Abstract | AIM: The authors aimed to investigate whether nanotechnology-based delivery of antigenic peptides is feasible for efficiently inducing anti- tumor cytotoxic T lymphocyte responses through vaccination. MATERIALS & METHODS: RESULTS: The loading efficiency of hydrophilic peptides was greatly improved when lipids were introduced to formulate lipid-coated NPs. The lipid-coated NPs carrying a single peptide and/or combinations of multiple lipid-coated NPs carrying antigenic peptides were characterized in vitro and in vivo in a C57/BL6 (B6) mouse model. Both the single melanoma antigen peptide-loaded NPs and combinational delivery of lipid-coated NPs carrying different peptides could induce antigen-specific T-cell responses. However, single peptide-loaded NPs failed to significantly delay the growth of subcutaneously inoculated B16 melanoma cells in a prophylactic setting. By contrast, the combinational delivery of lipid-coated NPs carrying different peptides significantly suppressed growth of inoculated B16 melanoma cells.
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Authors | Songwei Tan, Tetsuro Sasada, Anna Bershteyn, Kunyu Yang, Tetsuya Ioji, Zhiping Zhang |
Journal | Nanomedicine (London, England)
(Nanomedicine (Lond))
Vol. 9
Issue 5
Pg. 635-47
(Apr 2014)
ISSN: 1748-6963 [Electronic] England |
PMID | 23905577
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cancer Vaccines
- Lipids
- Nanocapsules
- Peptides
- Polylactic Acid-Polyglycolic Acid Copolymer
- Polyglycolic Acid
- Lactic Acid
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Topics |
- Animals
- Antineoplastic Combined Chemotherapy Protocols
(administration & dosage, immunology)
- Cancer Vaccines
(administration & dosage, immunology)
- Cell Line, Tumor
- Lactic Acid
(chemistry)
- Lipids
(chemistry)
- Melanoma
(immunology, pathology, prevention & control)
- Mice
- Mice, Inbred C57BL
- Nanocapsules
(chemistry, ultrastructure)
- Peptides
(administration & dosage, immunology)
- Polyglycolic Acid
(chemistry)
- Polylactic Acid-Polyglycolic Acid Copolymer
- Survival Rate
- Treatment Outcome
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