O'Neal C M, Crawford S E, Estes M K, Conner M E
Division of Molecular Virology, Baylor College of Medicine, Houston, Texas 77030, USA.
J Virol. 1997 Nov;71(11):8707-17. doi: 10.1128/JVI.71.11.8707-8717.1997.
We have evaluated the immunogenicity and protective efficacy of rotavirus subunit vaccines administered by mucosal routes. Virus-like particles (VLPs) produced by self-assembly of individual rotavirus structural proteins coexpressed by baculovirus recombinants in insect cells were the subunit vaccine tested. We first compared the immunogenicities and protective efficacies of VLPs containing VP2 and VP6 (2/6-VLPs) and G3 2/6/7-VLPs mixed with cholera toxin and administered by oral and intranasal routes in the adult mouse model of rotavirus infection. VLPs administered orally induced serum antibody and intestinal immunoglobulin A (IgA) and IgG. The highest oral dose (100 microg) of VLPs induced protection from rotavirus challenge (> or = 50% reduction in virus shedding) in 50% of the mice. VLPs administered intranasally induced higher serum and intestinal antibody responses than VLPs administered orally. All mice receiving VLPs intranasally were protected from challenge; no virus was shed after challenge. Since there was no difference in immunogenicity or protective efficacy between 2/6- and 2/6/7-VLPs, protection was achieved without inclusion of the neutralization antigens VP7 and VP4. We also tested the immunogenicities and protective efficacies of 2/6-VLPs administered intranasally without the addition of cholera toxin. 2/6-VLPs administered intranasally without cholera toxin induced lower serum and intestinal antibody titers than 2/6-VLPs administered with cholera toxin. The highest dose (100 microg) of 2/6-VLPs administered intranasally without cholera toxin resulted in a mean reduction in shedding of 38%. When cholera toxin was added, higher levels of protection were achieved with 10-fold less immunogen. VLPs administered mucosally offer a promising, safe, nonreplicating vaccine for rotavirus.
我们评估了通过黏膜途径接种的轮状病毒亚单位疫苗的免疫原性和保护效力。由杆状病毒重组体在昆虫细胞中共表达的单个轮状病毒结构蛋白自组装产生的病毒样颗粒(VLPs)是所测试的亚单位疫苗。我们首先在轮状病毒感染的成年小鼠模型中,比较了含有VP2和VP6的VLPs(2/6-VLPs)以及与霍乱毒素混合并通过口服和鼻内途径接种的G3 2/6/7-VLPs的免疫原性和保护效力。口服的VLPs可诱导血清抗体以及肠道免疫球蛋白A(IgA)和IgG。最高口服剂量(100微克)的VLPs可使50%的小鼠免受轮状病毒攻击(病毒排泄减少≥50%)。鼻内接种的VLPs比口服接种的VLPs诱导更高的血清和肠道抗体反应。所有鼻内接种VLPs的小鼠均受到保护而免受攻击;攻击后未出现病毒排泄。由于2/6-VLPs和2/6/7-VLPs在免疫原性或保护效力方面没有差异,因此在不包含中和抗原VP7和VP4的情况下也实现了保护。我们还测试了不添加霍乱毒素鼻内接种2/6-VLPs的免疫原性和保护效力。不添加霍乱毒素鼻内接种的2/6-VLPs诱导的血清和肠道抗体滴度低于添加霍乱毒素接种的2/6-VLPs。不添加霍乱毒素鼻内接种的最高剂量(100微克)2/6-VLPs导致排泄平均减少38%。添加霍乱毒素后,使用少10倍的免疫原即可实现更高水平的保护。通过黏膜途径接种的VLPs为轮状病毒提供了一种有前景、安全的非复制型疫苗。