Fujiwara M, Watanabe H
Laboratory of Immunology, Niigata University School of Medicine, Japan.
Scand J Immunol. 1988 Mar;27(3):311-8. doi: 10.1111/j.1365-3083.1988.tb02352.x.
Proliferative response of splenic T cells of C57BL/6 mice to mutant major histocompatibility complex (MHC) class I antigen (H-2Kbm1) was examined with regard to the role of accessory cells. T cell proliferation in mixed lymphocyte culture (MLC) was not induced when accessory cells were removed from stimulator spleen cells by passage through Sephadex G-10 or nylon-wool column. Anti-Iab antibodies did not inhibit the proliferative response to class I antigen, whereas the same antibodies completely blocked the response to class II antigen (Iabm12). Accessory cells may not be mere presenters of MHC class I antigen because stimulator cells fixed with 0.05% paraformaldehyde lost the stimulating function. The proliferative response was partially recovered by the addition of recombinant interleukin 1 (IL-1) and/or IL-2 to MLC devoid of stimulator type accessory cells. It is concluded that stimulatory type accessory cells were obligatorily involved in the T cell proliferation, and the production of IL-1 by accessory cells is thought to play a critical role in this process.
就辅助细胞的作用而言,检测了C57BL/6小鼠脾T细胞对突变主要组织相容性复合体(MHC)I类抗原(H-2Kbm1)的增殖反应。当通过Sephadex G-10或尼龙毛柱从刺激脾细胞中去除辅助细胞时,混合淋巴细胞培养(MLC)中的T细胞增殖未被诱导。抗Iab抗体不抑制对I类抗原的增殖反应,而相同抗体完全阻断对II类抗原(Iabm12)的反应。辅助细胞可能不仅仅是MHC I类抗原的呈递者,因为用0.05%多聚甲醛固定的刺激细胞失去了刺激功能。通过向缺乏刺激型辅助细胞的MLC中添加重组白细胞介素1(IL-1)和/或IL-2,增殖反应部分恢复。结论是,刺激型辅助细胞必然参与T细胞增殖,辅助细胞产生IL-1被认为在此过程中起关键作用。