Department of Dermatology, Southwest Hospital, Army Medical University, Chongqing, China.
Front Immunol. 2024 Oct 21;15:1464474. doi: 10.3389/fimmu.2024.1464474. eCollection 2024.
Bullous pemphigoid (BP) is a rare, life-threatening autoimmune blistering disease with pruritus and tension blisters/bullous as the main clinical manifestations. Glucocorticosteroids are the main therapeutic agents for it, but their efficacy is poor in some patients. Tofacitinib, a small molecule agent that inhibits JAK1/3, has shown incredible efficacy in a wide range of autoimmune diseases and maybe a new valuable treatment option for refractory BP.
To report a case of refractory BP successfully treated with tofacitinib, then explore the underlying mechanism behind the treatment, and finally review similarities to other cases reported in the literature.
Case report and literature review of published cases of successful BP treatment with JAK inhibitors. The case report describes a 73-year-old male with refractory BP that was successfully managed with the combination therapy of tofacitinib and low-dose glucocorticoids for 28 weeks. Immunohistochemistry and RNA sequencing were performed to analyze the underlying mechanism of tofacitinib therapy. A systematic literature search was conducted to identify other cases of treatment with JAK inhibitors.
Throughout the 28-week treatment period, the patient experienced clinical, autoantibody and histologic resolution. Immunohistochemical analysis showed tofacitinib significantly decreased the pSTAT3 and pSTAT6 levels in the skin lesions of this patient. RNA sequencing and immunohistochemical testing of lesion samples from other BP patients identified activation of the JAK-STAT signaling pathway. Literature review revealed 17 previously reported cases of BP treated with four kinds of JAK inhibitors successfully, including tofacitinib (10), baricitinib (1), upadacitinib (3) and abrocitinib (3).
Our findings support the potential of tofacitinib as a safe and effective treatment option for BP. Larger studies are underway to better understand this efficacy and safety.
大疱性类天疱疮(BP)是一种罕见的、危及生命的自身免疫性水疱病,以瘙痒和紧张性水疱/大疱为主要临床表现。糖皮质激素是其主要治疗药物,但在某些患者中疗效不佳。托法替尼是一种抑制 JAK1/3 的小分子药物,在广泛的自身免疫性疾病中显示出令人难以置信的疗效,也许是治疗难治性 BP 的一种新的有价值的治疗选择。
报告 1 例用托法替尼成功治疗的难治性 BP 病例,探讨其治疗的潜在机制,并与文献中报道的其他病例进行比较。
病例报告和已发表的 JAK 抑制剂成功治疗 BP 病例的文献复习。该病例报告描述了 1 例 73 岁男性难治性 BP,用托法替尼联合小剂量糖皮质激素治疗 28 周后成功控制。进行免疫组织化学和 RNA 测序分析以探讨托法替尼治疗的潜在机制。对 JAK 抑制剂治疗的其他病例进行了系统的文献检索。
在 28 周的治疗期间,患者的临床、自身抗体和组织学均得到缓解。免疫组织化学分析显示,托法替尼显著降低了该患者皮肤病变中的 pSTAT3 和 pSTAT6 水平。对其他 BP 患者病变样本的 RNA 测序和免疫组化检测显示 JAK-STAT 信号通路的激活。文献复习共发现 17 例以前用 4 种 JAK 抑制剂成功治疗 BP 的病例报告,包括托法替尼(10 例)、巴瑞替尼(1 例)、乌帕替尼(3 例)和阿布昔替尼(3 例)。
我们的研究结果支持托法替尼作为 BP 安全有效的治疗选择的潜力。正在进行更大规模的研究以更好地了解其疗效和安全性。