Thoman M L, Morgan E L, Weigle W O
J Immunol. 1981 Feb;126(2):632-5.
Fc fragments of human IgG stimulate both proliferation and polyclonal antibody formation by B lymphocytes. T lymphocytes, although not proliferating in response to Fc fragments, are triggered to produce a T cell-replacing factor, which substitutes for T cells in the Fc fragment-induced polyclonal response. The factor is produced within 24 hr after Fc stimulation. Neither Fab fragments nor whole IgG have the capacity to stimulate the release of this activity. This material is a product of Lyt 1+23-, Ia-T lymphocytes and requires Ia+ adherent accessory cells for production. The role of the accessory cell is to process the Fc fragments to biologically active 14,000-daltons subfragments, which directly trigger T cells to factor production. This material has been called (Fc)TRF to distinguish it from other T cell factors.
人IgG的Fc片段可刺激B淋巴细胞增殖并形成多克隆抗体。T淋巴细胞虽然不会对Fc片段产生增殖反应,但会被触发产生一种T细胞替代因子,该因子在Fc片段诱导的多克隆反应中替代T细胞发挥作用。该因子在Fc刺激后24小时内产生。Fab片段和完整的IgG均无刺激这种活性释放的能力。这种物质是Lyt 1+23-、Ia-T淋巴细胞的产物,其产生需要Ia+黏附辅助细胞。辅助细胞的作用是将Fc片段加工成具有生物活性的14,000道尔顿亚片段,这些亚片段直接触发T细胞产生因子。这种物质被称为(Fc)TRF,以区别于其他T细胞因子。