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乌帕替尼治疗对白细胞介素-6和白细胞介素-17抑制难治的巨细胞动脉炎

Giant Cell Arteritis Refractory to Interleukin-6 and Interleukin-17 Inhibition Treated With Upadacitinib.

作者信息

Vest Luke S, Ahmad Anam, Valasareddy Sanhitha, Phillips Nancy, Kilian Adam

机构信息

Brigham and Women's Hospital, Boston, Massachusetts.

Saint Louis University School of Medicine, St Louis, Missouri.

出版信息

ACR Open Rheumatol. 2025 Aug;7(8):e70094. doi: 10.1002/acr2.70094.

Abstract

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.

摘要

巨细胞动脉炎(GCA)是一种可累及颅内和颅外血管的肉芽肿性血管炎。尽管白细胞介素-6(IL-6)受体阻断是一种既定的治疗方法,但对于药物难治性疾病的治疗选择仍然有限。我们报告了一例独特的颅外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)和司库奇尤单抗(IL-17A抑制剂)均难治,但对选择性JAK1抑制剂乌帕替尼有显著反应。据我们所知,这是第一例报道的GCA病例,显示对IL-6和IL-17抑制均耐药,但通过JAK抑制实现了临床和影像学缓解,突出了乌帕替尼作为GCA患者治疗方法的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/779d/12305451/702345621395/ACR2-7-e70094-g001.jpg

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