First School of Clinical Medicine, Southern Medical University, Guangzhou, China.
Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Front Immunol. 2022 Oct 24;13:967989. doi: 10.3389/fimmu.2022.967989. eCollection 2022.
Radiotherapy is one of the mainstream treatment modalities for several malignancies. However, radiation-induced injury to surrounding normal tissues limits its efficacy. The NLRP3 inflammasome is an essential mechanism of innate immunity that reacts to challenges from endogenous danger signals and pathological microbes. A growing body of evidence has demonstrated a key role of NLRP3 inflammasome in the pathogenesis of radiation-induced tissue injury. Despite accumulating evidence, the potential value of the NLRP3 inflammasome in the management of radiation-induced tissue injury is not adequately recognized. We conducted a literature review to characterize the relationship between NLRP3 inflammasome and radiation injury. By analyzing recent evidence, we identify NLRP3 inflammasome as one of the executioners of radiation-induced injury, since it responds to the challenges of radiation, induces cell pyroptosis and tissue dysfunction, and initiates non-resolving inflammation and fibrosis. Based on these concepts, we propose early intervention/prevention strategies targeting NLRP3 inflammasome in a radiation context, which may help resolve imperative clinical problems.
放射疗法是几种恶性肿瘤的主流治疗方法之一。然而,辐射对周围正常组织的损伤限制了其疗效。NLRP3 炎性小体是先天免疫的一个重要机制,对来自内源性危险信号和病理微生物的挑战作出反应。越来越多的证据表明 NLRP3 炎性小体在辐射诱导的组织损伤发病机制中起关键作用。尽管有大量证据,但 NLRP3 炎性小体在管理辐射诱导的组织损伤方面的潜在价值尚未得到充分认识。我们进行了文献回顾,以描述 NLRP3 炎性小体与辐射损伤之间的关系。通过分析最近的证据,我们确定 NLRP3 炎性小体是辐射诱导损伤的执行者之一,因为它对辐射的挑战作出反应,诱导细胞焦亡和组织功能障碍,并引发非解决性炎症和纤维化。基于这些概念,我们提出了针对放射环境中 NLRP3 炎性小体的早期干预/预防策略,这可能有助于解决迫切的临床问题。