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Evaluation of serotypes 5 and 8 capsular polysaccharides in protection against Staphylococcus aureus in murine models of infection

机译:血清型5和8荚膜多糖的评价在感染鼠模型中葡萄球菌保护中的保护

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Staphylococcus aureus is the leading cause of nosocomial and community-acquired infections, including soft tissue and skin infections and bacteremia. However, efforts to develop an effective vaccine against S. aureus infections have not been successful. We evaluated serotypes 5 and 8 capsule polysaccharides (CP) CRM197 conjugates as vaccine candidates in murine models of bacteremia, lethal sepsis, and skin infection. The conjugate vaccines elicited a good antibody response, and active immunization of CP5-CRM or CP8-CRM conjugates protected against staphylococcal bacteremia. In the skin infection model, CP8-CRM but not CP5-CRM protected against dermonecrosis, and CP8-CRM immunization significantly decreased the bacterial burden in the lesion. However, neither CP5-CRM nor CP8-CRM protected against mortality in the lethal sepsis model. The results indicate the capsular vaccines elicit protection against some, but not all, aspects of staphylococcal infection.
机译:金黄色葡萄球菌是医院和社区收养的感染的主要原因,包括软组织和皮肤感染和菌血症。 然而,努力制定有效疫苗的针对金黄色葡萄球菌感染没有成功。 我们评估了血清型和8粒多糖(CP)CRM197缀合物作为菌丝模型的疫苗候选菌,致死败血症和皮肤感染。 缀合物疫苗引发了良好的抗体反应,并且CP5-CRM或CP8-CRM缀合物的主动免疫保护免受葡萄球菌菌血症。 在皮肤感染模型中,CP8-CRM但不是CP5-CRM免受DermoNecros,CP8-CRM免疫显着降低了病变中的细菌负担。 然而,既不是CP5-CRM也没有CP8-CRM免受致死败血症模型中的死亡率。 结果表明,囊疫苗引发了对某些但不是全部的葡萄球菌感染方面的保护。

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