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Comparison of protective efficacies of plasmid DNAs encoding Japanese encephalitis virus proteins that induce neutralizing antibody or cytotoxic T lymphocytes in mice

机译:编码日本脑炎病毒蛋白的质粒DNA诱导小鼠中和抗体或细胞毒性T淋巴细胞的保护作用比较

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摘要

Mice immunized with a plasmid DNA encoding the premembrane (prM) and envelope (E) proteins of Japanese encephalitis (JE) virus (designated pcJEME) produce neutralizing antibodies and are protected from JE. To determine the role of the immune response to other viral proteins in protection, we constructed plasmid DNAs encoding other JE virus proteins and made a direct comparison among these plasmids using a Mouse model. Cytotoxic T lymphocytes (CTLs) were induced by plasmids encoding capsid (C) or nonstructural proteins, NS1, NS2A, NS2B, NS3 or NS5. However, these plasmids provided only a partial protection against intraperitoneal challenge with a lethal dose of JE virus, whereas mice immunized with pcJEME were fully protected. In mice inoculated with CTL-inducing plasmids, high virus titers were detected in plasma immediately (1 h) following challenge and in brain on day 4 post-challenge, but no virus infectivity was detected in plasma and brain of pcJEME-immunized mice during the 5 days following challenge. These results indicate that protection provided by the prM/E-encoding DNA consists of neutralizing antibody that prevents virus dissemination from the peripheral site to the brain, and that this antibody-mediated mechanism of protection is more efficient than the immunity induced by plasmids that generate CTL responses capable of killing JE virus-infected cells.
机译:用编码日本脑炎(JE)病毒(称为pcJEME)的前膜(prM)和包膜(E)蛋白的质粒DNA免疫的小鼠产生中和抗体,并受到了JE的保护。为了确定针对其他病毒蛋白的免疫应答在保护中的作用,我们构建了编码其他JE病毒蛋白的质粒DNA,并使用Mouse模型对这些质粒进行了直接比较。通过编码衣壳(C)或非结构蛋白NS1,NS2A,NS2B,NS3或NS5的质粒诱导细胞毒性T淋巴细胞(CTL)。然而,这些质粒仅提供了部分剂量的抗致命性JE病毒的腹膜内攻击的保护,而用pcJEME免疫的小鼠则得到了充分的保护。在接种了CTL诱导质粒的小鼠中,攻击后立即(1 h)和攻击后第4天在大脑中检测到高病毒滴度,但在免疫过程中pcJEME免疫小鼠的血浆和脑中未检测到病毒感染性。挑战后5天。这些结果表明,编码prM / E的DNA提供的保护作用是由中和抗体组成,该中和抗体可防止病毒从外围部位扩散到大脑,并且这种抗体介导的保护机制比产生质粒的免疫力更有效。能够杀死JE病毒感染细胞的CTL反应。

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