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阿司匹林通过抑制CD4 T淋巴细胞来阻止正畸复发。

Aspirin Blocks Orthodontic Relapse via Inhibition of CD4 T Lymphocytes.

作者信息

Liu Y, Zhang T, Zhang C, Jin S S, Yang R L, Wang X D, Jiang N, Gan Y H, Kou X X, Zhou Y H

机构信息

1 Department of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.

2 Center for Craniofacial Stem Cell Research and Regeneration, Peking University School and Hospital of Stomatology, Beijing, China.

出版信息

J Dent Res. 2017 May;96(5):586-594. doi: 10.1177/0022034516685527. Epub 2017 Jan 6.

Abstract

Immunologic response plays an important role in orthodontic tooth movement (OTM) and relapse. Nonsteroidal anti-inflammatory drugs, such as aspirin, affect immune cells and clinical orthodontic treatment. However, the mechanisms by which nonsteroidal anti-inflammatory drugs regulate immune cells to affect orthodontic relapse are unclear. In this study, male Sprague-Dawley rats were grouped as relapse and relapse + aspirin for 10 d after 14 d of OTM. Silicone impressions of the rats' maxillary dentitions were obtained to record the distance of OTM at the indicated time point. CD4 T lymphocytes in spleen were examined by flow cytometry. Serum levels of type 1 T-helper (Th1) cell-associated cytokines tumor necrosis factor α (TNF-α), and interferon γ (IFN-γ) were determined through enzyme-linked immunosorbent assay. The effects of aspirin on CD4 T and Th1 cells were also analyzed in vitro. Aspirin treatment significantly reduced the relapse rate. More interestingly, injection of CD25 neutralizing antibody basiliximab or TNF-α inhibitor etanercept can significantly reduce the relapse rate as well. Correspondingly, aspirin treatment significantly accelerated the decrease of orthodontic force-induced secretion of TNF-α and IFN-γ in serum and the expression of TNF-α and IFN-γ in periodontal ligament during relapse. Furthermore, aspirin treatment in vitro significantly repressed the differentiation of CD4 T and Th1 cells. Overall, results indicated that aspirin treatment can block orthodontic relapse by regulating Th1 cells.

摘要

免疫反应在正畸牙移动(OTM)和复发中起重要作用。非甾体抗炎药,如阿司匹林,会影响免疫细胞和临床正畸治疗。然而,非甾体抗炎药调节免疫细胞以影响正畸复发的机制尚不清楚。在本研究中,雄性Sprague-Dawley大鼠在OTM 14天后分为复发组和复发+阿司匹林组,持续10天。获取大鼠上颌牙列的硅橡胶印模,以记录指定时间点的OTM距离。通过流式细胞术检测脾脏中的CD4 T淋巴细胞。通过酶联免疫吸附测定法测定1型辅助性T(Th1)细胞相关细胞因子肿瘤坏死因子α(TNF-α)和干扰素γ(IFN-γ)的血清水平。还在体外分析了阿司匹林对CD4 T细胞和Th1细胞的影响。阿司匹林治疗显著降低了复发率。更有趣的是,注射CD25中和抗体巴利昔单抗或TNF-α抑制剂依那西普也能显著降低复发率。相应地,阿司匹林治疗显著加速了复发期间正畸力诱导的血清中TNF-α和IFN-γ分泌的减少以及牙周膜中TNF-α和IFN-γ的表达。此外,体外阿司匹林治疗显著抑制了CD4 T细胞和Th1细胞的分化。总体而言,结果表明阿司匹林治疗可通过调节Th1细胞来阻止正畸复发。

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