| Literature DB >> 30713801 |
Hector Terán-Navarro1, Ricardo Calderon-Gonzalez1, David Salcines-Cuevas1, Isabel García2, Marco Marradi2, Javier Freire3, Erwan Salmon1, Mar Portillo-Gonzalez1, Elisabet Frande-Cabanes1, Almudena García-Castaño4, Virginia Martinez-Callejo5, Javier Gomez-Roman3, Raquel Tobes6, Fernando Rivera4, Sonsoles Yañez-Diaz1,7, Carmen Álvarez-Domínguez1.
Abstract
Gold glyconanoparticles loaded with the listeriolysin O peptide 91-99 (GNP-LLO91-99), a bacterial peptide with anti-metastatic properties, are vaccine delivery platforms facilitating immune cell targeting and increasing antigen loading. Here, we present proof of concept analyses for the consideration of GNP-LLO91-99 nanovaccines as a novel immunotherapy for cutaneous melanoma. Studies using mouse models of subcutaneous melanoma indicated that GNP-LLO91-99 nanovaccines recruite and modulate dendritic cell (DC) function within the tumour, alter tumour immunotolerance inducing melanoma-specific cytotoxic T cells, cause complete remission and improve survival. GNP-LLO91-99 nanovaccines showed superior tumour regression and survival benefits, when combined with anti-PD-1 or anti-CTLA-4 checkpoint inhibitors, resulting in an improvement in the efficacy of these immunotherapies. Studies on monocyte-derived DCs from patients with stage IA, IB or IIIB melanoma confirmed the ability of GNP-LLO91-99 nanovaccines to complement the action of checkpoint inhibitors, by not only reducing the expression of cell-death markers on DCs, but also potentiating DC antigen-presentation. We propose that GNP-LLO91-99 nanovaccines function as immune stimulators and immune effectors and serve as safe cancer therapies, alone or in combination with other immunotherapies.Entities:
Keywords: Listeria; immunotherapy; melanoma; nanoparticles; therapeutic vaccination
Year: 2018 PMID: 30713801 PMCID: PMC6343812 DOI: 10.1080/2162402X.2018.1541534
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110