Harry T O, Nasidi A, Fritzell B, Akinlade H O, Nereli B, Rollin P, Sureau P, Adeiga A
National Institute for Medical Research, Yaba, Lagos, Nigeria.
Vaccine. 1989 Aug;7(4):329-32. doi: 10.1016/0264-410x(89)90195-3.
The suckling mouse brain rabies vaccine, recommended for production and routine use in Nigeria from our previous study, was investigated in the present study in an effort to reduce the cost of antirabies treatment in the country. This is needed for economic reasons. Instead of seven daily doses followed by three boosters, we tried five daily doses followed by three boosters, with or without equine hyperimmune serum given on day 0 (40 IU per kg body weight). Fifty dog-bite, victims, aged 3-81 years, were placed on this regimen, 25 with serum and 25 without serum, according to the history of the case. The serum had no effect on the kinetics of antibody development and both serum and vaccine were well tolerated. The geometric mean titres (GMTs) of antirabies antibodies in the sera of recipients of vaccine alone on days 10, 28 and 90 were 3.05 equivalent units ml-1 (EU ml-1), 4.35 EU ml-1 and 2.54 EU ml-1 respectively. Among those who had received antiserum and vaccine the titres were respectively 3.19 EU ml-1, 4.35 EU ml-1 and 3.02 EU ml-1. Of the 50 subjects, 49 showed detectable antibodies by day 28, and all the 50 survived. This regimen is therefore recommended for further trial in countries where rabies is endemic but potent antirabies vaccines are scarce and expensive. Another 23 subjects, considered not to be at risk of rabies, were given a one-tenth dose, two-site intradermal inoculation of the same vaccine on days 0, 3, 7, 14, 28 and 90.(ABSTRACT TRUNCATED AT 250 WORDS)
在本研究中,对我们之前的研究推荐用于尼日利亚生产和常规使用的乳鼠脑狂犬病疫苗进行了调查,目的是降低该国抗狂犬病治疗的成本。出于经济原因,这是必要的。我们尝试用每日五剂继以三剂加强针,而非之前的每日七剂继以三剂加强针,同时在第0天给予或不给予马超免疫血清(每千克体重40国际单位)。根据病例史,50名3至81岁的犬咬伤受害者接受了该方案治疗,25人使用血清,25人不使用血清。血清对抗体产生动力学没有影响,血清和疫苗耐受性良好。仅接种疫苗的受试者在第10天、第28天和第90天血清中抗狂犬病抗体的几何平均滴度(GMT)分别为3.05等效单位/毫升(EU/ml)、4.35 EU/ml和2.54 EU/ml。接受抗血清和疫苗的受试者的滴度分别为3.19 EU/ml、4.35 EU/ml和3.02 EU/ml。50名受试者中,49人在第28天显示出可检测到的抗体,所有50人均存活。因此,推荐该方案在狂犬病流行但高效抗狂犬病疫苗稀缺且昂贵的国家进行进一步试验。另外23名被认为无狂犬病风险的受试者,在第0天、第3天、第7天、第14天、第28天和第90天接受了同一疫苗十分之一剂量的两点皮内接种。(摘要截短至250字)