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Immunohistochemical analysis of FoxP3 + cells in periapical granulomas and radicular cysts

机译:根尖肉芽肿和根尖囊肿中FoxP3 +细胞的免疫组织化学分析

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Objectives: To compare the number of FoxP3 + cells between periapical granulomas (PGs) and radicular cysts (RCs), and to correlate this number with the intensity of the inflammatory infiltrate in these lesions and with epithelial thickness of RCs. Study design: Thirty PGs and 30 RCs were submitted to immunohistochemical analysis using an anti-FoxP3 polyclonal antibody. FoxP3 + cells were counted under a light microscope (×400 magnification) in five fields and the mean value was calculated for each specimen. Statistical tests were used to evaluate differences in the number of FoxP3 + cells according to type of lesion (PG vs. RC), intensity of the inflammatory infiltrate (grade I/II vs. grade III), and epithelial thickness of RCs (atrophic vs. hyperplastic). Results: FoxP3 + cells were detected in most PGs (93.3%) and RCs (93.3%). The median number of FoxP3 + cells was 2.40 in PGs and 1.00 in RCs, with this difference being statistically significant (P = 0.005). No significant differences in the number of FoxP3 + cells were observed in terms of the intensity of the inflammatory infiltrate (P = 0.465) or epithelial thickness of RCs (P = 0.737). Conclusions: The present results suggest a greater participation of regulatory T cells in the modulation of the inflammatory response in PGs. In addition, the presence of a less effective regulatory environment in RCs, together with the high levels of inflammatory mediators as reported in the literature, may contribute to the greater growth potential of these lesions.
机译:目的:比较根尖肉芽肿(PGs)和根尖囊肿(RCs)之间FoxP3 +细胞的数量,并将该数量与这些病灶中炎性浸润的强度以及RCs的上皮厚度相关联。研究设计:使用抗FoxP3多克隆抗体对30种PG和30个RC进行了免疫组织化学分析。在光学显微镜下(×400放大倍数)在五个视野中计数FoxP3 +细胞,并计算每个样品的平均值。统计测试用于根据病变类型(PG与RC),炎性浸润强度(I / II级与III级)和RCs的上皮厚度(萎缩性vs. (增生)。结果:在大多数PG(93.3%)和RC(93.3%)中检测到FoxP3 +细胞。 PGs中FoxP3 +细胞的中位数为2.40,RCs中为1.00,这一差异具有统计学意义(P = 0.005)。就炎症浸润的强度(P = 0.465)或RCs的上皮厚度(P = 0.737)而言,FoxP3 +细胞的数量没有观察到显着差异。结论:目前的结果表明调节性T细胞更多地参与了PGs炎症反应的调节。另外,如文献中所报道的那样,RC中较差的调节环境的存在以及高水平的炎性介质可能有助于这些病变的更大的生长潜力。

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