Mozzanica N, Cattaneo A, Legori A, Pigatto P, Finzi A F
Second Department of Dermatology, University of Milan, Italy.
J Am Acad Dermatol. 1991 Apr;24(4):550-4. doi: 10.1016/0190-9622(91)70080-l.
We have investigated immunohistologically the cutaneous immune infiltrate in the lesions of five patients with severe, extensive lichen planus of recent onset before and after 15 days of oral, low-dose cyclosporine therapy (3 mg/kg/day). Before therapy, we observed an abnormal bandlike cellular infiltrate localized in the papillary dermis, composed mostly of CD3+ cells, with a prevalence of CD4+ cells. Infiltrating lymphocytes showed markers of activation (HLA-DR antigens and interleukin 2 receptor), and there were many Langerhans (CD1+) cells in the dermal infiltrate. After 15 days of cyclosporine therapy, we observed a dramatic decrease in the total number of T cells and a corresponding decrease in interleukin 2 receptor-positive activated CD25+ cells and in antigen-presenting cells (CD1+ and CD14b+). These changes were concurrent with clinical improvement. Our results are compatible with the hypothesis that the inhibition of CD4 T cells by cyclosporine might explain the drug's therapeutic action and that the interaction between antigen-presenting cells and CD4 T cells is important in the pathogenesis of lichen planus.
我们采用免疫组织学方法,对5例近期起病的重度广泛性扁平苔藓患者在口服低剂量环孢素治疗(3mg/kg/天)15天前后皮损处的皮肤免疫浸润情况进行了研究。治疗前,我们观察到乳头真皮层有异常的带状细胞浸润,主要由CD3+细胞组成,其中CD4+细胞占优势。浸润的淋巴细胞显示出活化标记(HLA-DR抗原和白细胞介素2受体),并且真皮浸润中有许多朗格汉斯(CD1+)细胞。环孢素治疗15天后,我们观察到T细胞总数显著减少,白细胞介素2受体阳性的活化CD25+细胞以及抗原呈递细胞(CD1+和CD14b+)相应减少。这些变化与临床改善同时出现。我们的结果符合这样的假设,即环孢素对CD4 T细胞的抑制作用可能解释了该药物的治疗作用,并且抗原呈递细胞与CD4 T细胞之间的相互作用在扁平苔藓的发病机制中很重要。