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Liposomal Antitumor Vaccines Targeting Mucin 1 Elicit a Lipid-Dependent Immunodominant Response

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成果类型:
期刊论文
作者:
Du, Jing-Jing;Zou, Shi-Yao;Chen, Xiang-Zhao;Xu, Wen-Bo;Wang, Chang-Wei;...
通讯作者:
Liu, Zheng;Guo, Jun
作者机构:
[Zhang, Lian; Wang, Jian; Du, Jing-Jing; Zou, Shi-Yao; Yin, Xu-Guang; Zhou, Shi-Hao; Chen, Xiang-Zhao; Xu, Wen-Bo; Tang, Yuan-Kai; Liu, Zheng; Guo, J; Guo, Jun; Wang, Chang-Wei] Cent China Normal Univ, Int Joint Res Ctr Intelligent Biosensing Technol, Hubei Int Sci & Technol Cooperat Base Pesticide &, Key Lab Pesticide & Chem Biol,Minist Educ,Coll Ch, Wuhan 430079, Hubei, Peoples R China.
[Gao, Xiao-Fei] East China Univ Technol, Jiangxi Key Lab Mass Spectrometry & Instrumentat, Nanchang 330013, Jiangxi, Peoples R China.
通讯机构:
[Liu, Z; Guo, J] C
Cent China Normal Univ, Int Joint Res Ctr Intelligent Biosensing Technol, Hubei Int Sci & Technol Cooperat Base Pesticide &, Key Lab Pesticide & Chem Biol,Minist Educ,Coll Ch, Wuhan 430079, Hubei, Peoples R China.
语种:
英文
关键词:
MUC1 antigen;NKT cells;cancer;fully synthetic vaccines;liposomes;alphaGalCer
期刊:
CHEMISTRY-AN ASIAN JOURNAL
ISSN:
1861-4728
年:
2019
卷:
14
期:
12
页码:
2116-2121
基金类别:
We are grateful to the National Key Research and Development Program of China (No. 2017YFA0505200), the National Natural Science Foundation of China (Nos. 21772056 and 21402058), Wuhan Bureau of Science and Technology (2018060401011323), the self-determined research funds of CCNU from the colleges’ basic research and operation of MOE (Nos. CCNU18TS011 and CCNU19QN068), Program of Introducing Talents of Discipline to Universities of China (111 program, B17019), the Research Fund of East China University of Technology (No. DHBK2017114), and Chemical Biology Center of CCNU.
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
The tumor-associated antigen mucin 1 (MUC1) has been pursued as an attractive target for cancer immunotherapy, but the poor immunogenicity of the endogenous antigen hinders the development of vaccines capable of inducing effective anti-MUC1 immunodominant responses. Herein, we prepared synthetic anti-MUC1 vaccines in which the hydrophilic MUC1 antigen was N-terminally conjugated to one or two palmitoyl lipid chains (to form amphiphilic Pam-MUC1 or Pam2-MUC1). These amphiphilic lipid-tailed MUC1 antigens were self-assembled into liposomes contai...

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