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研究内体 Toll 样受体在小鼠胶原诱导性关节炎中的作用揭示 TLR7 在疾病维持中的潜在作用。

Investigation of the role of endosomal Toll-like receptors in murine collagen-induced arthritis reveals a potential role for TLR7 in disease maintenance.

机构信息

Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, London, W6 8LH, UK.

出版信息

Arthritis Res Ther. 2012 Jun 12;14(3):R142. doi: 10.1186/ar3875.

Abstract

INTRODUCTION

Endosomal toll-like receptors (TLRs) have recently emerged as potential contributors to the inflammation observed in human and rodent models of rheumatoid arthritis (RA). This study aims to evaluate the role of endosomal TLRs and in particular TLR7 in the murine collagen induced arthritis (CIA) model.

METHODS

CIA was induced by injection of collagen in complete Freund's adjuvant. To investigate the effect of endosomal TLRs in the CIA model, mianserin was administered daily from the day of disease onset. The specific role of TLR7 was examined by inducing CIA in TLR7-deficient mice. Disease progression was assessed by measuring clinical score, paw swelling, serum anti-collagen antibodies histological parameters, cytokine production and the percentage of T regulatory (Treg) cells.

RESULTS

Therapeutic administration of mianserin to arthritic animals demonstrated a highly protective effect on paw swelling and joint destruction. TLR7-/- mice developed a mild arthritis, where the clinical score and paw swelling were significantly compromised in comparison to the control group. The amelioration of arthritis by mianserin and TLR7 deficiency both corresponded with a reduction in IL-17 responses, histological and clinical scores, and paw swelling.

CONCLUSIONS

These data highlight the potential role for endosomal TLRs in the maintenance of inflammation in RA and support the concept of a role for TLR7 in experimental arthritis models. This study also illustrates the potential benefit that may be afforded by therapeutically inhibiting the endosomal TLRs in RA.

摘要

简介

内体 Toll 样受体 (TLR) 最近被认为是人类和啮齿动物类风湿关节炎 (RA) 模型中观察到的炎症的潜在贡献者。本研究旨在评估内体 TLRs,特别是 TLR7 在胶原诱导性关节炎 (CIA) 模型中的作用。

方法

通过在完全弗氏佐剂中注射胶原诱导 CIA。为了研究内体 TLRs 在 CIA 模型中的作用,从疾病发病之日起每天给予米氮平。通过在 TLR7 缺陷型小鼠中诱导 CIA 来检查 TLR7 的特定作用。通过测量临床评分、爪肿胀、血清抗胶原抗体组织学参数、细胞因子产生和 T 调节 (Treg) 细胞的百分比来评估疾病进展。

结果

米氮平对关节炎动物的治疗性给药对爪肿胀和关节破坏具有高度保护作用。与对照组相比,TLR7-/- 小鼠发生轻度关节炎,其临床评分和爪肿胀明显受损。米氮平和 TLR7 缺乏症对关节炎的改善均与 IL-17 反应、组织学和临床评分以及爪肿胀的减少相对应。

结论

这些数据突出了内体 TLRs 在 RA 中维持炎症的潜在作用,并支持 TLR7 在实验性关节炎模型中发挥作用的概念。本研究还说明了在 RA 中通过治疗性抑制内体 TLRs 可能带来的益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa70/3446525/57895762c759/ar3875-1.jpg

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