摘要
目前,国内许多疫苗生产厂家都在致力于研制以无细胞组分百日咳-白喉-破伤风疫苗(diphtheria,tetanus,acelluar component pertussis vaccine,DTacP)为基础的联合疫苗,而国外不同厂家该类联合疫苗的临床试验,其免疫后抗体检测方法和保护性评判标准有较大差异。此文旨在通过比较不同DTacP-灭活脊髓灰质炎病毒疫苗的临床免疫原性结果,包括血清保护率/血清转换率和不同方法测定的抗体几何平均滴度,为临床试验方案设计提供依据和思路。
At present,many vaccine manufactories in China are focusing on the development of combined vaccines based on diphtheria, tetanus, component pertussis vaccine (DTacP). There are great differences in antibody detection methods and protective evaluation criteria in clinical trials of different manufacturers abroad.This paper is aimed to provide experimental evidence and ideas for the design protocol of clinical trial by comparing the immunogenity results of different DTacP-inactivated poliovirus vaccines including seropositive/seroconversion rates and geographic mean titers measured by various detection methods.
作者
潘殊男(综述)
肖詹蓉(审校)
Pan Shunan;Xiao Zhanrong(Research Division of Bacterial Vaccine,Beijing Biological Products Institute Co.,Ltd.,Beijing 100176,China)
出处
《国际生物制品学杂志》
CAS
2019年第2期84-87,共4页
International Journal of Biologicals
