Khan Ambereen, Farah Camile S, Savage Neil W, Walsh Laurence J, Harbrow Doug J, Sugerman Philip B
Oral Biology and Pathology, The University of Queensland, St Lucia, Brisbane, Queensland, Australia.
J Oral Pathol Med. 2003 Feb;32(2):77-83. doi: 10.1034/j.1600-0714.2003.00077.x.
Cell-mediated immune responses in oral lichen planus (OLP) may be regulated by cytokines and their receptors.
In situ cytokine expression and in vitro cytokine secretion in OLP were determined by immunohistochemistry and ELISA.
The majority of subepithelial and intraepithelial mononuclear cells in OLP were CD8+. In some cases, intraepithelial CD8+ cells were adjacent to degenerating keratinocytes. CD4+ cells were observed mainly in the deep lamina propria with occasional CD4+ cells close to basal keratinocytes. Mononuclear cells expressed IFN-gamma in the superficial lamina propria and TNF-alpha adjacent to basal keratinocytes. Basal keratinocytes expressed TNF-alpha as a continuous band. TNF R1 was expressed by mononuclear cells and basal and suprabasal keratinocytes. There was variable expression of TGF-beta1 in the subepithelial infiltrate while all intraepithelial mononuclear cells were TGF-beta1-. Keratinocytes in OLP stained weakly for TGF-beta1. Unstimulated OLP lesional T cells secreted IFN-gamma in vitro. TNF-alpha stimulation down-regulated IFN-gamma secretion and up-regulated TNF-alpha secretion. IL-4, IL-10 and TGF-beta1 secretion were not detected.
These data suggest the development of a T helper 1 immune response that may promote CD8+ cytotoxic T-cell activity in OLP.
口腔扁平苔藓(OLP)中的细胞介导免疫反应可能受细胞因子及其受体的调节。
通过免疫组织化学和酶联免疫吸附测定(ELISA)法测定OLP中的原位细胞因子表达和体外细胞因子分泌。
OLP中大多数上皮下和上皮内单核细胞为CD8 + 。在某些情况下,上皮内CD8 + 细胞与退变的角质形成细胞相邻。CD4 + 细胞主要见于固有层深部,偶尔有CD4 + 细胞靠近基底角质形成细胞。单核细胞在固有层浅层表达γ干扰素(IFN-γ),在基底角质形成细胞附近表达肿瘤坏死因子-α(TNF-α)。基底角质形成细胞呈连续带状表达TNF-α。单核细胞以及基底和基底上层角质形成细胞表达肿瘤坏死因子受体1(TNF R1)。上皮下浸润中转化生长因子-β1(TGF-β1)表达各异,而上皮内所有单核细胞均不表达TGF-β1。OLP中的角质形成细胞TGF-β1染色较弱。未受刺激的OLP损害性T细胞在体外分泌IFN-γ。TNF-α刺激下调IFN-γ分泌并上调TNF-α分泌。未检测到白细胞介素-4(IL-4)、白细胞介素-10(IL-10)和TGF-β1分泌。
这些数据提示可能在OLP中发生了辅助性T细胞1型免疫反应,该反应可能促进CD8 + 细胞毒性T细胞活性。