Hermsen Cornelus C, de Vlas Sake J, van Gemert Geert Jan A, Telgt Denise S C, Verhage Danielle F, Sauerwein Robert W
Department of Medical Microbiology, University Medical Center, Nijmegen, The Netherlands.
Am J Trop Med Hyg. 2004 Aug;71(2):196-201.
Clinical trials are an essential step in evaluation of safety and efficacy of malaria vaccines, and human experimental malaria infections have been used for evaluation of protective immunity of Plasmodium falciparum malaria. In this study, a quantitative real-time polymerase chain reaction was used to measure P. falciparum malaria parasitemia in non-immune volunteers who had been experimentally infected by mosquito bites. Based on a remarkably small variation in the kinetics of parasitemia, a statistical model was developed that provides detailed estimates of pre-patent periods and parasite multiplication of blood stages. Using this model, we could predict results on vaccine efficacy for 1) pre-erythrocytic vaccines in the asymptomatic incubation period and 2) asexual stage vaccines after a limited number of multiplication cycles. The model shows that stage-specific vaccines even with limited efficacy can be highly efficacious when used in combination. This P. falciparum challenge method significantly adds to the potential to evaluate efficacy of candidate malaria vaccines before going into field trials.
临床试验是评估疟疾疫苗安全性和有效性的重要步骤,人体实验性疟疾感染已被用于评估恶性疟原虫疟疾的保护性免疫。在本研究中,采用定量实时聚合酶链反应来测量经蚊虫叮咬实验性感染的非免疫志愿者体内的恶性疟原虫血症。基于疟原虫血症动力学的显著微小变化,开发了一种统计模型,该模型可提供对潜伏期和血液阶段寄生虫增殖的详细估计。使用该模型,我们可以预测1)无症状潜伏期的红细胞前期疫苗和2)有限数量增殖周期后的无性阶段疫苗的疫苗效力结果。该模型表明,即使效力有限的阶段特异性疫苗联合使用时也可能具有高效力。这种恶性疟原虫攻击方法显著增加了在进行现场试验之前评估候选疟疾疫苗效力的可能性。