| Literature DB >> 33260400 |
Carmela Gallo1, Giusi Barra1, Marisa Saponaro1, Emiliano Manzo1, Laura Fioretto2, Marcello Ziaco3, Genoveffa Nuzzo1, Giuliana d'Ippolito1, Raffaele De Palma1,4, Angelo Fontana1,5.
Abstract
Immunotherapy takes advantage of the immune system to prevent, control, and eliminate neoplastic cells. The research in the field has already led to major breakthroughs to treat cancer. In this work, we describe a platform that integrates in vitro bioassays to test the immune response and direct antitumor effects for the preclinical discovery of anticancer candidates. The platform relies on the use of dendritic cells that are professional antigen-presenting cells (APC) able to activate T cells and trigger a primary adaptive immune response. The experimental procedure is based on two phenotypic assays for the selection of chemical leads by both a panel of nine tumor cell lines and growth factor-dependent immature mouse dendritic cells (D1). The positive hits are then validated by a secondary test on human monocyte-derived dendritic cells (MoDCs). The aim of this approach is the selection of potential immunotherapeutic small molecules from natural extracts or chemical libraries.Entities:
Keywords: anticancer; bioassay platform; chemical immunology; dendritic cell; drug discovery; high throughput; immunotherapy; screening guidelines
Mesh:
Substances:
Year: 2020 PMID: 33260400 PMCID: PMC7760914 DOI: 10.3390/md18120604
Source DB: PubMed Journal: Mar Drugs ISSN: 1660-3397 Impact factor: 5.118