Dykewicz M S, Patterson R, Cugell D W, Harris K E, Wu A F
Department of Medicine, Northwestern University Medical School, Chicago, Ill 60611.
J Allergy Clin Immunol. 1991 Jan;87(1 Pt 1):48-57. doi: 10.1016/0091-6749(91)90212-7.
Fifty-five subjects were studied to determine if the presence of IgE or IgG antibodies to formaldehyde (F)-human serum albumin (HSA) was associated with exposure to gaseous F or with respiratory or conjunctival symptoms from such exposure. The study population included cohorts exposed to F in the workplace, smokers, and normal subjects. IgE antibody specific for F-HSA was detected by ELISA in three subjects; immediate-type skin testing was negative in two of these subjects, and not interpretable because of dermatographism in one subject. One of these subjects had a history of respiratory symptoms when the subject was working in a histology laboratory that contained ambient F and xylene; a respiratory challenge with F at concentrations of up to 2 ppm failed to produce respiratory symptoms or significant changes in pulmonary function. Serum from the three subjects with IgE to F-HSA by ELISA failed to passively transfer skin reactivity to F-HSA to rhesus monkey recipients. These three subjects and two other subjects had IgG to F-HSA by ELISA, although this was of generally low titer. We could not define a relationship between the presence of antibodies and (1) a history of F exposure or (2) a history of adverse respiratory or conjunctival symptoms from F. This study is a continuum of 5 years of study in our laboratory attempting to define allergy to gaseous F, and the current study does not support an immunologic basis for respiratory or conjunctival symptoms from gaseous F exposure. Based on the findings of this and our other studies, it is possible that clinical IgE-mediated allergy to gaseous F does not exist, or if it does exist, it is extremely rare.
对55名受试者进行了研究,以确定针对甲醛(F)-人血清白蛋白(HSA)的IgE或IgG抗体的存在是否与气态F暴露相关,或与这种暴露引起的呼吸道或结膜症状相关。研究人群包括工作场所接触F的队列、吸烟者和正常受试者。通过ELISA在三名受试者中检测到了对F-HSA特异的IgE抗体;其中两名受试者的速发型皮肤试验为阴性,一名受试者因皮肤划痕症无法进行解读。这些受试者中有一名在组织学实验室工作时曾有呼吸道症状病史,该实验室含有环境F和二甲苯;对浓度高达2 ppm的F进行呼吸道激发试验未能产生呼吸道症状或肺功能的显著变化。通过ELISA检测出对F-HSA有IgE的三名受试者的血清未能将对F-HSA的皮肤反应性被动转移给恒河猴受体。这三名受试者和另外两名受试者通过ELISA检测出对F-HSA有IgG,尽管其滴度通常较低。我们无法确定抗体的存在与(1)F暴露史或(2)F引起的不良呼吸道或结膜症状史之间的关系。本研究是我们实验室5年研究的延续,旨在确定对气态F的过敏情况,目前的研究不支持气态F暴露引起的呼吸道或结膜症状存在免疫学基础。基于本研究及其他研究的结果,临床上IgE介导的对气态F的过敏可能不存在,或者即使存在,也极为罕见。