Mizoguchi Emiko, Subramaniam Renuka, Okada Toshiyuki, Mizoguchi Atsushi
Department of Immunology, Kurume University School of Medicine, 67 Asahi-machi, Fukuoka 830-0011, Japan.
Department of Molecular Microbiology and Immunology, Brown University Alpert Medical School, Providence, RI 02912, USA.
Diagnostics (Basel). 2021 Jan 30;11(2):207. doi: 10.3390/diagnostics11020207.
Inflammatory bowel disease (IBD) is a dysregulated inflammatory condition induced by multiple factors. The etiology of IBD is largely unknown, and the disease progression and prognosis are variable and unpredictable with uncontrolled disease behavior. Monitoring the status of chronic colitis closely is challenging for physicians, because the assessment of disease activity and severity require invasive methods. Using laboratory biomarkers may provide a useful alternative to invasive methods in the diagnosis and management of IBD. Furthermore, patients with ulcerative colitis or Crohn's disease are also at risk of developing cancer. Annual colonoscopies can help lower the risk for developing colorectal cancer. However, laboratory biomarkers may also be helpful as non-invasive indicators in predicting treatment responses, improving prognosis, and predicting possible tumors. This review addresses selected laboratory biomarkers (including ANCA, chitinase 3-like 1, S100A12/RAGE, calprotectin, and TNF/TNFR2), which are identified by utilizing two well-accepted animal models of colitis, dextran sodium sulfate-induced and T cell receptor alpha knockout colitis models. In addition to being useful for monitoring disease severity, these biomarkers are associated with therapeutic strategies. The factors may regulate the initiation and perpetuation of inflammatory factors in the gut.
炎症性肠病(IBD)是一种由多种因素引发的炎症调节失调病症。IBD的病因很大程度上尚不明确,且在疾病行为未得到控制的情况下,疾病进展和预后存在变数且不可预测。对医生而言,密切监测慢性结肠炎的状况颇具挑战性,因为疾病活动度和严重程度的评估需要采用侵入性方法。使用实验室生物标志物在IBD的诊断和管理中可能为侵入性方法提供一种有用的替代方案。此外,溃疡性结肠炎或克罗恩病患者也有患癌风险。每年进行结肠镜检查有助于降低患结直肠癌的风险。然而,实验室生物标志物作为非侵入性指标在预测治疗反应、改善预后以及预测可能发生的肿瘤方面也可能有所帮助。本综述探讨了选定的实验室生物标志物(包括抗中性粒细胞胞浆抗体、几丁质酶3样蛋白1、S100A12/晚期糖基化终末产物受体、钙卫蛋白以及肿瘤坏死因子/肿瘤坏死因子受体2),这些生物标志物是通过利用两种广泛认可并接受的结肠炎动物模型(葡聚糖硫酸钠诱导的结肠炎模型和T细胞受体α基因敲除结肠炎模型)得以确定的。除了有助于监测疾病严重程度外,这些生物标志物还与治疗策略相关。这些因素可能调节肠道中炎症因子的启动和持续存在。