Nantes Université, Centre Hospitalier Universitaire (CHU) Nantes, Institut des Maladies de l'Appareil Digestif (IMAD), Hépato-Gastro-Entérologie et Assistance Nutritionnelle, Institut national de la santé et de la recherche médicale (Inserm) CIC 1413, Nantes, France.
Nantes Université, Centre Hospitalier Universitaire (CHU) Nantes, Laboratoire d'Immunologie Biologique, Centre d'ImmunoMonitorage Nantes-Atlantique (CIMNA), Nantes, France.
Front Immunol. 2023 Aug 28;14:1243898. doi: 10.3389/fimmu.2023.1243898. eCollection 2023.
Patients with inflammatory bowel disease (IBD) may have a modified immune response to SARS-CoV-2. The objectives were to evaluate the prevalence of COVID-19 in patients treated with infliximab or vedolizumab, to analyze the factors associated with the infection, the impact of treatments and trough levels.
Patients with IBD treated with intravenous biologics in 14 French centers were included between March and June 2020 and followed-up for 6 months. Blood samples were collected for serologies and trough levels. The analysis of factors associated with COVID-19 was conducted in a matched 1:1 case-control sub-study with positive patients.
In total, 1026 patients were included (74.9% infliximab). Over the follow-up period, 420 patients reported the occurrence of COVID-19 symptoms; 342 had been tested of whom 18 were positive. At the end of follow-up, 38 patients had a positive serology. Considering both nasal tests and serologies together, 46 patients (4.5%) had been infected. The risk of COVID-19 was related neither to the use of treatments (whatever the trough levels) nor to disease activity. Infections were more frequent when using public transport or living in flats in urban areas.
The prevalence rate of COVID-19 in this IBD population treated with intravenous infliximab or vedolizumab was the same as the one in the French population before the start of the vaccination campaign. The risk was increased by urban living and was not influenced by disease activity or biologics. Sanitary barrier measures remain the best way to protect against SARS-CoV-2 in patients with IBD in biological therapy.
炎症性肠病(IBD)患者可能对 SARS-CoV-2 产生改变的免疫反应。目的是评估英夫利昔单抗或维得利珠单抗治疗的患者中 COVID-19 的患病率,分析感染的相关因素、治疗和药物谷浓度的影响。
2020 年 3 月至 6 月期间,14 家法国中心纳入接受静脉用生物制剂治疗的 IBD 患者,并进行 6 个月的随访。采集血样进行血清学和药物谷浓度检测。对阳性患者进行了匹配的 1:1 病例对照亚研究,以分析与 COVID-19 相关的因素。
共纳入 1026 例患者(74.9%为英夫利昔单抗)。随访期间,420 例患者报告出现 COVID-19 症状;342 例接受了检测,其中 18 例阳性。随访结束时,38 例患者血清学阳性。同时考虑鼻拭子和血清学结果,46 例(4.5%)患者感染。COVID-19 的风险与治疗(无论药物谷浓度如何)或疾病活动度无关。使用公共交通工具或居住在市区公寓时感染更频繁。
在接受静脉用英夫利昔单抗或维得利珠单抗治疗的 IBD 人群中,COVID-19 的患病率与疫苗接种前法国人群的患病率相同。城市居住会增加风险,且不受疾病活动度或生物制剂的影响。卫生防护措施仍是生物治疗中 IBD 患者预防 SARS-CoV-2 的最佳方法。