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评估利特昔替尼治疗斑秃的治疗潜力。

Evaluating the Therapeutic Potential of Ritlecitinib for the Treatment of Alopecia Areata.

机构信息

Department of Dermatology, Weill Cornell Medical College, New York, NY, USA.

Dr. Philip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

Drug Des Devel Ther. 2022 Feb 17;16:363-374. doi: 10.2147/DDDT.S334727. eCollection 2022.

Abstract

Alopecia areata (AA) is an autoimmune condition that causes patchy hair loss, affecting up to 147 million people globally. Currently, there are no treatments approved by US Food and Drug Administration (FDA) specific for AA, and there are few effective therapeutic options for widespread and persistent illness. There is an ongoing need for a treatment that demonstrates a good clinical response with a benefit-risk ratio that is suitable for long-term use, especially for patients with chronic, extensive disease. Several clinical trials and case studies that have assessed Janus kinase inhibitors have had encouraging results. Ritlecitinib, a selective JAK3/TEC kinase inhibitor has been demonstrated to inhibit the action of signaling molecules and immune cells that are responsible for hair loss in people with alopecia areata. Furthermore, several clinical trials are investigating the utility of ritlecitinib in patients with vitiligo, rheumatoid arthritis, Crohn's disease, and ulcerative colitis. Advantages of using ritlecitinib when compared with other non-selective JAK inhibitors include avoiding JAK1/JAK2 inhibition's clinical repercussions, which include pharmacodynamic effects such as increased cholesterol and liver enzymes, and those related to JAK2 inhibition (thrombocytopenia, anemia). Treatment with Ritlecitinib 50 mg and 30 mg daily for 24 weeks has been shown to induce hair regrowth with a significant proportion of patients reaching SALT 20 (≤20% scalp hair loss) after six months of therapy compared to placebo. Additional research is needed for long-term effects.

摘要

斑秃(AA)是一种自身免疫性疾病,会导致斑块状脱发,影响全球多达 1.47 亿人。目前,美国食品和药物管理局(FDA)尚未批准任何专门用于 AA 的治疗方法,对于广泛和持续的疾病,有效的治疗选择很少。人们一直需要一种治疗方法,该方法具有良好的临床反应,且获益风险比适合长期使用,尤其是对于患有慢性、广泛疾病的患者。几项评估 Janus 激酶抑制剂的临床试验和案例研究取得了令人鼓舞的结果。选择性 JAK3/TEC 激酶抑制剂 ritlecitinib 已被证明可抑制信号分子和免疫细胞的作用,这些分子和免疫细胞负责导致斑秃患者脱发。此外,几项临床试验正在研究 ritlecitinib 在白癜风、类风湿性关节炎、克罗恩病和溃疡性结肠炎患者中的应用。与其他非选择性 JAK 抑制剂相比,使用 ritlecitinib 的优势包括避免 JAK1/JAK2 抑制的临床影响,包括药效学影响,如胆固醇和肝酶升高,以及与 JAK2 抑制相关的影响(血小板减少症、贫血症)。在 24 周的时间里,每天使用 Ritlecitinib 50mg 和 30mg 治疗 24 周,与安慰剂相比,在治疗六个月后,有相当比例的患者达到 SALT 20(≤20%头皮脱发),从而诱导头发生长。需要进一步研究长期影响。

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