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作为轮状病毒亚单位疫苗的病毒样颗粒

Virus-like particles as a rotavirus subunit vaccine.

作者信息

Conner M E, Zarley C D, Hu B, Parsons S, Drabinski D, Greiner S, Smith R, Jiang B, Corsaro B, Barniak V, Madore H P, Crawford S, Estes M K

机构信息

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

出版信息

J Infect Dis. 1996 Sep;174 Suppl 1:S88-92. doi: 10.1093/infdis/174.supplement_1.s88.

Abstract

Rotavirus subunit vaccines are being evaluated for use in humans. The virus-like particles (VLPs) for these vaccines are produced in insect cells coinfected with combinations of baculovirus recombinants expressing bovine RIF VP2 and simian SA11, VP4, VP6, or VP7 rotavirus proteins. VLPs were administered parenterally to mice and rabbits, and the immunogenicity and protective efficacy of the vaccines were evaluated. Rabbits vaccinated with VP2/4/6/7 or VP2/6/7 VLP combinations developed high levels of rotavirus-specific serum antibody and fecal IgG but not fecal IgA. The induction of fecal IgG was associated with total or partial protection from oral challenge with ALA rotavirus. Heterotypic serum and fecal neutralizing antibody was induced in mice vaccinated parenterally with G1 VP2/6/7 or VP2/4/6n VLPs. VLPs were highly immunogenic when administered in QS21 adjuvant, inducing serum neutralizing antibody titers comparable to those induced by SA11 virus. VLPs are effective immunogens when administered parenterally and may be an effective subunit vaccine.

摘要

轮状病毒亚单位疫苗正在进行人体试验评估。这些疫苗的病毒样颗粒(VLP)是在昆虫细胞中产生的,该昆虫细胞被表达牛RIF VP2和猿猴SA11、VP4、VP6或VP7轮状病毒蛋白的杆状病毒重组体组合共同感染。将VLP通过肠胃外途径给予小鼠和兔子,并评估疫苗的免疫原性和保护效力。用VP2/4/6/7或VP2/6/7 VLP组合接种的兔子产生了高水平的轮状病毒特异性血清抗体和粪便IgG,但未产生粪便IgA。粪便IgG的诱导与对ALA轮状病毒口服攻击的全部或部分保护相关。用G1 VP2/6/7或VP2/4/6n VLP通过肠胃外途径接种的小鼠诱导产生了异型血清和粪便中和抗体。当在QS21佐剂中给予时,VLP具有高度免疫原性,诱导的血清中和抗体滴度与SA11病毒诱导的相当。当通过肠胃外途径给予时,VLP是有效的免疫原,可能是一种有效的亚单位疫苗。

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