Schultz J C
University of Wisconsin, Department of Pathology and Laboratory Medicine, Madison, USA.
J Clin Lab Anal. 1999;13(2):82-9. doi: 10.1002/(sici)1098-2825(1999)13:2<82::aid-jcla7>3.0.co;2-c.
Radial immunodiffusion (RID), alkaline cellulose acetate electrophoresis, and high-performance liquid chromatography (HPLC) were compared for quantitating the elevated (> 10%) level of fetal hemoglobin (HbF) found in the red blood cells of sickle cell disease patients undergoing treatment with hydroxyurea. HPLC- and electrophoresis-determined values were comparable. The RID-determined values were higher, in many cases twofold higher. False high HbF values would be misleading in assessing the effectiveness of hydroxyurea therapy in sickle cell disease patients. We subsequently initiated an examination of the variation in HbF values due to the use of different HbF radial immunodiffusion QUIPlates and different positions within a single plate in an attempt to determine the cause of these discrepancies. Within-run precision studies indicated that significantly different size precipitin rings were obtained depending upon which area of the plate the hemolysate containing antigen (HbF) was applied. A common feature associated with poor precision plates was a marked difference in degree of coloration of gel throughout the plate. Spuriously high HF concentrations were obtained with antigen (HbF) placed in wells located in the lighter colored gel area while antigen placed in wells in the darker colored area of the agarose gel bed were more in agreement with the electrophoretically determined HbF concentrations. The variation in HbF values was significantly greater in the diluted (HbF QUIPlate Diluent) samples than in the neat samples even on plates of uniform gel coloration. As a result of this study, we will continue to monitor high HbF levels by densitometry following alkaline cellulose acetate electrophoresis.
对接受羟基脲治疗的镰状细胞病患者红细胞中发现的胎儿血红蛋白(HbF)水平升高(>10%)进行定量时,比较了径向免疫扩散(RID)、碱性醋酸纤维素电泳和高效液相色谱(HPLC)。HPLC和电泳测定的值具有可比性。RID测定的值更高,在许多情况下高出两倍。在评估羟基脲疗法对镰状细胞病患者的有效性时,错误的高HbF值会产生误导。随后,我们开始研究由于使用不同的HbF径向免疫扩散QUIPlates以及单个板内不同位置而导致的HbF值变化,以试图确定这些差异的原因。批内精密度研究表明,根据含有抗原(HbF)的溶血产物施加在板的哪个区域,会获得明显不同大小的沉淀素环。与精密度差的板相关的一个共同特征是整个板上凝胶的着色程度存在明显差异。当抗原(HbF)置于颜色较浅的凝胶区域的孔中时,会得到假性高HF浓度,而置于琼脂糖凝胶床颜色较深区域的孔中的抗原与电泳测定的HbF浓度更一致。即使在凝胶颜色均匀的板上,稀释(HbF QUIPlate稀释剂)样品中HbF值的变化也比纯样品中的变化明显更大。这项研究的结果是,我们将继续通过碱性醋酸纤维素电泳后的光密度测定法监测高HbF水平。