Postgraduate Program in Dental Sciences, Departments of Dentistry.
Anatomy, Institute of Biomedical Sciences, Federal University of Alfenas, MG, Brazil.
Appl Immunohistochem Mol Morphol. 2022 Apr 1;30(4):291-297. doi: 10.1097/PAI.0000000000001005.
Radicular cysts (RCs) and residual radicular cysts (RRCs) are the sequelae of dental caries and that leads to proliferation of epithelial rests of Malassez in periapical tissues.
The aim was to evaluate the relationship between Langerhans cells, macrophages, matrix metalloproteinases (MMP-9, MMP-13), and tumor necrosis factor-alpha (TNF-α) in the capsule and lining epithelium of cystic lesions.
Twenty RCs and 20 RRCs were submitted to immunohistochemical analysis with anti-CD68, anti-CD1a, anti-MMP-9, anti-MMP-13, and anti-TNF-α antibodies. The Mann-Whitney test and the Spearman correlation test were used for analysis of the data (P<0.05).
The immunoexpression of MMP-13 and CD68 was significantly higher in RCs when compared with RRCs (P=0.011 and 0.012, respectively). The presence of an intense inflammatory infiltrate was significantly correlated with the immunoexpression of CD68 in RCs (P=0.025). Expression of CD68 showed a significant positive correlation with MMP-13 (P=0.015). A moderate correlation was observed between MMP-9 and MMP-13 (P=0.010). TNF-α expression was more common in RCs (P=0.001). CD1a was more frequently expressed in atrophic epithelium (P=0.041) and was significantly correlated with TNF-α (P=0.014).
Langerhans cells induce a greater release of TNF-α which, in turn, is responsible for the stimulation of M1 macrophages. Higher immunoexpression of MMP-13 and MMP-9 is observed in the early stages of RCs compared with RRCs. Therefore, the toxins of microorganisms present in highly inflamed RCs are the main factors triggering a proinflammatory immune response and greater cystic expansion in the early stages of these lesions.
根囊肿(RCs)和残余根囊肿(RRCs)是龋齿的后遗症,导致根尖组织中 Malassez 上皮剩余的增殖。
评估朗格汉斯细胞、巨噬细胞、基质金属蛋白酶(MMP-9、MMP-13)和肿瘤坏死因子-α(TNF-α)在囊性病损的囊壁和衬里上皮中的关系。
对 20 例 RCs 和 20 例 RRCs 进行免疫组织化学分析,使用抗 CD68、抗 CD1a、抗 MMP-9、抗 MMP-13 和抗 TNF-α 抗体。采用曼-惠特尼检验和斯皮尔曼相关检验对数据进行分析(P<0.05)。
与 RRC 相比,RC 中 MMP-13 和 CD68 的免疫表达显著更高(P=0.011 和 0.012)。强烈的炎症浸润与 RC 中 CD68 的免疫表达显著相关(P=0.025)。CD68 的表达与 MMP-13 呈显著正相关(P=0.015)。MMP-9 与 MMP-13 之间观察到中度相关性(P=0.010)。TNF-α在 RC 中更为常见(P=0.001)。CD1a 在萎缩性上皮中表达更为频繁(P=0.041),与 TNF-α显著相关(P=0.014)。
朗格汉斯细胞诱导 TNF-α的大量释放,而 TNF-α又负责刺激 M1 巨噬细胞。与 RRC 相比,RC 的早期 MMP-13 和 MMP-9 的免疫表达更高。因此,高度炎症性 RC 中存在的微生物毒素是触发促炎免疫反应和这些病变早期囊腔更大扩张的主要因素。