Glycopeptide-functionalized gold nanoparticles for antibody induction against the tumor associated mucin-1 glycoprotein

被引:48
作者
Cai, Hui [1 ]
Degliangeli, Federica [2 ]
Palitzsch, Bjoern [3 ]
Gerlitzki, Bastian [4 ]
Kunz, Horst [3 ]
Schmitt, Edgar [4 ]
Fiammengo, Roberto [2 ]
Westerlind, Ulrika [1 ]
机构
[1] Leibniz Inst Analyt Sci, Gesell Forderung Analyt Wissensch eV ISAS, Otto Hahn Str 6b, D-44227 Dortmund, Germany
[2] IIT, Ctr Biomol Nanotechnol UniLe, Via Barsanti, I-73010 Lecce, Italy
[3] Johannes Gutenberg Univ Mainz, Inst Organ Chem, Duesbergweg 10-14, D-55128 Mainz, Germany
[4] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Immunol, Langenbeckstr 1,Geb 708, D-55101 Mainz, Germany
关键词
Glycopeptides; Nanoparticles; Vaccines; Antibodies; Cancer; SYNTHETIC ANTITUMOR VACCINES; IMMUNE-RESPONSE; CANCER-IMMUNOTHERAPY; MUC1; GLYCOPEPTIDES; DENDRITIC CELLS; IN-VIVO; ANTIGENS; BREAST; GLYCOSYLATION; IMPROVE;
D O I
10.1016/j.bmc.2016.01.044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
We report the preparation of gold nanoparticle (AuNP)-based vaccine candidates against the tumor-associated form of the mucin-1 (MUC1) glycoprotein. Chimeric peptides, consisting of a glycopeptide sequence derived from MUC1 and the T-cell epitope P30 sequence were immobilized on PEGylated AuNPs and the ability to induce selective antibodies in vivo was investigated. After immunization, mice showed significant MHC-II mediated immune responses and their antisera recognized human MCF-7 breast cancer cells. Nanoparticles designed according to this report may become key players in the development of anticancer vaccines. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1132 / 1135
页数:4
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