ZHANG Cai-hong, JIANG Xiu-li, WANG Min, ZHANG Yan-ming, WANG Jian-wei and HONG Tao. Immune Response Induced by Recombinant Adenoviruses Expressing Serotype G2 or G3 VP7 of Group A Human Rotavirus in Mice[J]. Virologica Sinica, 2005, 20(4): 352-356.
Citation: ZHANG Cai-hong, JIANG Xiu-li, WANG Min, ZHANG Yan-ming, WANG Jian-wei, HONG Tao. Immune Response Induced by Recombinant Adenoviruses Expressing Serotype G2 or G3 VP7 of Group A Human Rotavirus in Mice .VIROLOGICA SINICA, 2005, 20(4) : 352-356.

表达轮状病毒G2和G3型vp7基因重组腺病毒的免疫效果

  • 为探索以非复制型腺病毒为表达载体的多价轮状病毒(Rotavirus,RV)基因工程疫苗的可行性,在前期工作的基础上,对表达我国G2和G3型RV流行毒株vp7基因的重组腺病毒的免疫效果进行了研究。分别用表达G2和G3型vp7基因的重组腺病毒rvAdG2VP7、rvAdG3VP7经滴鼻和灌胃两种途径免疫Balb/c小鼠,对免疫后小鼠的血清抗体、黏膜抗体和相关的细胞因子水平进行了检测和比较。结果表明,用表达G2和G3型vp7基因的重组腺病毒经滴鼻和灌胃两种途径免疫小鼠后,均可诱导机体产生较强的RV特异性免疫反应,包括体液免疫、细胞免疫和黏膜免疫,并能产生中和抗体。但免疫反应以Th2类为主,Th1类反应也占有相当的比例。本研究为新型RV基因工程疫苗的深入研究奠定了基础。

Immune Response Induced by Recombinant Adenoviruses Expressing Serotype G2 or G3 VP7 of Group A Human Rotavirus in Mice

  • In order to clarify the feasibility of adenovirus vector-based multivalent genetic engineering vaccine of Rotavirus (RV), we investigated the immune responses induced by the adenoviruses expressing serotype G2 or G3 VP7 of group A rotavirus on the basis of our previous reports. Balb/c mice were immunized with recombinant adenovirus rvAdG2VP7 or rvAdG3VP7, which expressing G2 or G3 type VP7,respectively, via intranasal or oral route for 3 times and serum antibodies, mucosal antibodies as well as the level of related cytokines were determinated. The results demonstrated that immunizing with the adenoviruses expressing serotype G2 or G3 RV VP7 intranasally or orally could induce strong rotavirus-specific immune response in mice, including humoral immunity, cell-mediated immunity, mucosal immunity as well as protective neutralizing antibody. The results also implied that Th2-like response triggered by the immunization is probably the primary response compared to Th1-like response. In summary, this study laid a fo

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    Immune Response Induced by Recombinant Adenoviruses Expressing Serotype G2 or G3 VP7 of Group A Human Rotavirus in Mice

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    Abstract: In order to clarify the feasibility of adenovirus vector-based multivalent genetic engineering vaccine of Rotavirus (RV), we investigated the immune responses induced by the adenoviruses expressing serotype G2 or G3 VP7 of group A rotavirus on the basis of our previous reports. Balb/c mice were immunized with recombinant adenovirus rvAdG2VP7 or rvAdG3VP7, which expressing G2 or G3 type VP7,respectively, via intranasal or oral route for 3 times and serum antibodies, mucosal antibodies as well as the level of related cytokines were determinated. The results demonstrated that immunizing with the adenoviruses expressing serotype G2 or G3 RV VP7 intranasally or orally could induce strong rotavirus-specific immune response in mice, including humoral immunity, cell-mediated immunity, mucosal immunity as well as protective neutralizing antibody. The results also implied that Th2-like response triggered by the immunization is probably the primary response compared to Th1-like response. In summary, this study laid a fo

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