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首页> 外文期刊>Case Reports in Gastroenterology >Combination Therapy with Intensive Granulocyte and Monocyte Adsorptive Apheresis plus Adalimumab: Therapeutic Outcomes in 5 Cases with Refractory Crohn’s Disease
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Combination Therapy with Intensive Granulocyte and Monocyte Adsorptive Apheresis plus Adalimumab: Therapeutic Outcomes in 5 Cases with Refractory Crohn’s Disease

机译:密集粒细胞和单核细胞吸附性疗法联合阿达木单抗联合治疗:难治性克罗恩病5例治疗结果

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摘要

Adalimumab (ADA) is applied to induce remission in patients with Crohn’s disease (CD) na?ve to chimeric anti-tumor necrosis factor-α (anti-TNF-α), infliximab or patients with loss of response to scheduled maintenance infliximab. Adsorptive granulocyte and monocyte apheresis (GMA) depletes elevated/activated myeloid lineage leucocytes as sources of inflammatory cytokines and has been used to treat patients with CD. This study was to investigate the efficacy of intensive GMA in combination with ADA as remission induction therapy in cases of CD refractory to medications including anti-TNF-α therapies. Between December 2010 and February 2012, 5 consecutive cases with refractory CD were treated with intensive GMA (2 sessions per week) plus ADA to induce remission. CD activity index (CDAI), C-reactive protein (CRP), and endoscopic findings based on the simple endoscopic score for CD (SES-CD) at baseline and 10 weeks post 5 ADA injections were applied to determine treatment efficacy outcomes. At week 10 post ADA treatment, clinical remission together with normal CRP levels were achieved in all 5 cases, while SES-CD scores reflected marked improvement in 3 cases and partial improvement in 2 cases who had extensive deep longitudinal CD lesions. The CDAI and CRP values at baseline were 324 ± 118 and 4.9 ± 3.3 mg/dl, respectively. The corresponding values after treatment were 100 ± 28 (p = 0.024) and 0.2 ± 0.2 mg/dl (p = 0.038). In these 5 cases with medication-refractory CD, combination therapy with intensive GMA followed by 5 ADA shots appeared to be an effective and safe intervention for inducing clinical remission.
机译:阿达木单抗(ADA)用于诱导初治克罗恩病(CD)的患者抗嵌合抗肿瘤坏死因子-α(anti-TNF-α),英夫利昔单抗或对计划维持的英夫利昔单抗无反应的患者缓解。吸附性粒细胞和单核细胞单采(GMA)消耗升高/激活的髓系谱系白细胞作为炎症细胞因子的来源,已被用于治疗CD患者。这项研究旨在探讨强化GMA联合ADA在诱导CD抗药性(包括抗TNF-α疗法)难治性病例中的疗效。在2010年12月至2012年2月之间,连续5例难治性CD患者接受了强化GMA(每周2次治疗)和ADA治疗,以诱导缓解。在基线和5次ADA注射后10周,基于CD的简单内窥镜评分(SES-CD)的CD活性指数(CDAI),C反应蛋白(CRP)和内窥镜检查结果被用来确定治疗效果。 ADA治疗后第10周,所有5例患者均达到临床缓解和CRP水平正常,而SES-CD评分反映3例患者明显改善,2例广泛的深部纵向CD病变患者部分改善。基线时的CDAI和CRP值分别为324±118和4.9±3.3 mg / dl。处理后的相应值为100±28(p = 0.024)和0.2±0.2 mg / dl(p = 0.038)。在这5例药物难治性CD患者中,加用GMA加5次ADA针的联合治疗似乎是诱导临床缓解的有效且安全的干预措施。

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