Roujeau Jean-Claude, Gélard Kristel, Bensussan Armand
Service de Dermatologie et Inserm U.659, Hôpital Henri Mondor, Université Paris XII, Faculté de Médecine, 8, rue du Général Sarrail, 94010 Créteil Cedex, France.
Med Sci (Paris). 2006 Feb;22(2):188-91. doi: 10.1051/medsci/2006222188.
Toxic epidermal necrolysis and Stevens-Johnson syndrome are acute and severe adverse reaction to drugs, characterized by the widespread destruction of the epithelium of the skin and mucous membranes. This destruction by massive apoptosis leads to a clinical pattern of epidermal necrolysis resembling second degree burns, with sheets of necrotic epidermis detached from the underlying dermis. The mechanisms of acute and extensive destruction of the skin are not yet fully understood. At the onset of the reaction blisters develop from the fluid that accumulates between the dead epidermis and the dermis. High concentrations of mononuclear cells are present in this blister fluid, principally CD8 T-lymphocytes that may exhibit a drug specific MHC class I restricted cytotoxicity against autologous cells. The intervention of soluble mediators such as TNFalpha, perforin/granzyme, or Fas-Ligand may be necessary for amplifying the apoptosis of keratinocytes. A strong association between epidermal necrolysis to certain drugs and rare HLA-B genotypes suggests that direct interaction between these drugs and HLA-B molecules may initiate a reaction resembling the acute rejection of allogeneic epidermis.
中毒性表皮坏死松解症和史蒂文斯 - 约翰逊综合征是药物引起的急性严重不良反应,其特征是皮肤和黏膜上皮广泛破坏。这种由大量细胞凋亡导致的破坏会引发一种类似二度烧伤的表皮坏死松解临床症状,坏死的表皮大片从下层真皮脱落。皮肤急性广泛破坏的机制尚未完全明确。在反应初期,水泡由积聚在死亡表皮和真皮之间的液体形成。水泡液中存在高浓度的单核细胞,主要是CD8 T淋巴细胞,它们可能对自体细胞表现出药物特异性的MHC I类限制性细胞毒性。可溶性介质如肿瘤坏死因子α、穿孔素/颗粒酶或Fas配体的介入可能是放大角质形成细胞凋亡所必需的。表皮坏死松解与某些药物以及罕见的HLA - B基因型之间存在强烈关联,这表明这些药物与HLA - B分子之间的直接相互作用可能引发一种类似于同种异体表皮急性排斥的反应。