Halperin S A, Davies H D, Barreto L, Guasparini R, Meekison W, Humphreys G, Eastwood B J
Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia.
J Pediatr. 1997 Apr;130(4):525-31. doi: 10.1016/s0022-3476(97)70233-6.
To compare the safety and immunity of an acellular pertussis vaccine containing pertussis toxoid, filamentous hemagglutinin, 69 kd protein, fimbriae 2 and 3 combined with diphtheria and tetanus toxoids given as single or separate injection with inactivated poliovirus vaccine (MRC-5-or Vero cell-derived) or live attenuated polio vaccine.
A total of 425 healthy children between 17 and 19 months of age who were receiving the fourth dose of their routine immunization series were randomly allocated to receive either the acellular pertussis vaccine and oral poliovirus vaccine or one of two inactivated poliovirus vaccines as a combined injection or separate injections.
Although minor adverse events were commonly reported, differences between the groups were few. Fever and decreased feeding were less common in recipients of live attenuated poliovirus vaccine than the combination vaccine containing MRC-5 cell-derived inactivated poliovirus vaccine. A significant antibody response was demonstrated in all groups against all the antigens contained in the vaccines. Antibodies against poliovirus were higher in the groups immunized with the inactivated poliovirus vaccine than the live attenuated vaccine. Anti-69 kd protein antibodies were higher in the group given the MRC-5 cell-derived inactivated poliovirus vaccine as a combined injection than in the group given the separate injection or the group immunized with the live attenuated poliovirus vaccine.
The five-component acellular pertussis vaccine combined with diphtherid and tetanus toxoids is safe and immunogenic when combined with either MRC-5- or Vero cell-derived inactivated poliovirus vaccine. This will facilitate the implementation of acellular pertussis vaccine and the movement to inactivated poliovirus vaccine programs.
比较含有百日咳毒素、丝状血凝素、69kd蛋白、2型和3型菌毛的无细胞百日咳疫苗与白喉和破伤风类毒素联合使用时,单剂或分开注射与灭活脊髓灰质炎疫苗(MRC-5细胞或Vero细胞衍生)或减毒活脊髓灰质炎疫苗的安全性和免疫效果。
共有425名17至19个月大正在接受常规免疫系列第四剂接种的健康儿童被随机分配,接受无细胞百日咳疫苗和口服脊髓灰质炎疫苗,或两种灭活脊髓灰质炎疫苗之一进行联合注射或分开注射。
尽管常见轻微不良事件报告,但各组之间差异较少。减毒活脊髓灰质炎疫苗接种者中发热和进食减少的情况比含有MRC-5细胞衍生的灭活脊髓灰质炎疫苗的联合疫苗更少。所有组对疫苗中包含的所有抗原均表现出显著的抗体反应。接种灭活脊髓灰质炎疫苗组的脊髓灰质炎病毒抗体高于减毒活疫苗组。接受MRC-5细胞衍生的灭活脊髓灰质炎疫苗联合注射组的抗69kd蛋白抗体高于分开注射组或接种减毒活脊髓灰质炎疫苗组。
与MRC-5细胞或Vero细胞衍生的灭活脊髓灰质炎疫苗联合使用时,五组分无细胞百日咳疫苗与白喉和破伤风类毒素联合使用是安全且具有免疫原性的。这将有助于无细胞百日咳疫苗的实施以及向灭活脊髓灰质炎疫苗计划的转变。