Department of Oral and Maxillofacial Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.
School of Stomatology of Qingdao University, Qingdao, China.
Front Immunol. 2021 Feb 25;12:606043. doi: 10.3389/fimmu.2021.606043. eCollection 2021.
Medication-related osteonecrosis of the jaw (MRONJ) is a rare but serious adverse drug effect. There are multiple hypotheses to explain the development of MRONJ. Reduced bone remodeling and infection or inflammation are considered central to the pathogenesis of MRONJ. In recent years, increasing evidence has shown that bisphosphonates (BPs)-mediated immunity dysfunction is associated with the pathophysiology of MRONJ. In a healthy state, mucosal immunity provides the first line of protection against pathogens and oral mucosal immune cells defense against potentially invading pathogens by mediating the generation of protective immunoinflammatory responses. In addition, the immune system takes part in the process of bone remodeling and tissue repair. However, the treatment of BPs disturbs the mucosal and osteo immune homeostasis and thus impairs the body's ability to resist infection and repair from injury, thereby adding to the development of MRONJ. Here, we present the current knowledge about immunity dysfunction to shed light on the role of local immune disorder in the development of MRONJ.
药物相关性颌骨坏死(MRONJ)是一种罕见但严重的药物不良反应。有多种假说可以解释 MRONJ 的发生发展。目前认为,骨重建减少和感染或炎症是 MRONJ 发病机制的核心。近年来,越来越多的证据表明,双膦酸盐(BPs)介导的免疫功能障碍与 MRONJ 的病理生理学有关。在健康状态下,黏膜免疫为抵抗病原体提供了第一道防线,口腔黏膜免疫细胞通过介导保护性免疫炎症反应来抵御潜在的入侵病原体。此外,免疫系统参与骨重建和组织修复的过程。然而,BPs 的治疗扰乱了黏膜和骨免疫稳态,从而损害了机体抵抗感染和损伤修复的能力,从而促进了 MRONJ 的发展。在这里,我们介绍了目前关于免疫功能障碍的知识,以阐明局部免疫紊乱在 MRONJ 发生发展中的作用。