Wiedermann G, Ambrosch F, Vanura H
Institut für Spezifische Prophylaxe und Tropenmedizin, Universität Wien.
Wien Med Wochenschr. 1991;141(12):270-2.
Acellular pertussis vaccines contain antigen components of B. pertussis, usually lymphocytosis promoting factor (LPF) which is also called pertussis-toxin (PT) or pertussigen, filamentous hemagglutinin (FH) and, eventually, agglutinogens 2 and 3. Acellular vaccines are being used in Japan since 1981. Several Phase II studies have been performed and showed a better tolerability than whole cell vaccines and antibody responses of at least equal magnitude. In some of these studies good protection rates were observed. The latter were not satisfactory in a Phase III study in Sweden. This study, however, might cause some criticism in as much as only 2 vaccine doses were given and a control group with whole cell vaccine was missing. Moreover, the significance of bacterial infections in vaccinated children is doubtful, similar observations have not been made in other trials nor in Japan since introduction of the vaccine in 1981. Preliminary results of our own study with a newly developed acellular vaccine which has been permitted by the Austrian Drug Commission have shown good tolerability.
无细胞百日咳疫苗含有百日咳杆菌的抗原成分,通常包括淋巴细胞增多促进因子(LPF),也称为百日咳毒素(PT)或百日咳原、丝状血凝素(FH),以及最终的凝集原2和3。自1981年起,日本开始使用无细胞疫苗。已经进行了多项II期研究,结果显示其耐受性优于全细胞疫苗,且抗体反应至少具有同等强度。在其中一些研究中,观察到了良好的保护率。然而,在瑞典进行的一项III期研究中,保护率并不令人满意。不过,这项研究可能会受到一些批评,因为只接种了两剂疫苗,且缺少全细胞疫苗对照组。此外,接种疫苗儿童中细菌感染的意义尚不确定,自1981年该疫苗引入以来,在其他试验或日本均未观察到类似情况。我们自己对一种新开发的、已获奥地利药品委员会批准的无细胞疫苗的研究初步结果显示,其耐受性良好。