Università degli Studi di Milano, Milan, Italy.
Pediatric Clinic, Department of Medicine and Surgery, University of Parma, Parma, Italy.
Int Immunopharmacol. 2024 Nov 15;141:113017. doi: 10.1016/j.intimp.2024.113017. Epub 2024 Aug 27.
Recurrent pericarditis (RP) is defined by the European Society of Cardiology (ESC) as an instance of acute pericarditis (AP) that occurs at least 4-6 weeks after the resolution of a previous episode of the same ailment. To mitigate the risk of RP, it is advised to administer accurate and prolonged pharmacological treatment for both the initial AP and subsequent RP. ESC guidelines recommend commencing treatment for any single episode of AP, including those that contribute to RP, with non-steroidal anti-inflammatory drugs (NSAIDs) in conjunction with colchicine for several months, often followed by gradual tapering. If there is an inadequate response, corticosteroids (CS) may be introduced cautiously. However, in a minority of cases, even when NSAIDs, colchicine, and CS are administered together at the highest recommended dosages, they may prove ineffective. In such instances, treatment with immunosuppressive drugs or biologics is advised. Among biologics, interleukin (IL)-1 inhibitors have been extensively studied, although certain gaps remain. This narrative review delves into the rationale for employing IL-1 inhibitors and presents findings from existing studies regarding their efficacy, tolerability, and safety. Analysis of the literature indicates that there is currently insufficient data to ascertain the true therapeutic role of IL-1 inhibitors in managing and preventing RP. However, theoretically, drugs targeting both IL-1α and IL-1β may offer superior efficacy compared to those solely targeting IL-1β due to the significant involvement of both cytokines in inflammation. Further research is warranted to determine the comparative effectiveness of IL-1α and IL-1β inhibitors.
复发性心包炎 (RP) 被欧洲心脏病学会 (ESC) 定义为急性心包炎 (AP) 的一个实例,其发生在前一次相同疾病发作后至少 4-6 周。为了降低 RP 的风险,建议对初始 AP 和随后的 RP 进行准确和长期的药物治疗。ESC 指南建议对任何单一的 AP 发作进行治疗,包括那些导致 RP 的发作,使用非甾体抗炎药 (NSAIDs) 联合秋水仙碱治疗数月,通常随后逐渐减少剂量。如果反应不足,可以谨慎地引入皮质类固醇 (CS)。然而,在少数情况下,即使 NSAIDs、秋水仙碱和 CS 以最高推荐剂量联合使用,它们也可能无效。在这种情况下,建议使用免疫抑制剂或生物制剂进行治疗。在生物制剂中,白细胞介素 (IL)-1 抑制剂已得到广泛研究,尽管仍存在一些空白。这篇叙述性综述探讨了使用 IL-1 抑制剂的基本原理,并介绍了现有研究关于其疗效、耐受性和安全性的发现。对文献的分析表明,目前尚无足够的数据确定 IL-1 抑制剂在管理和预防 RP 中的真正治疗作用。然而,从理论上讲,靶向 IL-1α 和 IL-1β 的药物可能比仅靶向 IL-1β 的药物具有更高的疗效,因为这两种细胞因子都在炎症中起重要作用。需要进一步研究来确定 IL-1α 和 IL-1β 抑制剂的比较效果。