CVID Enteropathy Is Difficult To Treat and Shows a Heterogeneous Histopathology.

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Noah M Juliana, Mirjam Severs, Jan Willem Marsden, Joris M van Montfrans, Pauline M Ellerbroek, Miangela M Lacle, Virgil A S H Dalm, Amir Abelmoumen, Helen L Leavis
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Abstract

Purpose: Enteropathy is a non-infectious complication in Common Variable Immune Deficiency (CVID) associated with increased morbidity and mortality. We characterized this group of CVID enteropathy (CVID-E) patients and investigated the effectiveness of immunosuppressive treatments on its clinical course.

Method: We identified patients with CVID-E in two academic teaching hospitals and obtained informed consents. Using electronic patient health care records, we retrospectively collected clinical information in the national Primary immunodeficiency disorder database until 01-2023.

Results: We included 39 patients with CVID-E. Bronchiectasis (69.2%) and lymphoproliferation (46.1%) were the most frequent co-occurring symptoms. The most common endoscopy findings concerned inflammation (72.2%) and erythema (69.4%); The most prevalent histopathologic findings were IBD-like inflammation (55.6%), indiscriminate chronic inflammation (47.2%) and indiscriminate active inflammation (38.9%). We assessed 88 events of treatment response in the 25 treated patients. Overall treatment response was poor, however there were 31 events of remission observed, ranging from partial to sustained remission. Of these 26 were the result of tumor necrosis factor inhibitors (TNFi) or thiopurines, either as monotherapy or in combination with other immunosuppressive treatment. 10 patients achieved complete remission.

Conclusion: In this study, we describe a cohort of CVID-E patients including related comorbidity, clinical course and response to therapy. CVID-E patients frequently develop other, sometimes severe comorbidities. Our study confirms the alleged heterogeneity regarding endoscopic and histopathological findings, and in one third of patients even multiple distinct abnormalities co-occurred in the same biopsy. We found azathioprine and/or TNFi to be the most effective current treatment.

CVID肠病难以治疗,并表现出异质性的组织病理学。
目的:肠病是常见可变免疫缺陷(CVID)的一种非感染性并发症,与发病率和死亡率增高相关。我们对这组CVID肠病(CVID- e)患者进行了特征描述,并研究了免疫抑制治疗对其临床病程的有效性。方法:选取两所专科教学医院的CVID-E患者并取得知情同意。使用电子患者医疗记录,我们回顾性地收集了国家原发性免疫缺陷疾病数据库中直到01-2023年的临床信息。结果:纳入39例CVID-E患者。支气管扩张(69.2%)和淋巴细胞增生(46.1%)是最常见的合并症状。最常见的内窥镜检查结果涉及炎症(72.2%)和红斑(69.4%);最常见的组织病理学表现为ibd样炎症(55.6%)、不加区分的慢性炎症(47.2%)和不加区分的活动性炎症(38.9%)。我们评估了25名接受治疗的患者的88个治疗反应事件。总体治疗反应较差,但观察到31个缓解事件,从部分缓解到持续缓解。其中26例是肿瘤坏死因子抑制剂(TNFi)或硫嘌呤单独治疗或与其他免疫抑制治疗联合治疗的结果。10例患者完全缓解。结论:在本研究中,我们描述了一组CVID-E患者,包括相关合并症、临床病程和对治疗的反应。covid - e患者经常出现其他,有时是严重的合并症。我们的研究证实了所谓的内窥镜和组织病理学结果的异质性,在三分之一的患者中,甚至在同一活检中同时发生多种明显的异常。我们发现硫唑嘌呤和/或TNFi是目前最有效的治疗方法。
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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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