Boehncke W H, Zollner T M, Dressel D, Kaufmann R
Dept. of Dermatology, Ulm University, Germany.
J Cutan Pathol. 1997 Jan;24(1):1-7. doi: 10.1111/j.1600-0560.1997.tb00778.x.
Psoriasis is a chronic skin disease affecting about 2% of the Caucasian population, characterized by co-existing inflammation and epidermal hyperproliferation. A T-lymphocyte-mediated autoimmune reaction induced by bacterial superantigens might be central in its pathogenesis. To model psoriasiform inflammation, we transplanted clinically uninvolved skin from psoriatic patients onto SCID mice. Repetitive intradermal injections with a bacterial superantigen and simultaneous intraperitoneal injections with the patients superantigen-stimulated peripheral mononuclear blood cells resulted in an inflammatory reaction exhibiting some of the hallmarks of psoriasis, e.g. epidermal hyperproliferation, papillomatosis, focal neo-expression of ICAMI, and an exocytotic T-lymphocytic infiltrate characterized by the expression of the cutaneous lymphocyte-associated antigen. These observations document the potential of superantigens to trigger psoriasiform dermatitis and provide a model to study lymphocyte homing.
银屑病是一种影响约2%白种人的慢性皮肤病,其特征为炎症和表皮过度增殖并存。由细菌超抗原诱导的T淋巴细胞介导的自身免疫反应可能在其发病机制中起核心作用。为了建立银屑病样炎症模型,我们将银屑病患者临床上未受累的皮肤移植到SCID小鼠身上。重复皮内注射细菌超抗原并同时腹腔注射患者超抗原刺激的外周单个核血细胞,导致出现了一些银屑病特征性的炎症反应,如表皮过度增殖、乳头瘤病、ICAM1的局灶性新表达,以及以皮肤淋巴细胞相关抗原表达为特征的外吐性T淋巴细胞浸润。这些观察结果证明了超抗原有引发银屑病样皮炎的可能性,并提供了一个研究淋巴细胞归巢的模型。