Umesaki Y, Setoyama H
Yakult Central Institute for Microbiological Research, Tokyo, Japan.
Immunology. 1992 Feb;75(2):386-8.
Cholera toxin (CT) has been shown to be a most potent mucosal immunogen and an adjuvant to orally administered unrelated antigens. We investigated the effect of the oral administration of substances with the ability to bind to intestinal epithelial cells on the immune responses against themselves in the presence or absence of CT. Mice were fed non-specific rabbit IgG (RGG) or rabbit IgG (a-GA1) specific to asialo GM1 glycolipid, a major component of the apical membrane of mouse small intestinal epithelial cells, with or without CT. Oral administration of a-GA1 evoked stronger antibody responses than that of RGG in both the serum and intestinal fluid in the presence of CT. However, when the antigens were administered singly without CT, no significant antibody response was detected. In this case, oral administration of RGG induced severe suppression of the systemic antibody response to a subsequent intraperitoneal injection of RGG. In contrast, a-GA1 could not induce oral tolerance. Together these findings suggest that substances with the ability to bind to intestinal epithelial cells are strong immunogens in the presence of CT and weak tolerogens in the absence of CT.
霍乱毒素(CT)已被证明是一种极其有效的黏膜免疫原,也是口服无关抗原的佐剂。我们研究了口服具有结合肠上皮细胞能力的物质,在有或没有CT存在的情况下,对自身免疫反应的影响。给小鼠喂食非特异性兔免疫球蛋白G(RGG)或针对去唾液酸GM1糖脂(小鼠小肠上皮细胞顶端膜的主要成分)的兔免疫球蛋白G(α-GA1),同时添加或不添加CT。在有CT存在的情况下,口服α-GA1在血清和肠液中引发的抗体反应比RGG更强。然而,当单独给予抗原而不添加CT时,未检测到明显的抗体反应。在这种情况下,口服RGG会严重抑制随后腹腔注射RGG所引发的全身抗体反应。相比之下,α-GA1不能诱导口服耐受。这些发现共同表明,具有结合肠上皮细胞能力的物质在有CT存在时是强免疫原,在没有CT存在时是弱耐受原。