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在日本,通过23年用于常规免疫接种对无细胞百日咳疫苗的安全性和有效性进行评估。

Safety and efficacy of acellular pertussis vaccine in Japan, evaluated by 23 years of its use for routine immunization.

作者信息

Kuno-Sakai Harumi, Kimura Mikio

机构信息

Department of Public Health and Social Medicine, Tokai University, Isehara City, Japan.

出版信息

Pediatr Int. 2004 Dec;46(6):650-5. doi: 10.1111/j.1442-200x.2004.01970.x.

Abstract

BACKGROUND

Real evaluation of any vaccine can only be done after the vaccine has been in routine use for a substantially long period of time. In Japan, acellular pertussis vaccine was introduced and totally replaced whole cell pertussis vaccine in 1981. From 1982 to 1988 40.3 million doses of acellular pertussis vaccine were given to 2-year-olds and from 1989 to 2001 59.3 million doses of acellular pertussis vaccine were given to 3-month-olds. It is now time to evaluate the efficacy and safety of acellular pertussis vaccine by the use of national data officially supplied by the Government.

METHODS

Government national surveillance of pertussis, which began in 1981, was used to analyze epidemiology of pertussis. Official Government reports on acceptance rates of pertussis were analyzed. A peer review has been made on all severe neurological illnesses/death occurring after pertussis immunization which have been applied for through the Vaccine Injury Compensation System, Ministry of Health Labor and Welfare, Japan.

RESULTS

High acceptance rates of acellular pertussis vaccine combined with diphtheria and tetanus toxoids (DTaP) has been maintained and a dramatic decrease in pertussis was noted over the past 23 years. Neurological illnesses temporally associated both with whole cell and with acellular pertussis vaccination has been a rare phenomenon. However, incidences of encephalopathy/encephalitis and status epileptics/frequent convulsions, febrile seizures/provocation of convulsions, and sudden deaths were significantly lower with acellular pertussis vaccination than with whole cell pertussis vaccination.

CONCLUSION

With the use of acellular pertussis vaccine which has been accepted by the public, pertussis has been well controlled in Japan.

摘要

背景

任何疫苗的实际评估只有在疫苗经过相当长时间的常规使用后才能进行。在日本,1981年引入了无细胞百日咳疫苗并完全取代了全细胞百日咳疫苗。1982年至1988年,向2岁儿童接种了4030万剂无细胞百日咳疫苗,1989年至2001年,向3个月大的婴儿接种了5930万剂无细胞百日咳疫苗。现在是时候利用政府官方提供的全国数据来评估无细胞百日咳疫苗的有效性和安全性了。

方法

利用始于1981年的政府对百日咳的全国监测来分析百日咳的流行病学情况。分析了政府关于百日咳疫苗接种率的官方报告。对通过日本厚生劳动省疫苗伤害补偿系统申请的所有百日咳免疫接种后发生的严重神经疾病/死亡病例进行了同行评审。

结果

无细胞百日咳疫苗与白喉和破伤风类毒素(DTaP)联合使用的接种率一直保持在较高水平,并且在过去23年中百日咳病例显著减少。与全细胞和无细胞百日咳疫苗接种在时间上相关的神经疾病一直是罕见现象。然而,无细胞百日咳疫苗接种后,脑病/脑炎、癫痫持续状态/频繁惊厥、热性惊厥/惊厥诱发以及猝死的发生率明显低于全细胞百日咳疫苗接种后。

结论

通过使用已被公众接受的无细胞百日咳疫苗,日本的百日咳得到了很好的控制。

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