Immunogenicity and safety of a pentavalent acellular pertussis combined vaccine including diphtheria, tetanus, inactivated poliovirus and conjugated Haemophilus Influenzae type b polysaccharide for primary vaccination at 2, 3, 4 or 3, 4, 5 months of age in infants in China

被引:14
|
作者
Li, Rong Cheng
Li, Feng Xiang
Li, Yan Ping
Hou, Qi Ming
Li, Chang Gui
Li, Ya Nan
Chen, Fu Sheng [2 ]
Hu, Xue Zhong [3 ]
Su, Wen Bin [4 ]
Zhang, Shu Min
Fang, Han Hua
Ye, Qiang
Zeng, Tian De [2 ]
Liu, Tao Xuan [3 ]
Li, Xiu Bi [4 ]
Huang, Yun Neng [5 ]
Deng, Man Ling [5 ]
Zhang, Yan Ping
Ortiz, Esteban [1 ]
机构
[1] Sanofi Pasteur, Global Med Affairs, F-69007 Lyon, France
[2] Ping Le Cty Ctr Dis Prevent & Control, Guangxi, Peoples R China
[3] Li Pu Cty Ctr Dis Prevent & Control, Guangxi, Peoples R China
[4] Yang Shuo Cty Ctr Dis Prevent & Control, Guangxi, Peoples R China
[5] Gui Lin City Ctr Dis Prevent & Control, Guangxi, Peoples R China
关键词
Pentavalent vaccine; China; Immunogenicity; Safety; Primary series; COMBINATION VACCINES; FOLLOW-UP; CHILDREN; POLIOMYELITIS; PNEUMONIA; DISEASE; BOOSTER;
D O I
10.1016/j.vaccine.2010.12.103
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The aim was to demonstrate the immunogenicity and safety of a DTaP-IPV//PRP-T combined vaccine (Pentaxim (R)) compared to individual vaccines in infants in the People's Republic of China. Infants (N=792) were randomly assigned to receive DTaP-IPV//PRP-T at 2, 3 and 4 months of age (Group A) or 3, 4 and 5 months of age (Group B), or DTaP (Wuhan Institute of Biological Products), PRP-T (Act-Hib (R)) and IPV (Imovax (R) Polio) at 3,4 and 5 months of age (Group C). Antibody titers were measured pre- and 1 month after the third vaccination; non-inferiority analyses were performed for seroprotection/seroconversion (SP/SC) rates. Safety was assessed 1 month after the primary series. SP/SC rates for the DTaP-IPV//PRP-T vaccine were high and non-inferior to the controls. Reactogenicity was low for each group and no hypotonic hyporesponsive episode or seizure was reported. In conclusion, the DTaP-IPV//PRP-T vaccine was highly immunogenic, non-inferior to the commercially available control vaccines and had a good safety profile for both primary administration schedules. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1913 / 1920
页数:8
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