ArticleMolecular therapy. Oncology2026
mRNA-LNP vaccine providing antigen and co-stimulation in the tumor microenvironment enhances CAR T cell function (CART-Vac).
Article in Molecular therapy. Oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Despite advances in multimodal therapies, outcomes for pediatric patients with relapsed or refractory cancers remain poor. Chimeric antigen receptor (CAR) T cell therapy has demonstrated limited efficacy in solid tumors due to the immunosuppressive tumor microenvironment (TME), which promotes T cell exhaustion and restricts CAR T cell expansion. This study evaluated a combinatorial approach to enhance CAR T function by reprogramming the TME to overexpress target antigens (TAs) and co-stimulatory molecules (CSMs) through a lipid nanoparticle-based CAR-T vaccination (CART-Vac). As proof of concept, rhabdomyosarcoma cells (Rh30) engineered to overexpress TAs and CSMs (Rh30-TACS) were examined. EPHB4-directed CAR T cells demonstrated enhanced cytotoxicity, proliferation, and cytokine secretion
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