Pérez-Lorenzo R, Zambrano-Zaragoza J F, Saul A, Jiménez-Zamudio L, Reyes-Maldonado E, García-Latorre E
Departamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Hospital General de México, Mexico.
Int J Dermatol. 1998 Jul;37(7):524-31. doi: 10.1046/j.1365-4362.1998.00512.x.
Psoriasis is a chronic disease of the skin that appears to be of autoimmune nature. It has a strong association with throat streptococcal infections, as well as with stressful events. Although many groups consider psoriasis to be a T-cell-mediated autoimmune disease, autoantibodies could also play a role in the development of this process.
In this work, we looked for autoantibodies to psoriatic skin in 21 psoriatic patients and four healthy donors (controls). The immunoperoxidase technique was used to look for autoantibodies in autologous sera in skin sections obtained from lesions or from healthy areas of the same patient, before and after immunoadsorption with a Streptococcus pyogenes extract. The skin biopsies were also analyzed with a pool of sera from mice immunized with the streptococcal extract.
We found that all psoriatic patients had autoantibodies to antigens present in keratinocytes, whereas healthy subjects did not. These antibodies did not recognize epitopes on healthy skin from the same psoriatic patients or controls. Immunoadsorption of autologous sera removed the reactivity to antigens in skin lesions in all cases. Mouse anti-streptococcal sera recognized epidermal antigens present in lesional psoriatic skin, but not in healthy skin from psoriatic patients or controls. Deposits of immunoglobulin G (IgG) were not detected in the lesions.
It seems that autoantibodies, although they do not appear to participate in the pathogenesis of psoriasis, are an important feature, and that skin antigens, which appear in lesional immature keratinocytes, cross-react with S. pyogenes and contribute to the autoimmune process in psoriasis.
银屑病是一种慢性皮肤疾病,似乎具有自身免疫性质。它与咽喉部链球菌感染以及应激事件密切相关。尽管许多研究小组认为银屑病是一种T细胞介导的自身免疫性疾病,但自身抗体在这一过程的发展中也可能发挥作用。
在本研究中,我们检测了21例银屑病患者和4名健康供者(对照)血清中针对银屑病皮肤的自身抗体。采用免疫过氧化物酶技术,在同一患者病变部位或健康部位获取的皮肤切片中,检测自体血清中的自身抗体,检测前和用化脓性链球菌提取物进行免疫吸附后均进行检测。还用链球菌提取物免疫的小鼠血清池对皮肤活检标本进行分析。
我们发现所有银屑病患者血清中均存在针对角质形成细胞中抗原的自身抗体,而健康受试者则没有。这些抗体不能识别同一银屑病患者或对照的健康皮肤中的表位。自体血清的免疫吸附在所有病例中均消除了对皮肤病变中抗原的反应性。小鼠抗链球菌血清可识别银屑病病变皮肤中的表皮抗原,但不能识别银屑病患者或对照的健康皮肤中的表皮抗原。病变部位未检测到免疫球蛋白G(IgG)沉积。
自身抗体似乎虽不参与银屑病的发病机制,但却是一个重要特征,且病变部位未成熟角质形成细胞中出现的皮肤抗原与化脓性链球菌发生交叉反应,促进了银屑病的自身免疫过程。