Black R E, Levine M M, Ferreccio C, Clements M L, Lanata C, Rooney J, Germanier R
Center for Vaccine Development, University of Maryland School of Medicine, Baltimore.
Vaccine. 1990 Feb;8(1):81-4. doi: 10.1016/0264-410x(90)90183-m.
Typhoid fever remains an important public health problem in many areas of the world and an effective, non-reactogenic vaccine would be useful to control this disease. An attenuated Salmonella typhi strain (Ty21a), which has shown promise in previous trials, was evaluated in a controlled field trial in Santiago, Chile. In this trial, 82,543 schoolchildren were randomly assigned to receive one or two doses of Ty21a vaccine in enteric-coated capsules or placebo. The enteric-coated vaccine formulation was well tolerated and practical for mass oral immunization. In the first two years of surveillance, 213 cases of bacteriologically-confirmed typhoid fever were found in schoolchildren participating in the trial; annual rates in the placebo group were 139 and 227 per 100,000. Vaccine efficacy in the first two years after vaccination was 59% for two doses and 29% for one dose; no efficacy was found 3-5 years after vaccination. These results indicate that it will be necessary to identify a vaccine formulation and schedule for Ty21a S. typhi that is practical and provides high level protection for greater than 2 years.
伤寒热在世界许多地区仍然是一个重要的公共卫生问题,一种有效且无反应原性的疫苗对于控制这种疾病将很有用。一种减毒伤寒杆菌菌株(Ty21a),在之前的试验中已显示出前景,在智利圣地亚哥进行的一项对照现场试验中进行了评估。在该试验中,82543名学童被随机分配接受一剂或两剂肠溶胶囊形式的Ty21a疫苗或安慰剂。肠溶疫苗制剂耐受性良好,适用于大规模口服免疫。在监测的头两年,在参与试验的学童中发现了213例细菌学确诊的伤寒热病例;安慰剂组的年发病率分别为每10万人139例和227例。接种疫苗后头两年的疫苗效力,两剂为59%,一剂为29%;接种疫苗3至5年后未发现效力。这些结果表明,有必要确定一种针对Ty21a伤寒杆菌的实用疫苗制剂和接种方案,该方案能提供超过两年的高水平保护。