Holt P G, Batty J E, Turner K J
Immunology. 1981 Mar;42(3):409-17.
Exposure of mice to aerosolized ovalbumin (OA) once weekly for 5 min, or once weekly to 10 microgram OA in PBS intranasally, elicited transient IgE responses which declined by the seventh week. When these animals were challenged intraperitoneally (i.p.) with soluble or alum-precipitated OA, their subsequent IgE responses were markedly suppressed relative to controls. In contrast, i.p. challenge provoked hemaagglutinating antibody (HA) responses to OA in the same animals which were considerably more vigorous than in controls. Adoptive transfer experiments employing splenocytes from mice repeatedly exposed to OA via the respiratory tract revealed the presence of suppressor cells active against OA-specific IgE but not HA responses. Radiotracer studies employing 125I-OA, administered intranasally and by aerosol, indicated that much of the antigen rapidly became associated with the gut.
每周一次让小鼠暴露于雾化卵清蛋白(OA)中5分钟,或每周一次经鼻给予10微克溶于磷酸盐缓冲液(PBS)的OA,可引发短暂的IgE反应,该反应在第七周时下降。当用可溶性或明矾沉淀的OA对这些动物进行腹腔注射(i.p.)攻击时,相对于对照组,它们随后的IgE反应受到明显抑制。相比之下,腹腔注射攻击在相同动物中引发了针对OA的血凝抗体(HA)反应,该反应比对照组更为强烈。采用经呼吸道反复暴露于OA的小鼠脾细胞进行的过继转移实验显示,存在对OA特异性IgE有活性但对HA反应无活性的抑制细胞。采用经鼻和雾化给予125I - OA的放射性示踪研究表明,大部分抗原迅速与肠道结合。