Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA
Infect Immun. 2019 Sep 19;87(10). doi: 10.1128/IAI.00253-19. Print 2019 Oct.
Acute otitis media is one of the most common childhood infections worldwide. Currently licensed vaccines against the common otopathogen target the bacterial capsular polysaccharide and confer no protection against nonencapsulated strains or capsular types outside vaccine coverage. Mucosal infections such as acute otitis media remain prevalent, even those caused by vaccine-covered serotypes. Here, we report that a protein-based vaccine, a fusion construct of epitopes of CbpA to pneumolysin toxoid, confers effective protection against pneumococcal acute otitis media for non-PCV-13 serotypes and enhances protection for PCV-13 serotypes when coadministered with PCV-13. Having cross-reactive epitopes, the fusion protein also induces potent antibody responses against nontypeable and , engendering protection against acute otitis media caused by emerging unencapsulated otopathogens. These data suggest that augmenting capsule-based vaccination with conserved, cross-reactive protein-based vaccines broadens and enhances protection against acute otitis media.
急性中耳炎是全球最常见的儿童感染病之一。目前已获得许可的针对常见耳病原体的疫苗针对细菌荚膜多糖,对非囊膜菌株或疫苗覆盖范围之外的荚膜型没有保护作用。即使是由疫苗覆盖的血清型引起的黏膜感染,如急性中耳炎,仍然很普遍。在这里,我们报告说,一种基于蛋白质的疫苗,即 CbpA 表位与肺炎球菌溶素类毒素的融合构建体,为非 PCV-13 血清型的肺炎球菌急性中耳炎提供了有效保护,并在与 PCV-13 共同给药时增强了对 PCV-13 血清型的保护作用。由于具有交叉反应表位,融合蛋白还诱导针对不可分型和的有效抗体反应,从而针对新出现的非囊膜耳病原体引起的急性中耳炎提供保护。这些数据表明,用保守的、具有交叉反应性的基于蛋白质的疫苗来增强基于荚膜的疫苗接种,可以扩大和增强对急性中耳炎的保护作用。