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A general strategy towards personalized nanovaccines based on fluoropolymers for post-surgical cancer immunotherapy
in
Animal growth
/ Animal models
/ Antigen presentation
/ Antigens
/ Breast cancer
/ Cancer
/ Cancer immunotherapy
/ Cancer vaccines
/ Cell membranes
/ Customization
/ Cytosol
/ Dendritic cells
/ Dendritic structure
/ Fluoropolymers
/ Immune checkpoint
/ Immunological memory
/ Immunotherapy
/ Melanoma
/ Metastases
/ Metastasis
/ Nanoparticles
/ Ovalbumin
/ Signal transduction
/ Strategy
/ TLR4 protein
/ Toll-like receptors
/ Tumors
2020
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A general strategy towards personalized nanovaccines based on fluoropolymers for post-surgical cancer immunotherapy
by
in
Animal growth
/ Animal models
/ Antigen presentation
/ Antigens
/ Breast cancer
/ Cancer
/ Cancer immunotherapy
/ Cancer vaccines
/ Cell membranes
/ Customization
/ Cytosol
/ Dendritic cells
/ Dendritic structure
/ Fluoropolymers
/ Immune checkpoint
/ Immunological memory
/ Immunotherapy
/ Melanoma
/ Metastases
/ Metastasis
/ Nanoparticles
/ Ovalbumin
/ Signal transduction
/ Strategy
/ TLR4 protein
/ Toll-like receptors
/ Tumors
2020
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A general strategy towards personalized nanovaccines based on fluoropolymers for post-surgical cancer immunotherapy
in
Animal growth
/ Animal models
/ Antigen presentation
/ Antigens
/ Breast cancer
/ Cancer
/ Cancer immunotherapy
/ Cancer vaccines
/ Cell membranes
/ Customization
/ Cytosol
/ Dendritic cells
/ Dendritic structure
/ Fluoropolymers
/ Immune checkpoint
/ Immunological memory
/ Immunotherapy
/ Melanoma
/ Metastases
/ Metastasis
/ Nanoparticles
/ Ovalbumin
/ Signal transduction
/ Strategy
/ TLR4 protein
/ Toll-like receptors
/ Tumors
2020
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A general strategy towards personalized nanovaccines based on fluoropolymers for post-surgical cancer immunotherapy
Journal Article
A general strategy towards personalized nanovaccines based on fluoropolymers for post-surgical cancer immunotherapy
2020
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Overview
Cancer metastases and recurrence after surgical resection remain an important cause of treatment failure. Here we demonstrate a general strategy to fabricate personalized nanovaccines based on a cationic fluoropolymer for post-surgical cancer immunotherapy. Nanoparticles formed by mixing the fluoropolymer with a model antigen ovalbumin, induce dendritic cell maturation via the Toll-like receptor 4 (TLR4)-mediated signalling pathway, and promote antigen transportation into the cytosol of dendritic cells, which leads to an effective antigen cross-presentation. Such a nanovaccine inhibits established ovalbumin-expressing B16-OVA melanoma. More importantly, a mix of the fluoropolymer with cell membranes from resected autologous primary tumours synergizes with checkpoint blockade therapy to inhibit post-surgical tumour recurrence and metastases in two subcutaneous tumour models and an orthotopic breast cancer tumour. Furthermore, in the orthotopic tumour model, we observed a strong immune memory against tumour rechallenge. Our work offers a simple and general strategy for the preparation of personalized cancer vaccines to prevent post-operative cancer recurrence and metastasis.A fluoropolymer-based cancer nanovaccine that delivers antigens directly to the cytosol of dendritic cells and elicits strong antitumour immune responses inhibiting tumour growth in animal models can be used to produce personalized treatment for post-surgical immunotherapy.
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