维生素D与自身免疫性甲状腺疾病(第1部分)

N. Volkova, A. Solntseva
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摘要

自身免疫性甲状腺炎(AIT)和Graves病(GD)是常见的自身免疫性疾病,其患病率估计为普通人群的5%。目前,用于自身免疫病理病理治疗的选择性免疫抑制剂正在开发中。维生素D具有抗炎和免疫调节的特性,也引起了人们的极大兴趣。本文的第一部分综述了各种免疫细胞在自身免疫性甲状腺疾病发病机制中的作用,这是揭示骨化三醇在这些疾病中的治疗潜力的必要条件。传统上认为,AIT是由t辅助型1 (Th1)介导的,GD -是由t辅助型2 (Th2)介导的。这种误解是基于体液免疫由Th2细胞因子控制,而细胞免疫由Th1控制。在过去的几十年里,新的免疫细胞亚群在自身免疫性甲状腺疾病发病机制中的作用正在被研究,取代了传统的Th1/Th2二分法。已经确定t辅助型17 (Th17)在各种炎症和自身免疫性疾病的发展中起重要作用,以前被归类为th1依赖性病理。T和b调节淋巴细胞在自身免疫过程中的参与也引起了特别的兴趣。发现这些细胞在甲状腺病变患者的炎症甲状腺组织中积聚,但它们不能有效地抑制免疫反应。进一步的研究将有助于发现在自身免疫性疾病的复杂治疗中,哪些免疫细胞可以成为维生素D激动剂的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vitamin D and autoimmune thyroid diseases (part 1)
Autoimmune thyroiditis (AIT) and Graves’ disease (GD) are common autoimmune diseases, and their prevalence assessed as 5 % of general population. Currently, selective immunosuppressive agents for pathogenetic treatment of autoimmune pathology are being developed. Vitamin D with the known anti­inflammatory and immunoregulatory properties, is also of great interest. The first part of the article reviews the roles of various immune cells in the pathogenesis of autoimmune thyroid diseases, which is necessary to reveal the therapeutic potential of calcitriol in these disorders. Classically, AIT was considered to be mediated by T­helpers type 1 (Th1), and GD — by T­helpers type 2 (Th2). This misunderstanding was based on the idea that humoral immunity is controlled by Th2 cytokines, and cellular immunity — by Th1. In the past decades, the role of new subsets of immune cells in the pathogenesis of autoimmune thyroid diseases is being studied, displacing the traditional paradigm of Th1/Th2 dichotomy. It has been established that T­helpers type 17 (Th17) play an important role in the development of various inflammatory and autoimmune diseases, previously classified as Th1­dependent pathologies. The involvement of T­ and B­regulatory lymphocytes in the autoimmune process is also of particular interest. It was found that these cells accumulate in inflamed thyroid tissue in patients with thyroid pathology, but they are unable to suppress the immune response effectively. Further research will help to find out which immune cells can become targets for vitamin D agonists in the complex treatment of autoimmune diseases.
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