Shields J G, Parrott D M
Immunology. 1985 Apr;54(4):771-6.
Feeding of a protein antigen, human gamma globulin (HGG), to BALB/c mice prior to parenteral immunization resulted in the abrogation of a delayed-type hypersensitivity (DTH) response to challenge with that antigen. Unlike parenterally immunized mice, HGG-fed mice were unable to transfer DTH to naive syngeneic recipients using peripheral lymph node lymphocytes. Co-transfer experiments ruled out the possibility of a suppressor cell in the orally immunized mice operating on DTH effector cells. Intra-epithelial lymphocytes (IELs) from mice immunized either orally or parenterally were able to transfer a DTH reaction to unimmunized recipients, while mesenteric lymph node lymphocytes from orally, but not parenterally, immunized donors were capable of transferring DTH. The implications of these results for investigations of gastrointestinal disorders with a suspected immunological aetiology are discussed.
在肠胃外免疫之前给BALB/c小鼠喂食蛋白质抗原人γ球蛋白(HGG),会导致对该抗原激发的迟发型超敏反应(DTH)被消除。与肠胃外免疫的小鼠不同,喂食HGG的小鼠无法使用外周淋巴结淋巴细胞将DTH转移给同基因的未致敏受体。共转移实验排除了口服免疫小鼠中存在作用于DTH效应细胞的抑制细胞的可能性。来自经口服或肠胃外免疫小鼠的上皮内淋巴细胞(IEL)能够将DTH反应转移给未免疫的受体,而来自口服免疫而非肠胃外免疫供体的肠系膜淋巴结淋巴细胞能够转移DTH。本文讨论了这些结果对于疑似免疫病因的胃肠道疾病研究的意义。