Gomes Margarida, Mendes Ana, Ferreira Filipa, Branco Joana, Tonin Fernanda S, Pedro M Elisa
Serviço de Imunoalergologia, Hospital de Santa Maria, Centro Hospitalar e Universitário Lisboa Norte, Lisbon, Portugal.
Serviço de Gastroenterologia, Hospital Professor Doutor Fernando Fonseca, EPE, Amadora, Portugal.
Case Rep Med. 2023 Apr 24;2023:8832242. doi: 10.1155/2023/8832242. eCollection 2023.
In the past years, the knowledge of eosinophils playing a primary pathophysiologic role in several associated conditions has led to the development of biologics targeting therapies aiming at normalizing the immune response, reducing chronic inflammation, and preventing tissue damage. To better illustrate the potential relationship between different eosinophilic immune dysfunctions and the effects of biological therapies in this scenario, here, we present a case of a 63-year-old male first referred to our department in 2018 with a diagnosis of asthma, polyposis, and rhinosinusitis and presenting a suspicion of nonsteroidal anti-inflammatory drugs' allergy. He also had a past medical history of eosinophilic gastroenteritis/duodenitis (eosinophilia counts >50 cells/high-power field HPF). The use of multiple courses of corticosteroid therapy failed to completely control these conditions. In October 2019, after starting benralizumab (an antibody directed against the alpha chain of the IL-5 cytokine receptor) as add-on treatment for severe eosinophilic asthma, important clinical improvements were reported both on the respiratory (no asthma exacerbations) and gastrointestinal systems (eosinophilia count 0 cells/HPF). Patients' quality of life also increased. Since June 2020, systemic corticosteroid therapy was reduced without worsening of gastrointestinal symptoms or eosinophilic inflammation. This case warns of the importance of early recognition and appropriate individualized treatment of eosinophilic immune dysfunctions and suggests the conduction of further larger studies on the use of benralizumab in gastrointestinal syndromes aiming at better understanding its relying mechanisms of action in the intestinal mucosa.
在过去几年中,嗜酸性粒细胞在几种相关病症中发挥主要病理生理作用这一认识,促使了旨在使免疫反应正常化、减轻慢性炎症并预防组织损伤的生物靶向治疗的发展。为了更好地说明在这种情况下不同嗜酸性粒细胞免疫功能障碍与生物治疗效果之间的潜在关系,在此,我们介绍一例63岁男性病例,该患者于2018年首次转诊至我科,诊断为哮喘、息肉病和鼻窦炎,疑似非甾体抗炎药过敏。他既往还有嗜酸性胃肠炎/十二指肠炎症病史(嗜酸性粒细胞计数>50个/高倍视野HPF)。使用多疗程皮质类固醇治疗未能完全控制这些病症。2019年10月,在开始使用贝那利珠单抗(一种针对IL-5细胞因子受体α链的抗体)作为重度嗜酸性粒细胞性哮喘的附加治疗后,据报告呼吸(无哮喘发作)和胃肠道系统(嗜酸性粒细胞计数为0个/HPF)均有重要临床改善。患者的生活质量也有所提高。自2020年6月以来,全身皮质类固醇治疗减少,而胃肠道症状或嗜酸性粒细胞炎症并未恶化。该病例警示了早期识别和适当个体化治疗嗜酸性粒细胞免疫功能障碍的重要性,并建议针对贝那利珠单抗在胃肠道综合征中的应用开展进一步更大规模的研究,以更好地了解其在肠黏膜中的作用机制。