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Toll 样受体 2 和 4 在系统性红斑狼疮和慢性牙周炎患者唾液中的表达。

Expression of Toll-like receptors 2 and 4 in the saliva of patients with systemic lupus erythematosus and chronic periodontitis.

机构信息

Dentistry Graduate Program, Federal University of Maranhão, São Luís, Maranhão, Brazil.

School of Medicine, Federal University of Maranhão, Pinheiro, Maranhão, Brazil.

出版信息

Clin Rheumatol. 2021 Jul;40(7):2727-2734. doi: 10.1007/s10067-020-05560-z. Epub 2021 Feb 11.

DOI:10.1007/s10067-020-05560-z
PMID:33570702
Abstract

OBJECTIVE

The aim of this study was to investigate the expression of salivary Toll-like receptors (TRL) 2 and 4 in patients with systemic lupus erythematosus (SLE) and chronic periodontitis (CP).

METHODS

A case-control study was conducted with 77 participants (42 SLE and 35 non-SLE) stratified according to CP diagnosis criteria. Periodontal parameters consisted of clinical attachment level (CAL), probing depth (PD), the visible plaque index (VPI), and the gingival bleeding index (GBI). Salivary TRL 2 and 4 expressions were determined by quantitative real-time polymerase chain reaction (RT-PCR). Statistical analysis included Mann-Whitney U test, Kruskal-Wallis test, Spearman's correlation rank, and multiple linear regression.

RESULTS

Patients with isolated SLE or CP had higher TLR 2 and TLR 4 expression in their saliva samples (P < 0.05). The group with both SLE and CP had lower TLR 2 and 4 expressions (P < 0.05). TLR 2 and TLR 4 showed significant negative correlations with PD, CAL, and GBI in SLE patients, and a significant positive correlation with periodontal parameters in non-SLE patients. CP was independently associated with reduction of TLR2 and TLR4 expression, even after adjusting for clinical data and current drug use.

CONCLUSION

Reduced TRL 2 and 4 expression in saliva was associated with the presence of CP in SLE patients. Key Points • Patients affected by isolated CP or SLE had higher TLR2 and TLR4 expression. • TLR under-expression may be associated with a worse periodontal status in SLE. • Abnormalities in TLRs expression may increase the susceptibility to periodontitis.

摘要

目的

本研究旨在探讨系统性红斑狼疮(SLE)和慢性牙周炎(CP)患者唾液 Toll 样受体(TLR)2 和 4 的表达。

方法

采用病例对照研究,根据 CP 诊断标准将 77 名参与者(42 名 SLE 和 35 名非 SLE)分层。牙周参数包括临床附着水平(CAL)、探诊深度(PD)、可见菌斑指数(VPI)和牙龈出血指数(GBI)。通过实时定量聚合酶链反应(RT-PCR)测定唾液 TLR 2 和 4 的表达。统计分析包括 Mann-Whitney U 检验、Kruskal-Wallis 检验、Spearman 秩相关和多元线性回归。

结果

孤立性 SLE 或 CP 患者的唾液 TLR 2 和 TLR 4 表达较高(P<0.05)。同时患有 SLE 和 CP 的患者 TLR 2 和 TLR 4 表达较低(P<0.05)。TLR 2 和 TLR 4 与 SLE 患者的 PD、CAL 和 GBI 呈显著负相关,与非 SLE 患者的牙周参数呈显著正相关。CP 与 TLR2 和 TLR4 表达降低独立相关,即使在调整临床数据和当前药物使用后也是如此。

结论

SLE 患者唾液中 TLR 2 和 TLR 4 表达减少与 CP 有关。

关键点

  1. 单纯 CP 或 SLE 患者的 TLR2 和 TLR4 表达较高。

  2. TLR 低表达可能与 SLE 患者牙周状况较差有关。

  3. TLR 表达异常可能增加牙周炎的易感性。

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本文引用的文献

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Host-Microbial Interactions in Systemic Lupus Erythematosus and Periodontitis.系统性红斑狼疮和牙周炎中的宿主-微生物相互作用。
Front Immunol. 2019 Nov 12;10:2602. doi: 10.3389/fimmu.2019.02602. eCollection 2019.
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Clinical, immunological and microbial gingival profile of juvenile systemic lupus erythematosus patients.青少年系统性红斑狼疮患者的临床、免疫学和微生物学牙龈特征
Lupus. 2019 Feb;28(2):189-198. doi: 10.1177/0961203318819134. Epub 2018 Dec 18.
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The Oral Microbiota Is Modified by Systemic Diseases.口腔微生物群受全身性疾病影响而改变。
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Anticardiolipin (aCL) in sera from periodontitis subjects activate Toll-like receptor 4 (TLR4).牙周炎患者血清中的抗心磷脂抗体(aCL)可激活 Toll 样受体 4 (TLR4)。
PLoS One. 2018 Sep 7;13(9):e0203494. doi: 10.1371/journal.pone.0203494. eCollection 2018.
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Immunological signatures in saliva of systemic lupus erythematosus patients: influence of periodontal condition.系统性红斑狼疮患者唾液中的免疫特征:牙周状况的影响。
Clin Exp Rheumatol. 2019 Mar-Apr;37(2):208-214. Epub 2018 Jul 19.
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Antibodies to periodontogenic bacteria are associated with higher disease activity in lupus patients.针对牙周病原菌的抗体与狼疮患者较高的疾病活动度相关。
Clin Exp Rheumatol. 2019 Jan-Feb;37(1):106-111. Epub 2018 Jun 25.
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Association between Systemic Lupus Erythematosus and Periodontitis: A Systematic Review and Meta-analysis.系统性红斑狼疮与牙周炎之间的关联:一项系统评价与荟萃分析
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Periodontal disease in Chinese patients with systemic lupus erythematosus.中国系统性红斑狼疮患者的牙周疾病
Rheumatol Int. 2017 Aug;37(8):1373-1379. doi: 10.1007/s00296-017-3759-5. Epub 2017 Jun 19.
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