Thrane P S, Halstensen T S, Haanaes H R, Brandtzaeg P
Laboratory for Immunohistochemistry and Immunopathology (LIIPAT), Rikshospitalet, Oslo, Norway.
Clin Exp Immunol. 1993 May;92(2):256-62. doi: 10.1111/j.1365-2249.1993.tb03389.x.
Salivary gland specimens from 10 patients with primary Sjögren's syndrome (pSS) were examined by two-colour immunofluorescence with various combinations of monoclonal and polyclonal antibody reagents of the following specificities: human leucocyte antigen (HLA) class I and II (DR, DP and DQ), CD3, CD45 (leucocyte common antigen), various cytokeratins, and factor VIII-related antigen. Tissue specimens from 10 normal glands and 10 glands with obstructive sialadenitis (no known autoimmunity) served as controls. Only some intercalated ducts and scattered acini of the normal major glands expressed HLA class II determinants (< 5% of total epithelial area); the relative proportion of positive elements indicated differential expression (DR > DP > DQ). SS glands contained substantial T cell infiltrates and increased numbers of activated (DR+) T cells; adjacent epithelium showed extensive differential expression of HLA class II determinants (DR > DP > DQ). Glands with obstructive sialadenitis showed similarly increased epithelial expression of HLA-DR but with surprisingly small amounts of concomitant HLA-DP and -DQ expression. Epithelial HLA class II expression probably depends on cytokines as an inductive event, which is not unique for SS but particularly prominent in this disorder. Our results suggest that epithelial expression of HLA-DP or -DQ, rather than -DR, might be a prerequisite for the autoimmune process of SS to develop in genetically susceptible individuals.
采用双色免疫荧光法,使用具有以下特异性的单克隆和多克隆抗体试剂的各种组合,对10例原发性干燥综合征(pSS)患者的唾液腺标本进行检测:人类白细胞抗原(HLA)I类和II类(DR、DP和DQ)、CD3、CD45(白细胞共同抗原)、各种细胞角蛋白以及因子VIII相关抗原。来自10个正常腺体和10个患有阻塞性涎腺炎(无已知自身免疫性疾病)的腺体的组织标本作为对照。正常大唾液腺中只有一些闰管和散在的腺泡表达HLA II类决定簇(占上皮总面积的<5%);阳性成分的相对比例显示出差异表达(DR>DP>DQ)。干燥综合征患者的腺体含有大量T细胞浸润,且活化(DR +)T细胞数量增加;相邻上皮显示HLA II类决定簇广泛差异表达(DR>DP>DQ)。阻塞性涎腺炎患者的腺体显示HLA-DR的上皮表达同样增加,但伴随的HLA-DP和-DQ表达量惊人地少。上皮HLA II类表达可能依赖于细胞因子作为诱导事件,这并非干燥综合征所特有,但在该疾病中尤为突出。我们的结果表明,HLA-DP或-DQ而非-DR的上皮表达可能是干燥综合征自身免疫过程在遗传易感个体中发生发展的一个先决条件。