Coico R F, Xue B, Wallace D, Siskind G W, Thorbecke G J
J Exp Med. 1985 Dec 1;162(6):1852-61. doi: 10.1084/jem.162.6.1852.
We show that the IgD-induced augmentation of the immune response to trinitrophenylated keyhole limpet hemocyanin can be transferred to syngeneic mice with spleen cells from IgD-injected donors. The augmenting activity is present in the Lyt-1+2-, L3T4+ T cell population and is absent from B cells. The ability of transferred T cells to augment the immune response correlates with the presence of a high frequency of Lyt-1+2- T cells that form rosettes with IgD-coated sheep erythrocytes (T delta cells). Such rosette-forming cells can also be induced by incubation of spleen cells from normal donors in IgD-coated petri dishes. Injection of normal spleen cells exposed to IgD-coated petri dishes together with antigen also augments the immune response of recipients. The existence of a regulatory circuit based upon interactions between T delta cells, antigen, B cell surface IgD, and serum IgD, is proposed.
我们发现,IgD诱导的对三硝基苯化钥孔戚血蓝蛋白免疫反应的增强作用,可以通过将来自注射IgD的供体的脾细胞转移给同基因小鼠来实现。增强活性存在于Lyt-1+2-、L3T4+ T细胞群体中,而B细胞中不存在。转移的T细胞增强免疫反应的能力与形成IgD包被的绵羊红细胞玫瑰花结的Lyt-1+2- T细胞(Tδ细胞)的高频率存在相关。这种形成玫瑰花结的细胞也可以通过将正常供体的脾细胞在IgD包被的培养皿中孵育来诱导。将暴露于IgD包被培养皿的正常脾细胞与抗原一起注射也能增强受体的免疫反应。我们提出存在一种基于Tδ细胞、抗原、B细胞表面IgD和血清IgD之间相互作用的调节回路。