Matthews J B, Pitigala-Arachchi A, Crane I J, Scully C, Prime S S
Department of Oral Pathology, Dental School, University of Birmingham, St Chads Queensway, UK.
Virchows Arch A Pathol Anat Histopathol. 1988;413(6):521-8. doi: 10.1007/BF00750393.
The development of oral epithelial expression of Ia antigens and its relationship to the presence of IL-2r+ (CD25+) cells was investigated in rats treated with the water soluble carcinogen 4-nitroquinoline-N-oxide (4NQO). Acetone fixed frozen sections of the palate and tongue were stained using an indirect immunoperoxidase technique and monoclonal antibodies to rat Ia (I-A & I-E) and IL-2 receptor. After 4 weeks 4NQO treatment all rats expressed oral epithelial Ia but thereafter (2-9 months) expression was present in only 20-40% of animals. Epithelial expression of Ia by histologically normal, dysplastic and neoplastic epithelium was always associated with the presence of an underlying inflammatory cell infiltrate containing CD25+ cells. Overall there were significantly more CD25+ cells in tissue specimens containing Ia+ epithelium compared with Ia- epithelium. Furthermore, during the first 4 weeks of carcinogen treatment, a significant positive correlation was found between the CD25+ cell density and occurrence of focal epithelial Ia expression. These results, together with analysis of the T cell, NK cell, macrophage and B cell content of the infiltrates induced by 4NQO, suggest that the CD25+ cells represent activated T cells. Thus, our results in this experimental model are consistent with the idea that epithelial expression of Ia is the result of production of IFN-gamma by locally activated T cells.
在用水溶性致癌物4-硝基喹啉-N-氧化物(4NQO)处理的大鼠中,研究了Ia抗原的口腔上皮表达的发展及其与IL-2r +(CD25 +)细胞存在的关系。使用间接免疫过氧化物酶技术以及针对大鼠Ia(I-A和I-E)和IL-2受体的单克隆抗体,对腭和舌的丙酮固定冰冻切片进行染色。4NQO处理4周后,所有大鼠均表达口腔上皮Ia,但此后(2-9个月)仅20-40%的动物存在表达。组织学上正常、发育异常和肿瘤性上皮的Ia上皮表达总是与含有CD25 +细胞的潜在炎性细胞浸润的存在相关。总体而言,与Ia -上皮相比,含有Ia +上皮的组织标本中的CD25 +细胞明显更多。此外,在致癌物处理的前4周内,发现CD25 +细胞密度与局灶性上皮Ia表达的发生之间存在显著正相关。这些结果,连同对4NQO诱导的浸润中的T细胞、NK细胞、巨噬细胞和B细胞含量的分析,表明CD25 +细胞代表活化的T细胞。因此,我们在这个实验模型中的结果与以下观点一致,即Ia的上皮表达是局部活化的T细胞产生IFN-γ的结果。