炎症性肠病患者抗细胞因子治疗的原发性和继发性耐药发生率

L B Lazebnik, V E Sagynbaeva
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引用次数: 0

摘要

长期使用伊利利昔单抗治疗炎症性肠病(IBD)患者的经验表明,20-30%的患者不能达到临床改善(原发性失败)或出现获得性耐药(继发性失败)。英夫利昔单抗产生抗体的频率为28-61%,阿达木单抗产生抗体的频率为4-12%,塞妥珠单抗产生抗体的频率为12.3%,依那西普产生抗体的频率为2.5%。目前克服抗细胞因子治疗原发性和继发性无效的方法是:增加剂量,缩短基因工程生物药物的输注间隔,增加免疫抑制剂,以及切换到另一种生物药物。寻找IBD患者抗细胞因子治疗的原发性和继发性无效目前仍然是热门话题,需要新的方法来解决这一问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE INCIDENCE OF PRIMARY AND SECONDARY RESISTANCE TO THE ANTI-CYTOKINE THERAPY IN PATIENTS WITH INFLAMMATORY BOWEL DISEASE.

Long-term experience of using irifliximab in patients with inflammatory bowel disease (IBD) have shown that 20-30% of patients couldn't achieve clinical improvement (primary failure) or have developed acquired drug resistance (secondary failure). The frequency of antibody formation to infliximab is to 28-61%, for adalimumab 4-12%, to certolizumab the guests to 12.3%, for etanercept to 2.5%. The ways to overcome the primary and secondary inefficiency of anti-cytokine the(apy (loss of response to therapy) at the present time are: increasing the dose, shortening the interval between infusions of genetically engineered biological drugs, additional immunosuppressive agents, as well as switching to another biologic drug. Search of primary and secondary inefficiency of anti-cytokine therapy in patients with IBD currently remains topical and requires new approaches to the solution of this problem.

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