Shapiro Howard M, Apte Simon H, Chojnowski Grace M, Hänscheid Thomas, Rebelo Maria, Grimberg Brian T
The Center for Microbial Cytometry, West Newton, Massachusetts.
Queensland Institute of Medical Research, Brisbane, Queensland, Australia.
Curr Protoc Cytom. 2013 Jul;Chapter 11:11.20.1-11.20.23. doi: 10.1002/0471142956.cy1120s65.
Malaria, caused by protozoan Plasmodium parasites, kills ~800,000 people each year. Exact figures are uncertain because presumptive diagnoses are often made without identifying parasites in patients' blood either by microscopy, using Giemsa's century-old stain, or by simpler tests that are ultimately dependent on microscopy for quality control. Microscopy itself relies on trained observers' ability to detect subtle morphological features of parasitized red blood cells, only a few of which may be present on a slide. Quantitative and objective flow cytometric measurements of cellular constituents such as DNA, RNA, and the malaria pigment hemozoin are now useful in research in malaria biology and pharmacology, and can provide more reliable identification of parasite species and developmental stages and better detection of low-density parasitemia than could microscopy. The same measurements can now be implemented in much smaller, simpler, cheaper imaging cytometers, potentially providing a more accurate and precise diagnostic modality.
由原生动物疟原虫引起的疟疾每年导致约80万人死亡。确切数字尚不确定,因为通常在未通过显微镜检查(使用已有百年历史的吉姆萨染色法)在患者血液中识别寄生虫的情况下做出推定诊断,或者通过最终依赖显微镜进行质量控制的更简单测试来诊断。显微镜检查本身依赖于训练有素的观察者检测被寄生红细胞细微形态特征的能力,而载玻片上可能仅存在少数此类特征。现在,对细胞成分(如DNA、RNA和疟疾色素疟原虫血红素)进行定量和客观的流式细胞术测量在疟疾生物学和药理学研究中很有用,并且与显微镜检查相比,能够更可靠地识别寄生虫种类和发育阶段,以及更好地检测低密度疟原虫血症。现在,同样的测量可以在更小、更简单、更便宜的成像细胞仪中进行,这有可能提供一种更准确、精确的诊断方式。