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Monocyte-derived RANTES is intrinsically elevated in periodontal disease while MCP-1 levels are related to inflammation and are inversely correlated with IL-12 levels

机译:单核细胞衍生的RANTES在牙周疾病中固有升高而MCP-1水平与炎症相关与IL-12水平呈负相关

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摘要

Bacteria colonizing tooth surfaces are essential in the induction of an inflammatory response in the periodontal tissues, but do not cause periodontitis in everyone, implicating differences in the host immune response. These possible differences were studied using lipopolysaccharide (LPS)-stimulated whole blood cell cultures (WBCC), which revealed a down regulation of monocyte derived interleukin-12 (IL-12p70) in untreated periodontitis patients and an up regulation after therapy. IL-12p70 is a crucial factor in the differentiation of Th1 cell responses. Since CC chemokines are able to influence the T cell differentiation via cytokine secretion in antigen-presenting cells, the production of CC chemokines in periodontitis was evaluated. Therefore WBCC were stimulated with LPS from Escherichia coli for 18 h and the levels of IL-12p70 and CC chemokines were measured in the supernatants by ELISA. Untreated periodontitis patients released 2 fold more RANTES (regulated on activation normal T cell expressed and secreted) (P = 0·01) and lower levels of IL-12p70 in comparison to controls (P < 0·05). A trend towards higher levels of macrophage chemoattractant protein-1 (MCP-1) (P = 0·07) was also seen in untreated periodontitis patients; while similar levels of monocyte derived chemokine (MDC) and macrophage inflammatory proteins-1α and -1β (MIP-1α and -1β) were found. After periodontal therapy no changes were seen with regard to MDC, MIP-1α, MIP-1β and RANTES, whereas the MCP-1 levels decreased (P < 0·05) and the IL-12p70 levels strongly increased (P < 0·01). The data showed a consistent inverse correlation between the levels of MCP-1 and IL-12p70, and their proportional changes after therapy correlated with the clinical inflammatory response after therapy. This indicates that the disease state regulates the release of IL-12p70 and MCP-1 in E. coli LPS-stimulated WBCC. In contrast, the persistent augmented levels of RANTES after therapy are suggestive for an intrinsic behaviour.
机译:细菌在牙齿表面的定植对诱导牙周组织的炎症反应至关重要,但并不会在每个人中引起牙周炎,这暗示着宿主免疫反应的差异。使用脂多糖(LPS)刺激的全血细胞培养物(WBCC)研究了这些可能的差异,该结果显示未治疗的牙周炎患者中单核细胞衍生的白介素12(IL-12p70)的下调和治疗后的上调。 IL-12p70是Th1细胞反应分化的关键因素。由于CC趋化因子能够通过抗原呈递细胞中的细胞因子分泌影响T细胞分化,因此评估了牙周炎中CC趋化因子的产生。因此,用来自大肠杆菌的LPS刺激WBCC 18小时,并通过ELISA测量上清液中IL-12p70和CC趋化因子的水平。与对照组相比,未经治疗的牙周炎患者释放的RANTES(受激活的正常T细胞表达和分泌的调节)多2倍(P = 0·01),IL-12p70水平较低(P <0·05)。在未经治疗的牙周炎患者中也发现了巨噬细胞趋化蛋白-1(MCP-1)水平升高的趋势(P = 0·07)。而单核细胞趋化因子(MDC)和巨噬细胞炎症蛋白-1α和-1β(MIP-1α和-1β)的水平相似。牙周治疗后,MDC,MIP-1α,MIP-1β和RANTES均未见变化,而MCP-1水平下降(P <0·05),IL-12p70水平强烈上升(P <0·01) )。数据显示,MCP-1和IL-12p70的水平之间呈一致的负相关,其在治疗后的比例变化与治疗后的临床炎症反应相关。这表明疾病状态调节了大肠杆菌LPS刺激的WBCC中IL-12p70和MCP-1的释放。相比之下,治疗后RANTES水平的持续升高提示其固有行为。

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