IgA Nephropathy Associated With Infliximab Treatment in Patients With Crohn's Disease: Study of IgA1 and IgA2 Expression in Glomeruli.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-05-01 DOI:10.21873/invivo.13975
Akira Mima, Takahiro Nakamoto, Takamasa Matsuki, Suguru Kido, Yuta Saito, Takaaki Morikawa, Keishi Matsumoto, Hidemasa Gotoda, Shinji Lee
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引用次数: 0

Abstract

Background/aim: It is well known that infliximab is an anti-tumor necrosis factor chimeric factor that is effective in treating inflammatory bowel diseases, such as Crohn's disease. Recently, there have been reports of new onset or flare-ups of immunoglobulin A (IgA) nephropathy during infliximab therapy for Crohn's disease. Inflammatory bowel disease-associated IgA nephropathy has been associated with IgA2; However, its activation by infliximab is still unknown.

Case report: We report our experience with two patients who experienced acute exacerbations of pre-existing abnormal urinalysis and renal dysfunction 1-18 years following infliximab treatment for Crohn's disease. Renal biopsies at the time of renal disease flare-up revealed IgA nephropathy in one patient and mesangial proliferative nephropathy in the other. Immunostaining results showed no clear predominance of intraglomerular expression of IgA2, and the patient diagnosed with IgA nephropathy entered remission with high dose methylprednisolone pulse therapy and oral corticosteroids, without the need for tonsillectomy. In contrast, the patient with mesangial proliferative nephritis had many devastated glomeruli, thus corticosteroids were not administrated, and the patient was followed up.

Conclusion: The clinical course of our patients, along with similar cases reported in the literature, indicates that infliximab therapy for Crohn's disease is linked to a relatively high risk of new-onset IgA nephropathy or disease relapse. This report is notable because it is the first to compare the expression of IgA1 and IgA2 in glomeruli in nephritis associated with infliximab therapy.

克罗恩病患者IgA肾病与英夫利昔单抗治疗相关:肾小球中IgA1和IgA2表达的研究
背景/目的:众所周知,英夫利昔单抗是一种抗肿瘤坏死因子嵌合因子,可有效治疗炎症性肠病,如克罗恩病。最近,有报道称,在英夫利昔单抗治疗克罗恩病期间,免疫球蛋白A (IgA)肾病新发或突然发作。炎性肠病相关IgA肾病与IgA2相关;然而,英夫利昔单抗对其的激活作用尚不清楚。病例报告:我们报告了两例患者的经验,他们在英夫利昔单抗治疗克罗恩病后1-18年出现了先前存在的尿分析异常和肾功能障碍的急性加重。肾病发作时的肾活检显示一名患者为IgA肾病,另一名患者为系膜增生性肾病。免疫染色结果显示肾小球内IgA2的表达没有明显优势,诊断为IgA肾病的患者通过大剂量甲基强的松龙脉冲治疗和口服皮质类固醇进入缓解期,无需扁桃体切除术。而系膜增生性肾炎患者肾小球破坏较多,故未给予糖皮质激素治疗,并对患者进行随访。结论:我们患者的临床病程,以及文献中报道的类似病例,表明英夫利昔单抗治疗克罗恩病与新发IgA肾病或疾病复发的相对较高的风险相关。该报告值得注意,因为它首次比较了英夫利昔单抗治疗相关肾炎患者肾小球中IgA1和IgA2的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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