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基于腺病毒/甲病毒复制子嵌合载体的疫苗 rAdV-SFV-E2 对古典猪瘟的综合评估。

Comprehensive evaluation of the adenovirus/alphavirus-replicon chimeric vector-based vaccine rAdV-SFV-E2 against classical swine fever.

机构信息

State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China.

出版信息

Vaccine. 2013 Jan 7;31(3):538-44. doi: 10.1016/j.vaccine.2012.11.013. Epub 2012 Nov 12.

DOI:10.1016/j.vaccine.2012.11.013
PMID:23153441
Abstract

Classical swine fever (CSF) is an economically important, highly contagious swine disease caused by classical swine fever virus (CSFV). Marker vaccines and companion serological diagnostic tests are thought to be a promising strategy for future control and eradication of CSF. Previously, we have demonstrated that an adenovirus-vectored Semliki forest virus replicon construct expressing the E2 glycoprotein from CSFV, rAdV-SFV-E2, induced sterile immunity against a lethal CSFV challenge. In this study, we further evaluated the vaccine with respect to its safety, number and dose of immunization, and effects of maternally derived antibodies, re-immunization of the vaccine or co-administration with pseudorabies vaccine on the vaccine efficacy. The results showed that: (1) the vaccine was safe for mice, rabbits and pigs; (2) two immunizations with a dose as low as 6.25×10(5) TCID(50) or a single immunization with a dose of 10(7) TCID(50) rAdV-SFV-E2 provided complete protection against a lethal CSFV challenge; (3) maternally derived antibodies had no inhibitory effects on the efficacy of the vaccine; (4) the vaccine did not induce interfering anti-vector immunity; and (5) co-administration of rAdV-SFV-E2 with a live pseudorabies vaccine induced antibodies and protection indistinguishable from immunization with either vaccine administered alone. Taken together, the chimeric vaccine represents a promising marker vaccine candidate for control and eradication of CSF.

摘要

经典猪瘟(CSF)是一种经济上重要的、高度传染性的猪病,由经典猪瘟病毒(CSFV)引起。标记疫苗和伴随的血清学诊断测试被认为是未来控制和根除 CSF 的有前途的策略。先前,我们已经证明,表达 CSFV E2 糖蛋白的腺病毒载体 Semliki 森林病毒复制子构建体 rAdV-SFV-E2 诱导了针对致命 CSFV 挑战的无菌免疫力。在这项研究中,我们进一步评估了疫苗的安全性、免疫次数和剂量、母源抗体的影响、疫苗的再免疫或与伪狂犬病疫苗共同给药对疫苗效力的影响。结果表明:(1)该疫苗对小鼠、兔和猪是安全的;(2)两次免疫剂量低至 6.25×10(5)TCID(50)或单次免疫剂量为 10(7)TCID(50)rAdV-SFV-E2 可提供针对致命 CSFV 挑战的完全保护;(3)母源抗体对疫苗效力没有抑制作用;(4)疫苗不会诱导干扰抗载体免疫;(5)rAdV-SFV-E2 与活伪狂犬病疫苗共同给药诱导的抗体和保护作用与单独使用任何一种疫苗免疫相同。总之,嵌合疫苗代表了控制和根除 CSF 的有前途的标记疫苗候选物。

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