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Evaluation of Pneumococcal Surface Protein A as a Vaccine Antigen against Secondary Streptococcus pneumoniae Challenge during Influenza A Infection

机译:肺炎球菌表面蛋白A作为疫苗抗原抗甲型流感病毒继发性肺炎链球菌攻击的评估

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摘要

Secondary bacterial pneumonia is responsible for significant morbidity and mortality during seasonal and pandemic influenza. Due to the unpredictability of influenza A virus evolution and the time-consuming process of manufacturing strain-specific influenza vaccines, recent efforts have been focused on developing anti- immunity to prevent influenza-related illness and death. Bacterial vaccination to prevent viral-bacterial synergistic interaction during co-infection is a promising concept that needs further investigation. Here, we show that immunization with pneumococcal surface protein A (PspA) fully protects mice against low-dose, but not high-dose, secondary bacterial challenge using a murine model of influenza A virus- co-infection. We further show that immunization with PspA is more broadly protective than the pneumococcal conjugate vaccine (Prevnar). These results demonstrate that PspA is a promising vaccine target that can provide protection against a physiologically relevant dose of following influenza infection.
机译:在季节性和大流行性流感期间,继发性细菌性肺炎是造成高发病率和高死亡率的原因。由于甲型流感病毒进化的不可预测性以及制造菌株特异性流感疫苗的耗时过程,最近的努力集中在开发抗免疫性上,以预防与流感相关的疾病和死亡。在共同感染过程中预防细菌-细菌协同相互作用的细菌疫苗接种是一个有前途的概念,需要进一步研究。在这里,我们显示,使用A型流感病毒共感染的鼠模型,肺炎球菌表面蛋白A(PspA)免疫可完全保护小鼠免受小剂量但不是大剂量的次级细菌攻击。我们进一步表明,用PspA进行的免疫比肺炎球菌结合疫苗(Prevnar)具有更广泛的保护性。这些结果表明,PspA是一种有前途的疫苗靶标,可以针对流感相关的生理相关剂量提供保护。

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