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α干扰素作为委内瑞拉马脑炎病毒感染的腺病毒载体疫苗佐剂及抗病毒剂。

Alpha interferon as an adenovirus-vectored vaccine adjuvant and antiviral in Venezuelan equine encephalitis virus infection.

作者信息

O'Brien Lyn, Perkins Stuart, Williams Amanda, Eastaugh Lin, Phelps Amanda, Wu Josh, Phillpotts Robert

机构信息

Biomedical Sciences Department, Defence Science and Technology Laboratory, Porton Down, Salisbury, Wiltshire SP4 0JQ, UK.

Biotechnology Section, Defence Research and Development Canada - Suffield, Box 4000, Station Main, Medicine Hat, Alberta T1A 8K6, Canada.

出版信息

J Gen Virol. 2009 Apr;90(Pt 4):874-882. doi: 10.1099/vir.0.006833-0. Epub 2009 Mar 4.

DOI:10.1099/vir.0.006833-0
PMID:19264673
Abstract

There are no widely available vaccines or antiviral drugs capable of protecting against infection with Venezuelan equine encephalitis virus (VEEV), although an adenovirus vector expressing VEEV structural proteins protects mice from challenge with VEEV and is potentially a vaccine suitable for human use. This work examines whether alpha interferon (IFN-alpha) could act as an adjuvant for the adenovirus-based vaccine. IFN-alpha was either expressed by a plasmid linked to the adenovirus vaccine or encoded by a separate adenovirus vector administered as a mixture with the vaccine. In contrast to previous reports with other vaccines, the presence of IFN-alpha reduced the antibody response to VEEV. When IFN-alpha was encoded by adenovirus, the lack of a VEEV-specific response was accompanied by an increase in the immune response to the adenovirus vector. IFN-alpha also plays a direct role in defence against virus infection, inducing the expression of a large number of antiviral proteins. Adenovirus-delivered IFN-alpha protected mice from VEEV disease when administered 24 h prior to challenge, but not when administered 6 h post-challenge, suggesting that up to 24 h is required for the development of the IFN-mediated antiviral response.

摘要

目前尚无广泛可用的疫苗或抗病毒药物能够预防委内瑞拉马脑炎病毒(VEEV)感染,尽管一种表达VEEV结构蛋白的腺病毒载体可保护小鼠免受VEEV攻击,并且可能是一种适用于人类的疫苗。这项研究探讨了α干扰素(IFN-α)是否可作为基于腺病毒的疫苗的佐剂。IFN-α要么由与腺病毒疫苗相连的质粒表达,要么由作为与疫苗混合物施用的单独腺病毒载体编码。与先前关于其他疫苗的报道相反,IFN-α的存在降低了对VEEV的抗体反应。当IFN-α由腺病毒编码时,缺乏VEEV特异性反应伴随着对腺病毒载体免疫反应的增加。IFN-α在抵御病毒感染中也发挥直接作用,诱导大量抗病毒蛋白的表达。在攻击前24小时施用腺病毒递送的IFN-α可保护小鼠免受VEEV疾病,但在攻击后6小时施用则无效,这表明IFN介导的抗病毒反应的发展需要长达24小时。

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