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首页> 外文期刊>Microbial Pathogenesis >Protection against nasal colonization with Streptococcus pneumoniae by parenteral immunization with a DNA vaccine encoding PspA (Pneumococcal surface protein A)
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Protection against nasal colonization with Streptococcus pneumoniae by parenteral immunization with a DNA vaccine encoding PspA (Pneumococcal surface protein A)

机译:通过编码PspA(肺炎球菌表面蛋白A)的DNA疫苗的肠胃外免疫预防肺炎链球菌在鼻中定植

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摘要

Pneumococcal surface protein A (PspA) is an important candidate for a cost-effective vaccine with broad coverage against Streptococcus pneumoniae. We have previously shown that intramuscular immunization with PspA as a DNA vaccine induces an immune response characterized by the induction of a balanced IgG1/IgG2a antibody response in BALB/c mice, which was able to efficiently mediate complement deposition onto intact bacteria and to induce protection against an intraperitoneal challenge. We now confirm the results in C57BL/6 mice and further show that the response induced by the DNA vaccine expressing PspA is able to mediate protection against colonization of the nasopharyngeal mucosa even though immunization was given parenterally. Moreover, a positive correlation was observed between IgG1 and the numbers of CFU recovered, whereas an inverse correlation was observed between nasal CFU levels and IgG2a. A positive correlation was also found for IgG1/IgG2a antibody ratios with CFU recovered from the nasopharynx. Therefore, reduction of nasal colonization was strongly associated with increased levels of serum IgG2a complement fixing antibody and low levels of IgG1 antibody which has much less complement fixing activity. Passive transfer of serum from animals immunized with the DNA vaccine expressing PspA was also able to reduce the fraction of mice with high density of colonization of the nasopharynx. Secretion of IFN-gamma, but not IL-17, was observed in splenocytes from mice immunized with the DNA vaccine. (C) 2010 Elsevier Ltd. All rights reserved.
机译:肺炎球菌表面蛋白A(PspA)是具有成本效益的疫苗的重要候选者,该疫苗具有广泛的抗肺炎链球菌功能。先前我们已经证明,以PspA作为DNA疫苗的肌肉内免疫可诱导免疫反应,其特征是在BALB / c小鼠中诱导平衡的IgG1 / IgG2a抗体反应,从而能够有效介导补体沉积到完整细菌上并诱导保护作用应对腹膜内挑战。现在,我们证实了C57BL / 6小鼠的结果,并进一步表明,表达PspA的DNA疫苗诱导的应答能够介导针对鼻咽粘膜定居的保护,即使是非肠道免疫也是如此。此外,在IgG1和恢复的CFU数量之间观察到正相关,而在鼻CFU水平和IgG2a之间观察到负相关。 IgG1 / IgG2a抗体比例与从鼻咽中回收的CFU也呈正相关。因此,鼻部定植的减少与血清IgG2a补体固定抗体水平的升高和IgG1抗体水平低(补体固定活性低得多)密切相关。来自用表达PspA的DNA疫苗免疫的动物的血清被动转移也能够减少高密度鼻咽定居小鼠的比例。在用DNA疫苗免疫的小鼠的脾细胞中观察到IFN-γ的分泌,但没有IL-17的分泌。 (C)2010 Elsevier Ltd.保留所有权利。

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