Immunogenicity, safety and antibody persistence of a purified vero cell cultured rabies vaccine (Speeda) administered by the Zagreb regimen or Essen regimen in post-exposure subjects

被引:20
作者
Shi, Nianmin [1 ]
Zhang, Yibin [2 ]
Zheng, Huizhen [3 ]
Zhu, Zhenggang [4 ]
Wang, Dingming [5 ]
Li, Sihai [6 ]
Li, Yuhua [7 ]
Yang, Liqing [1 ]
Zhang, Junnan [1 ]
Bai, Yunhua [1 ]
Lu, Qiang [1 ]
Zhang, Zheng [1 ]
Luo, Fengji [1 ]
Yu, Chun [5 ]
Li, Li [1 ]
机构
[1] Chaoyang Dist Ctr Dis Control & Prevent, 25 Huaweili, Beijing 100021, Peoples R China
[2] Liaoning Chengda Biol Ltd Share Ltd, Shenyang, Peoples R China
[3] Guangdong Prov Ctr Dis Control & Prevent, Guangzhou, Guangdong, Peoples R China
[4] Wuhan City Ctr Dis Control & Prevent, Wuhan, Peoples R China
[5] Guizhou Prov Ctr Dis Control & Prevent, Guiyang, Peoples R China
[6] Hunan Prov Ctr Dis Control & Prevent, Changsha, Hunan, Peoples R China
[7] Natl Inst Food & Drug Control, Beijing, Peoples R China
关键词
Post-exposure; Protective effect; Rabies vaccine; Safety; Immunogenicity; PROPHYLAXIS; CHINA; SCHEDULE; EXPOSURE; PVRV;
D O I
10.1080/21645515.2017.1279770
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: To compare the safety, immunogenicity and long-term effect of a purified vero cell cultured rabies vaccine in post-exposure subjects following 2 intramuscular regimens, Zagreb or Essen regimen. Methods: Serum samples were collected before vaccination and on days 7, 14, 42, 180 and 365 post vaccination. Solicited adverse events were recorded for 7 d following each vaccine dose, and unsolicited adverse events throughout the entire study period. This study was registered with ClinicalTrials.gov (NCT01821911 and NCT01827917). Results: No serious adverse events were reported. Although Zagreb regimen had a higher incidence of adverse reactions than Essen regimen at the first and second injection, the incidence was similar at the third and fourth injection between these 2 groups as well. At day 42, 100% subjects developed adequate rabies virus neutralizing antibody concentrations ( 0.5IU/ml) for both regimens. At days 180 and 365, the antibody level decreased dramatically, however, the percentage of subjects with adequate antibody concentrations still remained high (above 75% and 50% respectively). None of confirmed rabies virus exposured subjects had rabies one year later, and percentage of subjects with adequate antibody concentrations reached 100% at days 14 and 42. Conclusions: Rabies post-exposure prophylaxis vaccination with PVRV following a Zagreb regimen had a similar safety, immunogenicity and long-term effect to the Essen regimen in China.
引用
收藏
页码:1338 / 1345
页数:8
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