University of Genoa, viale Benedetto XV, 16132, Genoa, Italy.
Eur J Dermatol. 2011 Jan-Feb;21(1):32-6. doi: 10.1684/ejd.2010.1150.
The pathophysiology of erythema multiforme (EM), Stevens-Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN) is unclear. Whether autoantibodies against desmoplakin (Dp) I and II play a pathogenic role or result from an epitope spreading phenomenon is uncertain. Our aim was to characterize the keratinocyte antigens recognized in EM, TEN and SJS. Of 33 patients studied, 2 had TEN, 1 SJS, 9 EM major and 21 EM minor, according to Roujeau's criteria. All sera were studied by indirect immunofluorescence (IIF), immunoblotting and immunoprecipitation. Twenty normal sera were used as controls. 10/33 sera reacted with polypeptides of 215 and/or 250-kDa molecular mass, which co-migrate with Dp I and II as assessed by an anti-Dp I and II monoclonal antibody on IB. In IP, none of the anti-Dp I and -Dp II 10 patient sera immunoprecipitated Dp I and/or II from radiolabeled keratinocyte extracts. Two of 10 patient sera (SJS, EM minor) reacted with DpI and II when denaturated by the IB procedure. The reactivity against intracellular antigens DpI and II as denaturated proteins may result from the epidermal damage produced by aggressive autoreactive T cells, playing therefore only a secondary role in the pathogenesis of the disease.
多形性红斑(EM)、史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死松解症(TEN)的病理生理学尚不清楚。自身抗体针对桥粒芯糖蛋白 I 和 II 是否发挥致病作用或是否由表位扩展现象引起尚不确定。我们的目的是描述 EM、TEN 和 SJS 中识别的角质形成细胞抗原。根据 Roujeau 的标准,研究的 33 例患者中,2 例为 TEN,1 例为 SJS,9 例为 EM 大疱,21 例为 EM 小疱。所有血清均通过间接免疫荧光(IIF)、免疫印迹和免疫沉淀进行研究。用 20 份正常血清作为对照。33 份血清中的 10 份与 215 和/或 250kDa 分子量的多肽反应,这与通过 IB 上的抗 Dp I 和 II 单克隆抗体评估的 Dp I 和 II 共同迁移。在 IP 中,没有 10 份患者血清中的抗 Dp I 和 -Dp II 免疫沉淀从放射性标记的角质形成细胞提取物中免疫沉淀 Dp I 和/或 II。10 份患者血清中的 2 份(SJS、EM 小疱)在 IB 过程中变性时与 DpI 和 II 反应。对变性蛋白内细胞抗原 Dp I 和 II 的反应可能是由侵袭性自身反应性 T 细胞引起的表皮损伤所致,因此在疾病发病机制中仅起次要作用。