Andrews Laura, Andersen Rikke F, Webster Daniel, Dunachie Susanna, Walther R Michael, Bejon Philip, Hunt-Cooke Angela, Bergson Gillian, Sanderson Frances, Hill Adrian V S, Gilbert Sarah C
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Am J Trop Med Hyg. 2005 Jul;73(1):191-8.
The demand for an effective malaria vaccine is high, with millions of people being affected by the disease every year. A large variety of potential vaccines are under investigation worldwide, and when tested in clinical trials, researchers need to extract as much data as possible from every vaccinated and control volunteer. The use of quantitative real-time polymerase chain reaction (PCR), carried out in real-time during the clinical trials of vaccines designed to act against the liver stage of the parasite's life cycle, provides more information than the gold standard method of microscopy alone and increases both safety and accuracy. PCR can detect malaria parasites in the blood up to 5 days before experienced microscopists see parasites on blood films, with a sensitivity of 20 parasites/mL blood. This PCR method has so far been used to follow 137 vaccinee and control volunteers in Phase IIa trials in Oxford and on 220 volunteer samples during a Phase IIb field trial in The Gambia.
对有效疟疾疫苗的需求很高,每年有数以百万计的人受到这种疾病的影响。全球正在研究各种各样的潜在疫苗,在临床试验中进行测试时,研究人员需要从每一位接种疫苗的志愿者和对照志愿者身上提取尽可能多的数据。在针对疟原虫生命周期肝期的疫苗临床试验期间实时进行的定量实时聚合酶链反应(PCR),比单独使用显微镜这一黄金标准方法能提供更多信息,同时提高了安全性和准确性。PCR能够在经验丰富的显微镜检查人员在血涂片上看到疟原虫之前5天就检测出血液中的疟原虫,灵敏度为每毫升血液20个疟原虫。到目前为止,这种PCR方法已用于牛津大学IIa期试验中对137名疫苗接种者和对照志愿者的跟踪,以及在冈比亚的IIb期现场试验中对220份志愿者样本的检测。