Revillard J P
Eur J Immunol. 1985 Jan;15(1):96-9. doi: 10.1002/eji.1830150119.
IgG-binding factors (IgG-BF) prepared from cell-free supernatant of human peripheral blood mononuclear cells interfere with the polyclonal activation of peripheral B cells by decreasing the numbers of IgG-containing cells and Ig plaque-forming cells. Using Nocardia opaca delipidated cell mitogen (NDCM), a T helper cell-independent polyclonal B cell activator, it was found that the suppressive effect of IgG-BF was no longer demonstrable after removal of T cells. In pokeweed mitogen-stimulated cultures, the suppression by IgG-BF required the presence of radiosensitive T cells. Selective depletion of OKT4+ or OKT8+ subsets in NDCM-stimulated cultures showed that IgG-BF required the presence of OKT4+ lymphocytes to induce suppression. It is concluded that the effect of human IgG-BF was mediated by one or several subsets of T cells.
从人外周血单个核细胞无细胞上清液制备的IgG结合因子(IgG-BF)通过减少含IgG细胞和Ig斑块形成细胞的数量,干扰外周B细胞的多克隆激活。使用不透明诺卡氏菌脱脂细胞促有丝分裂原(NDCM),一种不依赖T辅助细胞的多克隆B细胞激活剂,发现去除T细胞后,IgG-BF的抑制作用不再明显。在商陆促有丝分裂原刺激的培养物中,IgG-BF的抑制作用需要有放射敏感的T细胞存在。在NDCM刺激的培养物中对OKT4 +或OKT8 +亚群进行选择性清除表明,IgG-BF需要OKT4 +淋巴细胞的存在来诱导抑制。得出的结论是,人IgG-BF的作用是由T细胞的一个或几个亚群介导的。