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一种新型重组口疮病毒(ORFV,副痘病毒)可保护兔子免受兔出血症病毒(RHDV)的致死性感染。

A new recombinant Orf virus (ORFV, Parapoxvirus) protects rabbits against lethal infection with rabbit hemorrhagic disease virus (RHDV).

机构信息

Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Immunology, Paul-Ehrlich-Str. 28, D-72074 Tuebingen, FRG.

出版信息

Vaccine. 2011 Nov 15;29(49):9256-64. doi: 10.1016/j.vaccine.2011.09.121. Epub 2011 Oct 11.

Abstract

This report describes the generation of a new recombinant Orf virus (ORFV; Parapoxvirus) expressing the major capsid protein VP1 (VP60) of the calicivirus, rabbit hemorrhagic disease virus (RHDV). Authentic expression of VP1 could be demonstrated in cells infected with the recombinant D1701-V-VP1 without the need for production of infectious ORFV progeny. Notably, infected cells also released empty calicivirus-like particles (VLPs). Challenge experiments showed that even a single immunization with ≥10(5) PFU of D1701-V-VP1 protected rabbits against lethal RHDV infection. ELISA tests indicated that the protective immunity mediated by D1701-V-VP1 did not strictly depend on the presence of detectable RHDV-specific serum antibodies. The induction of interleukin-2 found only in the sera of rabbits immunized with the D1701-V-VP1, but not in sera of rabbits immunized with the inactivated commercial vaccine RIKA-VACC, might indicate also some involvement of T-cells in protection. Collectively, this work adds another example of the successful use of the ORFV vector system for the generation of a recombinant vaccine, and demonstrates its potential as an alternative vaccine to protect rabbits against RHDV infection.

摘要

本报告描述了一种新的重组口疮病毒(ORFV;副痘病毒)的产生,该病毒表达了杯状病毒、兔出血症病毒(RHDV)的主要衣壳蛋白 VP1(VP60)。在没有产生感染性 ORFV 后代的情况下,用重组 D1701-V-VP1 感染的细胞中可以证实 VP1 的真实表达。值得注意的是,受感染的细胞还释放了空的杯状病毒样颗粒(VLPs)。攻毒实验表明,即使单次免疫 ≥10(5)PFU 的 D1701-V-VP1 也能保护兔子免受致死性 RHDV 感染。ELISA 试验表明,D1701-V-VP1 介导的保护免疫并不严格依赖于可检测到的 RHDV 特异性血清抗体的存在。仅在 D1701-V-VP1 免疫的兔子血清中发现的白细胞介素-2 的诱导,而在 RIKA-VACC 灭活商业疫苗免疫的兔子血清中没有发现,这可能表明 T 细胞也参与了保护。总的来说,这项工作增加了另一个成功利用 ORFV 载体系统生成重组疫苗的例子,并证明了它作为替代疫苗保护兔子免受 RHDV 感染的潜力。

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