Maron R, Palanivel V, Weiner H L, Harn D A
Center for Neurologic Diseases, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Clin Immunol Immunopathol. 1998 Apr;87(1):85-92. doi: 10.1006/clin.1997.4506.
In murine Schistosoma mansoni, parenteral administration of parasite eggs or saline-soluble egg antigens (SEA), generates Th2 T-cell responses to both schistosome-specific and unrelated third-party antigens. Oral administration of insulin to NOD mice suppresses or delays the onset of diabetes by skewing the response toward CD4+ Th2 cells and TGF-beta producing cells. From these two independent sets of observations, we initiated the present study to determine if oral administration of SEA would stimulate Th2-type cytokine responses when mice were fed SEA alone or in tandem with insulin B-chain. Our results show that feeding NOD mice with either insulin B-chain or SEA alone significantly inhibits proliferation to the immunizing antigen. When cytokine profiles were examined, feeding led to a predominance of IL-10 and TGF-beta production. Furthermore, feeding SEA in combination with insulin B-chain augmented the level of IL-10 production to insulin. T-cell lines established from SEA-fed and -immunized mice secreted IL-4 and IL-10 cytokines whereas the T-cell lines from control-fed mice immunized with SEA secreted predominantly IL-2 and IFN-gamma. These results demonstrate that orally administered insulin can induce regulatory T-cells secreting IL-4, IL-10, and TGF-beta and that Th2 responses to oral insulin could be augmented in a synergistic way by feeding SEA and insulin B-chain together.
在小鼠曼氏血吸虫感染模型中,经肠外途径给予寄生虫卵或盐溶性虫卵抗原(SEA),可引发针对血吸虫特异性抗原和无关第三方抗原的Th2型T细胞应答。给非肥胖糖尿病(NOD)小鼠口服胰岛素,通过使免疫应答偏向CD4 + Th2细胞和产生转化生长因子β(TGF-β)的细胞,从而抑制或延缓糖尿病的发病。基于这两组独立的观察结果,我们开展了本研究,以确定当单独给小鼠喂食SEA或与胰岛素B链同时喂食时,口服SEA是否会刺激Th2型细胞因子应答。我们的结果表明,单独给NOD小鼠喂食胰岛素B链或SEA,均能显著抑制对免疫抗原的增殖反应。检测细胞因子谱时发现,喂食会导致白细胞介素10(IL-10)和TGF-β的产生占主导地位。此外,将SEA与胰岛素B链联合喂食,可提高对胰岛素的IL-10产生水平。从经SEA喂食和免疫的小鼠建立的T细胞系分泌IL-4和IL-10细胞因子,而用SEA免疫的对照喂食小鼠的T细胞系主要分泌IL-2和干扰素γ(IFN-γ)。这些结果表明,口服胰岛素可诱导分泌IL-4、IL-10和TGF-β的调节性T细胞,并且通过将SEA和胰岛素B链一起喂食,可协同增强对口服胰岛素的Th2应答。