| Literature DB >> 21084463 |
Jun-Jun Shao1, Chung Kai Wong, Tong Lin, Shuk Kwan Lee, Guo-Zheng Cong, Fion Wai Yee Sin, Jun-Zheng Du, Shan-Dian Gao, Xiang-Tao Liu, Xue-Peng Cai, Yong Xie, Hui-Yun Chang, Ji-Xing Liu.
Abstract
In order to develop a completely safe immunogen to replace the traditional inactivated vaccine, a tandem-repeat multiple-epitope recombinant vaccine against foot-and-mouth disease (FMD) virus (FMDV) type O was developed. It contained three copies each of residues 141 to 160 and 200 to 213 of VP1 of the O/China/99 strain of FMDV coupled with a swine immunoglobulin G heavy-chain constant region (scIgG). The data showed that the multiple-epitope recombinant vaccine elicited high titers of anti-FMDV specific antibodies in swine at 30 days postvaccination (dpv) and conferred complete protection against a challenge with 10³ 50% swine infective doses of the O/China/99 strain. The anti-FMDV specific antibody titers were not significantly different between the multiple-epitope recombinant vaccine and the traditional vaccine (t test, P > 0.05). The number of 50% pig protective doses was 6.47, which is higher than the number recommended by the World Organization for Animal Health. The multiple-epitope recombinant vaccine resulted in a duration of immunity of at least 6 months. We speculate that the multiple-epitope recombinant vaccine is a promising vaccine that may replace the traditional inactivated vaccine for the prevention and control of FMD in swine in the future.Entities:
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Year: 2010 PMID: 21084463 PMCID: PMC3019777 DOI: 10.1128/CVI.00236-10
Source DB: PubMed Journal: Clin Vaccine Immunol ISSN: 1556-679X