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牛病毒性腹泻病毒(BVDV) E2 糖蛋白重组复制子疫苗的研制与评价

Development and evaluation of a replicon particle vaccine expressing the E2 glycoprotein of bovine viral diarrhea virus (BVDV) in cattle.

机构信息

Harrisvaccines, Inc, 1102 Southern Hills Dr, Suite 101, Ames, IA 50010, USA.

出版信息

Virol J. 2013 Jan 28;10:35. doi: 10.1186/1743-422X-10-35.

Abstract

BACKGROUND

Bovine viral diarrhea virus is one of the most significant and costly viral pathogens of cattle worldwide. Alphavirus-derived replicon particles have been shown to be safe and highly effective vaccine vectors against a variety of human and veterinary pathogens. Replicon particles are non-propagating, DIVA compatible, and can induce both humoral and cell mediated immune responses. This is the first experiment to demonstrate that Alphavirus-based replicon particles can be utilized in a standard prime/boost vaccination strategy in calves against a commercially significant bovine pathogen.

FINDINGS

Replicon particles that express bovine viral diarrhea virus sub-genotype 1b E2 glycoprotein were generated and expression was confirmed in vitro using polyclonal and monoclonal antibodies specific to E2. Vaccine made from particles was generated in Vero cells and administered to BVDV free calves in a prime/boost regimen at two dosage levels. Vaccination resulted in neutralizing antibody titers that cross-neutralized both type 1 and type 2 BVD genotypes following booster vaccination. Additionally, high dose vaccine administration demonstrated some protection from clinical disease and significantly reduced the degree of leukopenia caused by viral infection.

CONCLUSIONS

Replicon particle vaccines administered in a prime/boost regimen expressing BVDV E2 glycoprotein can induce cross-neutralizing titers, reduce leukopenia post challenge, and mitigate clinical disease in calves. This strategy holds promise for a safe and effective vaccine to BVDV.

摘要

背景

牛病毒性腹泻病毒是全球范围内对牛群影响最大、代价最高的病毒病原体之一。已证明源自甲病毒的复制子颗粒是针对多种人类和兽医病原体的安全且高效的疫苗载体。复制子颗粒是非增殖性的、DIVA 兼容的,可诱导体液和细胞介导的免疫反应。这是首次证明基于甲病毒的复制子颗粒可用于针对具有商业重要性的牛病原体的小牛标准初免-加强免疫接种策略的实验。

结果

生成了表达牛病毒性腹泻病毒亚群 1b E2 糖蛋白的复制子颗粒,并使用针对 E2 的多克隆和单克隆抗体在体外证实了其表达。使用颗粒制备的疫苗在 Vero 细胞中生成,并在两种剂量水平下以初免-加强方案施用于无 BVDV 的小牛。接种疫苗后,中和抗体滴度可中和 1 型和 2 型 BVD 基因型,加强接种后可交叉中和。此外,高剂量疫苗接种显示出对临床疾病的一定保护作用,并显著减轻了病毒感染引起的白细胞减少症的严重程度。

结论

在初免-加强方案中施用表达 BVDV E2 糖蛋白的复制子颗粒疫苗可诱导交叉中和抗体滴度,减少攻毒后白细胞减少症,并减轻小牛的临床疾病。该策略为 BVDV 提供了一种安全有效的疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c42f/3565941/aaa1b4a98fd4/1743-422X-10-35-1.jpg

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