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强化粒细胞和单核细胞吸附性血液成分分离术联合乌帕替尼用于难治性克罗恩病的诱导治疗

Intensive Granulocyte and Monocyte Adsorptive Apheresis Plus Upadacitinib for Induction Treatment of Refractory Crohn's Disease.

作者信息

Tanida Satoshi, Imura Naoto, Sasoh Shun, Kubota Yoshimasa, Ban Tesshin, Ando Tomoaki, Nakamura Makoto, Joh Takashi

机构信息

Education and Research Center for Community Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.

Division of Gastroenterology, Gamagori City Hospital, Gamagori, Aichi 443-8501, Japan.

出版信息

J Clin Med Res. 2025 Apr;17(4):240-246. doi: 10.14740/jocmr6188. Epub 2025 Apr 5.

Abstract

Case 1 involved a 34-year-old woman who had been diagnosed with Crohn's disease (CD) at 30 years old. After deciding to discontinue CD treatment, she was diagnosed with moderate flare-up of CD based on disease activity and endoscopic findings. Inadequate response was seen 7 days after starting oral prednisolone (PSL) at 30 mg/day, so combination therapy was started with intensive granulocyte and monocyte adsorptive apheresis (GMA) plus upadacitinib (UPA) at 45 mg/day. Twelve weeks after starting this combination therapy, clinical remission and endoscopic and histological improvements of the inflamed mucosa were achieved with no adverse events. Case 2 involved a 26-year-old man who had been diagnosed with CD at 13 years old. He was diagnosed with severe flare-up of CD based on disease activity and endoscopic findings due to loss of response to double doses of infliximab (IFX). Combination therapy was started with intensive GMA plus UPA at 45 mg/day. Twelve weeks after starting this therapy, clinical remission and endoscopic and histological improvements of the inflamed mucosa were achieved with no adverse events. The combination of intensive GMA plus UPA appears to have provided an effective therapeutic option for refractory CD in a patient with a 4-year history of CD and refractoriness to systemic corticosteroids, and in another patient with a 13-year history of CD and loss of response to IFX.

摘要

病例1涉及一名34岁女性,她在30岁时被诊断出患有克罗恩病(CD)。在决定停止CD治疗后,根据疾病活动度和内镜检查结果,她被诊断为CD中度发作。开始口服泼尼松龙(PSL)30毫克/天7天后,疗效不佳,因此开始联合强化粒细胞和单核细胞吸附性血浆置换术(GMA)加乌帕替尼(UPA)45毫克/天进行治疗。开始这种联合治疗12周后,实现了临床缓解,炎症黏膜的内镜和组织学改善,且无不良事件发生。病例2涉及一名26岁男性,他在13岁时被诊断出患有CD。由于对双倍剂量英夫利昔单抗(IFX)失去反应,根据疾病活动度和内镜检查结果,他被诊断为CD重度发作。开始联合强化GMA加UPA 45毫克/天进行治疗。开始该治疗12周后,实现了临床缓解,炎症黏膜的内镜和组织学改善,且无不良事件发生。强化GMA加UPA的联合治疗似乎为一名有4年CD病史且对全身皮质类固醇难治的患者以及另一名有13年CD病史且对IFX失去反应的患者的难治性CD提供了一种有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/136f/12045780/b86e30a71918/jocmr-17-04-240-g001.jpg

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