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'Multicopy Multivalent' Glycopolymer-Stabilized Gold Nanoparticles as Potential Synthetic Cancer Vaccines
被引:176
|作者:
Parry, Alison L.
[1
,2
,3
]
Clemson, Natasha A.
[1
,2
]
Ellis, James
[1
,2
]
Bernhard, Stefan S. R.
[1
,2
]
Davis, Benjamin G.
[3
]
Cameron, Neil R.
[1
,2
]
机构:
[1] Univ Durham, Dept Chem, Durham DH1 3LE, England
[2] Univ Durham, Biophys Sci Inst, Durham DH1 3LE, England
[3] Univ Oxford, Dept Chem, Chem Res Lab, Oxford OX1 3TA, England
基金:
英国生物技术与生命科学研究理事会;
英国工程与自然科学研究理事会;
关键词:
FRAGMENTATION CHAIN-TRANSFER;
THOMSEN-FRIEDENREICH DISACCHARIDE;
T-CELL EPITOPE;
GLYCOPEPTIDE ANTIGENS;
ANTICANCER VACCINE;
MUC1;
GLYCOPEPTIDES;
CONJUGATE VACCINE;
BREAST-CANCER;
PLUS QS21;
GLYCONANOPARTICLES;
D O I:
10.1021/ja4046857
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Mucin-related carbohydrates are overexpressed on the surface of cancer cells, providing a disease-specific target for cancer immunotherapy. Here, we describe the design and construction of peptide-free multivalent glycosylated nanoscale constructs as potential synthetic cancer vaccines that generate significant titers of antibodies selective for aberrant mucin glycans. A polymerizable version of the Tn-antigen glycan was prepared and converted into well-defined glycopolymers by Reversible Addition Fragmentation chain Transfer (RAFT) polymerization. The polymers were then conjugated to gold nanoparticles, yielding 'multicopy-multivalent nanoscale glycoconjugates. Immunological studies indicated that these nanomaterials generated strong and long-lasting production of antibodies that are selective to the Tn-antigen glycan and cross-reactive toward mucin proteins displaying Tn. The results demonstrate proof-of-concept of a simple and modular approach toward synthetic anticancer vaccines based on multivalent glycosylated nanomaterials without the need for a typical vaccine protein component.
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页码:9362 / 9365
页数:4
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