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Comparison of immune responses against foot-and-mouth disease virus induced by fusion proteins using the swine IgG heavy chain constant region or beta-galactosidase as a carrier of immunogenic epitopes

文献类型: 外文期刊

作者: Li, GJ 1 ; Chen, WZ 2 ; Yan, WY 2 ; Zhao, K 2 ; Liu, MQ 2 ; Zhang, J 2 ; Fei, L 2 ; Xu, QX 2 ; Sheng, ZT 2 ; Lu, YG 2 ; Zheng, ZX 2 ;

作者机构: 1.Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China

2.Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China; Shanghai Acad Agr Sci, Inst Anim Husb & Vet Med, Shanghai 201106, Peoples R China; Zhejiang Acad Agr Sci, Inst Virol, Hangzhou 310021, Peoples R China; Inst Vet Lanzhou, Lanzhou 730046, Peoples R China

关键词: FMDV;IgG;vaccine;immune response;T-CELL EPITOPE;IMMUNOGLOBULIN MOLECULES;SYNTHETIC PEPTIDE;VACCINE CANDIDATE;CAPSID PROTEINS;PROTECTION;CATTLE;FMDV;ANTIBODIES;IMMUNIZATION

期刊名称:VIROLOGY ( 影响因子:3.616; 五年影响因子:3.967 )

ISSN:

年卷期:

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收录情况: SCI

摘要: Previously, we demonstrated that a fusion protein (Gal-FMDV) consisting of beta-galactosidase and an immunogenic peptide, amino acids (141-160)-(21-40)-(141-160), of foot-and-mouth disease virus (FMDV) VP1 protein induced protective immune responses in guinea pigs and swine. We now designed a new potential recombinant protein vaccine against FMDV in swine. The immunogenic peptide, amino acids (141-160)-(21-40)-(141-160) from the VP1 protein of serotype O FMDV, was fused to the carboxy terminus of a swine immunoglobulin G single heavy chain constant region and expressed in Escherichia coli. The expressed fusion protein (IgG-FMDV) was purified and emulsified with oil adjuvant. Vaccination twice at an interval of 3 weeks with the emulsified IgG-FMDV fusion protein induced an FMDV-specific spleen proliferative T-cell response in guinea pigs and elicited high levels of neutralizing antibody in guinea pigs and swine. All of the immunized animals were efficiently protected against FMDV challenge. There was no significant difference between IgG-FMDV and Gal-FMDV in eliciting immunity after vaccination twice in swine. However, when evaluating the efficacy of a single inoculation of the fusion proteins, we found that IgG-FMDV could elicit a protective immune response in swine, while Gal-FMDV only elicited a weak neutralizing activity and could not protect the swine against FMDV challenge. Our results suggest that the IgG-FMDV fusion protein is a promising vaccine candidate for FMD in swine. (C) 2004 Elsevier Inc. All rights reserved.

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