Cumberbatch M, Scott R C, Basketter D A, Scholes E W, Hilton J, Dearman R J, Kimber I
ICI Central Toxicology Laboratory, Macclesfield, Cheshire, UK.
Toxicology. 1993 Jan 29;77(1-2):181-91. doi: 10.1016/0300-483x(93)90148-l.
The influence of the anionic surfactant sodium lauryl sulphate (SLS) on the ability of the contact allergen 2,4-dinitrochlorobenzene (DNCB) to provoke draining lymph node cell proliferative responses, a correlate of skin sensitizing potential, has been examined in mice. Topical application of 10% SLS with 0.1% DNCB caused a more vigorous proliferative response than did exposure to 0.1% DNCB alone. Lower concentrations (0.1% or 1%) of SLS were ineffective and 10% SLS failed to influence proliferative responses to higher concentrations (0.5% or 1%) of DNCB. Using an in vitro model for measurement of percutaneous absorption 10% SLS was shown not to increase the skin penetration of 0.1% DNCB. We therefore examined the influence of SLS on the accumulation of dendritic cells (DC) in lymph nodes draining the site of exposure, an important early event during the induction phase of skin sensitization. The frequency of DC in draining nodes was measured following topical application of SLS, DNCB or a combination of both. Epicutaneous exposure to 0.1% DNCB caused only a modest increase in the number of lymph node DC. However, 10% SLS or a mixture of 10% SLS with 0.1% DNCB each resulted in a significant elevation of DC numbers. It is proposed that SLS augments the skin sensitizing potential of sub-irritant concentrations of DNCB via an increase in the number of immunostimulatory DC which reach the draining nodes.
已在小鼠中研究了阴离子表面活性剂十二烷基硫酸钠(SLS)对接触性变应原2,4 - 二硝基氯苯(DNCB)引发引流淋巴结细胞增殖反应能力的影响,该反应是皮肤致敏潜力的一个相关指标。与单独接触0.1% DNCB相比,局部应用10% SLS与0.1% DNCB会引发更强烈的增殖反应。较低浓度(0.1%或1%)的SLS无效,且10% SLS未能影响对较高浓度(0.5%或1%)DNCB的增殖反应。使用体外经皮吸收测量模型表明,10% SLS不会增加0.1% DNCB的皮肤渗透率。因此,我们研究了SLS对暴露部位引流淋巴结中树突状细胞(DC)积累的影响,这是皮肤致敏诱导阶段的一个重要早期事件。在局部应用SLS、DNCB或两者组合后,测量引流淋巴结中DC的频率。经皮暴露于0.1% DNCB仅使淋巴结DC数量略有增加。然而,10% SLS或10% SLS与0.1% DNCB的混合物均导致DC数量显著升高。有人提出,SLS通过增加到达引流淋巴结的免疫刺激性DC数量,增强了亚刺激性浓度DNCB的皮肤致敏潜力。