Nagai H, Sakurai T, Inagaki N, Mori H
Department of Pharmacology, Gifu Pharmaceutical University, Japan.
Biol Pharm Bull. 1995 Feb;18(2):239-45. doi: 10.1248/bpb.18.239.
Biphasic skin reactions, with peaks at 1 and 24 h after epicutaneous challenge with antigen (immediate phase response: IPR and late phase response: LPR, respectively), were induced in ddY, ICR, Balb/c and Balb/c-nu/nu mice passively sensitized with monoclonal IgE antibody 24 h before. In WBB6F1-W/Wv mice, which lack mast cells, only the LPR was observed. The IPR was characterized by a rapid increase in capillary permeability and the LPR by skin thickening with significant infiltration of eosinophils and other inflammatory cells in Balb/c mice. Histamine H1 receptor antagonists, including diphenhydramine and homochlorcyclizine, and the allergic histamine release inhibitors, tranilast and amlexanox, clearly inhibited the IPR, but not the LPR. Prednisolone and dexamethasone, however, inhibited both. Prednisolone also inhibited the LPR in WBB6F1-W/Wv mice. These results indicate that IgE antibody-dependent biphasic skin reactions consist of a mast cell- and histamine-dependent IPR and a mast cell-independent LPR.
在用抗原进行表皮攻击后1小时和24小时出现峰值的双相皮肤反应(分别为即刻相反应:IPR和迟发相反应:LPR),在用单克隆IgE抗体在24小时前被动致敏的ddY、ICR、Balb/c和Balb/c-nu/nu小鼠中被诱导。在缺乏肥大细胞的WBB6F1-W/Wv小鼠中,仅观察到迟发相反应。在Balb/c小鼠中,即刻相反应的特征是毛细血管通透性迅速增加,迟发相反应的特征是皮肤增厚,伴有嗜酸性粒细胞和其他炎症细胞的显著浸润。包括苯海拉明和氯环利嗪在内的组胺H1受体拮抗剂以及过敏组胺释放抑制剂曲尼司特和氨来呫诺,明显抑制即刻相反应,但不抑制迟发相反应。然而,泼尼松龙和地塞米松两者均有抑制作用。泼尼松龙也抑制WBB6F1-W/Wv小鼠的迟发相反应。这些结果表明,IgE抗体依赖性双相皮肤反应由肥大细胞和组胺依赖性的即刻相反应以及肥大细胞非依赖性的迟发相反应组成。