The tumor-targeted CD40 agonist CEA-CD40 promotes T cell priming via a dual mode of action by increasing antigen delivery to dendritic cells and enhancing their activation

التفاصيل البيبلوغرافية
العنوان: The tumor-targeted CD40 agonist CEA-CD40 promotes T cell priming via a dual mode of action by increasing antigen delivery to dendritic cells and enhancing their activation
المؤلفون: Eva Sum, Moritz Rapp, Harald Dürr, Alekhya Mazumdar, Pedro J Romero, Christine Trumpfheller, Pablo Umaña
المصدر: Journal for immunotherapy of cancer. 10(3)
سنة النشر: 2022
مصطلحات موضوعية: Pharmacology, Cancer Research, Immunology, hemic and immune systems, Dendritic Cells, CD8-Positive T-Lymphocytes, digestive system diseases, Carcinoembryonic Antigen, Oncology, Neoplasms, Molecular Medicine, Immunology and Allergy, Humans, CD40 Antigens
الوصف: Tumor-targeted CD40 agonism represents an attractive strategy for cancer immunotherapy (CIT) as it promotes dendritic cell (DC) activation and concomitant tumor-specific T cell priming without causing systemic side effects. We developed the bispecific CD40 agonistic antibody CEA-CD40, which triggers CD40 stimulation exclusively in the presence of carcinoembryonic antigen (CEA), a glycoprotein specifically expressed on tumor cells. In this study, we demonstrate that CEA-CD40 can enable potent in vitro DC activation and consecutive T cell cross-priming in a CEA-specific manner. Furthermore, we provide evidence that CEA-CD40 increases colocalization of CEA+ tumor material and DCs. Using CEA+ tumor-derived extracellular vesicles (EVs), which are known to be an excellent tumor antigen source, we show that CEA-CD40 mediates delivery of CEA+ EVs to DCs. Importantly, our data indicates that this fosters acquisition of tumor EV major histocompatibility complex I/peptide complexes by DCs, consequently improving CD8+ T cell priming against EV-associated antigen in vitro. Thus, we provide mechanistic evidence for a dual mode of action of CEA-CD40 for CIT: we suggest that CEA-CD40 has the potential to activate DCs and in addition can promote their loading with tumor antigen derived from EVs to trigger tumor-specific T cell cross-priming.
تدمد: 2051-1426
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::142e434fe0ce69ae51e7b44fce74b5dc
https://pubmed.ncbi.nlm.nih.gov/35292514
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....142e434fe0ce69ae51e7b44fce74b5dc
قاعدة البيانات: OpenAIRE