Sweis Jaleel Jerry G, Sweis Nabil W G, Alnaimat Fatima, Jansz Jacqueline, Liao Ting-Wei Ernie, Alsakaty Alaa, Azam Abeera, Elmergawy Hesham, Hanson Hali A, Ascoli Christian, Rubinstein Israel, Sweiss Nadera
School of Medicine, The University of Jordan, Amman, Jordan.
Division of Rheumatology, Department of Internal Medicine, The University of Jordan, Amman, Jordan.
Front Med (Lausanne). 2023 Apr 6;10:1160755. doi: 10.3389/fmed.2023.1160755. eCollection 2023.
The role of immunity in the pathogenesis of various pulmonary diseases, particularly interstitial lung diseases (ILDs), is being increasingly appreciated as mechanistic discoveries advance our knowledge in the field. Immune-mediated lung diseases demonstrate clinical and immunological heterogeneity and can be etiologically categorized into connective tissue disease (CTD)-associated, exposure-related, idiopathic, and other miscellaneous lung diseases including sarcoidosis, and post-lung transplant ILD. The immunopathogenesis of many of these diseases remains poorly defined and possibly involves either immune dysregulation, abnormal healing, chronic inflammation, or a combination of these, often in a background of genetic susceptibility. The heterogeneity and complex immunopathogenesis of ILDs complicate management, and thus a collaborative treatment team should work toward an individualized approach to address the unique needs of each patient. Current management of immune-mediated lung diseases is challenging; the choice of therapy is etiology-driven and includes corticosteroids, immunomodulatory drugs such as methotrexate, cyclophosphamide and mycophenolate mofetil, rituximab, or other measures such as discontinuation or avoidance of the inciting agent in exposure-related ILDs. Antifibrotic therapy is approved for some of the ILDs (e.g., idiopathic pulmonary fibrosis) and is being investigated for many others and has shown promising preliminary results. A dire need for advances in the management of immune-mediated lung disease persists in the absence of standardized management guidelines.
随着机制研究的进展增进了我们对该领域的认识,免疫在各种肺部疾病,尤其是间质性肺疾病(ILD)发病机制中的作用越来越受到重视。免疫介导的肺部疾病表现出临床和免疫异质性,病因上可分为结缔组织病(CTD)相关、暴露相关、特发性以及其他包括结节病和肺移植后ILD在内的杂类肺部疾病。这些疾病中的许多免疫发病机制仍不清楚,可能涉及免疫失调、异常愈合、慢性炎症或这些因素的组合,通常是在遗传易感性背景下。ILD的异质性和复杂的免疫发病机制使治疗变得复杂,因此协作治疗团队应采取个体化方法来满足每位患者的独特需求。免疫介导的肺部疾病目前的治疗具有挑战性;治疗选择由病因驱动,包括皮质类固醇、免疫调节药物如甲氨蝶呤、环磷酰胺和霉酚酸酯、利妥昔单抗,或其他措施,如在暴露相关ILD中停用或避免接触诱发因素。抗纤维化治疗已被批准用于某些ILD(如特发性肺纤维化),并且正在对许多其他ILD进行研究,已显示出有希望的初步结果。在缺乏标准化管理指南的情况下,对免疫介导的肺部疾病治疗进展的迫切需求依然存在。