Literature DB >> 31827051

The proportion of peripheral blood Tregs among the CD4+ T cells of autoimmune thyroid disease patients: a meta-analysis.

Ziyi Chen1, Yue Wang1, Xi Ding1, Meng Zhang1, Mingqian He1, Yang Zhao1, Shiqian Hu1, Fengyi Zhao1, Jingya Wang1, Baosong Xie1, Bingyin Shi1.   

Abstract

Autoimmune thyroid disease (AITD) is characterized by a loss of self-tolerance to thyroid antigen. Tregs, whose proportions are controversial among CD4+ T cell from AITD patients (AITDs), are crucial in immune tolerance. Considering that drugs might affect Treg levels, we assumed that the differences originated from different treatment statuses. Thus, we performed a meta-analysis to explore proportions of Tregs in untreated and treated AITDs. PubMed, Embase and ISI Web of Knowledge were searched for relevant studies. Review Manager 5.3 and Stata 14.0 were used to conduct the meta-analysis. Subgroup analysis based on different diseases and cell surface markers was performed. Egger linear regression analysis was used to assess publication bias. Approximately 1,100 AITDs and healthy controls (HCs) from fourteen studies were included. Proportions of Tregs among CD4+ T cells of untreated AITDs were significantly lower than those in HCs (p = 0.002), but were not in treated patients (p = 0.40). Subgroup analysis revealed lower proportions of Tregs in untreated Graves' disease patients (GDs) (p = 0.001) but did not show obvious differences in untreated Hashimoto's thyroiditis patients (HTs) (p = 0.62). Furthermore, proportions of circulating FoxP3+ Tregs were reduced in untreated GDs (p < 0.00001) and HTs (p = 0.04). No publication bias was found. In this first meta-analysis exploring proportions of circulating Tregs among CD4+ T cells of AITDs with different treatment statuses, we found that Tregs potentially contribute to the pathogenesis of AITD but function differently in GD and HT. Remarkably, FoxP3+ Tregs, which were decreased in both diseases, might be promising targets for novel therapies.

Entities:  

Keywords:  Autoimmune thyroid diseases; Graves’ disease; Hashimoto’s thyroiditis; Meta-analysis; Regulatory T cells

Mesh:

Year:  2019        PMID: 31827051     DOI: 10.1507/endocrj.EJ19-0307

Source DB:  PubMed          Journal:  Endocr J        ISSN: 0918-8959            Impact factor:   2.349


  4 in total

1.  Decreased Treg Cell and TCR Expansion Are Involved in Long-Lasting Graves' Disease.

Authors:  Ziyi Chen; Yufeng Liu; Shiqian Hu; Meng Zhang; Bingyin Shi; Yue Wang
Journal:  Front Endocrinol (Lausanne)       Date:  2021-04-12       Impact factor: 5.555

2.  The changes in peripheral blood Th17 and Treg ratios in Hashimoto's thyroiditis are accompanied by differential PD-1/PD-L1 expression.

Authors:  Jun Fang; Lei Yu; Lan-Gen Zhuang; Xiao-Yan Pei; Qiong Wang; Guo-Xi Jin
Journal:  Front Endocrinol (Lausanne)       Date:  2022-08-25       Impact factor: 6.055

Review 3.  Immunological Drivers in Graves' Disease: NK Cells as a Master Switcher.

Authors:  Daniela Gallo; Eliana Piantanida; Matteo Gallazzi; Luigi Bartalena; Maria Laura Tanda; Antonino Bruno; Lorenzo Mortara
Journal:  Front Endocrinol (Lausanne)       Date:  2020-07-17       Impact factor: 5.555

Review 4.  The exploration of Hashimoto's Thyroiditis related miscarriage for better treatment modalities.

Authors:  Yu Min; Xing Wang; Hang Chen; Guobing Yin
Journal:  Int J Med Sci       Date:  2020-08-29       Impact factor: 3.738

  4 in total

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