Yamamoto M, McDaniel L S, Kawabata K, Briles D E, Jackson R J, McGhee J R, Kiyono H
Department of Oral Biology, The University of Alabama at Birmingham, 35294-2170, USA.
Infect Immun. 1997 Feb;65(2):640-4. doi: 10.1128/iai.65.2.640-644.1997.
Streptococcus pneumoniae is a major respiratory mucosal pathogen affecting infants and children. Although a polysaccharide-based vaccine has been useful in adult populations, it does not elicit protective immunity in infants and young children. Pneumococcal surface protein A (PspA) is a highly immunogenic surface protein produced by all strains of Streptococcus pneumoniae. Previous studies have shown that systemic immunization of mice with PspA can elicit protective immunity against fatal pneumococcal infection. In this study, we demonstrated that oral immunization with PspA could elicit protective immune responses against pneumococcal infection. When mice were orally immunized with PspA alone, low levels of PspA-specific immunoglobulin G (IgG) responses were induced in serum; none was induced in secretion. On the other hand, when PspA was given orally with the mucosal adjuvant cholera toxin (CT), significant levels of IgG and IgA anti-PspA responses were induced in serum. The major IgG subclass was IgG1, followed by IgG2b, a profile of antibody response supported by Th2-type cells. In addition, all mice orally immunized with PspA and CT were protected from the lethal challenge with capsular serotype 3 S. pneumoniae A66. These results suggested that an oral PspA vaccine may be a useful means of preventing pneumococcal disease.
肺炎链球菌是一种影响婴幼儿的主要呼吸道黏膜病原体。尽管基于多糖的疫苗对成人有效,但它不能在婴幼儿中引发保护性免疫。肺炎球菌表面蛋白A(PspA)是由所有肺炎链球菌菌株产生的一种高度免疫原性的表面蛋白。先前的研究表明,用PspA对小鼠进行全身免疫可引发针对致命性肺炎球菌感染的保护性免疫。在本研究中,我们证明用PspA进行口服免疫可引发针对肺炎球菌感染的保护性免疫反应。当单独用PspA对小鼠进行口服免疫时,血清中诱导出低水平的PspA特异性免疫球蛋白G(IgG)反应;分泌物中未诱导出反应。另一方面,当PspA与黏膜佐剂霍乱毒素(CT)一起口服时,血清中诱导出显著水平的抗PspA IgG和IgA反应。主要的IgG亚类是IgG1,其次是IgG2b,这是由Th2型细胞支持的抗体反应谱。此外,所有用PspA和CT进行口服免疫的小鼠都受到了荚膜3型肺炎链球菌A66致死性攻击的保护。这些结果表明,口服PspA疫苗可能是预防肺炎球菌疾病的一种有用手段。