Dunn S J, Fiore L, Werner R L, Cross T L, Broome R L, Ruggeri F M, Greenberg H B
Division of Gastroenterology, Stanford University School of Medicine, California, USA.
Arch Virol. 1995;140(11):1969-78. doi: 10.1007/BF01322686.
Rhesus rotavirus (RRV) VP4 trypsin cleavage product VP5(1), a truncated form of VP5, was expressed in baculovirus and found by immunoprecipitation to be antigenically similar to VP5* on the virion. Immunization of mice with VP5(1)* elicited neutralizing antibody that was found to be cross-reactive with viruses representing P genotypes 1, 3, 4, 6, 7, and 8. Baculovirus expressed trypsin cleavage products, VP8* (amino acids 1-246) and VP5(1)* (amino acids 247-474), were tested for their ability to elicit a protective response in a murine model of passive protection. These results were compared to those obtained with baculovirus expressed RRV VP4. Dams immunized with baculovirus expressed RRV VP4 gave birth to pups protected from RRV virus challenge. Neither VP5(1)* nor VP8* was as effective at generating protective immunity as full length VP4. However, antibody to VP5(1)* was more effective than antibody to VP8* at mediating protection even though the neutralizing antibody titers as measured by hemagglutination inhibition and focus reduction neutralization were similar.
恒河猴轮状病毒(RRV)VP4经胰蛋白酶切割后的产物VP5(1)是VP5的截短形式,在杆状病毒中表达,通过免疫沉淀发现其在抗原性上与病毒体上的VP5相似。用VP5(1)免疫小鼠可诱导产生中和抗体,该抗体被发现与代表P基因型1、3、4、6、7和8的病毒具有交叉反应性。对杆状病毒表达的胰蛋白酶切割产物VP8(氨基酸1 - 246)和VP5(1)(氨基酸247 - 474)在被动保护小鼠模型中引发保护性反应的能力进行了测试。将这些结果与杆状病毒表达的RRV VP4所获得的结果进行比较。用杆状病毒表达的RRV VP4免疫的母鼠产下的幼崽受到保护,免受RRV病毒攻击。VP5(1)和VP8在产生保护性免疫方面都不如全长VP4有效。然而,尽管通过血凝抑制和蚀斑减少中和法测得的中和抗体滴度相似,但针对VP5(1)的抗体在介导保护方面比针对VP8的抗体更有效。