Pattnaik Bijay, Sryma P B, Mittal Saurabh, Agrawal Anurag, Guleria Randeep, Madan Karan
Department of Pulmonary, Critical Care and Sleep Medicine, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
Centre of Excellence in Asthma and Lung Disease, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Respir Investig. 2020 Jul;58(4):232-238. doi: 10.1016/j.resinv.2020.02.008. Epub 2020 Apr 15.
Sarcoidosis is a multisystemic granulomatous disorder of unknown etiology. Diagnosis of sarcoidosis is made by correlating clinical and radiological features along with the histopathological demonstration of non-necrotizing granulomas in tissue samples. Diagnosis is often challenging as the clinical profile may mimic other granulomatous disorders, including infections, inflammatory diseases, and lymphoid malignancies. Differentiation from tuberculosis is especially crucial in endemic regions where exclusion of mediastinal tuberculosis is necessary before any immunosuppressant treatment can be initiated for symptomatic sarcoidosis. Identification of biomarkers, which can aid in diagnosis as well as prognosis, can be helpful in clinical decision making. MicroRNAs are small non-coding regulatory RNAs that serve as post-transcriptional regulators of gene expression and have been studied as emerging biomarkers in many other respiratory diseases, including lung cancer, asthma, idiopathic pulmonary fibrosis, and chronic obstructive pulmonary disease. In the context of sarcoidosis, miRNA expression has been studied in the lungs, lymph nodes, bronchoalveolar lavage fluid, and peripheral blood mononuclear cells. A comprehensive search of the PubMed database was performed by two authors independently, and relevant studies were retrieved for review. This systematic review summarizes the current information on miRNAs in sarcoidosis, the biological mechanisms involved in CD4 T-helper 1 and macrophage polarization, and the use of exhaled breath condensate as an alternative, noninvasive and potential source of miRNAs.
结节病是一种病因不明的多系统肉芽肿性疾病。结节病的诊断是通过将临床和放射学特征与组织样本中非坏死性肉芽肿的组织病理学表现相结合来做出的。由于临床特征可能模仿其他肉芽肿性疾病,包括感染、炎症性疾病和淋巴系统恶性肿瘤,因此诊断往往具有挑战性。在流行地区,将结节病与结核病区分开来尤为关键,因为在对有症状的结节病开始任何免疫抑制治疗之前,必须排除纵隔结核。识别有助于诊断和预后的生物标志物有助于临床决策。微小RNA是小的非编码调节RNA,作为基因表达的转录后调节因子,在许多其他呼吸系统疾病中,包括肺癌、哮喘、特发性肺纤维化和慢性阻塞性肺疾病,已被作为新兴的生物标志物进行研究。在结节病的背景下,已经在肺、淋巴结、支气管肺泡灌洗液和外周血单核细胞中研究了微小RNA的表达。两位作者独立对PubMed数据库进行了全面检索,并检索了相关研究进行综述。本系统综述总结了结节病中微小RNA的当前信息、CD4辅助性T细胞1和巨噬细胞极化所涉及的生物学机制,以及呼出气冷凝物作为微小RNA的替代、非侵入性和潜在来源的应用。