Serum CXCL 9 as a Potential Biomarker for Patients with Ulcerative Colitis

Mohammed A. Qusay, Sarmad M.H. Zeiny, Haider J.M. Al-Maraashi
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Abstract

Background: Ulcerative colitis (UC) is an inflammatory bowel disease restricted to the large intestine, characterized by superficial ulceration. It is a progressive and chronic disease requiring long-term treatment. Although its etiology remains unknown, it is suggested that environmental factors influence genetically susceptible individuals, leading to the onset of the disease. (C-X-C) ligand 9 is a chemokine that belongs to the CXC chemokine family, it plays a role in the differentiation of immune cells such as cytotoxic lymphocytes, natural killer T cells, and macrophages. Its interaction with its corresponding receptor CXCR3 which is expressed by a variety of cells such as effector T cells, CD8+ cytotoxic T cells, and macrophage, leads to stimulation of the production of IFN-γ and TNF-α and in turn, stimulates the production of Th1 chemokines which results in promoting the inflammation. Objectives: To assess the significance of serum chemokine (C-X-C) ligand 9 as a potential marker for identifying ulcerative colitis in adults with inflammatory bowel disease. Patients and Methods:  This is a case-control study that included 50 patients diagnosed with UC, aged between 18 and 75 years, compared to 50 healthy controls, aged between 18 and 60 years. The study was conducted between November 2022 and March 2023, at the Gastroenterology and Hepatology Teaching Hospital at the Medical City Complex in Baghdad. The serum samples were analyzed using the Enzyme-Linked Immunosorbent Assay (ELISA) technique. Results: The mean ± SD in pg/ml of serum CXCL9 in patient group was 26.9 ± 9.05 and in control group was 6.4 ± 2.37 (p< 0.0001) which indicates a highly significant difference. Conclusion: CXCL 9 may be employed as a biomarker for identifying ulcerative colitis and it can be used as a tool for measuring disease activity, in addition to the possibility of being a potential therapeutic target.  
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血清 CXCL 9 是溃疡性结肠炎患者的潜在生物标记物
背景:溃疡性结肠炎(UC)是一种局限于大肠的炎症性肠病,以浅表溃疡为特征。它是一种进展性慢性疾病,需要长期治疗。虽然其病因尚不清楚,但有人认为是环境因素影响了易感基因个体,导致发病。(C-X-C)配体 9 是一种趋化因子,属于 CXC 趋化因子家族,在细胞毒性淋巴细胞、自然杀伤 T 细胞和巨噬细胞等免疫细胞的分化过程中发挥作用。它与效应 T 细胞、CD8+ 细胞毒性 T 细胞和巨噬细胞等多种细胞表达的相应受体 CXCR3 相互作用,导致刺激 IFN-γ 和 TNF-α 的产生,进而刺激 Th1 趋化因子的产生,从而促进炎症的发生:评估血清趋化因子(C-X-C)配体 9 作为识别成人炎症性肠病患者溃疡性结肠炎潜在标志物的意义: 这是一项病例对照研究,包括 50 名年龄在 18 岁至 75 岁之间的确诊为溃疡性结肠炎的患者,以及 50 名年龄在 18 岁至 60 岁之间的健康对照者。研究于 2022 年 11 月至 2023 年 3 月期间在巴格达医疗城综合医院的胃肠病学和肝病学教学医院进行。血清样本采用酶联免疫吸附试验(ELISA)技术进行分析:结果:患者组血清中 CXCL9 的平均值(以 pg/ml 为单位)为 26.9 ± 9.05(P< 0.0001),对照组为 6.4 ± 2.37(P< 0.0001),差异非常显著:结论:CXCL 9 可用作识别溃疡性结肠炎的生物标记物,也可用作测量疾病活动性的工具,此外还可能成为潜在的治疗靶点。
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