Holmlund Emma, Quiambao Beatriz, Ollgren Jukka, Nohynek Hanna, Käyhty Helena
Vaccine Immunology Laboratory, National Public Health Institute, Mannerheimintie 166, 00300 Helsinki, Finland.
Vaccine. 2006 Jan 9;24(1):57-65. doi: 10.1016/j.vaccine.2005.07.055. Epub 2005 Aug 3.
For vaccine development it is important to know how antibodies develop after natural pneumococcal contacts. This work was done to receive information about the development of natural antibodies to pneumococcal surface protein A (PspA), pneumococcal surface adhesin A (PsaA) and pneumolysin (Ply), in early infancy and to receive information on how nasopharyngeal carriage of Streptococcus pneumoniae in infants affects the antibody concentrations. The antibody concentrations to PspA, PsaA and Ply were measured by EIA in serum samples of 51 pregnant women, in six consecutive serum samples of 173 infants (samples from 7 to 48 weeks of age), as well as in 39 cord bloods. Nasopharyngeal swabs were also collected from the infants and cultured for pneumococci. The geometric mean concentration (GMC) of anti-PspA and -Ply decreased until 18 weeks of age and started to increase thereafter, but was still at 48 weeks lower than in the mothers. The GMC of anti-PsaA in the infants increased significantly by age and reached the GMC of the mothers already at 14 weeks of age. The increase in antibody concentration in the infants was associated with pneumococcal carriage, but followed the different kinetics depending on the antigen. High maternal anti-Ply antibodies were negatively associated with the risk of pneumococcal carriage (OR 0.78, 0.61-0.99). This indicates that high maternal anti-Ply could be associated with lower pneumococcal carriage acquisition in infants.
对于疫苗研发而言,了解自然接触肺炎球菌后抗体如何产生非常重要。开展这项研究是为了获取有关婴儿早期针对肺炎球菌表面蛋白A(PspA)、肺炎球菌表面黏附素A(PsaA)和肺炎溶血素(Ply)的天然抗体产生情况的信息,并了解婴儿肺炎链球菌鼻咽部携带情况如何影响抗体浓度。通过酶免疫测定法(EIA)检测了51名孕妇血清样本、173名婴儿连续6份血清样本(7至48周龄样本)以及39份脐带血中针对PspA、PsaA和Ply的抗体浓度。还从婴儿采集了鼻咽拭子并培养肺炎球菌。抗PspA和抗Ply的几何平均浓度(GMC)在18周龄前下降,此后开始上升,但在48周龄时仍低于母亲的水平。婴儿抗PsaA的GMC随年龄显著增加,在14周龄时已达到母亲的GMC。婴儿抗体浓度的增加与肺炎球菌携带有关,但根据抗原不同遵循不同的动力学。母亲高抗Ply抗体与肺炎球菌携带风险呈负相关(比值比0.78,0.61 - 0.99)。这表明母亲高抗Ply可能与婴儿较低的肺炎球菌携带获得率有关。