The Expression of T Cell FOXP3 and T-Bet Is Upregulated in Severe but Not Euthyroid Hashimoto's Thyroiditis

Mediators Inflamm. 2016:2016:3687420. doi: 10.1155/2016/3687420. Epub 2016 Jul 5.

Abstract

Hashimoto's thyroiditis (HT) is an organ-specific autoimmune disorder characterized by progressive thyroid failure. Th1 and Treg subset of CD4(+) cells have been implicated in the pathogenesis; however, less is known about their respective roles across the spectrum of HT clinical presentations. To shed more light on CD4(+) subsets role in HT, we investigated the mRNA expression levels of several Th1/Treg-associated transcription factors (T-bet/ETS1, HIF1α/BLIMP1/FOXP3) in peripheral blood T cells of 10 hypothyroid, untreated HT patients, 10 hypothyroid patients undergoing hormone replacement therapy, 12 euthyroid HT subjects, and 11 healthy controls by the qRT-PCR. Compared to euthyroid HT patients and controls, both hypothyroid (2.34-fold difference versus controls, P < 0.01) and thyroxine-supplemented patients (2.5-fold, P < 0.001) showed an increased FOXP3 mRNA expression in T cells. Similarly, mRNA expression levels of T-bet were upregulated in severely affected but not in euthyroid HT subjects (2.37-fold and 3.2-fold, hypothyroid and thyroxine-supplemented HT patients versus controls, resp., P < 0.01). By contrast, no differences in mRNA expression levels of ETS1, BLIMP1, and HIF1α were observed across the study groups. In summary, severe but not euthyroid HT was associated with robust upregulation of T-bet and FOXP3 mRNA in peripheral T cells, independent of the thyroid hormone status but proportional to disease activity.

MeSH terms

  • Adult
  • Autoimmune Diseases / metabolism
  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / metabolism*
  • Case-Control Studies
  • Cohort Studies
  • Female
  • Forkhead Transcription Factors / metabolism*
  • Gene Expression Regulation
  • Hashimoto Disease / immunology
  • Hashimoto Disease / metabolism*
  • Hormones / therapeutic use
  • Humans
  • Hypothyroidism / immunology
  • Hypothyroidism / metabolism
  • Leukocytes, Mononuclear / cytology
  • Male
  • Middle Aged
  • RNA, Messenger / metabolism
  • T-Box Domain Proteins / metabolism*
  • Up-Regulation

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Hormones
  • RNA, Messenger
  • T-Box Domain Proteins
  • T-box transcription factor TBX21