Kondo S, Pastore S, Fujisawa H, Shivji G M, McKenzie R C, Dinarello C A, Sauder D N
Division of Dermatology, Sunnybrook Health Science Centre, University of Toronto, Canada.
J Invest Dermatol. 1995 Sep;105(3):334-8. doi: 10.1111/1523-1747.ep12320329.
Interleukin-1 receptor antagonist (IL-1ra), a naturally occurring inhibitor of interleukin-1 (IL-1), blocks IL-1 binding to its receptors but has no agonistic activity. IL-1 is thought to play an important role in contact hypersensitivity (CHS), although the effects of exogenously administered IL-1 in CHS have been somewhat controversial. To clarify the role of IL-1 in CHS, we studied the effect of IL-1 receptor blockade using exogenous IL-1ra and evaluated these effects on CHS. We examined the in vivo effects of local administration of recombinant human IL-1ra in the murine CHS model. Local injection of IL-1ra to sensitized BALB/c mice just before challenge with dinitrofluorobenzene resulted in a significant reduction in the intensity of CHS responses, assessed by ear swelling. A dose-response study revealed that maximal inhibition of ear swelling (36% to 43%) was observed after intradermal injection of IL-1ra at doses of 10 to 100 micrograms/ear. This reduction in ear swelling in IL-1ra-injected ears consisted of less inflammatory cell infiltration and decreased edema in the dermis compared with controls. Suppression of CHS was observed when IL-1ra was applied in the 24-h interval preceding challenge with dinitrofluorobenzene, whereas no suppressive effect was observed when IL-1ra was applied 48 h before or after the challenge. Local administration of IL-1ra to naive mice 5 h before sensitization also suppressed CHS responses. However, IL-1ra injection did not suppress phenol-induced inflammation. These results suggest that IL-1ra is an effective inhibitor of both the sensitization and elicitation phases of CHS expression in mice, thus emphasizing the role of IL-1 as an immunologic potentiator of responses associated with CHS.
白细胞介素-1受体拮抗剂(IL-1ra)是白细胞介素-1(IL-1)的天然抑制剂,可阻断IL-1与其受体的结合,但无激动活性。尽管外源性给予IL-1在接触性超敏反应(CHS)中的作用存在一定争议,但IL-1被认为在CHS中起重要作用。为阐明IL-1在CHS中的作用,我们研究了使用外源性IL-1ra阻断IL-1受体的效果,并评估了其对CHS的影响。我们在小鼠CHS模型中检测了局部给予重组人IL-1ra的体内效应。在用二硝基氟苯攻击致敏的BALB/c小鼠之前立即局部注射IL-1ra,通过耳肿胀评估发现CHS反应强度显著降低。剂量反应研究表明,皮内注射剂量为10至100微克/耳的IL-1ra后,观察到耳肿胀的最大抑制率为36%至43%。与对照组相比,注射IL-1ra的耳朵耳肿胀减轻,包括真皮中炎症细胞浸润减少和水肿减轻。当在二硝基氟苯攻击前24小时内应用IL-1ra时观察到CHS受到抑制,而在攻击前48小时或攻击后应用IL-1ra则未观察到抑制作用。在致敏前5小时对未致敏小鼠局部给予IL-1ra也抑制了CHS反应。然而,IL-1ra注射并未抑制苯酚诱导的炎症。这些结果表明,IL-1ra是小鼠CHS表达致敏和激发阶段的有效抑制剂,从而强调了IL-1作为与CHS相关反应的免疫增强剂的作用。