Immunogenicity and safety of concomitant administration of the chinese inactivated poliovirus vaccine with the diphtheria-tetanus-acellular pertussis (DTaP) vaccine in children: A multicenter, randomized, non-inferiority, controlled trial

被引:5
作者
Sun, Xiang [1 ]
Xu, Yan [1 ]
Tang, Fenyang [1 ]
Xiao, Yanhui [2 ]
Wang, Zhiguo [1 ]
Wang, Binbing [3 ]
Zhu, Xiaoping [4 ]
Yang, Xiaoming [2 ]
Chen, Haiping [2 ]
机构
[1] Jiangsu Prov Ctr Dis Control & Prevent, Expanded Program Immunizat, Nanjing, Jiangsu, Peoples R China
[2] China Natl Biotec Grp Co Ltd, Med Affairs, Beijing, Peoples R China
[3] Anhui Prov Ctr Dis Control & Prevent, Expanded Program Immunizat, Hefei, Anhui, Peoples R China
[4] Sichuan Prov Ctr Dis Control & Prevent, Expanded Program Immunizat, Chengdu, Sichuan, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
sIPV; DTaP; concomitant administration; vaccine interference; safety; immunogenicity; DTPA-HBV-IPV/HIB; POSTMARKETING SURVEILLANCE; CLINICAL-TRIAL; OPEN-LABEL; REACTOGENICITY; IMMUNIZATION;
D O I
10.3389/fimmu.2022.905634
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Key point: Considering that vaccination with the sIPV and DTaP overlap at the ages of 3 and 4 months in China, to reduce the burden of treatment on parents and increase vaccination coverage rates, we designed a postmarket clinical study of co-administration. Background: The Sabin-strain-based inactivated poliovirus vaccine (sIPV) and the diphtheria-tetanus-acellular pertussis vaccine (DTaP) have been licensed in China for many years. To conduct a clinical study on the safety and immunogenicity of the sIPV when administered concomitantly with the DTaP. Methods: The study population was divided into three groups: group 1 was the sl PV+ DTaP concomitant administration group, group 2 was the sIPV inoculation group, and group 3 was the DTaP inoculation group. Blood samples were collected prevaccination and 30 days postvaccination, and serum antibody levels were detected. Results: This study showed that the seropositive and seroconversion rates of type 1, 2 and 3 poliovirus in group 1 were higher than those in group 2, with no statistically significant difference after vaccination (P>0.05). Groups 1 and 3 also showed similar responses for all vaccine antigens except anti-FHA (97.65 (94.09-99.36) vs. 100 (97.89-100)). The geometric mean titers (GMTs) for the DTaP and sIPV among the groups were comparable, and the non-inferiority t test result was P<0.001. The number of local adverse events (AEs) reported in group 1 (29.91%) were larger than those in group 2 (12.39%) and group 3 (21.93%), among which the most common was redness. Similarly, the most common systemic AE was fever. All 5 severe AE (SAE) cases were determined by experts to be unrelated to the vaccines during the study. Conclusions: The evidence of similar seroconversion and safety with co-administered DTaP and sIPV supports the co-administration supports the introduction of a strategy of simultaneous administration of both vaccines into routine infant immunization, and it could increase vaccination coverage and protect more infants from morbidity and mortality from these related diseases.
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页数:11
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