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The **pp65-LAMP mRNA vaccine** is an investigational cancer immunotherapy consisting of mRNA encoding the cytomegalovirus (CMV) pp65 protein fused to lysosomal-associated membrane protein (LAMP), loaded into autologous dendritic cells (DCs) or monocytes via electroporation. Developed primarily by researchers at the University of Florida and Duke University, it targets CMV antigens expressed in glioblastoma multiforme (GBM) tumors to elicit antitumor CD4+ and CD8+ T-cell responses. The LAMP fusion enhances MHC class II presentation, promoting robust cellular immunity during lymphodepletion from dose-intensified temozolomide (DI-TMZ). Administered subcutaneously with GM-CSF adjuvant post-standard chemoradiation, it has shown feasibility, safety, and immune activation in phase I/II trials, with potential survival benefits in newly diagnosed GBM.[1][7][11]
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