接受抗 CD20 疗法的中枢神经系统炎症性脱髓鞘疾病患者感染 COVID-19 引起的继发性组织化肺炎。

IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY
René Carvajal, Breogán Rodríguez-Acevedo, Lorena García-Vasco, Ana Zabalza, Helena Ariño, Luca Bollo, Noemí Cabello-Clotet, Joaquín Castilló, Álvaro Cobo-Calvo, Manuel Comabella, Anna Falcó-Roget, Ingrid Galán, Alexis García-Sarreón, Irene Gómez-Estévez, Galo Granados, Delon La Puma, Gloria Mato Chain, Luciana Midaglia, Asunción Nieto-García, Susana Otero-Romero, Agustín Pappolla, Marta Rodriguez, Irene Sansano, Jordi Río, Paula Tagliani, Carmen Tur, Ángela Vidal-Jordana, Andreu Vilaseca, Ana Villar, Jaume Sastre-Garriga, Celia Oreja-Guevara, Mar Tintoré, Xavier Montalban, Georgina Arrambide
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引用次数: 0

摘要

背景:组织性肺炎(OP)是一种间质性肺部疾病,在接受抗CD20治疗的炎症性脱髓鞘疾病(IDDs)患者中已经观察到,尤其是在COVID-19治疗后,但数据有限。目的:详细描述接受抗CD20治疗的IDD患者中COVID-19相关OP的特征:方法:双中心回顾性队列研究,纳入2020年3月至2023年10月期间接受抗CD20治疗并被诊断为COVID-19相关OP的多发性硬化症(MS)、水光素-4阳性神经脊髓炎视神经谱系障碍(AQP4 + NMOSD)和髓鞘少突胶质细胞糖蛋白抗体病(MOGAD)患者:共纳入19名患者(平均年龄46.8岁;52.6%为女性;63%为利妥昔单抗,37%为奥克立珠单抗)。其中 16 人患有多发性硬化症,2 人患有 MOGAD,1 人患有 AQP4 + NMOSD。间歇性发热是主要症状。除一名患者外,其他患者均住院治疗,但无死亡病例。胸部 CT 一致显示 OP 模式。13 名患者的支气管肺泡灌洗液中严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)PCR 呈阳性。治疗方法包括皮质类固醇、抗病毒药物、单克隆抗体和康复血浆。14 名患者推迟了输液时间;9 名患者在康复后恢复了输液(中位 11.9 个月),2 名患者因低丙种球蛋白血症而更换了输液,3 名患者停止了输液。在平均 1.5 年的随访后,18 名患者的肺部异常和临床表现得到缓解;但 13 名患者出现了长期 COVID:结论:抗CD20治疗后反复发热且CT特征明显的患者,应考虑与COVID-19相关的OP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Secondary organising pneumonia associated to COVID-19 infection in patients with central nervous system inflammatory demyelinating diseases treated with anti-CD20 therapies.

Background: Organizing pneumonia (OP), an interstitial lung disease, has been observed in patients with inflammatory demyelinating diseases (IDDs) treated with anti-CD20, particularly after COVID-19, but data are limited.

Aim: To provide a detailed characterization of COVID-19-associated OP in IDD patients treated with anti-CD20.

Methods: Bi-centric retrospective cohort study including patients with multiple sclerosis (MS), aquaporin-4-positive neuromyelitis optica spectrum disorder (AQP4 + NMOSD), and myelin oligodendrocyte glycoprotein antibody disease (MOGAD) who received anti-CD20 and were diagnosed with COVID-19-associated OP between March 2020 and October 2023.

Results: Nineteen patients were included (mean age 46.8 years; 52.6% female; 63% rituximab, 37% ocrelizumab). Sixteen had MS, two MOGAD, and one AQP4 + NMOSD. Intermittent fever was the predominant symptom. Hospitalization occurred in all but one patient, without fatalities. Chest CT consistently showed OP patterns. Thirteen patients had positive severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) PCR in bronchoalveolar lavage. Treatments included corticosteroids, antivirals, monoclonal antibodies, and convalescent plasma. Fourteen patients postponed infusions; nine resumed post-recovery (median 11.9 months), two switched due to hypogammaglobulinemia, and three stopped. After a mean follow-up of 1.5 years, lung abnormalities and clinical manifestations resolved in 18 patients; however, 13 experienced long-COVID.

Conclusions: In anti-CD20-treated patients with recurrent fever and distinctive CT features, COVID-19-associated OP should be considered.

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来源期刊
Multiple Sclerosis Journal
Multiple Sclerosis Journal 医学-临床神经学
CiteScore
10.90
自引率
6.90%
发文量
186
审稿时长
3-8 weeks
期刊介绍: Multiple Sclerosis Journal is a peer-reviewed international journal that focuses on all aspects of multiple sclerosis, neuromyelitis optica and other related autoimmune diseases of the central nervous system. The journal for your research in the following areas: * __Biologic basis:__ pathology, myelin biology, pathophysiology of the blood/brain barrier, axo-glial pathobiology, remyelination, virology and microbiome, immunology, proteomics * __Epidemology and genetics:__ genetics epigenetics, epidemiology * __Clinical and Neuroimaging:__ clinical neurology, biomarkers, neuroimaging and clinical outcome measures * __Therapeutics and rehabilitation:__ therapeutics, rehabilitation, psychology, neuroplasticity, neuroprotection, and systematic management Print ISSN: 1352-4585
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