Bratel J, Dahlgren U, Simark Mattsson C, Jontell M
Department of Endodontology/Oral Diagnosis, Faculty of Odontology, Göteborg University, Sweden.
J Oral Pathol Med. 1998 Oct;27(9):415-9. doi: 10.1111/j.1600-0714.1998.tb01978.x.
Oral lichen planus (OLP) and lichenoid contact lesions (CL) are recognized as different pathological conditions of the oral mucosa. Cutaneous delayed-type hypersensitivity to mercury displayed by patients with CL but not by OLP patients supports the concept of different etiological mechanisms behind the two lesions. It is not possible to reveal this difference by histopathological assessments, and differences in clinical appearances are at present the only way to discriminate between the two conditions. It has recently been observed that T cells in OLP lesions express T-cell receptors (TCR) belonging to the Vbeta3 family in a higher frequency than expected from a random distribution, suggesting an involvement of superantigens as an etiologic factor behind this condition. In an effort to discriminate more clearly between OLP and CL, and to provide clues to the etiological mechanisms behind the two lesions, the TCR V-family distributions in the inflammatory infiltrates of OLP and CL were compared. Biopsies were taken from 10 patients with manifest OLP and 10 patients with CL. Frozen sections were incubated with antibodies against TCR Vbeta3, Valpha2 and Vbeta5a utilizing a standard immunoperoxidase technique. The frequency of Vbeta3.1 (clone 8F10) was calculated as 7%, and for Valpha2 less than 3%, and the results did not reveal any differences between OLP and CL regarding the frequencies of T-cell V-families. Thus, it was not possible to discriminate between OLP and CL by immunohistochemistry staining for different V families.
口腔扁平苔藓(OLP)和苔藓样接触性病变(CL)被认为是口腔黏膜的不同病理状况。CL患者表现出对汞的皮肤迟发型超敏反应,而OLP患者则无此反应,这支持了两种病变背后存在不同病因机制的观点。通过组织病理学评估无法揭示这种差异,目前临床外观的差异是区分这两种情况的唯一方法。最近观察到,OLP病变中的T细胞表达属于Vbeta3家族的T细胞受体(TCR)的频率高于随机分布预期的频率,这表明超抗原作为这种情况的病因因素参与其中。为了更清楚地区分OLP和CL,并为两种病变背后的病因机制提供线索,比较了OLP和CL炎症浸润中TCR V家族的分布。从10例显性OLP患者和10例CL患者中获取活检组织。利用标准免疫过氧化物酶技术,将冰冻切片与抗TCR Vbeta3、Valpha2和Vbeta5a的抗体孵育。计算出Vbeta3.1(克隆8F10)的频率为7%,Valpha2的频率小于3%,结果未显示OLP和CL在T细胞V家族频率方面存在任何差异。因此,通过对不同V家族进行免疫组织化学染色无法区分OLP和CL。