Thomson S P, Rose J B, McMahon L J
Immunol Commun. 1979;8(3):313-23. doi: 10.3109/08820137909050045.
Highly reproducible peripheral blood lymphocyte (PBL) count and percent E-rosette forming lymphocyte (%E-RFL) assays were developed by modifying existing procedures. PBL count assay variation was reduced by using replicate electronic white blood cell (WBC) counting and 2,000 WBC differentials. The %E-RFL assay modifications reduced variation and include the use of: (a) a capillary buffy coat isolation procedure that recovered more than 85% of the PBL without the use of chemical separation media, (b) centrifugation temperatures of 20--22 degrees C, and (c) toluidine blue staining that allowed enumeration of %E-RFL and not E-rosette forming cells, by exclusion of nonlymphoid cells. Day-to-day variation of PBL count and %E-RFL was defined by making serial determinations over a period of months. The data indicate that healthy adults maintain PBL counts and %E-RFL within narrow ranges that are specific for each individual.
通过改进现有程序,开发出了高度可重复的外周血淋巴细胞(PBL)计数和E花环形成淋巴细胞百分比(%E-RFL)检测方法。通过使用重复电子白细胞(WBC)计数和2000个WBC分类,减少了PBL计数检测的变异。%E-RFL检测的改进减少了变异,包括使用:(a)一种毛细血管血沉棕黄层分离程序,该程序在不使用化学分离介质的情况下可回收超过85%的PBL;(b)20-22摄氏度的离心温度;(c)甲苯胺蓝染色,通过排除非淋巴细胞来计数%E-RFL而非E花环形成细胞。通过在数月内进行系列测定来定义PBL计数和%E-RFL的每日变异。数据表明,健康成年人的PBL计数和%E-RFL维持在每个个体特定的狭窄范围内。