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A Synthetic Multi-epitope Antigen Enhances Hepatitis C Virus-Specific B- and T-Cell Responses
被引:1
|作者:
Yang, Guimei
[1
]
Chen, Shuwen
[1
]
Zhu, Xiangying
[1
]
Liang, Shenghua
[1
]
Liu, Longding
[2
]
Ren, Daming
[1
]
机构:
[1] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll, Inst Med Biol, Kunming, Peoples R China
关键词:
IMMUNE-RESPONSES;
NONSTRUCTURAL PROTEIN-3;
LYMPHOCYTE-RESPONSES;
VACCINE ADJUVANTS;
HCV INFECTION;
MULTIEPITOPE;
PARTICLES;
MICE;
GLYCOPROTEINS;
CD4(+);
D O I:
10.1089/vim.2010.0096
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Combining results from previous studies, a multi-epitope antigen PCXZ against the hepatitis C virus was synthesized in this study. The antigenic specificity of PCXZ was determined by recognizing antibodies in serum samples from hepatitis C virus patients, but not from healthy subjects or subjects who had the hepatitis B virus. The characteristics of PCXZ immunogenicity were evaluated in BALB/c mice. Strong antibody responses were generated in mice immunized with either naked PCXZ or PCXZ in Freund's adjuvant. As for the T-cell responses, Freund's adjuvant significantly increased interferon-g secretion and enhanced the lytic activity of cytotoxic T lymphocytes. The epitope Pa, one component of PCXZ, made the most significant contribution to specific CTL lysis; this epitope was also a B-cell epitope and was able to induce high IgG titers. In summary, PCXZ was found to be highly immunogenic, and elicited both humoral and cellular immune responses in mice.
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页码:109 / 118
页数:10
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