Zimmerman Peter A, Howes Rosalind E
The Center for Global Health and Diseases, Case Western Reserve University, Cleveland, Ohio, USA.
Curr Opin Infect Dis. 2015 Oct;28(5):446-54. doi: 10.1097/QCO.0000000000000191.
Limitations of blood smear microscopy contributed to failure of the 1950-1960s WHO Global Programme to Eliminate Malaria. All diagnostic methods encounter limits of detection (LOD) beyond which it will not be possible to identify infected individuals. When this occurs, it becomes difficult to continue evaluating progress of malaria elimination. The purpose of this review is to compare available diagnostic technologies, factors that underlie their LOD, and their potential roles related to the goal of elimination.
Parasite-containing cells, parasite proteins, hemozoin, nucleic acids, and parasite-specific human antibodies are targets of diagnosis. Many studies report advantages of technologies to detect these diagnostic targets. Nucleic acid amplification tests and strategies for enriching capture of malaria diagnostic targets have consistently identified a parasite reservoir not detected by methods focused on the other biological targets. Exploiting magnetic properties of hemozoin may open new strategies for noninvasive malaria diagnosis.
Microscopy and rapid diagnostic tests provide effective surveillance for malaria control. Strategies that detect a reservoir of submicroscopic infection must be developed and standardized to guide malaria elimination.
血涂片显微镜检查的局限性导致了20世纪50 - 60年代世界卫生组织全球疟疾根除计划的失败。所有诊断方法都存在检测限(LOD),超过此限就无法识别感染者。当出现这种情况时,继续评估疟疾根除进展就变得困难。本综述的目的是比较现有的诊断技术、其检测限的潜在因素以及它们与根除目标相关的潜在作用。
含寄生虫细胞、寄生虫蛋白、疟原虫色素、核酸和寄生虫特异性人类抗体是诊断的靶点。许多研究报告了检测这些诊断靶点的技术的优势。核酸扩增试验和富集捕获疟疾诊断靶点的策略一直能够识别出专注于其他生物学靶点的方法所未检测到的寄生虫库。利用疟原虫色素的磁性特性可能为非侵入性疟疾诊断开辟新策略。
显微镜检查和快速诊断测试为疟疾控制提供了有效的监测手段。必须开发并标准化检测亚显微感染库的策略,以指导疟疾根除工作。