Department of Microbiology and Immunology, Medical School of Southeast University, 87 Dingjiaqiao Rd., Nanjing, Jiangsu 210009, China.
Virus Res. 2010 Aug;151(2):162-9. doi: 10.1016/j.virusres.2010.04.011. Epub 2010 May 6.
Previous studies have identified that a hepatits E virus peptide (HEV-p179), spanning amino acids (aa) 439-617 in the 660-aa protein encoded by open reading frame 2(ORF2) of the Chinese epidemic strain (genotype 4), is the minimal size fragment of conformation-dependent neutralization epitope(s). We report here the successful immunization of mice with DNA vaccines expressing the secreted form of HEV-p179 (fused with a human tissue plasminogen activator (tPA) signal sequence) and the tPA-p179-C3d fusion protein (fused with three tandem copies of the murine complement C3d). Analysis of antibody responses in vaccinated mice revealed that immunizations with tPA-p179-C3d3 DNA vaccine dramatically increased both the level and avidity maturation of antibodies against HEV-p179 compared to p179 and tPA-p179 DNA vaccines. In addition, this increased antibody response correlated with neutralizing titers in a PCR-based cell culture neutralization assay. These results indicate that vaccination with C3d conjugated p179 DNA vaccine enhances antibody responses to HEV, and this approach may be applied to overcome the poor immunogenicity of DNA vaccines to generate HEV neutralizing antibodies.
先前的研究已经确定,来自中国流行株(基因型 4)ORF2 编码的 660 个氨基酸的蛋白中,跨越 439-617 个氨基酸的一个戊型肝炎病毒肽(HEV-p179)是构象依赖性中和表位的最小片段。我们在此报告,用表达分泌型 HEV-p179(与人组织型纤溶酶原激活物(tPA)信号序列融合)和 tPA-p179-C3d 融合蛋白(与三个串联的鼠补体 C3d 融合)的 DNA 疫苗成功地对小鼠进行了免疫。对疫苗接种小鼠的抗体反应分析表明,与 p179 和 tPA-p179 DNA 疫苗相比,tPA-p179-C3d3 DNA 疫苗免疫显著提高了针对 HEV-p179 的抗体水平和亲和成熟度。此外,这种增加的抗体反应与基于 PCR 的细胞培养中和测定中的中和效价相关。这些结果表明,用 C3d 缀合的 p179 DNA 疫苗接种可增强对 HEV 的抗体反应,并且该方法可用于克服 DNA 疫苗对产生 HEV 中和抗体的低免疫原性。