Tofacitinib Treatment and Molecular Analysis of Cutaneous Sarcoidosis

被引:124
|
作者
Damsky, William [1 ,2 ]
Thakral, Durga [1 ]
Emeagwali, Nkiruka [4 ]
Galan, Anjela [1 ,3 ]
King, Brett [1 ]
机构
[1] Yale Sch Med, Dept Dermatol, 333 Cedar St,LCI 501,POB 208059, New Haven, CT 06520 USA
[2] Yale Sch Med, Dept Immunobiol, New Haven, CT USA
[3] Yale Sch Med, Dept Pathol, New Haven, CT USA
[4] Yale Sch Med, Dept Internal Med, Sect Pulm Crit Care & Sleep Med, New Haven, CT USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2018年 / 379卷 / 26期
基金
美国国家卫生研究院;
关键词
ALVEOLAR MACROPHAGES; GRANULOMA-FORMATION; HELPER;
D O I
10.1056/NEJMoa1805958
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is evidence that Janus kinase (JAK)-signal transducer and activator of transcription (STAT) signaling plays a role in the pathogenesis of sarcoidosis. We treated a patient with cutaneous sarcoidosis with the JAK inhibitor tofacitinib; the patient had not previously had a response to medications and had not received systemic glucocorticoids. This treatment resulted in clinical and histologic remission of her skin disease. Sequencing of RNA and immunohistochemical examination of skin-lesion samples obtained from the patient before and during therapy and immunohistochemical testing of lesion samples obtained from other patients with cutaneous sarcoidosis support a role for JAK-STAT signaling in cutaneous sarcoidosis.
引用
收藏
页码:2540 / 2546
页数:7
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