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重组诺如病毒样颗粒作为口服疫苗。

Recombinant Norwalk virus-like particles as an oral vaccine.

作者信息

Ball J M, Estes M K, Hardy M E, Conner M E, Opekun A R, Graham D Y

机构信息

Division of Molecular Virology, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Arch Virol Suppl. 1996;12:243-9. doi: 10.1007/978-3-7091-6553-9_26.

Abstract

Viruses that infect cells in the gastrointestinal tract are well suited for examining the immune response to oral delivery of antigen and for exploring the advantages and pitfalls of oral vaccines. Norwalk virus (NV) (family Caliciviridae, genus Calicivirus) causes acute gastroenteritis in all age groups. The NV capsid is composed of 180 copies of a single 58000 molecular weight protein which spontaneously forms virus-like particles (VLPs) that can be purified in extremely high yields (22 mg per 300 ml culture) when produced using the baculovirus expression system. We are testing the potential of these recombinant NV (rNV) particles for use as an oral vaccine by administering them to mice and volunteers. Mice were orally inoculated four times with rNV particles in concentrations ranging from 5 to 500 micrograms in the absence of adjuvant or from 5 to 200 micrograms with 10 micrograms of cholera toxin. Serum IgG and fecal IgA immune responses were monitored. rNV particles were found to be immunogenic when orally given to mice with or without adjuvant. These particles also were safe and immunogenic when orally given to volunteers. These studies show that rNV particles are an excellent model to test the oral delivery of mucosal immunogens in general, and that rNV particles are ideal candidates for vaccine development in particular.

摘要

感染胃肠道细胞的病毒非常适合用于研究口服抗原后的免疫反应,以及探索口服疫苗的优缺点。诺如病毒(NV)(杯状病毒科,杯状病毒属)可导致各年龄组的急性肠胃炎。NV衣壳由180个拷贝的单一分子量为58000的蛋白质组成,该蛋白质能自发形成病毒样颗粒(VLP),当使用杆状病毒表达系统生产时,这些颗粒可以极高的产量进行纯化(每300毫升培养物可获得22毫克)。我们正在通过将这些重组NV(rNV)颗粒给予小鼠和志愿者来测试其作为口服疫苗的潜力。在无佐剂的情况下,用浓度为5至500微克的rNV颗粒对小鼠进行四次口服接种,或在含有10微克霍乱毒素的情况下,用浓度为5至200微克的rNV颗粒进行口服接种。监测血清IgG和粪便IgA免疫反应。结果发现,无论有无佐剂,给小鼠口服rNV颗粒时都具有免疫原性。给志愿者口服这些颗粒时也安全且具有免疫原性。这些研究表明,rNV颗粒总体上是测试黏膜免疫原口服递送的极佳模型,尤其是rNV颗粒是疫苗开发的理想候选物。

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