Thomas D W, Matthews J B, Prime S S
Department of Oral Dental Science, Bristol Dental Hospital & School, University of Bristol, England.
J Oral Pathol Med. 1996 Apr;25(4):145-50. doi: 10.1111/j.1600-0714.1996.tb00211.x.
This study examined the histological changes and local cellular immune response induced within the lingual mucosa in an allogeneic F1 hybrid rat model of graft-versus-host disease (GvHD) with a view to studying oral lymphocyte-epithelial cell reactions. Highest levels of disease, as reflected by both a GvHD index and the extent of the oral mucosal changes, were obtained using primed donor (Lewis rats) splenocytes and irradiated hosts (Lew/Da rats). The lingual mucosae of test animals were characterised by irregular epithelial keratosis, an absence of basal cell liquefaction and a diffuse inflammatory cell infiltrate, histological features consistent with an oral lichenoid tissue reaction. Immunohistochemical studies showed that mucosal involvement was characterised by infiltration of the lamina propria by NK cells (CD8+, CD5-), "activated" cells (CD25+) and T cells (CD5+) with selective migration of the latter, including a CD5+, CD8- subset (helper/inducer T cell), into the epithelium. Epithelial expression of Ia was invariably associated with these inflammatory cell infiltrates and correlated with the GvHD index. These findings suggest the presence of local mucosal T cell activation in the absence of detectable epithelial cell damage, which may be equivalent to the early initiating events in the pathogenesis of oral lichen planus. However, whilst experimental graft-versus-host disease appears to be a useful model for studying lymphocyte-epithelial interactions, the induced oral mucosal changes are more consistent with a lichenoid reaction rather than lichen planus.
本研究在移植物抗宿主病(GvHD)的同种异体F1杂交大鼠模型中,检查了舌黏膜内诱导的组织学变化和局部细胞免疫反应,旨在研究口腔淋巴细胞与上皮细胞的反应。使用经预处理的供体(Lewis大鼠)脾细胞和经照射的宿主(Lew/Da大鼠),获得了由GvHD指数和口腔黏膜变化程度所反映的最高疾病水平。试验动物的舌黏膜特征为上皮角化不规则、无基底细胞液化以及弥漫性炎性细胞浸润,这些组织学特征与口腔苔藓样组织反应一致。免疫组织化学研究表明,黏膜受累的特征是固有层有NK细胞(CD8 +、CD5 -)、“活化”细胞(CD25 +)和T细胞(CD5 +)浸润,后者选择性迁移,包括CD5 +、CD8 -亚群(辅助/诱导性T细胞)迁移至上皮内。Ia在上皮中的表达总是与这些炎性细胞浸润相关,并与GvHD指数相关。这些发现表明,在未检测到上皮细胞损伤的情况下存在局部黏膜T细胞活化,这可能等同于口腔扁平苔藓发病机制中的早期起始事件。然而,虽然实验性移植物抗宿主病似乎是研究淋巴细胞与上皮相互作用的有用模型,但诱导的口腔黏膜变化更符合苔藓样反应而非扁平苔藓。