Flores J, Perez-Schael I, Gonzalez M, Garcia D, Perez M, Daoud N, Cunto W, Chanock R M, Kapikian A Z
Lancet. 1987 Apr 18;1(8538):882-4. doi: 10.1016/s0140-6736(87)92858-3.
The efficacy of the rhesus rotavirus vaccine candidate MMU-18006 was evaluated in a longitudinal double-blind field trial in Caracas, Venezuela. 247 infants aged 1-10 months were studied and followed for up to 1 year (201 completed the 1-year surveillance): 123 received a dose of 10(4) plaque-forming units of the vaccine orally and 124 received placebo. 21 episodes of rotavirus diarrhoea were detected, 16 in the controls and 5 in the vaccines: vaccine efficacy against any rotavirus diarrhoea was thus 68%. In the 1-5-month-old group the vaccine efficacy was 93%; only 1 episode of rotavirus diarrhoea was detected in 68 vaccinees and 15 such illnesses were observed in 65 controls (p less than 0.0001). For the entire study group vaccine efficacy was 100% against the most severe rotavirus diarrhoeal episodes.
在委内瑞拉加拉加斯进行的一项纵向双盲现场试验中,对恒河猴轮状病毒候选疫苗MMU - 18006的疗效进行了评估。研究了247名1至10个月大的婴儿,并对其进行了长达1年的随访(201人完成了1年的监测):123人口服了一剂含10(4)个空斑形成单位的疫苗,124人接受了安慰剂。检测到21例轮状病毒腹泻病例,其中对照组16例,疫苗组5例:因此,疫苗对任何轮状病毒腹泻的疗效为68%。在1至5个月大的组中,疫苗疗效为93%;在68名接种疫苗的婴儿中仅检测到1例轮状病毒腹泻病例,而在65名对照组婴儿中观察到15例此类疾病(p小于0.0001)。对于整个研究组,疫苗对最严重的轮状病毒腹泻发作的疗效为100%。