Sakurai T, Inagaki N, Nagai H
Department of Pharmacology, Gifu Pharmaceutical University, Japan.
Life Sci. 1994;54(17):PL291-5. doi: 10.1016/0024-3205(94)00859-0.
Biphasic cutaneous reaction with peak response at 1 (early phase) and 24 to 48 hour (late phase) was elicited by epicutaneous challenge with antigen in actively and passively sensitized mice. Mice were actively immunized with dinitrophenylated (DNP) ascaris antigen and challenged with dinitrofluorobenzene (DNFB). Passively sensitization was carried out by the injection of monoclonal anti-DNP-IgE antibody into mice and challenge was elicited with DNFB. Prednisolone at doses of 3 to 10 mg/kg clearly inhibited both early and late phase reactions in either sensitized mice. Monoclonal anti-tumor necrosis factor (TNF)-alpha antibody inhibited the late phase cutaneous reaction in actively sensitized mice. Anti-interleukin-5 (IL-5) monoclonal antibody has no effect on both phase reactions in either actively and passively sensitized animals. These results indicate the possible participation of TNF-alpha in allergic cutaneous late phase reaction in actively sensitized mice.
在主动和被动致敏小鼠中,通过抗原皮内激发可引发双相皮肤反应,其峰值反应分别出现在1小时(早期)和24至48小时(晚期)。小鼠用二硝基苯基化(DNP)蛔虫抗原进行主动免疫,并用二硝基氟苯(DNFB)激发。通过向小鼠注射单克隆抗DNP-IgE抗体进行被动致敏,并用DNFB激发。剂量为3至10mg/kg的泼尼松龙明显抑制了致敏小鼠的早期和晚期反应。单克隆抗肿瘤坏死因子(TNF)-α抗体抑制了主动致敏小鼠的晚期皮肤反应。抗白细胞介素-5(IL-5)单克隆抗体对主动和被动致敏动物的两个阶段反应均无影响。这些结果表明TNF-α可能参与了主动致敏小鼠的过敏性皮肤晚期反应。