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Long-term clinical studies of varicella vaccine at a regional hospital in Japan and proposal for a varicella vaccination program

机译:水痘疫苗在日本地方医院的长期临床研究以及水痘疫苗接种计划的建议

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In 1974, a live varicella vaccine (Oka strain) was developed in Japan for the prevention of varicella. It has been commercially available since 1987 for the voluntary vaccination program, in which children over the age of 1 year with no history of previous varicella infection receive a single dose. From before approval up to the present, we have been carrying out long-term studies in healthy children at a regional hospital to assess the immunogenicity, safety, and efficacy of the varicella vaccine. This vaccine is very safe, and serious adverse reactions have not been observed since the year 2000 when it changed gelatin-free. In the past three studies, seroconversion was detected in around 95% of subjects by the immune adherence hemagglutination (IAHA) test, and this high rate was considered to indicate good immunogenicity. Breakthrough varicella is observed in approximately 20-30% of children who receive a single dose of the vaccine, but most cases are mild. Although recent vaccination has generally been effective, the IAHA test has shown that immunogenicity is somewhat lower than was previously demonstrated. The sensitivity of the IAHA test has been shown to be adequate when compared with the neutralization test, so the current testing system is sufficient for the maintenance of immunity levels. An additional vaccination increased the IAHA antibody level in subjects who failed to seroconvert after a single dose vaccination. According to another clinical study, additional varicella vaccination at 3-5 years after the initial vaccination achieved stronger immunogenicity. Because it is administered as part of the voluntary vaccination program, the varicella vaccination coverage rate has remained low in Japan, with no sign of a decrease in the number of varicella patients. We consider that implementation of routine varicella vaccination program based on the Preventive Vaccination Law would be the most effective approach for improvement of the coverage rate. Along with this, introduction of a two-dose schedule would also be desirable. In addition to decreasing the prevalence of characteristic breakthrough varicella infection, the vaccination coverage rate would also be expected to improve with a two-dose schedule due to an increase in opportunities for vaccination
机译:1974年,日本为预防水痘而研发了活水痘疫苗(冈株)。自1987年以来,该疫苗已在市场上出售,用于自愿性疫苗接种计划,其中1岁以上无水痘以前感染史的儿童接受单剂治疗。从批准之前到现在,我们一直在区域医院对健康儿童进行长期研究,以评估水痘疫苗的免疫原性,安全性和功效。该疫苗非常安全,自从2000年改用无明胶以来,从未观察到严重的不良反应。在过去的三项研究中,通过免疫粘附血凝试验(IAHA)在大约95%的受试者中检测到了血清转化,这种高发生率被认为表明了良好的免疫原性。接受单剂疫苗的儿童中约有20-30%会观察到突破性水痘,但大多数情况是轻度的。尽管最近的疫苗接种总体上是有效的,但IAHA测试表明免疫原性略低于先前证明的水平。与中和测试相比,IAHA测试的灵敏度已被证明是足够的,因此当前的测试系统足以维持免疫力水平。在单剂疫苗接种后未能血清转化的受试者中,额外的疫苗接种增加了IAHA抗体水平。根据另一项临床研究,在初次接种疫苗后3-5年进行额外的水痘疫苗接种可获得更强的免疫原性。由于水痘疫苗是自愿性疫苗接种计划的一部分,因此在日本水痘疫苗的覆盖率一直很低,没有迹象表明水痘患者的数量有所减少。我们认为,根据预防接种法实施常规水痘疫苗接种计划将是提高覆盖率的最有效方法。伴随此,引入两剂量时间表也是理想的。除了减少特征性突破性水痘感染的患病率外,由于接种机会增加,预计接种两剂的疫苗接种率也会提高

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  • 来源
    《Vaccine》 |2013年第51期|共6页
  • 作者

    Ozaki Takao;

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