D'Alessandro U, Leach A, Drakeley C J, Bennett S, Olaleye B O, Fegan G W, Jawara M, Langerock P, George M O, Targett G A
Medical Research Council Laboratories, Banjul, The Gambia.
Lancet. 1995 Aug 19;346(8973):462-7. doi: 10.1016/s0140-6736(95)91321-1.
SPf66 malaria vaccine is a synthetic protein with aminoacid sequences derived from pre-erythrocytic and asexual blood-stage proteins of Plasmodium falciparum. SPf66 was found to have a 31% protective efficacy in an area of intensive malaria transmission in Tanzanian children, 1-5 years old. We report a randomised, double-blind, placebo-controlled trial of SPf66 against clinical P falciparum malaria in Gambian infants. 630 children, aged 6-11 months at time of the first dose, received three doses of SPf66 or injected polio vaccine (IPV). Morbidity was monitored during the following rainy season by means of active and passive case detection. Cross-sectional surveys were carried out at the beginning and at the end of the rainy season. An episode of clinical malaria was defined as fever (> or = 37.5 degrees C) and a parasite density of 6000/microL or more. Analysis of efficacy was done on 547 children (316 SPf66/231 IPV). No differences in mortality or in health centre admissions were found between the two groups of children. 347 clinical episodes of malaria were detected during the three and a half months of surveillance. SPf66 vaccine was associated with a protective efficacy against the first or only clinical episode of 8% (95% CI -18 to 29, p = 0.50) and against the overall incidence of clinical episodes of malaria of 3% (95% CI -24 to 24, p = 0.81). No significant differences in parasite rates or in any other index of malaria were found between the two groups of children. The findings of this study differ from previous reports on SPf66 efficacy from South America and from Tanzania. In The Gambia, protection against clinical attacks of malaria during the rainy season after immunisation in children 6-11 months old at time of the first dose was not achieved.
SPf66疟疾疫苗是一种合成蛋白,其氨基酸序列源自恶性疟原虫的前红细胞期和无性血液期蛋白。在坦桑尼亚1至5岁密集疟疾传播地区的儿童中,发现SPf66具有31%的保护效力。我们报告了一项针对冈比亚婴儿的SPf66预防恶性疟原虫临床疟疾的随机、双盲、安慰剂对照试验。630名首次接种时年龄为6至11个月的儿童接受了三剂SPf66或注射用脊髓灰质炎疫苗(IPV)。在接下来的雨季通过主动和被动病例检测来监测发病率。在雨季开始和结束时进行横断面调查。临床疟疾发作定义为发热(≥37.5摄氏度)且寄生虫密度为每微升6000个或更多。对547名儿童(316名接种SPf66/231名接种IPV)进行了效力分析。两组儿童在死亡率或卫生中心入院率方面未发现差异。在三个半月的监测期间共检测到347例临床疟疾发作。SPf66疫苗对首次或仅有的临床发作的保护效力为8%(95%置信区间 -18至29,p = 0.50),对临床疟疾发作的总发病率的保护效力为3%(95%置信区间 -24至24,p = 0.81)。两组儿童在寄生虫率或任何其他疟疾指标方面未发现显著差异。本研究的结果与先前来自南美洲和坦桑尼亚的关于SPf66效力的报告不同。在冈比亚,对于首次接种时年龄为6至11个月的儿童,免疫后在雨季未能实现对疟疾临床发作的保护。