Comparative analysis of the expression of the soluble IL-7 receptor in patients with arthropathy

A. V. Kolerova, O. A. Angelskaya, O. Chumasova, A. Sizikov, I. Shirinsky, V. Shirinsky, E. Blinova
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Abstract

Arthropathy is one of the most prevalent diseases, which are based on the destruction and remodeling of cartilage and bone tissue. The inflammation that precedes destruction can be caused by mechanical stress on the joints, or by autoimmune reactions. Recently, IL-7 is considered as one of the key cytokines that promote the production of matrix metalloproteinases, catabolic enzymes, T cell-mediated activation of monocytes, and maturation of osteoclasts. The soluble form of the IL-7 receptor can help prolong the lifespan of IL-7 and thereby it ensures the bioavailability of the cytokine and mediates effect of IL-7 on cells. The aim of this study was to determine the soluble form of the IL-7 receptor (sIL-7R) in the blood plasma of patients with rheumatoid arthritis (RA), osteoarthritis (OA), psoriatic arthritis (PsA) and psoriasis vulgaris (PS), as well as healthy individuals. The RA patients included in the study had moderate to high disease activity according to the DAS28 index. Patients with PsA predominantly had moderate and low disease activity (DAS28) and were characterized by mild to moderate disease severity (PASI). In accordance with the PASI index, patients with PS with mild and severe severity of the disease were included in the study. All patients with OA had a metabolic phenotype that is accompanied by an elevated body mass index.sIL-7R was determined in blood plasma by enzyme-linked immunosorbent assay. It was found that in patients with arthropathy, the level of soluble form of IL-7 was increased relative to healthy individuals, with the exception of the group of patients with PsA. Also, a high concentration of sIL-7R was observed in patients with PS. Analyzing the clinical characteristics of the patients, we found that sIL-7R levels were elevated in RA and PsA patients with high disease activity by DAS28. In addition, positive correlations were found between the concentration of sIL-7R and DAS28 in RA and PsA. In patients with PsA with moderate severity of the disease (PASI), the concentration of sIL-7R was also increased relative to donor's values. On the contrary, in patients with PS, a high level of sIL-7R was noted regardless of the severity of the disease. In patients with OA, no relationship was found between sIL-7R levels and clinical parameters.Thus, an elevated level of sIL-7R in patients with arthropathy may indicate the involvement of IL-7 and its receptor system in the pathogenesis of joint diseases. The IL-7 receptor may become a promising target both in the treatment of joint diseases and other autoimmune diseases, including psoriasis.
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可溶性IL-7受体在关节病患者中表达的比较分析
关节病是最常见的疾病之一,其基础是软骨和骨组织的破坏和重塑。破坏之前的炎症可能是由关节上的机械应力或自身免疫反应引起的。近年来,IL-7被认为是促进基质金属蛋白酶、分解代谢酶、T细胞介导的单核细胞活化和破骨细胞成熟的关键细胞因子之一。IL-7受体的可溶性形式可以帮助延长IL-7的寿命,从而确保细胞因子的生物利用度,并介导IL-7对细胞的作用。本研究的目的是确定IL-7受体(sIL-7R)在类风湿关节炎(RA)、骨关节炎(OA)、银屑病关节炎(PsA)和寻常型银屑病(PS)患者以及健康个体血浆中的可溶性形式。根据DAS28指数,纳入研究的RA患者具有中度至高度的疾病活动性。PsA患者主要有中度和低疾病活动性(DAS28),并以轻至中度疾病严重程度(PASI)为特征。按照PASI指数,将病情轻重的PS患者纳入研究。所有OA患者都有代谢表型,伴有体重指数升高。采用酶联免疫吸附法测定血浆中sIL-7R的含量。结果发现,在关节病变患者中,除了PsA患者组外,可溶性IL-7水平相对于健康个体增加。此外,在PS患者中也观察到高浓度的sIL-7R。分析患者的临床特征,我们发现在疾病活动性高的RA和PsA患者中,DAS28使sIL-7R水平升高。此外,RA和PsA中sIL-7R和DAS28的浓度呈正相关。在具有中度疾病严重程度(PASI)的PsA患者中,sIL-7R的浓度相对于供者的值也有所增加。相反,在PS患者中,无论疾病的严重程度如何,都注意到高水平的sIL-7R。在OA患者中,sIL-7R水平与临床参数没有关系。因此,关节病变患者sIL-7R水平升高可能提示IL-7及其受体系统参与关节疾病的发病机制。IL-7受体可能成为治疗关节疾病和其他自身免疫性疾病(包括牛皮癣)的有希望的靶点。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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