Establishing China's national standards of antigen content and neutralizing antibody responses for evaluation of enterovirus 71 (EV71) vaccines

被引:103
作者
Liang, Zhenglun [1 ]
Mao, Qunying [1 ]
Gao, Qiang [2 ]
Li, Xiuling [3 ]
Dong, Chenghong [4 ]
Yu, Xiang [5 ]
Yao, Xin [1 ]
Li, Fengxiang [1 ]
Yin, Weidong [2 ]
Li, Qihan [4 ]
Shen, Xinliang [3 ]
Wang, Junzhi [1 ]
机构
[1] Natl Inst Control Pharmaceut & Biol Prod, Beijing 100050, Peoples R China
[2] Sinovac Biotech Co Ltd, Beijing 100085, Peoples R China
[3] Natl Vaccine & Serum Inst, Beijing 100024, Peoples R China
[4] Chinese Acad Med Sci, Inst Med Biol, Kunming 650118, Peoples R China
[5] Hualan Biol Engn Inc, Hualan 453003, Henan, Peoples R China
关键词
Enterovirus 71 (EV71); Vaccine; Antigen; Neutralizing antibody (NTAb); NEWBORN MICE; ELISA METHOD; LETHAL; PROTECTION; IMMUNIZATION; INFECTION; STRAINS;
D O I
10.1016/j.vaccine.2011.10.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Enterovirus 71 (EV71) is a highly infectious agent that causes hand-foot-mouth disease (HFMD) in humans. Effective vaccination against EV71 infection is critically important, given the recent outbreak of HFMD in the Asia-Pacific region, where it has shown significant mortality and morbidity. There is currently no approved anti-viral therapy available to treat the disease. While several vaccine manufacturers are actively developing EV71 vaccines, there are no international reference standards available to conduct quality control on EV71 vaccines or to assess the effectiveness of EV71 vaccines in immunized populations. in the current report, antigen reference standard based on the C4 subtype of the EV71 vaccine strain was developed. In addition, neutralizing antibody (NTAb) reference panels were analyzed and standards with various neutralizing titers were selected. These reference antigens were used to calibrate vaccine samples from several producers and found that five EV71 antigens and the national reference standards showed good linearity and parallelism. Moreover, mice immunized with various vaccines at doses standardized by these national references showed comparable NTAb responses. Finally, the national NTAb reference panels were found to effectively reduce assay discrepancy between different labs. Taken together, these national reference standards are highly valuable for the standardization and evaluation of EV71 vaccines. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9668 / 9674
页数:7
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