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日本白喉类毒素-破伤风类毒素-无细胞百日咳疫苗的使用经验。

Experience with diphtheria toxoid-tetanus toxoid-acellular pertussis vaccine in Japan.

作者信息

Sato H, Sato Y

机构信息

National Institute of Health, Tokyo, Japan.

出版信息

Clin Infect Dis. 1999 Jun;28 Suppl 2:S124-30. doi: 10.1086/515063.

Abstract

In Japan, the morbidity rate for pertussis per 100,000 population was 147.6 in 1950 when whole cell pertussis vaccine was introduced but dropped to 0.2 in 1972 when routine immunization with a combined vaccine consisting of diphtheria toxoid, tetanus toxoid, and whole cell pertussis had been widely accepted. Thereafter, adverse reactions to the whole cell pertussis vaccine became a social problem and lowered the acceptance of the vaccine. As a result, the morbidity rate increased to 11.3 in 1979. Introduction of the safer yet efficacious acellular pertussis vaccine, consisting of mainly pertussis toxoid and filamentous hemagglutinin, into the routine childhood vaccination in combination with diphtheria and tetanus toxoids in 1981 increased the acceptance rate. The lowest morbidity rate, 0.1, was achieved in 1993. During the next 16 years, almost all cases were in unvaccinated or incompletely vaccinated persons. Regardless of whether whole cell or acellular pertussis vaccine was used, > 90% of the reported pertussis cases were in children < 10 years of age until 1990. However, since 1991, the rate of pertussis in young adults 20-44 years of age has been clearly increasing. To control pertussis, booster vaccination with diphtheria toxoid-tetanus toxoid-acellular pertussis vaccine in adults should be considered.

摘要

在日本,1950年引入全细胞百日咳疫苗时,每10万人口中的百日咳发病率为147.6,但在1972年,当由白喉类毒素、破伤风类毒素和全细胞百日咳组成的联合疫苗的常规免疫被广泛接受时,发病率降至0.2。此后,全细胞百日咳疫苗的不良反应成为一个社会问题,降低了疫苗的接受度。结果,1979年发病率升至11.3。1981年,将主要由百日咳类毒素和丝状血凝素组成的更安全且有效的无细胞百日咳疫苗引入儿童常规疫苗接种,并与白喉和破伤风类毒素联合使用,提高了接受率。1993年达到了最低发病率0.1。在接下来的16年里,几乎所有病例都发生在未接种疫苗或未完全接种疫苗的人群中。直到1990年,无论使用全细胞还是无细胞百日咳疫苗,报告的百日咳病例中>90%发生在10岁以下儿童中。然而,自1991年以来,20至44岁的年轻成年人中的百日咳发病率一直在明显上升。为了控制百日咳,应考虑对成年人进行白喉类毒素-破伤风类毒素-无细胞百日咳疫苗的加强接种。

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