Teranishi T, Hirano T, Arima N, Onoue K
J Immunol. 1982 Apr;128(4):1903-8.
IgG-PFC was induced in Epstein-Barr virus-transformed B lymphoblastoid cell lines (LCL) by the addition of allogeneic T cells. T cells involved in the induction of IgG-PFC were shown to belong to the Leu 3a+/2a- T cell subset. Furthermore, partially purified soluble factors obtained from the culture supernatant of PPD-stimulated pleural T cells or PWM-stimulated tonsillar mononuclear cells was shown to induce IgG-PFC in LCL across the major histocompatibility complex barrier. The induction of IgG-PFC was observed only in surface IgG-positive LCL cell populations and was not accompanied by the increase in the number of LCL cells. The factors with such a TRF-like activity were found in two fractions corresponding to the m.w. range of 18,000 to 25,000 (22K fraction) and 28,000 to 38,000 (36K fraction) by gel filtration. Isoelectric focusing of these fractions revealed that TRF-like activity of both 22K and 36K fractions distributed in the pI range of 5.0 to 6.0, and both fractions were found to be devoid of TCGF activity. These results appear to indicate that the factors act on the B cells in terminal stages to trigger final differentiation to Ig-producing cells.
通过添加同种异体T细胞,在爱泼斯坦-巴尔病毒转化的B淋巴母细胞系(LCL)中诱导产生IgG-PFC。参与诱导IgG-PFC的T细胞被证明属于Leu 3a+/2a-T细胞亚群。此外,从PPD刺激的胸腔T细胞或PWM刺激的扁桃体单核细胞的培养上清液中获得的部分纯化的可溶性因子,被证明可在主要组织相容性复合体屏障的LCL中诱导IgG-PFC。仅在表面IgG阳性的LCL细胞群体中观察到IgG-PFC的诱导,并且不伴有LCL细胞数量的增加。通过凝胶过滤在对应于分子量范围18,000至25,000(22K组分)和28,000至38,000(36K组分)的两个组分中发现了具有这种TRF样活性的因子。这些组分的等电聚焦显示,22K和36K组分的TRF样活性分布在pI范围5.0至6.0,并且发现这两个组分均缺乏TCGF活性。这些结果似乎表明这些因子作用于终末阶段的B细胞,以触发向产生Ig的细胞的最终分化。