Reshef A, Kagey-Sobotka A, Adkinson N F, Lichtenstein L M, Norman P S
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
J Allergy Clin Immunol. 1989 Nov;84(5 Pt 1):678-87. doi: 10.1016/0091-6749(89)90296-0.
To investigate the kinetics and pattern of allergenically induced mediator release in the human skin, we have studied 24 ragweed- and grass-allergic patients with a blister-chamber technique. Chambers sealed to the skin around a denuded area, formed by unroofing a blister, were challenged with 0.5 ml of either diluent or 10 or 100 times the concentration of allergen required for 4+ early intradermal reaction. Chamber fluids were removed hourly 1 to 8 hours after antigen challenge and examined for the presence of histamine, leukotriene C4 (LTC4), and prostaglandin D2 to compare inflammatory mediator levels with the clinical early response and late-phase response (LPR), as assessed by erythema around the chamber. An initial erythema developed rapidly and began to subside after 1 hour in all patients, but a late-phase local erythema and subcutaneous swelling around the chamber (i.e., greater than 2.5 cm, the outside diameter of the chamber) developed in 13/15 challenges only when the higher concentration of antigen was used. At both allergen concentrations, histamine levels peaked sharply at the first hour (20.6 +/- 2.3 ng/ml) and progressively declined during the next 4 hours by 75%, but remained above control levels for at least 7 hours. Despite high control values, LTC4 levels were significantly elevated (p less than 0.01) 4 to 6 hours after challenge. In visible reactions, maximal LPR around the chamber correlated with LTC4 levels obtained 6 and 7 hours after challenge (p less than 0.05). Prostaglandin D2 rose gradually in antigen-challenged chambers to a peak at 5 to 6 hours. Thus, early rises in histamine were temporally related to the immediate erythema, whereas the arachidonic acid metabolites from both cyclooxygenase and lipoxygenase pathways that appeared in the skin after allergen challenge followed kinetics that corresponded to the time course of cutaneous LPR.
为了研究变应原诱导的介质在人体皮肤中释放的动力学和模式,我们采用水疱腔技术对24例豚草和草类过敏患者进行了研究。在通过去除水疱顶部形成的裸露区域周围将腔室密封在皮肤上,用0.5 ml稀释剂或4+早期皮内反应所需变应原浓度的10倍或100倍进行激发。抗原激发后1至8小时每小时收集腔室液,检测组胺、白三烯C4(LTC4)和前列腺素D2的存在,以将炎症介质水平与临床早期反应和迟发相反应(LPR)进行比较,LPR通过腔室周围的红斑进行评估。所有患者均迅速出现初始红斑,并在1小时后开始消退,但仅在使用较高浓度抗原时,13/15次激发中出现了腔室周围的迟发局部红斑和皮下肿胀(即大于2.5 cm,腔室的外径)。在两种变应原浓度下,组胺水平在第1小时急剧达到峰值(20.6±2.3 ng/ml),并在接下来的4小时内逐渐下降75%,但至少7小时内仍高于对照水平。尽管对照值较高,但激发后4至6小时LTC4水平显著升高(p<0.01)。在可见反应中,腔室周围最大的LPR与激发后6和7小时获得的LTC4水平相关(p<0.05)。前列腺素D2在抗原激发的腔室中逐渐升高,在5至6小时达到峰值。因此,组胺的早期升高在时间上与即刻红斑相关,而变应原激发后皮肤中出现的来自环氧化酶和脂氧化酶途径的花生四烯酸代谢产物遵循与皮肤LPR时间进程相对应的动力学。