Turner K J, Holt P G, Holt B J, Cameron K J
Clin Exp Immunol. 1983 Feb;51(2):387-94.
The appearance of IgE in supernatant fluids from cultures of human peripheral blood leucocytes (PBL) is employed in many laboratories as an index of antibody 'synthesis'. This study demonstrates that, unlike IgG, the majority of cell associated IgE is sequestered by PBL in a tightly bound form, which resists extraction via the freeze-thawing (F/T) techniques in current use. A method is presented for the quantitative extraction of cell associated IgE, involving brief acid treatment of whole cells, and is shown to yield up to 100% more IgE than the F/T procedure. The use of this extraction process on PBL before and after culture permits discrimination between release of pre-formed IgE and de novo synthesis, both of which are demonstrated to occur to widely differing degrees in PBL cultures from different donors.
在许多实验室中,人外周血白细胞(PBL)培养上清液中IgE的出现被用作抗体“合成”的指标。本研究表明,与IgG不同,大多数细胞相关IgE以紧密结合的形式被PBL隔离,这种形式可抵抗目前使用的冻融(F/T)技术的提取。本文介绍了一种定量提取细胞相关IgE的方法,该方法涉及对全细胞进行短暂酸处理,结果显示其产生的IgE比F/T程序多100%。在培养前后对PBL使用这种提取方法,可以区分预先形成的IgE的释放和从头合成,结果表明,在来自不同供体的PBL培养物中,这两种情况的发生程度差异很大。