Ukkonen P, Hovi T, von Bonsdorff C H, Saikku P, Penttinen K
J Med Virol. 1984;13(2):131-48. doi: 10.1002/jmv.1890130204.
The age-specific prevalence of CF antibodies against 16 viral antigens was determined by using the computerized data registry of the routine diagnostic laboratory of the authors' department. The material consisted of data based on serum specimens from about 58,500 patients. All ages from newborn infants to 90-year-olds were represented. The sera had been collected and tested with a CF screening test over a period of 8 years (1971-1978). Several different antibody prevalence patterns were distinguished in regard to the rapidity and timing of the initial increase of the prevalence, as well as to the mode of later changes in prevalence. For most respiratory viruses a rapid increase of the prevalence was seen through the childhood continuing, for some of them, up to the 30s (influenza A and coronavirus), while rather variable patterns were found in the older age groups. Herpes simplex and cytomegaloviruses showed, interestingly, another type of pattern: a slow increase of prevalence continuing through the whole age range. The frequency of herpes simplex antibodies reached 90% by the age of 80 years. Antibody levels against any antigen in infants less than one-month-old were equal to those in 20- to 40-year-old adults, and the expected rapid decrease of antibodies took place within the first 6 months of life. Possible influences of epidemics and repeated exposures to different viruses (external boosting), and of latent or chronic infections (internal boosting), as well as of technical variations, on the observed prevalence patterns are discussed.
利用作者所在科室常规诊断实验室的计算机化数据登记系统,确定了针对16种病毒抗原的CF抗体在不同年龄组中的流行率。材料包括约58500名患者血清标本的数据。涵盖了从新生儿到90岁的所有年龄段。这些血清是在8年期间(1971 - 1978年)收集的,并通过CF筛查试验进行检测。根据流行率初始上升的速度和时间以及流行率后期变化的模式,区分出几种不同的抗体流行模式。对于大多数呼吸道病毒,流行率在儿童期迅速上升,并持续到30多岁(甲型流感和冠状病毒),而在老年组中发现的模式则相当多变。有趣的是,单纯疱疹病毒和巨细胞病毒呈现出另一种模式:流行率在整个年龄范围内持续缓慢上升。到80岁时,单纯疱疹抗体的频率达到90%。小于1个月的婴儿针对任何抗原的抗体水平与20至40岁成年人的抗体水平相当,并且抗体预期的快速下降发生在生命的前6个月内。文中讨论了疫情、反复接触不同病毒(外部增强)、潜伏或慢性感染(内部增强)以及技术差异对观察到的流行模式可能产生的影响。