Gastroenterology Unit, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-IP), Universidad Autónoma de Madrid, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
J Crohns Colitis. 2019 Mar 26;13(3):374-384. doi: 10.1093/ecco-jcc/jjy158.
The protein domain is probably the most ubiquitously affected in disease, response and recovery, and therefore proteomics holds special promise for biomarker discovery in general, and particularly in inflammatory bowel disease [IBD], i.e. ulcerative colitis and Crohn's disease. Tremendous progress has been made over the past decade in the development and refinement of proteomics technologies. These advances provide opportunities for a long-anticipated personalized medicine approach to the treatment of IBD. The present review examines the current state of IBD proteomics research and its usefulness in clinical practice. We performed a systematic bibliographic search to identify studies investigating the use of proteomics in patients with IBD, and we then summarized the current 'state of the art' in the applications of proteomic technologies in the study of IBD. In particular, in the present review we provide: [1] a brief introduction to proteomics in health and disease; [2] a review of the different stages from biomarker discovery to clinical application; and [3] a comprehensive review of the clinical usefulness and application of proteomics in IBD, including: [a] screening to differentiate IBD from healthy controls; [b] differentiating Crohn's disease from ulcerative colitis; [c] prediction of the behaviour or the IBD course; [d] prediction of IBD response to biological treatment; and [e] monitoring response to treatment. We also review the importance of the type of sample-blood vs intestinal tissue-for the study of proteomics in IBD patients. Finally, we emphasize the current limitations of proteomic studies in IBD.
蛋白质结构域可能是最普遍受到疾病、反应和恢复影响的结构域,因此蛋白质组学在生物标志物发现方面具有特殊的应用前景,特别是在炎症性肠病(IBD)中,即溃疡性结肠炎和克罗恩病。在过去的十年中,蛋白质组学技术的发展和完善取得了巨大的进展。这些进展为期待已久的个性化医疗方法治疗 IBD 提供了机会。本综述检查了 IBD 蛋白质组学研究的现状及其在临床实践中的应用。我们进行了系统的文献检索,以确定研究 IBD 患者蛋白质组学应用的研究,并总结了蛋白质组学技术在 IBD 研究中的应用的“当前状态”。特别是,在本综述中,我们提供了:[1] 健康和疾病中蛋白质组学的简要介绍;[2] 从生物标志物发现到临床应用的不同阶段的回顾;[3] 蛋白质组学在 IBD 中的临床应用和应用的全面回顾,包括:[a] 筛选以区分 IBD 与健康对照;[b] 区分克罗恩病与溃疡性结肠炎;[c] 预测 IBD 的行为或病程;[d] 预测 IBD 对生物治疗的反应;[e] 监测治疗反应。我们还回顾了在 IBD 患者中研究蛋白质组学时样本类型(血液与肠道组织)的重要性。最后,我们强调了蛋白质组学研究在 IBD 中的当前局限性。