白细胞介素-6和白细胞介素-17抑制难治性巨细胞动脉炎。

IF 2.8 Q2 RHEUMATOLOGY
Luke S Vest, Anam Ahmad, Sanhitha Valasareddy, Nancy Phillips, Adam Kilian
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引用次数: 0

摘要

巨细胞动脉炎(GCA)是一种肉芽肿性血管炎,可累及颅内和颅外血管。虽然白细胞介素-6 (IL-6)受体阻断是一种既定的治疗方法,但对于医学上难治性疾病的治疗选择仍然有限。我们报告了一个独特的颅外GCA病例,该病例对糖皮质激素、硫唑嘌呤、托珠单抗(IL-6抑制剂)和secukinumab (IL-17A抑制剂)难治,但对选择性JAK1抑制剂upadacitinib有强烈反应。据我们所知,这是首次报道的GCA对IL-6和IL-17抑制均有耐药性,但对JAK抑制有临床和影像学缓解的病例,突出了upadacitinib作为GCA患者治疗的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant Cell Arteritis Refractory to Interleukin-6 and Interleukin-17 Inhibition Treated With Upadacitinib.

Giant cell arteritis (GCA) is a granulomatous vasculitis that can involve both cranial and extracranial vessels. Although interleukin-6 (IL-6) receptor blockade is an established therapy, treatment options for medically refractory disease remain limited. We report a unique case of extracranial GCA refractory to glucocorticoids, azathioprine, tocilizumab (IL-6 inhibitor), and secukinumab (IL-17A inhibitor) that responded robustly to upadacitinib, a selective JAK1 inhibitor. To our knowledge, this is the first reported case of GCA demonstrating resistance to both IL-6 and IL-17 inhibition but clinical and imaging remission with JAK inhibition, highlighting the role of upadacitinib as a therapy for patients with GCA.

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CiteScore
5.80
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