Frontiers in Immunology (Dec 2016)

Increased Toll-Like Receptors Activity and TLR Ligands in Patients with Autoimmune Thyroid Diseases

  • Shiqiao Peng,
  • Chenyan Li,
  • Chenyan Li,
  • Xinyi Wang,
  • Xinyi Wang,
  • Xin Liu,
  • Xin Liu,
  • Cheng Han,
  • Ting Jin,
  • Ting Jin,
  • Shanshan Liu,
  • Shanshan Liu,
  • Xiaowen Zhang,
  • Hanyi Zhang,
  • Xue He,
  • Xiaochen Xie,
  • Xiaohui Yu,
  • Xiaohui Yu,
  • Chuyuan Wang,
  • Chuyuan Wang,
  • Ling Shan,
  • Chenling Fan,
  • Zhongyan Shan,
  • Zhongyan Shan,
  • Weiping Teng,
  • Weiping Teng

DOI
https://doi.org/10.3389/fimmu.2016.00578
Journal volume & issue
Vol. 7

Abstract

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ObjectiveAutoimmune thyroid disease (AITD) is an organ-specific disorder due to the interplay between environmental and genetic factors. Toll-like receptors (TLRs) are pattern recognition receptors expressed abundantly on monocytes. There is a paucity of data on TLR expression in AITD. The aim of this study was to examine TLR expression, activation, ligands, and downstream signaling adaptors in peripheral blood mononuclear cells (PBMCs) extracted from untreated AITD patients and healthy controls.MethodWe isolated PBMC of 30 healthy controls, 36 patients with untreated Hashimoto’s thyroiditis, and 30 patients with newly onset Graves’ disease. TLR mRNA, protein expression, TLR ligands, and TLR adaptor molecules were measured using real-time PCR, Western blot, flow cytometry, and enzyme-linked immunosorbent assay (ELISA). PBMC was simulated with TLR agonists. The effects of TLR agonists on the viability of human PBMC were evaluated using the MTT assay. The supernatants of cell cultures were measured for the pro-inflammatory cytokines, interleukin (IL)-6, tumor necrosis factor alpha (TNF-α), and IL-10 by ELISA.ResultsTLR2, TLR3, TLR9, and TLR10 mRNA were significantly increased in AITD patients compared with controls. TLR2, TLR3, TLR9, high mobility group box 1 (HMGB1), and RAGE expression on monocytes was higher in patients than control at baseline and TLR agonists’ stimulation. The release of TNF-α and IL-6 was significantly increased in PBMCs from AITD patients with TLR agonists, while IL-10 was significantly decreased. Downstream targets of TLR, myeloid differentiation factor 88 (MyD88), and myeloid toll/IL-1 receptor-domain containing adaptor-inducing interferon-β were significantly elevated in AITD patients. Levels of TLR2 ligands, HMGB1, and heat shock protein 60 were significantly elevated in AITD patients compared with those in controls and positively correlated with TgAb and TPOAb, while sRAGE concentration was significantly decreased in AITD patients.ConclusionThis work is the first to show that TLR2, TLR3, and TLR9 expression and activation are elevated in the PBMCs of patients with AITD and TLRs may participate in the pathogenesis of AITD.

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