Kamiya H, Nii R
Department of Pediatrics, Mie National Hospital, Japan.
Tokai J Exp Clin Med. 1988;13 Suppl:45-9.
Acellular pertussis diphtheria, tetanus vaccine (APDT) was licensed in 1981 in Japan. This vaccine contains pertussis toxin (PT), filamentous hemagglutinin (FHA) and agglutinogen (AGG) as the main protective antigens. The new APDT vaccine produced by each company differs slightly in composition. There are two representative types of vaccine. One vaccine (B type) contains PT and FHA in a ratio of 1 to 1 and the other one (T type) contains PT and FHA in a ratio of 4 to 1 or 9 to 1 and also contains different amounts of AGG. We have been comparing the effectiveness of these two types of vaccine. The adverse reactions of APDT were local reactions such as redness and swelling, with a few febrile cases. No central nervous system adverse reactions were observed. The antibody protective level of this vaccine is also being investigated. After we changed from conventional vaccine to APDT, the frequency of serious adverse reactions was reduced and the number of pertussis infections also gradually decreased. This vaccine should be used for the children world-wide.
无细胞百日咳、白喉、破伤风疫苗(APDT)于1981年在日本获得许可。该疫苗含有百日咳毒素(PT)、丝状血凝素(FHA)和凝集原(AGG)作为主要保护性抗原。各公司生产的新型APDT疫苗在成分上略有不同。有两种代表性的疫苗类型。一种疫苗(B型)中PT和FHA的比例为1比1,另一种(T型)中PT和FHA的比例为4比1或9比1,并且还含有不同量的AGG。我们一直在比较这两种疫苗的有效性。APDT的不良反应为局部反应,如发红和肿胀,有少数发热病例。未观察到中枢神经系统不良反应。这种疫苗的抗体保护水平也在研究中。我们从传统疫苗改用APDT后,严重不良反应的发生率降低,百日咳感染数量也逐渐减少。这种疫苗应在全球范围内用于儿童。