co-financed by Fondo Europeo de Desarrollo Regional (FEDER) PI21/00208 and CIBERONC no. CB16/12/00228 from the Instituto de Salud Carlos III (ISCIII); and a grant from Fundación Anemia de Fanconi to R.G.-E. The work has been conducted within the framework of an Agreement between Instituto de Salud Carlos III and CIEMAT for the creation of a Mixed Unit on Advanced Therapies (Resolution 27/1/2025).
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Medicaments antineoplàstics - Ús terapèutic; Cap - Càncer - Tractament; Coll - Càncer - Tractament; Anèmia de Fanconi; DISEASES::Hemic and Lymphatic Diseases::Hematologic Diseases::Anemia::Anemia, Aplastic::Anemia, Hypoplastic, Congenital::Fanconi Anemia; DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Glandular and Epithelial::Carcinoma::Carcinoma, Squamous Cell; DISEASES::Neoplasms::Neoplasms by Site::Head and Neck Neoplasms; Other subheadings::Other subheadings::Other subheadings::/drug therapy; ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Biological Therapy::Immunomodulation::Immunotherapy::Immunization::Immunization, Passive::Adoptive Transfer::Immunotherapy, Adoptive; ENFERMEDADES::enfermedades hematológicas y linfáticas::enfermedades hematológicas::anemia::anemia aplásica::anemia hipoplásica congénita::anemia de Fanconi; ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias glandulares y epiteliales::carcinoma::carcinoma de células escamosas; ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de cabeza y cuello; Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia; TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::terapia biológica::inmunomodulación::inmunoterapia::inmunización::inmunización pasiva::transferencia adoptiva::inmunoterapia adoptiva
Elsevier
Molecular Therapy Oncology;33(4)
https://doi.org/10.1016/j.omton.2025.201060
Attribution 4.0 International
http://creativecommons.org/licenses/by/4.0/
Articles científics - HVH [3396]