摘要
应用抗HLADR、CD3、CD4、CD8、CD20的单克隆抗体和streptravidinperoxidasestaining(SP)技术对10名正常人皮肤,16例SLE皮损和19例DLE皮损进行了免疫组化研究。观察到正常人皮肤角质形成细胞未见HLADR抗原表达,而SLE(6/16),DLE(8/19)皮损处角质形成细胞可以表达HLADR抗原。在SLE、DLE真皮内浸润细胞主要为T淋巴细胞(CD3+浸润细胞),且以TH细胞(CD4+浸润细胞)占优势。另外,还发现在两种LE表皮角质形成细胞表达HLADR抗原处,真皮内可见CD3+浸润细胞和激活的T淋巴细胞(HLADR+浸润细胞)。讨论了LE皮损角质形成细胞HLADR抗原表达及其与病损内浸润细胞免疫表型的关系。LE皮损处HLADR+角质形成细胞可能具有抗原递呈作用,而角质形成细胞异常表达HLADR抗原则可能与真皮内浸润单个核细胞或淋巴细胞释放的IFNα,TNFγ等有关。
To investigate the expression of HLA DR antigens on lesional keratinocytes in LE, and its relationship with the dermal infiltrating cells in LE lesions, HLA DR, CD3,CD4,CD8,CD20 monoclonal antibodies and streptravidin peroxidase staining technique were employed. The results showed that the expression of HLA DR antigens on lesional keratinocytes (KCs) could be observed in SLE (6/16) and DLE (8/19), but not in normal skin . Most of the keratinocytes expressing HLA DR antigens were basal cells. In addition, 51%~54%of mononuclear cells (MNC) infiltrating in superficial dermis were found to be T lymphocytes (CD3+cells), and CD4+lymphocytes which were more than CD8+lymphocytes among the CD3+T lymphocytes. 29%~30%of dermal infiltrating cells were HLA DR+lymphocytes (activated cells). The numbers of CD3+, CD4+, CD8+and HLA DR+cells were significantly higher in LE than in normal skin(P< 0 05). There were no significant differences in CD20+cells among the three groups. The results indicate that keratinocytes may have antigen presenting function and the T lymphocytes might play a significant role in mediating the inflammatory reaction in LE lesions.
出处
《临床皮肤科杂志》
CSCD
北大核心
1999年第3期150-153,共4页
Journal of Clinical Dermatology