Brüssow H, Baensch M, Sidoti J
Nestlé Research Centre, Nestec Ltd., Vers-chez-les-Blanc, Lausanne, Switzerland.
J Clin Microbiol. 1992 Nov;30(11):2765-71. doi: 10.1128/jcm.30.11.2765-2771.1992.
The age-specific prevalence of serum immunoglobulin M (IgM) antibody to capsular polysaccharides of Streptococcus pneumoniae, as detected by enzyme-linked immunosorbent assay, was studied in 1,301 Ecuadorian children enrolled in a national nutrition and health survey. This prevalence was 6% in infants < 6 months old and increased to 28% in children 6 to 11 months old, 49% in those 12 to 17 months old, and 58% in those 18 to 23 months old. About 80% of the 5-year-old children had this antibody. When tested separately against six different capsular polysaccharides, serum IgM antibody reacted with decreasing frequency with serotype 3, 8, 19, 6, 23, and 1 capsular polysaccharides. We did not observe a broadening of the antibody response with increasing age in the sense that more and more serotypes were recognized. A similar age-related prevalence was found for IgM antibody to the species-specific C-polysaccharide of S. pneumoniae and for IgG antibody to capsular polysaccharides of S. pneumoniae. A smaller German serum collection showed a comparable age-related prevalence of pneumococcus-specific serum IgG and IgM antibodies. The highest incidence of respiratory diseases was observed in 1- and 2-year-old Ecuadorian children. It thus seems that acquisition of serum antibody to S. pneumoniae reflects more the developmental maturation of an immune response than an actual exposure to different pneumococcal serotypes.
在一项全国营养与健康调查中,对1301名厄瓜多尔儿童进行了研究,通过酶联免疫吸附测定法检测了针对肺炎链球菌荚膜多糖的血清免疫球蛋白M(IgM)抗体的年龄特异性患病率。6个月以下婴儿的患病率为6%,6至11个月大儿童的患病率增至28%,12至17个月大儿童的患病率为49%,18至23个月大儿童的患病率为58%。约80%的5岁儿童有这种抗体。当分别针对六种不同的荚膜多糖进行检测时,血清IgM抗体与3型、8型、19型、6型、23型和1型荚膜多糖反应的频率逐渐降低。我们没有观察到随着年龄增长抗体反应范围扩大,即识别出越来越多血清型的情况。针对肺炎链球菌种特异性C多糖的IgM抗体以及针对肺炎链球菌荚膜多糖的IgG抗体也发现了类似的年龄相关患病率。一份规模较小的德国血清样本显示,肺炎球菌特异性血清IgG和IgM抗体的年龄相关患病率与之相当。在1岁和2岁的厄瓜多尔儿童中观察到呼吸道疾病的发病率最高。因此,似乎获得肺炎链球菌血清抗体更多地反映了免疫反应的发育成熟,而非实际接触不同的肺炎球菌血清型。