Center for Global Health and Diseases, Case Western Reserve, University, Wolstein Research Building, 4-134 Cleveland, OH 44106-7286, United States.
J Immunol Methods. 2011 Mar 31;367(1-2):1-16. doi: 10.1016/j.jim.2011.01.015. Epub 2011 Feb 4.
Historically, examinations of the inhibition of malaria parasite growth/invasion, whether using drugs or antibodies, have relied on the use of microscopy or radioactive hypoxanthine uptake. These are considered gold standards for measuring the effectiveness of antimalarial treatments, however, these methods have well known shortcomings. With the advent of flow cytometry coupled with the use of fluorescent DNA stains allowed for increased speed, reproducibility, and qualitative estimates of the effectiveness of antibodies and drugs to limit malaria parasite growth which addresses the challenges of traditional techniques. Because materials and machines available to research facilities are so varied, different methods have been developed to investigate malaria parasites by flow cytometry. This review is intended to serve as a reference guide for advanced users and importantly, as a primer for new users, to support expanded use and improvements to malaria flow cytometry, particularly in endemic countries.
从历史上看,无论是使用药物还是抗体来抑制疟原虫生长/入侵的检测,都依赖于显微镜或放射性次黄嘌呤摄取的使用。这些被认为是衡量抗疟治疗效果的金标准,但这些方法有明显的缺点。随着流式细胞术的出现,结合使用荧光 DNA 染料,可以提高速度、重现性和定性估计抗体和药物限制疟原虫生长的效果,从而解决了传统技术的挑战。由于研究机构可用的材料和机器差异很大,因此已经开发出不同的方法来通过流式细胞术研究疟原虫。本综述旨在为高级用户提供参考指南,重要的是,为新用户提供入门指南,以支持在疟疾流行国家扩大流式细胞术的使用和改进。