Deguchi H, Suemura M, Ishizaka A, Ozaki Y, Kishimoto S, Yamamura Y, Kishimoto T
J Immunol. 1983 Dec;131(6):2751-6.
An in vitro experimental system for the induction of IgE production has been established with human peripheral blood lymphocytes (PBL). The stimulation of human PBL with PWM plus Cowan I induced IgM-, IgG-, and IgE- producing cells when assessed by reverse plaque assay. T cells, which had been isolated from patients with pulmonary tuberculosis and incubated with PPD plus IgE for 5 days, showed a suppressive effect on the polyclonal IgE response induced by PWM plus Cowan I. The direct addition of activated T cells, as well as the culture supernatant from activated T cells, abrogated the IgE response; the IgG response was not affected. The IgE-specific suppressive activity in the supernatant was specifically absorbed by an IgE column and could be eluted with acid buffer. The results demonstrated the presence of a human IgE binding factor(s), which showed its suppressive effect selectively in the IgE antibody response.
已经建立了一种用人外周血淋巴细胞(PBL)诱导IgE产生的体外实验系统。用PWM加考恩I刺激人PBL时,通过反向空斑试验评估可诱导产生IgM、IgG和IgE的细胞。从肺结核患者中分离出的T细胞与PPD加IgE一起孵育5天,对PWM加考恩I诱导的多克隆IgE反应显示出抑制作用。直接加入活化的T细胞以及活化T细胞的培养上清液可消除IgE反应;IgG反应不受影响。上清液中的IgE特异性抑制活性可被IgE柱特异性吸附,并用酸性缓冲液洗脱。结果表明存在人IgE结合因子,其在IgE抗体反应中选择性地发挥抑制作用。