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Salivary concentrations of macrophage activation-related chemokines are influenced by non-surgical periodontal treatment: a 12-week follow-up study

机译:巨噬细胞活化相关趋化因子的唾液浓度受非手术牙周治疗的影响:为期12周的后续研究

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ABSTRACT Background: During periodontal inflammation, bacteria induces chemokine expression and migration of various inflammatory cells. The aim of the study was to learn if periodontal treatment alters salivary concentrations of macrophage activation-related chemokines and if such alterations correlate with abundance of periodontitis-associated bacteria. Methods: Twenty-five patients with periodontitis completed the study (NCT02913248 at clinicaltrials.gov). Periodontal parameters and stimulated saliva samples were obtained at baseline and 2, 6 and 12 weeks after non-surgical periodontal treatment. Salivary concentrations of monocyte chemoattractant proteins (MCP-1-4), macrophage-derived chemokine (MDC), macrophage migration inhibitory factor (MIF), monokine induced by interferon-gamma (MIG), macrophage inflammatory protein (MIP-1α) and interferon-inducible protein (IP-10) were quantified using the Luminex? xMAP? technique and abundance of bacteria was quantified using next-generation sequencing. Results: The treatment improved all periodontal parameters and caused an increase in the concentrations of MCP-2, MDC and MIP-1α at week 12 compared to baseline, week 2 and week 6, respectively. Salivary concentrations of MCP-1-2, MDC, MIG, MIP-1α and IP-10 correlated with the abundance of specific periodontitis-associated bacteria. Conclusions: Periodontal treatment impacts salivary concentrations of MCP-2, MDC and MIP-1α, which correlate with the abundance of specific periodontitis-associated bacteria. This indicates that these chemokines reflect periodontal status and possess potential in illustrating a response to treatment.
机译:摘要背景:牙周炎症期间,细菌诱导趋化因子表达和各种炎症细胞的迁移。该研究的目的是学习,如果牙周治疗改变了巨噬细胞活化相关的趋化因子的唾液浓度,并且如果这种改变与丰富的牙周炎相关细菌相关。方法:25例牙周炎患者完成了该研究(Clinicaltrials.gov的NCT02913248)。在非手术牙周治疗后的基线和2,6和12周内获得牙周参数和刺激的唾液样品。单核细胞趋化蛋白(MCP-1-4),巨噬细胞衍生趋化因子(MDC),巨噬细胞迁移抑制因子(MIF),由干扰素 - γ(MIG),巨噬细胞炎症蛋白(MIP-1α)和干扰素诱导的单孔使用Luminex量化剩余的蛋白质(IP-10)? XMAP?使用下一代测序定量了细菌的技术和丰度。结果:治疗改善了所有牙周参数,并分别与基线,第2周和第6周相比,在第12周的MCP-2,MDC和MIP-1α浓度增加。 MCP-1-2,MDC,MIG,MIP-1α和IP-10的唾液浓度与特定牙周炎相关细菌的丰度相关。结论:牙周治疗会影响MCP-2,MDC和MIP-1α的唾液浓度,其与特定牙周炎相关细菌的丰度相关。这表明这些趋化因子反映了牙周地位,并且具有施加对治疗的反应的潜力。

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