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.
引用
收藏
页码:109 / 118
页数:10
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