Polymeric inhibitor of influenza virus attachment protects mice from experimental influenza infection

被引:54
作者
Gambaryan, AS
Tuzikov, AB
Chinarev, AA
Juneja, LR
Bovin, NV
Matrosovich, MN
机构
[1] Russian Acad Med Sci, MP Chumakov Inst Poliomyelitis & Viral Encephalit, Moscow 142782, Russia
[2] Russian Acad Sci, MM Shemyakin Bioorgan Chem Inst, Moscow 117871, Russia
[3] Taiyo Kagaky Co Ltd, Nutr Foods Div, Yokaichi, Mie 5100825, Japan
基金
俄罗斯基础研究基金会;
关键词
influenza; attachment inhibitor; sialylglycopolymer; antiviral therapy; mice;
D O I
10.1016/S0166-3542(02)00020-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Synthetic sialic acid-containing macromolecules inhibit influenza virus attachment to target cells and suppress the virus-mediated hemagglutination and neutralize virus infectivity in cell culture. To test the protective effects of attachment inhibitors in vivo, mice were infected with mouse-adapted influenza virus A/Aichi/2/68 (H3N2) and treated with synthetic polyacrylamide-based sialylglycopolymer PAA-YDS bearing moieties of (Neu5Acalpha2-6Ga1beta1-4GlcNAcbeta1-2Manalpha1)(2)-3,6Manbeta1-4GlcNAcbeta1-4GlcNAc. Single intranasal inoculations with PAA-YDS 30 min before or 10 min after infection increased the survival of mice (P < 0.01). Multiple treatments with aerosolized PAA-YDS on days 2-5 post infection also increased survival (P < 0.01), alleviated disease symptoms, and decreased lesions in the mouse lungs. These data suggest that synthetic polyvalent inhibitors of virus attachment can be used for prevention and treatment of influenza. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:201 / 205
页数:5
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