Colby W D, Strejan G H
Eur J Immunol. 1980 Aug;10(8):602-8. doi: 10.1002/eji.1830100806.
Immunological tolerance was induced in CBA mice with respect to both anti-hapten and anti-carrier IgE antibody production, following pretreatment of the animals with deaggregated ovalbumin. IgG antibody production was also affected. The tolerance was antigen-specific, was stable upon adoptive transfer to irradiated syngeneic recipients, but was reversed following booster. The extent and duration of the tolerant state depended on the dosage and number of tolerogen injections. Tolerogen administered after the initiation of the primary response was without effect. The pattern and duration of this tolerance suggested that T suppressor cells were not involved. The adoptive transfer of spleen cells from tolerogen-treated donors while being themselves unresponsive, failed to interfere with the induction of an immune response in the recipient. Evidence of T suppressor cell function was found in adoptive transfers, only after prolonged pretreatment of donors with a combination of tolerogenic and immunogenic forms of the carrier. These results suggested that T cell-dependent tolerance of the IgE antibody response operates via two distinct mechanisms, of which only one is provided by suppressor cell function.
在用去聚合卵清蛋白对CBA小鼠进行预处理后,它们针对抗半抗原和抗载体IgE抗体产生均诱导出了免疫耐受。IgG抗体产生也受到了影响。这种耐受具有抗原特异性,在将其过继转移至经照射的同基因受体后仍保持稳定,但在加强免疫后会被逆转。耐受状态的程度和持续时间取决于耐受原注射的剂量和次数。在初次应答开始后给予耐受原则没有效果。这种耐受的模式和持续时间表明不涉及T抑制细胞。来自经耐受原处理的供体的脾细胞在自身无反应的情况下进行过继转移,未能干扰受体中免疫应答的诱导。仅在供体用载体的耐受原性和免疫原性形式的组合进行长时间预处理后,在过继转移中才发现T抑制细胞功能的证据。这些结果表明,IgE抗体应答的T细胞依赖性耐受通过两种不同机制起作用,其中只有一种由抑制细胞功能提供。