Boerrigter G H, Bril H, Scheper R J
Department of Pathology, Free University Hospital, Amsterdam, The Netherlands.
Int Arch Allergy Appl Immunol. 1988;85(4):385-91. doi: 10.1159/000234539.
A guinea pig model was used to investigate the potential role of hapten-specific antibodies in allergic contact dermatitis. Hapten-specific antibodies of both the IgG1, IgG2 and IgM (sub)classes could be readily detected by ELISA in sera obtained after single or repeated exposure to the allergens 2,4-dinitrochlorobenzene (DNCB) or 4-ethoxymethylene-2-phenyloxazolone. Experiments in which animals were strongly boostered with Freund's complete adjuvant support previous reports that hapten-specific antibodies are able to transfer contact skin reactions with a delayed time course into naive recipients. In contrast, epicutaneous sensitization procedures never allowed transfer of such reactivity. Upon transfer of immune sera to previously sensitized animals, existing allergic contact dermatitis was unaffected, except for a distinct suppression of induration, but not erythema, in the DNCB system. In actively sensitized animals, antibody-related suppression of induration was never observed. Hapten-specific hyposensitivity, as induced by repeated epicutaneous exposure, was also not related to circulating antibody levels. Our findings do not support the view that hapten-specific antibodies should be reconsidered as playing a potentially important role in allergic contact dermatitis.
采用豚鼠模型研究半抗原特异性抗体在过敏性接触性皮炎中的潜在作用。通过ELISA法可轻松检测到,在单次或反复接触过敏原2,4-二硝基氯苯(DNCB)或4-乙氧基亚甲基-2-苯基恶唑酮后获得的血清中,IgG1、IgG2和IgM(亚类)的半抗原特异性抗体。用弗氏完全佐剂对动物进行强力加强免疫的实验支持了先前的报道,即半抗原特异性抗体能够将具有延迟时程的接触性皮肤反应转移给未致敏的受体。相比之下,经皮致敏程序从未允许这种反应性的转移。将免疫血清转移到先前致敏的动物后,现有的过敏性接触性皮炎未受影响,除了在DNCB系统中硬结明显受到抑制,但红斑不受影响。在主动致敏的动物中,从未观察到与抗体相关的硬结抑制。反复经皮暴露诱导的半抗原特异性低敏反应也与循环抗体水平无关。我们的研究结果不支持以下观点,即半抗原特异性抗体应被重新视为在过敏性接触性皮炎中发挥潜在重要作用。