Finkelman F D, Snapper C M, Mountz J D, Katona I M
J Immunol. 1987 May 1;138(9):2826-30.
The possibility that injection of mice with an affinity-purified goat antibody to mouse IgD (GaM delta) that stimulates polyclonal IgG1 secretion might also stimulate differentiation of B cells into IgE-secreting cells was suggested by the observation that such treatment induces T cells from those mice to secrete a lymphokine, B cell stimulatory factor 1 (BSF-1), that can stimulate both IgG1 and IgE secretion in vitro. Studies described in this paper show that injection of BALB/c mice with 200 to 3200 micrograms of GaM delta greatly increased the quantity of splenic epsilon chain-encoding mRNA, the number of spleen cells with cytoplasmic IgE, and the concentration of serum IgE 7 days after injection. Serum IgE levels obtained in these mice were approximately 100 times baseline levels and were comparable with those found in mice infected with the nematode parasite Nippostrongylus brasiliensis, but were approximately 2000-fold less than the peak serum IgG1 levels induced by GaM delta injection. Both IgE and IgG1 secretion in GaM delta injected mice were T dependent (blocked by anti-L3T4 antibody). These observations are consistent with the hypothesis that BSF-1 may play a role in the in vivo stimulation of IgE secretion and provide an easy to apply model for the investigation of in vivo regulation of IgE responses.
用亲和纯化的抗小鼠IgD山羊抗体(GaMδ)注射小鼠可刺激多克隆IgG1分泌,鉴于这种处理能诱导这些小鼠的T细胞分泌一种淋巴因子——B细胞刺激因子1(BSF-1),而该因子在体外既能刺激IgG1分泌也能刺激IgE分泌,因此有人提出这种处理也可能刺激B细胞分化为分泌IgE的细胞。本文所述研究表明,给BALB/c小鼠注射200至3200微克GaMδ,在注射7天后,脾脏中编码ε链的mRNA数量、胞质内有IgE的脾细胞数量以及血清IgE浓度都大幅增加。这些小鼠的血清IgE水平约为基线水平的100倍,与感染巴西日圆线虫的小鼠的血清IgE水平相当,但比GaMδ注射诱导的血清IgG1峰值水平低约2000倍。注射GaMδ的小鼠中IgE和IgG1的分泌都依赖T细胞(被抗L3T4抗体阻断)。这些观察结果与BSF-1可能在体内刺激IgE分泌中起作用的假说一致,并为研究IgE反应的体内调节提供了一个易于应用的模型。