Pepys M B, Sategna-Guidetti C, Mirjah D D, Wansbrough-Jones M H, Dash A C
Clin Exp Immunol. 1976 Oct;26(1):91-4.
A new method is described for the detection by immunofluorescence of lymphocyte populations in whole peripheral blood. Lymphocytes are identified by their lack of intracellular peroxidase, and the absolute number of different populations can be accurately enumerated by avoiding procedures for isolating mononuclear cells before fluorescent staining. Among twenty-two normal individuals the mean +/- s.d. percentage and absolute number of lymphocytes with stable surface immunoglobulin were as follows: IgM, 8-1+/-2-3%, 142+/-60/mu1; IgD,8-9+/-2-2%, 212+/-85/mu1;IgA, 2-2+/-1-0%, 41+/-24/mu1; IgG, 2-3+/-1-6%, 60+/-47/mu1. It was confirmed that the detection of true IgG-bearing lymphocytes depends on washing the blood at 37degrees before staining or the use of F(ab)2 anti-IgG antibodies. The proportion of lymphocytes stained by whole IgG polyvalent anti-immunoglobulin antibody, which detects both true immunoglobulin-bearing lymphocytes (B cells) and Fc receptor cells was constant (20-5+/-1-0%) both in and between individuals, but the absolute numbers (380+/-117/mu1) varied with the lymphocyte count.
本文描述了一种通过免疫荧光检测全外周血中淋巴细胞群体的新方法。淋巴细胞通过缺乏细胞内过氧化物酶来识别,并且通过避免在荧光染色前分离单核细胞的程序,可以准确计数不同群体的绝对数量。在22名正常个体中,具有稳定表面免疫球蛋白的淋巴细胞的平均±标准差百分比和绝对数量如下:IgM,8.1±2.3%,142±60/μl;IgD,8.9±2.2%,212±85/μl;IgA,2.2±1.0%,41±24/μl;IgG,2.3±1.6%,60±47/μl。已证实,检测真正携带IgG的淋巴细胞取决于在染色前于37℃洗涤血液或使用F(ab)2抗IgG抗体。全IgG多价抗免疫球蛋白抗体染色的淋巴细胞比例,该抗体可检测真正携带免疫球蛋白的淋巴细胞(B细胞)和Fc受体细胞,在个体内部和个体之间均恒定(20.5±1.0%),但绝对数量(380±117/μl)随淋巴细胞计数而变化。