在炎症性肠病中克服抗肿瘤坏死因子药物抗体的策略:病例系列和文献回顾。

Mansi M Kothari, Douglas L Nguyen, Nimisha K Parekh
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引用次数: 17

摘要

抗肿瘤坏死因子(TNF)生物制剂是目前应用最广泛和最有效的治疗炎症性肠病(IBD)的药物之一。英夫利昔单抗和阿达木单抗治疗药物监测的发展已经允许测量药物水平和抗药物抗体。这些信息可以用于操纵药物治疗和预测反应。研究表明,治疗性抗肿瘤坏死因子药物水平与缓解的维持有关,抗药物抗体的产生可预测反应的丧失。然而,研究表明,低水平的药物抗体有时可以通过增加抗肿瘤坏死因子治疗的剂量或添加免疫调节剂来克服。我们描述了在加州大学欧文分校治疗的12例IBD患者的回顾性病例系列,这些患者接受英夫利昔单抗或阿达木单抗治疗,并发现可检测到但低水平的抗药物抗体。这些患者接受药物剂量增加或添加免疫调节剂,随后随访药物水平。12名患者中有8名(75%)表现出抗药物抗体的消退,并注意到疾病活动有所改善。虽然关于克服低水平抗肿瘤坏死因子药物抗体的数据仍然有限,但文献中描述的病例以及我们自己的经验表明,这可能是保留抗肿瘤坏死因子药物使用的可行策略。低水平的抗tnf药物抗体可以通过剂量增加和/或添加免疫调节剂来克服,并且可以允许疾病状态的临床改善。治疗药物监测是指导这一战略的重要工具。
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Strategies for overcoming anti-tumor necrosis factor drug antibodies in inflammatory bowel disease: Case series and review of literature.

Anti-tumor necrosis factor (TNF) biologics are currently amongst the most widely used and efficacious therapies for inflammatory bowel disease (IBD). The development of therapeutic drug monitoring for infliximab and adalimumab has allowed for measurement of drug levels and antidrug antibodies. This information can allow for manipulation of drug therapy and prediction of response. It has been shown that therapeutic anti-TNF drug levels are associated with maintenance of remission, and development of antidrug antibodies is predictive of loss of response. Studies suggest that a low level of drug antibodies, however, can at times be overcome by dose escalation of anti-TNF therapy or addition of an immunomodulator. We describe a retrospective case series of twelve IBD patients treated at the University of California-Irvine, who were on infliximab or adalimumab therapy and were found to have detectable but low-level antidrug antibodies. These patients underwent dose escalation of the drug or addition of an immunomodulator, with subsequent follow-up drug levels obtained. Eight of the twelve patients (75%) demonstrated resolution of antidrug antibodies, and were noted to have improvement in disease activity. Though data regarding overcoming low-level anti-TNF drug antibodies remains somewhat limited, cases described in the literature as well as our own experience suggest that this may be a viable strategy for preserving the use of an anti-TNF drug. Low-level anti-TNF drug antibodies may be overcome by dose escalation and/or addition of an immunomodulator, and can allow for clinical improvement in disease status. Therapeutic drug monitoring is an important tool to guide this strategy.

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