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用杆状病毒展示的H6血凝素疫苗免疫可保护小鼠免受致死性H6流感病毒攻击。

Immunization with baculovirus displayed H6 hemagglutinin vaccine protects mice against lethal H6 influenza virus challenge.

作者信息

Musthaq Syed Khader Syed, Kumar S Rajesh, Szyporta Milene, Kwang Jimmy

机构信息

Animal Health Biotechnology, Temasek Lifesciences Laboratory, 1 Research Link, National University of Singapore, Singapore 117604, Singapore.

Animal Health Biotechnology, Temasek Lifesciences Laboratory, 1 Research Link, National University of Singapore, Singapore 117604, Singapore; Department of Microbiology, Faculty of Medicine, National University of Singapore, Singapore.

出版信息

Antiviral Res. 2014 Sep;109:42-53. doi: 10.1016/j.antiviral.2014.06.002. Epub 2014 Jun 25.

Abstract

Low pathogenic influenza viruses of H6 hemagglutinin (HA) subtype have a high prevalence among aquatic and domestic birds and have caused outbreaks in poultry worldwide. The first human infection with wild avian influenza H6N1 virus was reported in Taiwan and these subtype viruses may continue to evolve and accumulate changes which increasing the potential risk of human-to-human transmission. To develop a vaccine against influenza viruses of the H6 subtype, we displayed the HA gene on the baculovirus surface (Bac-HA), and studied its vaccine efficacy against a lethal challenge with mouse-adapted RG-H6(Shorebird) virus carrying the H6 HA gene from A/shorebird/DE/12/2004 (H6N8) virus and 7 genes from A/Puerto Rico/8/1934 (H1N1) virus. Immunization with 256 HA units of Bac-HA via the intranasal route triggered HA-specific serum and mucosal antibodies in mice besides increased HA inhibition titers compared to mice immunized subcutaneously. Moreover, we observed an increase in cellular immune response (IL-4) and improved in vitro neutralization activity in the mice immunized intranasally with live Bac-HA compared to mice immunized with inactivated influenza virus (IV). Interestingly, Bac-HA intranasal immunized mice showed one fold higher neutralization titer against heterologous H6 influenza virus compared to inactivated IV immunized mice. In addition, the live Bac-HA, administered through either immunization route, as well as the adjuvanted inactivated Bac-HA, administered subcutaneously, conferred 100% protection to mice challenged with homologous mouse-adapted RG-H6(Shorebird) virus. The reduction in viral titers and extend of histopathological changes of Bac-HA immunized mice lungs further demonstrated the protective efficacy of Bac-HA. Hence, the recombinant baculovirus subunit vaccine is an alternative candidate against H6 subtypes that could be propagated and administered with minimal biosafety concerns.

摘要

H6血凝素(HA)亚型的低致病性流感病毒在水禽和家禽中广泛存在,并在全球范围内引发了家禽疫情。台湾地区报告了首例人类感染野生禽流感H6N1病毒的病例,这些亚型病毒可能会继续进化并积累变异,从而增加人际传播的潜在风险。为了研发针对H6亚型流感病毒的疫苗,我们将HA基因展示在杆状病毒表面(Bac-HA),并研究了其对携带来自A/shorebird/DE/12/2004(H6N8)病毒的H6 HA基因和来自A/波多黎各/8/1934(H1N1)病毒的7个基因的小鼠适应型RG-H6(滨鸟)病毒致死性攻击的疫苗效力。与皮下免疫的小鼠相比,通过鼻内途径用256个HA单位的Bac-HA免疫小鼠,除了提高HA抑制效价外,还引发了小鼠体内HA特异性血清和黏膜抗体。此外,与用灭活流感病毒(IV)免疫的小鼠相比,我们观察到用活的Bac-HA鼻内免疫的小鼠细胞免疫反应(IL-4)增强,体外中和活性提高。有趣的是,与灭活IV免疫的小鼠相比,Bac-HA鼻内免疫的小鼠对异源H6流感病毒的中和效价高1倍。此外,通过任何一种免疫途径给予的活Bac-HA,以及皮下给予的佐剂化灭活Bac-HA,都能为受到同源小鼠适应型RG-H6(滨鸟)病毒攻击的小鼠提供100%的保护。Bac-HA免疫小鼠肺部病毒滴度的降低和组织病理学变化范围的缩小进一步证明了Bac-HA的保护效力。因此,重组杆状病毒亚单位疫苗是针对H6亚型的另一种候选疫苗,其生产和给药过程中的生物安全问题最小。

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