Snounou G, Beck H P
Department of Infection and Tropical Medicine, Imperial College School of Medicine, Lister Unit, Northwick Park Hospital, Harrow, Middlesex, UK HA1 3UJ.
Parasitol Today. 1998 Nov;14(11):462-7. doi: 10.1016/s0169-4758(98)01340-4.
In the past, assessment of drug efficacy against Plasmodium falciparum malaria has been performed by microscopy, screening for parasites in blood smears. However, in areas of high endemicity, reappearing parasites might be derived from new inoculations and could be classified falsely as treatment failures. Recently, a number of studies have used polymerase chain reaction (PCR) analysis of detectable parasites after drug administration to discriminate new infections from true recrudescence. The feasibility, high sensitivity and high resolution of this technique proves that it will be practical and highly valuable in studies on both drug resistance and vaccine efficacy as well as the testing of novel antimalarial drugs. In this article, Georges Snounou and Hans-Peter Beck discuss the uncertainties in the interpretation of data inherent to the technical limitations of the PCR technique, and the constraints imposed by the biology of the parasite. They suggest that although genotyping can provide strong evidence for differentiating between true recrudescence and reinfection, it must be interpreted with caution. They also propose strategies that might help minimize these uncertainties.
过去,针对恶性疟原虫疟疾的药物疗效评估是通过显微镜检查,即在血涂片中筛查寄生虫来进行的。然而,在高流行地区,再次出现的寄生虫可能源自新的感染,可能会被错误地归类为治疗失败。最近,一些研究在给药后对可检测到的寄生虫进行聚合酶链反应(PCR)分析,以区分新感染与真正的复发。该技术的可行性、高灵敏度和高分辨率证明,它在耐药性和疫苗疗效研究以及新型抗疟药物测试中都将是实用且极具价值的。在本文中,乔治·斯诺努和汉斯 - 彼得·贝克讨论了PCR技术的技术局限性所固有的数据解释中的不确定性,以及寄生虫生物学所带来的限制。他们指出,尽管基因分型可为区分真正的复发和再感染提供有力证据,但必须谨慎解释。他们还提出了可能有助于将这些不确定性降至最低的策略。