Wright P F, Belshe R B, Kim H W, Van Voris L P, Chanock R M
Infect Immun. 1982 Jul;37(1):397-400. doi: 10.1128/iai.37.1.397-400.1982.
A highly attenuated respiratory syncytial virus (RSV) experimental vaccine, RSV ts-2, was sequentially evaluated in adults, seropositive children, and finally, fully susceptible seronegative children. The vaccine was administered intranasally in doses ranging from 10(5.2) to 10(6.3) PFU/ml. In both adults and children, the vaccine proved to be poorly infectious. Although poor infectivity would not have been predicted from tissue culture studies of RSV ts-2 growth, the human experience closely parallels the experience in a series of animal models, including the chimpanzee. The poor infectivity of this RSV vaccine virus preparation suggests that the postulated defect in the RSV ts-2 fusion protein may be important in determining in vivo infectivity of RSV.
一种高度减毒的呼吸道合胞病毒(RSV)实验性疫苗RSV ts-2,先后在成人、血清学阳性儿童以及最终完全易感的血清学阴性儿童中进行了评估。该疫苗通过鼻内给药,剂量范围为10(5.2)至10(6.3) PFU/ml。在成人和儿童中,该疫苗的传染性均较差。尽管根据RSV ts-2生长的组织培养研究无法预测其传染性较差,但人体试验结果与包括黑猩猩在内的一系列动物模型的试验结果非常相似。这种RSV疫苗病毒制剂的传染性较差表明,推测的RSV ts-2融合蛋白缺陷可能在决定RSV的体内传染性方面具有重要作用。