Zaidi Ahmar Urooj, Buck Steven, Gadgeel Manisha, Herrera-Martinez Miguel, Mohan Araathi, Johnson Kenya, Bagla Shruti, Johnson Robert M, Ravindranath Yaddanapudi
Children's Hospital of Michigan, Detroit, MI, United States.
Wayne State University School of Medicine, Detroit, MI, United States.
Front Physiol. 2020 Jun 19;11:636. doi: 10.3389/fphys.2020.00636. eCollection 2020.
The measurement of band 3 (AE1, SLC4A1, CD233) content of red cells by eosin-5- maleimide (EMA) staining is swiftly replacing conventional osmotic fragility (OF) test as a tool for laboratory confirmation of hereditary spherocytosis across the globe. Our group has systematically evaluated the EMA test as a method to screen for a variety of anemias in the last 10 years, and compared these results to those obtained with the osmotic gradient ektacytometry (osmoscans) which we have used over three decades. Our overall experience allowed us to characterize the distinctive patterns with the two tests in several congenital erythrocyte membrane disorders, such as hereditary spherocytosis (HS), hereditary elliptocytosis (HE), Southeast Asian Ovalocytosis (SAO), hereditary pyropoikilocytosis (HPP) variants, erythrocyte volume disorders, various red cell enzymopathies, and hemoglobinopathies. A crucial difference between the two methodologies is that osmoscans measure red blood cell deformability of the entire sample of RBCs, while the EMA test examines the band 3 content of individual RBCs. EMA content is influenced by cell size as smaller red cells have lower amount of total membrane than larger cells. The SAO mutation alters the EMA binding site resulting in a lower EMA MCF even as the band 3 content itself is unchanged. Thus, EMA scan results should be interpreted with caution and both the histograms and dot plots should be analyzed in the context of the clinical picture and morphology.
通过嗜酸性-5-马来酰亚胺(EMA)染色测量红细胞带3(AE1、SLC4A1、CD233)含量,正迅速取代传统的渗透脆性(OF)试验,成为全球范围内实验室确诊遗传性球形红细胞增多症的工具。在过去十年中,我们团队系统地评估了EMA试验作为筛查多种贫血症的方法,并将这些结果与我们使用了三十多年的渗透梯度血细胞变形性测定法(渗透扫描)所获得的结果进行比较。我们的总体经验使我们能够描绘出这两种检测方法在几种先天性红细胞膜疾病中的独特模式,如遗传性球形红细胞增多症(HS)、遗传性椭圆形红细胞增多症(HE)、东南亚椭圆形红细胞增多症(SAO)、遗传性热异形红细胞增多症(HPP)变体、红细胞体积异常、各种红细胞酶病和血红蛋白病。这两种方法的一个关键区别在于,渗透扫描测量的是整个红细胞样本的红细胞变形性,而EMA试验检测的是单个红细胞的带3含量。EMA含量受细胞大小影响,因为较小的红细胞总膜量比较大的细胞少。SAO突变改变了EMA结合位点,即使带3含量本身不变,也会导致较低的EMA平均荧光强度(MCF)。因此,EMA扫描结果应谨慎解读,直方图和点图均应结合临床情况和形态学进行分析。