Van Broeck Dorien, Steelant Brecht, Scadding Glenis, Hellings Peter W
Department of Microbiology, Immunology and Transplantation, KULeuven, Leuven, Belgium.
Royal National ENT Hospital and Division of Infection and Immunity, University College, London, United Kingdom.
Front Allergy. 2023 Apr 12;4:1080951. doi: 10.3389/falgy.2023.1080951. eCollection 2023.
Nonsteroidal anti-inflammatory drug (NSAID)-exacerbated respiratory disease (N-ERD) is a clinical syndrome characterized by nasal polyposis, asthma, and intolerance to aspirin/NSAID. It affects approximately 15% cases of severe asthma, 10% of nasal polyps and 9% of rhinosinusitis. N-ERD results in associated asthma exacerbations, oral corticosteroids bursts, corticosteroid-dependent disease, and multiple endoscopic sinus surgeries. Unknown influences cause polyp epithelium to release alarmins, such as IL-33 and TSLP. These cytokines activate lymphoid cells, both Th2 and ILC2, to release cytokines such as IL5, IL4 and IL13, resulting in complex type 2 inflammation involving mast cells, eosinophils and platelets. Arachidonic acid released from such cells is metabolized into mediators. N-ERD is characterized by an imbalance in eicosanoid levels, especially CysLTs, PDG and PGE2. Patients with N-ERD present nasal symptoms (congestion, hyposmia/anosmia, nasal discharge) and lower airways symptoms (cough, sneezing, shortness of breath, chest tightness), anosmia, severe hyposmia as well as severe asthma which impacts the quality of life in this disease and leads to safety concerns in patients daily lives. Despite the variety of treatment strategies, the likelihood of recurrence of symptoms is high in patients with N-ERD. The most important strategies for treating N-ERD are listed as following: drug therapies, aspirin desensitization, monoclonal antibodies and other therapies associated. N-ERD treatment remains a major challenge in the current situation. Selecting the appropriate patient for aspirin desensitization, monoclonal antibodies or both is essential. This review provides an overview on aspirin desensitization and biologics in N-ERD and might help in decision making from both the perspective of the physician and patient. Patient characteristics, safety, efficacy, health care costs, but also patient preferences are all factors to take into account when it comes to a choice between biologics or aspirin desensitization.
非甾体抗炎药(NSAID)加重的呼吸道疾病(N-ERD)是一种临床综合征,其特征为鼻息肉、哮喘以及对阿司匹林/NSAID不耐受。它影响约15%的重度哮喘病例、10%的鼻息肉病例和9%的鼻窦炎病例。N-ERD会导致相关的哮喘加重、口服糖皮质激素冲击治疗、糖皮质激素依赖型疾病以及多次鼻内镜鼻窦手术。未知因素促使息肉上皮释放警报素,如白细胞介素-33(IL-33)和胸腺基质淋巴细胞生成素(TSLP)。这些细胞因子激活Th2和2型固有淋巴细胞(ILC2)等淋巴细胞,释放白细胞介素-5(IL-5)、白细胞介素-4(IL-4)和白细胞介素-13等细胞因子,导致涉及肥大细胞、嗜酸性粒细胞和血小板的复杂2型炎症。此类细胞释放的花生四烯酸被代谢为介质。N-ERD的特征是类花生酸水平失衡,尤其是白三烯(CysLTs)、血小板衍生生长因子(PDG)和前列腺素E2(PGE2)。N-ERD患者会出现鼻部症状(鼻塞、嗅觉减退/嗅觉丧失、流涕)和下呼吸道症状(咳嗽、打喷嚏、呼吸急促、胸闷)、嗅觉丧失、严重嗅觉减退以及严重哮喘,这会影响该疾病患者的生活质量,并导致患者日常生活中的安全问题。尽管有多种治疗策略,但N-ERD患者症状复发的可能性很高。治疗N-ERD的最重要策略如下:药物治疗、阿司匹林脱敏、单克隆抗体及其他相关治疗。在当前情况下,N-ERD的治疗仍然是一项重大挑战。为阿司匹林脱敏、单克隆抗体或两者选择合适的患者至关重要。本综述概述了N-ERD中的阿司匹林脱敏和生物制剂,可能有助于从医生和患者的角度进行决策。在生物制剂或阿司匹林脱敏之间做出选择时,患者特征、安全性、疗效、医疗费用以及患者偏好都是需要考虑的因素。