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首页> 外文期刊>Acta tropica: Journal of Biomedical Sciences >Characterization of antibody responses to the Sj23 antigen of Schistosoma japonicum after infection and immunization.
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Characterization of antibody responses to the Sj23 antigen of Schistosoma japonicum after infection and immunization.

机译:感染和免疫后对日本血吸虫Sj23抗原抗体反应的表征。

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Sj23, a member of the tetraspanin protein family, is a 23-kDa surface-exposed protein of Schistosoma japonicum and expressed in all infective parasite stages, which has been regarded as a potential candidate in vaccine development for schistosomiasis. In this study, we found that, in the BALB/c mouse model, Sj23 elicited rapid humoral responses after parasite infection and the dominant antibodies were of IgG2a subclass. Immunization with Sj23 by priming with recombinant SFV RNA virus particles followed by a boost with recombinant protein also generated strong IgG2a responses which did not provide protection against challenge with cercariae. Our data indicated that one of the functions of Sj23 of S. japonicum is to facilitate parasite immune regulation. Sj23 antigen-based vaccine may require strong adjuvant that can drive IgG1 responses which are more critical in resistance to helminth infection.
机译:Sj23是四跨膜蛋白家族的成员,是一种日本血吸虫的23 kDa表面暴露蛋白,在所有感染性寄生虫阶段均表达,被认为是血吸虫病疫苗开发的潜在候选者。在这项研究中,我们发现,在BALB / c小鼠模型中,Sj23在寄生虫感染后引起快速的体液反应,并且主要抗体属于IgG2a亚类。通过用重组SFV RNA病毒颗粒引发,随后用重组蛋白加强免疫而用Sj23免疫也产生了强烈的IgG2a反应,该反应没有提供针对尾c的攻击的保护作用。我们的数据表明,日本血吸虫Sj23的功能之一是促进寄生虫的免疫调节。基于Sj23抗原的疫苗可能需要强佐剂,可以驱动IgG1反应,这在抵抗蠕虫感染中更为关键。

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