Rapola S, Jäntti V, Haikala R, Syrjänen R, Carlone G M, Sampson J S, Briles D E, Paton J C, Takala A K, Kilpi T M, Käyhty H
National Public Health Institute, Dept. of Vaccines, 00300 Helsinki, Finland.
J Infect Dis. 2000 Oct;182(4):1146-52. doi: 10.1086/315822. Epub 2000 Sep 5.
Pneumococcal surface protein A (PspA), pneumococcal surface adhesin A (PsaA), and pneumolysin (Ply) are common to virtually all Streptococcus pneumoniae isolates. They are immunogenic and protective against pneumococcal challenge in animals and are the major candidates for a protein-based pneumococcal vaccine for humans. However, little is known of the natural development of antibodies to these proteins in humans. The objective of this study was to evaluate the natural development of antibodies to PspA, PsaA, and Ply in relation to pneumococcal infection and carriage in young children. Serum antibodies to these proteins were measured by EIA in children at ages 6, 12, 18, and 24 months and in their mothers. All age groups were capable of producing antibodies to the 3 proteins. The antibody concentrations increased with age and were strongly associated with pneumococcal exposure, whether by carriage or infection (acute otitis media).
肺炎球菌表面蛋白A(PspA)、肺炎球菌表面黏附素A(PsaA)和肺炎球菌溶血素(Ply)几乎存在于所有肺炎链球菌分离株中。它们具有免疫原性,可保护动物免受肺炎球菌攻击,是人类基于蛋白质的肺炎球菌疫苗的主要候选物。然而,对于人类针对这些蛋白质的抗体的自然产生情况知之甚少。本研究的目的是评估幼儿中针对PspA、PsaA和Ply的抗体的自然产生情况与肺炎球菌感染和携带的关系。通过酶免疫测定法(EIA)检测了6、12、18和24个月大儿童及其母亲血清中针对这些蛋白质的抗体。所有年龄组都能够产生针对这3种蛋白质的抗体。抗体浓度随年龄增加,并且无论通过携带还是感染(急性中耳炎),都与肺炎球菌暴露密切相关。