[CXCR3 and CXCL10 in autoimmune thyroiditis].

CXCL10型 CXCR3型 医学 自身免疫性甲状腺炎 免疫学 甲状腺炎 趋化因子 甲状腺 自身免疫 自身免疫性疾病 免疫系统 趋化因子受体 内科学 抗体
作者
Ilaria Ruffilli,Silvia Martina Ferrari,Michele Colaci,Claudio Ferri,Ugo Politti,Alessandro Antonelli,Poupak Fallahi
出处
期刊:PubMed [National Institutes of Health]
卷期号:165 (3): e237-42 被引量:11
标识
DOI:10.7417/ct.2014.1727
摘要

The chemokine (C-X-C motif) ligand 10 (CXCL10, also called IP-10) was initially identified as a chemokine that is induced by interferon (IFN)-γ. CXCL10 exerts its function through binding to chemokine (C-X-C motif) receptor 3 (CXCR3). CXCL10 and its receptor, CXCR3, appear to contribute to the pathogenesis of many autoimmune diseases, organ specific (such as type 1 diabetes, Graves' disease and ophthalmopathy), or systemic (such as systemic lupus erythematosus, mixed cryoglobulinemia, Sjogren syndrome, or systemic sclerosis). The secretion of CXCL10 by CD4+, CD8+, and natural killer is dependent on IFN-γ. Under the influence of IFN-γ, CXCL10 is secreted by thyrocytes. Determination of high level of CXCL10 in peripheral fluids is therefore a marker of a T helper 1 orientated immune response. High levels of circulating CXCL10, have been shown in patients with autoimmune thyroiditis (AT). Among patients with AT, CXCL10 levels were significantly higher in those with a hypoechoic ultrasonographic pattern, that is a sign of a more severe lympho-monocytic infiltration, and in those with hypothyroidism. For these reasons it has been postulated that CXCL10 could be a marker of a stronger and more aggressive inflammatory response in the thyroid, subsequently leading to thyroid destruction and hypothyroidism. Further studies are needed to investigate whether CXCL10 is a novel therapeutic target in AT.

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