Leynadier F, Tran Xuan T, Dry J
Hôpital Rothschild, Internal Medicine Service, Paris, France.
Allergy. 1991 Nov;46(8):619-25. doi: 10.1111/j.1398-9995.1991.tb00633.x.
By a revised manufacturing process we aimed to obtain latex surgical gloves without immediate allergenicity, and also to determine a simple physical technique by which to estimate this allergenicity. Five glove samples were evaluated for allergenicity by physical and biochemical methods and by skin tests at the University Allergy Centre. Three groups of allergic patients with documented anaphylaxis to surgical gloves, positive skin tests to latex extract and specific IgE to latex (RAST Pharmacia greater than or equal to class II), volunteered for the study. The protein content, the in vitro allergenic potency of glove supernatants (RAST inhibition) and the skin test results with glove supernatants were lower in washed gloves than in non-washed samples (P less than 0.02 to P less than 0.009). The supplementary effect of glove sterilization at 120 degrees C (for 1 h in saturated steam) was obvious. The protein content became undetectable in four of the five glove supernatants, and skin tests results with sample supernatants were decreased (M +/- SEM = 0.68 +/- 0.29 mm vs 3.06 +/- 0.61 mm with non-sterilized gloves), P less than 0.009 by Wilcoxon test. With the Spearman test there was a significant correlation (P = 0.029) between the mean wheal size, obtained with supernatants (Groups 1 and 2) and electrical conductivity. Skin tests through pieces of gloves randomly distributed and coded were decreased by sterilization: 0.66 +/- 0.25 mm vs 2.86 +/- 0.45 mm, P less than 0.0001. Thus, it is possible to decrease glove allergenicity by washing them after mould forming and then sterilizing with steam. Electrical conductivity may be a simple parameter for revealing allergenicity.
我们旨在通过改进制造工艺获得无即刻致敏性的乳胶手术手套,并确定一种评估这种致敏性的简单物理技术。在大学过敏中心,通过物理和生化方法以及皮肤试验对五个手套样品的致敏性进行了评估。三组有手术手套过敏反应记录、乳胶提取物皮肤试验阳性以及乳胶特异性IgE(RAST法,Pharmacia,大于或等于II级)的过敏患者自愿参与了这项研究。清洗后的手套中,蛋白质含量、手套上清液的体外致敏效力(RAST抑制)以及手套上清液的皮肤试验结果均低于未清洗的样品(P小于0.02至P小于0.009)。120摄氏度(饱和蒸汽中1小时)手套灭菌的补充效果明显。五个手套上清液中有四个的蛋白质含量变得无法检测,样品上清液的皮肤试验结果降低(M +/- SEM = 0.68 +/- 0.29毫米,未灭菌手套为3.06 +/- 0.61毫米),Wilcoxon检验P小于0.009。通过Spearman检验,上清液(第1组和第2组)获得的平均风团大小与电导率之间存在显著相关性(P = 0.029)。通过随机分布和编码的手套片进行的皮肤试验因灭菌而降低:0.66 +/- 0.25毫米对2.86 +/- 0.45毫米,P小于0.0001。因此,在成型后清洗手套然后进行蒸汽灭菌有可能降低手套的致敏性。电导率可能是揭示致敏性的一个简单参数。