Ekström Nina, Ahman Heidi, Palmu Arto, Grönholm Sinikka, Kilpi Terhi, Käyhty Helena
National Institute for Health and Welfare THL, Helsinki, Finland.
Clin Vaccine Immunol. 2013 Jul;20(7):1034-40. doi: 10.1128/CVI.00039-13. Epub 2013 May 8.
To provide more extensive evidence of long-term effects of vaccination on immunity against Streptococcus pneumoniae, a follow-up study of the Finnish Otitis Media (FinOM) Vaccine Trial was conducted. One of the objectives was to assess the persistence and avidity of pneumococcal antibodies 4 years after pneumococcal vaccination given in infancy. Children with complete follow-up in the FinOM trial up to 24 months of age were invited to a single visit in their fifth year of life. A blood sample was taken from all children for determination of anticapsular antibody concentrations to vaccine serotypes and avidity of antibodies to three serotypes. Children had been vaccinated at 2, 4, 6, and 12 months of age with 7-valent pneumococcal capsular polysaccharide, CRM197 conjugate vaccine (PCV7), or a control vaccine. Serum IgG antibody concentrations to vaccine serotypes remained significantly higher in children who had received PCV7 than in control children for 4 years after the fourth PCV7 dose. Concentrations of antibodies to frequently carried serotypes (6B and 19F) declined less than those of antibodies to a rarely carried serotype (4), suggesting that natural boosting contributed to antibody persistence. Furthermore, antibody avidity was significantly higher in PCV7 than control vaccine recipients. Four doses of PCV7 given in infancy elicit long-lasting antibody responses with high avidity. (This study has been registered at ClinicalTrials.gov under registration no. NCT00378417.).
为了提供更多关于疫苗接种对肺炎链球菌免疫力长期影响的广泛证据,开展了一项芬兰中耳炎(FinOM)疫苗试验的随访研究。其中一个目标是评估婴儿期接种肺炎球菌疫苗4年后肺炎球菌抗体的持久性和亲和力。邀请在FinOM试验中至24个月龄时进行完整随访的儿童在其5岁时进行单次就诊。采集所有儿童的血样,以测定针对疫苗血清型的抗荚膜抗体浓度以及针对三种血清型的抗体亲和力。儿童在2、4、6和12月龄时接种了7价肺炎球菌荚膜多糖、CRM197结合疫苗(PCV7)或对照疫苗。在第四剂PCV7接种后4年,接受PCV7的儿童中针对疫苗血清型的血清IgG抗体浓度仍显著高于对照儿童。针对常见携带血清型(6B和19F)的抗体浓度下降幅度小于针对罕见携带血清型(4)的抗体浓度,这表明自然增强作用有助于抗体的持久性。此外,PCV7接种者的抗体亲和力显著高于对照疫苗接种者。婴儿期接种四剂PCV7可引发具有高亲和力的持久抗体反应。(本研究已在ClinicalTrials.gov注册,注册号为NCT00378417。)