Department of Physiology, University of Porto, Porto, Portugal.
Pathol Oncol Res. 2011 Sep;17(3):677-83. doi: 10.1007/s12253-011-9368-9. Epub 2011 Apr 1.
TLRs are important innate immunity receptors. Even though TLR2, 4 and 5 appear to be important for Helicobacter pylori (HP) recognition, their role in the evolution of gastritis to more advanced lesions is still unknown. To compare the expression of TLR2, 4 and 5 in normal gastric mucosa, HP+ gastritis, intestinal metaplasia, dysplasia and adenocarcinoma. Immunohistochemistry for TLR2, 4 and 5 was performed with anti-TLR2-TLR4-TLR5 antibodies in 117 histological samples of normal gastric mucosa (n = 22), HP+ gastritis (n = 20), intestinal metaplasia (n = 33), dysplasia (mucosectomy specimens, n = 20) and intestinal type adenocarcinoma (surgery specimens,n = 22); quantification of expression was performed independently by two pathologists taking into account the percentage of positive epithelial cells and the degree of expression (zero to three score). A statistically significant trend for progressive increase of TLRs expression from normal mucosa to gastric dysplasia was found (mean expression: normal mucosa 0.1; gastritis 1.0; metaplasia 2.2; dysplasia 2.8, p < 0.01). All dysplasia samples presented more than 90% positive epithelial cells with strong expression (2.8;95%CI2.7-3). There was less TLRs expression in carcinomas (TLR2:1.0; TLR4:2.0 and TLR5:1.2, p < 0.05) when compared with dysplasia, with TLR4 being more expressed than TLR2 and 5 in these lesions (p = 0.03). A score of all markers' expression of eight leads to a low (4%) false positive rate in patients with precancerous conditions. Progression of gastric lesions associated with gastric carcinogenesis is associated with increased TLRs expression. Gastric dysplasia presents a high level of TLRs expression, suggesting that these receptors may play a role in adenocarcinoma development.
TLRs 是重要的先天免疫受体。尽管 TLR2、4 和 5 似乎对幽门螺杆菌 (HP) 的识别很重要,但它们在胃炎向更高级病变发展中的作用仍不清楚。为了比较 TLR2、4 和 5 在正常胃黏膜、HP+胃炎、肠上皮化生、异型增生和腺癌中的表达。采用 TLR2-TLR4-TLR5 抗体对 117 例正常胃黏膜组织标本(n=22)、HP+胃炎(n=20)、肠上皮化生(n=33)、异型增生(黏膜切除术标本,n=20)和肠型腺癌(手术标本,n=22)进行 TLR2、4 和 5 的免疫组织化学检测;两位病理学家分别对表达进行定量,考虑到上皮细胞阳性百分比和表达程度(0-3 分)。从正常黏膜到胃异型增生,TLRs 表达呈逐渐增加的趋势(平均表达:正常黏膜 0.1;胃炎 1.0;化生 2.2;异型增生 2.8,p<0.01)。所有异型增生标本均有超过 90%的上皮细胞呈强阳性表达(2.8;95%CI2.7-3)。与异型增生相比,癌组织中 TLRs 的表达较少(TLR2:1.0;TLR4:2.0 和 TLR5:1.2,p<0.05),而在这些病变中 TLR4 的表达高于 TLR2 和 5(p=0.03)。8 种标志物表达评分均为高(4%)时,癌前病变患者的假阳性率较低。与胃癌发生相关的胃病变进展与 TLRs 表达增加有关。胃异型增生表现出高水平的 TLRs 表达,提示这些受体可能在腺癌发展中起作用。