A new marine-derived sulfoglycolipid triggers dendritic cell activation and immune adjuvant response
- Creators
- Manzo, Emiliano
- Cutignano, Adele
- Pagano, Dario
- Gallo, Carmela
- Barra, Giusi
- Nuzzo, Genoveffa
- Sansone, Clementina
- Ianora, Adrianna
- Urbanek, Konrad
- Fenoglio, Daniela
- Ferrera, Francesca
- Bernardi, Cinzia
- Parodi, Alessia
- Pasquale, Giuseppe
- Leonardi, Antonio
- Filaci, Gilberto
- DE PALMA, RAFFAELE
- Fontana, Angelo
- Others:
- Manzo, Emiliano
- Cutignano, Adele
- Pagano, Dario
- Gallo, Carmela
- Barra, Giusi
- Nuzzo, Genoveffa
- Sansone, Clementina
- Ianora, Adrianna
- Urbanek, Konrad
- Fenoglio, Daniela
- Ferrera, Francesca
- Bernardi, Cinzia
- Parodi, Alessia
- Pasquale, Giuseppe
- Leonardi, Antonio
- Filaci, Gilberto
- DE PALMA, Raffaele
- Fontana, Angelo
Description
Dendritic Cells (DCs) recognize infectious non-self molecules and engage the adaptive immune system thereby initiating long lasting, antigen-specific responses. As such, the ability to activate DCs is considered a key tool to enhance the efficacy and quality of vaccination. Here we report a novel immunomodulatory sulfolipid named β-SQDG18 that prototypes a class of natural-derived glycolipids able to prime human DCs by a TLR2/TLR4-independent mechanism and trigger an efficient immune response in vivo. β-SQDG18 induces maturation of DC with the upregulation of MHC II molecules and co-stimulatory proteins (CD83, CD86), as well as pro-inflammatory cytokines (IL-12 and INF-γ). Mice immunized with OVA associated to β-SQDG18 (1:500) produced a titer of anti-OVA Ig comparable to traditional adjuvants. In an experimental model of melanoma, vaccination of C57BL/6 mice with β-SQDG18-adjuvanted hgp10 peptide elicited a protective response with a reduction in tumour growth and increase in survival.
Additional details
- URL
- http://hdl.handle.net/11567/889110
- URN
- urn:oai:iris.unige.it:11567/889110
- Origin repository
- UNIGE