Istituto di Microbiologia, Facoltà di Medicina e Chirurgia, Seconda Università degli Studi di Napoli, Italy.
Inflammopharmacology. 1998;6(4):311-20. doi: 10.1007/s10787-998-0015-3.
In this study, changes were investigated in release of IL-1alpha, IFN-gamma and IL-4 from mouse splenocytes stimulated with staphylococcal protein A (SpA), toxic shock syndrome toxin-1 (TSST-1) or streptococcal lysin S (SLS) in the presence of insulin. The results show that insulin-treated splenocytes stimulated by SpA had a 25% increase in IFN-gamma release and a 50% decrease in IL-4 compared with splenocytes treated with SpA alone. IL-1alpha release was unchanged compared with controls. Insulintreated splenocytes stimulated with TSST-1 had a 30% fall in IL-1alpha and IFN-gamma release compared with controls. There were no changes in IL-4 release. Splenocytes stimulated with SLS after insulin treatment increased their release of IL-1alpha and IFN-gamma by 50%, whereas IL-4 release was unchanged. The data suggest that the insulin may have important functional implications in immunoregulation.
在这项研究中,研究人员研究了在胰岛素存在的情况下,金黄色葡萄球菌蛋白 A(SpA)、中毒性休克综合征毒素-1(TSST-1)或链球菌溶素 S(SLS)刺激小鼠脾细胞后,白细胞介素-1α(IL-1α)、干扰素-γ(IFN-γ)和白细胞介素-4(IL-4)的释放变化。结果表明,与单独用 SpA 处理的脾细胞相比,用 SpA 刺激的经胰岛素处理的脾细胞 IFN-γ释放增加了 25%,IL-4 释放减少了 50%。与对照相比,IL-1α释放没有变化。用 TSST-1 刺激的经胰岛素处理的脾细胞与对照相比,IL-1α 和 IFN-γ 的释放分别下降了 30%。IL-4 释放没有变化。经胰岛素处理后,用 SLS 刺激的脾细胞增加了 50%的 IL-1α 和 IFN-γ 释放,而 IL-4 释放没有变化。这些数据表明,胰岛素可能在免疫调节中具有重要的功能意义。