Favorable Response to Adjuvant Tofacitinib in a Case of Anti-Melanoma Differentiation-Associated Gene-5 Antibody Positive Clinically Amyopathic Dermatomyositis.

IF 1.9 Q3 DERMATOLOGY
Indian Dermatology Online Journal Pub Date : 2024-04-23 eCollection Date: 2024-09-01 DOI:10.4103/idoj.idoj_399_23
Nayankumar H Patel, Jigna K Padhiyar, Jahnvi R Patel, Keval V Pandya
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引用次数: 0

Abstract

Anti-melanoma differentiation-associated gene-5 antibody (anti-MDA-5 Ab) associated with clinically amyopathic dermatomyositis (CADM) is characterized by vasculopathic ulcers, mechanic's hands, and progressive interstitial lung disease (ILD). We present a case of 38-year-old female who presented with all these classical clinical features. Her investigations revealed normal serum muscle enzyme levels and the presence of anti-Mi2 and anti-MDA-5 antibodies by immunoblot. Imaging study revealed changes suggestive of ILD. She was treated with rituximab along with oral glucocorticoid and other supportive treatment to which she didn't respond adequately. Recently, it has been postulated that plasmacytoid dendritic cells produce interferon which is responsible for tissue injury in dermatomyositis (DM). Tofacitinib, by inhibiting JAK-STAT pathway, inhibits downstream cytokines, mainly type 1 interferon. So, we added tofacitinib as adjuvant therapy in our patient. Post-six months of commencement of adjuvant tofacitinib, patient experienced remarkable improvement in cutaneous features as well as in pulmonary fibrosis.

一例抗黑素瘤分化相关基因-5抗体阳性的临床肌病性皮肌炎患者对托法替尼辅助治疗的良好反应
抗黑色素瘤分化相关基因-5 抗体(anti-MDA-5 Ab)与临床淀粉样变性皮肌炎(CADM)相关,表现为血管病变性溃疡、机械手和进行性间质性肺病(ILD)。我们接诊了一例 38 岁的女性患者,她具有所有这些典型的临床特征。她的检查结果显示血清肌酶水平正常,免疫印迹显示存在抗 Mi2 和抗 MDA-5 抗体。影像学检查发现了提示 ILD 的变化。她接受了利妥昔单抗治疗以及口服糖皮质激素和其他支持治疗,但效果不佳。最近,有人推测浆细胞树突状细胞产生的干扰素是皮肌炎(DM)组织损伤的原因。托法替尼通过抑制JAK-STAT通路,抑制下游细胞因子,主要是1型干扰素。因此,我们在患者身上添加了托法替尼作为辅助治疗。开始使用托法替尼辅助治疗6个月后,患者的皮肤特征和肺纤维化均有显著改善。
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来源期刊
CiteScore
2.00
自引率
11.80%
发文量
201
审稿时长
49 weeks
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