Division of Rheumatology, University of Colorado Denver, Aurora, CO, USA.
Clin Ther. 2019 Jul;41(7):1270-1278. doi: 10.1016/j.clinthera.2019.04.012. Epub 2019 Jun 10.
As the goal in rheumatoid arthritis (RA) management shifts toward the prevention of joint disease, it is important to consider the role of mucosal sites in the pathogenesis of RA because they may be potential targets for preventive interventions. Multiple mucosal sites demonstrate immune dysregulation and inflammation in individuals with classifiable RA as well as, importantly, in individuals with systemic autoimmunity related to RA. The lung, gingival, and gastrointestinal mucosae are most strongly implicated in RA pathogenesis and may be sites where autoimmunity in RA initially develops. Targeting the exact site where the initial immune dysregulation in RA occurs is an appealing approach to prevention because it could avoid unwanted side effects of systemic therapies. However, several challenges must be addressed before mucosa-targeted interventions are a readily available option for RA prevention. Studies are needed to determine whether all RA-related immune dysregulation at mucosal sites will progress to joint disease and whether one or multiple mucosal sites demonstrate dysregulation prior to the development of classifiable RA. These areas of future research are likely to provide crucial pieces in the understanding of RA pathogenesis and ultimately RA prevention.
随着类风湿关节炎 (RA) 管理目标向预防关节疾病转移,考虑黏膜部位在 RA 发病机制中的作用非常重要,因为它们可能是预防干预的潜在靶点。在可分类 RA 患者以及重要的 RA 相关系统性自身免疫患者中,多个黏膜部位表现出免疫失调和炎症。肺、牙龈和胃肠道黏膜与 RA 发病机制的关系最为密切,并且可能是 RA 中自身免疫最初发生的部位。针对 RA 中最初发生免疫失调的确切部位进行靶向治疗是一种有吸引力的预防方法,因为它可以避免全身性治疗的不必要副作用。然而,在黏膜靶向干预成为 RA 预防的可行选择之前,还必须解决几个挑战。需要研究来确定所有 RA 相关的黏膜部位免疫失调是否都会进展为关节疾病,以及在可分类 RA 发生之前是否一个或多个黏膜部位表现出失调。这些未来研究领域可能为理解 RA 发病机制并最终预防 RA 提供关键信息。