Reversal of Alopecia Areata Following Treatment With the JAK1/2 Inhibitor Baricitinib

被引:197
作者
Jabbari, Ali [1 ]
Dai, Zhenpeng [1 ]
Xing, Luzhou [2 ]
Cerise, Jane E. [1 ]
Ramot, Yuval [3 ]
Berkun, Yackov [4 ]
Sanchez, Gina A. Montealegre [5 ]
Goldbach-Mansky, Raphaela [5 ]
Christiano, Angela M. [1 ,6 ]
Clynes, Raphael [1 ,2 ,7 ]
Zlotogorski, Abraham [3 ]
机构
[1] Columbia Univ, Dept Dermatol, New York, NY 10032 USA
[2] Columbia Univ, Dept Pathol, New York, NY 10032 USA
[3] Hadassah Hebrew Univ, Med Ctr, Dept Dermatol, Jerusalem, Israel
[4] Hadassah Hebrew Univ, Med Ctr, Dept Pediat, Jerusalem, Israel
[5] NIAMS, Translat Autoinflammatory Dis Sect, NIH, Bethesda, MD USA
[6] Columbia Univ, Dept Genet & Dev, New York, NY USA
[7] Columbia Univ, Dept Med, New York, NY 10032 USA
关键词
Alopecia areata; Interferon gamma; JAK inhibitor; CANDLE syndrome; Autoimmune disease; Baricitinib; Gene expression profiling; Autoinflammatory; ATYPICAL NEUTROPHILIC DERMATOSIS; PROTEASOME SUBUNIT; PLAQUE PSORIASIS; LIPODYSTROPHY; TOFACITINIB; UNIVERSALIS; EFFICACY; PATIENT; SAFETY; TRIAL;
D O I
10.1016/j.ebiom.2015.02.015
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: Alopecia areata (AA) is an autoimmune disease resulting in hair loss with devastating psychosocial consequences. Despite its high prevalence, there are no FDA-approved treatments for AA. Prior studies have identified a prominent interferon signature in AA, which signals through JAK molecules. Methods: A patient with AA was enrolled in a clinical trial to examine the efficacy of baricitinib, a JAK1/2 inhibitor, to treat concomitant CANDLE syndrome. In vivo, preclinical studieswere conducted using the C3H/HeJ AA mouse model to assess the mechanism of clinical improvement by baricitinib. Findings: The patient exhibited a striking improvement of his AA on baricitinib over several months. In vivo studies using the C3H/HeJ mouse model demonstrated a strong correlation between resolution of the interferon signature and clinical improvement during baricitinib treatment. Interpretation: Baricitinib may be an effective treatment for AA and warrants further investigation in clinical trials. (C) 2015 The Authors. Published by Elsevier B.V.
引用
收藏
页码:351 / 355
页数:5
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