中华皮肤科杂志 ›› 2019, Vol. 52 ›› Issue (5): 343-346.doi: 10.3760/cma.j.issn.0412-4030.2019.05.014
余丽娟,吕中法
收稿日期:
2018-04-20
修回日期:
2018-12-25
出版日期:
2019-05-15
发布日期:
2019-04-30
通讯作者:
吕中法
E-mail:lzfskin@zju.edu.cn
基金资助:
Yu Lijuan, Lyu Zhongfa
Received:
2018-04-20
Revised:
2018-12-25
Online:
2019-05-15
Published:
2019-04-30
Contact:
Lyu Zhongfa
E-mail:lzfskin@zju.edu.cn
Supported by:
摘要: 【摘要】 斑秃是一种突然发生的局限性脱发,严重者可进展为全秃或普秃。目前认为斑秃是一种具有遗传背景的器官特异性自身免疫性疾病,毛囊免疫赦免结构的破坏是重要的发病机制。目前,斑秃的治疗方法有口服、外用、肌内或局部皮损内注射糖皮质激素、外用米诺地尔酊等,但仍有一部分患者治疗无效。近年来,国外开展了很多有关JAK抑制剂治疗斑秃的临床试验。研究显示,在采用口服JAK抑制剂治疗的患者中,约半数中重度斑秃患者在治疗后毛发几乎完全长出,疗效较明显。也有报道外用鲁索替尼治疗斑秃,但疗效不一。尽管部分患者在停药后复发或是在治疗过程中出现感染等不良反应,JAK抑制剂确实为有效治疗中重度斑秃提供了一种选择。
余丽娟 吕中法. JAK抑制剂治疗斑秃的研究进展[J]. 中华皮肤科杂志, 2019, 52(5): 343-346.
Yu Lijuan, Lyu Zhongfa. JAK inhibitors for the treatment of alopecia areata[J]. Chinese Journal of Dermatology, 2019, 52(5): 343-346.
[1] | Villasante FAC, Miteva M. Epidemiology and burden of alopecia areata: a systematic review[J]. Clin Cosmet Investig Dermatol, 2015,8:397⁃403. doi: 10.2147/CCID.S53985. |
[2] | Mitra D, Agarwal R, Chopra A, et al. Rare presentation of alopecia universalis congenita and twenty⁃nail dystrophy in siblings[J]. Int J Trichology, 2017,9(2):63⁃66. doi: 10.4103/ijt.ijt_48_17. |
[3] | Petukhova L, Duvic M, Hordinsky M, et al. Genome⁃wide association study in alopecia areata implicates both innate and adaptive immunity[J]. Nature, 2010,466(7302):113⁃117. doi: 10.1038/nature09114. |
[4] | Price VH, Colombe BW. Heritable factors distinguish two types of alopecia areata[J]. Dermatol Clin, 1996,14(4):679⁃689. |
[5] | Betz RC, Petukhova L, Ripke S, et al. Genome⁃wide meta⁃analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci[J]. Nat Commun, 2015,6:5966. doi: 10.1038/ncomms6966. |
[6] | Billingham RE, Silvers WK. A biologist′s reflections on dermatology[J]. J Invest Dermatol, 1971,57(4):227⁃240. |
[7] | Westgate GE, Craggs RI, Gibson WT. Immune privilege in hair growth[J]. J Invest Dermatol, 1991,97(3):417⁃420. |
[8] | Kinori M, Bertolini M, Funk W, et al. Calcitonin gene⁃related peptide (CGRP) may award relative protection from interferon⁃γ⁃induced collapse of human hair follicle immune privilege[J].Exp Dermatol, 2012,21(3):223⁃226. doi: 10.1111/j.1600⁃0625. 2011.01432.x. |
[9] | Arita T, Nomiyama T, Asai J, et al. Successful treatment of refractory alopecia universalis by persuading a patient not to sleep with her dog[J]. Allergol Int, 2018,67(1):156⁃157. doi: 10.1016/j.alit.2017.06.011. |
[10] | Tsai TY, Huang YC. Vitamin D deficiency in patients with alopecia areata: a systematic review and meta⁃analysis[J]. J Am Acad Dermatol, 2018,78(1):207⁃209. doi: 10.1016/j.jaad.2017. 07.051. |
[11] | Gupta AK, Carviel JL, Abramovits W. Efficacy of tofacitinib in treatment of alopecia universalis in two patients[J]. J Eur Acad Dermatol Venereol, 2016,30(8):1373⁃1378. doi: 10.1111/jdv. 13598. |
[12] | Harel S, Higgins CA, Cerise JE, et al. Pharmacologic inhibition of JAK⁃STAT signaling promotes hair growth[J]. Sci Adv, 2015,1(9):e1500973. doi: 10.1126/sciadv.1500973. |
[13] | Craiglow BG, King BA. Killing two birds with one stone: oral tofacitinib reverses alopecia universalis in a patient with plaque psoriasis[J]. J Invest Dermatol, 2014,134(12):2988⁃2990. doi: 10.1038/jid.2014.260. |
[14] | Xing L, Dai Z, Jabbari A, et al. Alopecia areata is driven by cytotoxic T lymphocytes and is reversed by JAK inhibition[J]. Nat Med, 2014,20(9):1043⁃1049. doi: 10.1038/nm.3645. |
[15] | Craiglow BG, Tavares D, King BA. Topical ruxolitinib for the treatment of alopecia universalis[J]. JAMA Dermatol, 2016,152(4):490⁃491. doi: 10.1001/jamadermatol.2015.4445. |
[16] | Deeb M, Beach RA. A case of topical ruxolitinib treatment failure in alopecia areata[J]. J Cutan Med Surg, 2017,21(6):562⁃563. doi: 10.1177/1203475417716363. |
[17] | Mrowietz U, Gerdes S, Gläser R, et al. Successful treatment of refractory alopecia areata universalis and psoriatic arthritis, but not of plaque psoriasis with tofacitinib in a young woman[J]. Acta Derm Venereol, 2017,97(2):283⁃284. doi: 10.2340/00015555⁃2491. |
[18] | Craiglow BG, Liu LY, King BA. Tofacitinib for the treatment of alopecia areata and variants in adolescents[J]. J Am Acad Dermatol, 2017,76(1):29⁃32. doi: 10.1016/j.jaad.2016.09.006. |
[19] | Kennedy CM, Ko JM, Craiglow BG, et al. Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata[J]. JCI Insight, 2016,1(15):e89776. doi: 10.1172/jci.insight.89776. |
[20] | Liu LY, Craiglow BG, Dai F, et al. Tofacitinib for the treatment of severe alopecia areata and variants: a study of 90 patients[J]. J Am Acad Dermatol, 2017,76(1):22⁃28. doi: 10.1016/j.jaad. 2016.09.007. |
[21] | Mackay⁃Wiggan J, Jabbari A, Nguyen N, et al. Oral ruxolitinib induces hair regrowth in patients with moderate⁃to⁃severe alopecia areata[J]. JCI Insight, 2016,1(15):e89790. doi: 10.1172/ jci.insight.89790. |
[22] | Jabbari A, Dai Z, Xing L, et al. Reversal of alopecia areata following treatment with the JAK1/2 inhibitor baricitinib[J]. EBioMedicine, 2015,2(4):351⁃355. doi: 10.1016/j.ebiom.2015. 02.015. |
[23] | Pieri L, Guglielmelli P, Vannucchi AM. Ruxolitinib⁃induced reversal of alopecia universalis in a patient with essential thrombocythemia[J]. Am J Hematol, 2015,90(1):82⁃83. doi: 10.1002/ajh.23871. |
[24] | Anzengruber F, Maul JT, Kamarachev J, et al. Transient efficacy of tofacitinib in alopecia areata universalis[J]. Case Rep Dermatol, 2016,8(1):102⁃106. doi: 10.1159/000445182. |
[25] | Jabbari A, Nguyen N, Cerise JE, et al. Treatment of an alopecia areata patient with tofacitinib results in regrowth of hair and changes in serum and skin biomarkers[J]. Exp Dermatol, 2016,25(8):642⁃643. doi: 10.1111/exd.13060. |
[26] | Castelo⁃Soccio L. Experience with oral tofacitinib in 8 adolescent patients with alopecia universalis[J]. J Am Acad Dermatol, 2017,76(4):754⁃755. doi: 10.1016/j.jaad.2016.11.038. |
[27] | Erduran F, Adışen E, Aksakal AB. Excellent response to tofacitinib treatment in a patient with alopecia universalis[J]. Acta Dermatovenerol Alp Pannonica Adriat, 2017,26(2):47⁃49. doi: 10.15570/actaapa.2017.15. |
[28] | Kim BY, Kim HS. Successful hair regrowth in a Korean patient with alopecia universalis following tofacitinib treatment[J]. Singapore Med J, 2017,58(5):279⁃280. doi: 10.11622/smedj. 2017039. |
[29] | Scheinberg M, de Lucena Couto Océa RA, Cruz BA, et al. Brazilian experience of the treatment of alopecia universalis with the novel antirheumatic therapy tofacitinib: a case series[J]. Rheumatol Ther, 2017,4(2):503⁃508. doi: 10.1007/s40744⁃017⁃0069⁃z. |
[30] | Jabbari A, Sansaricq F, Cerise J, et al. An open⁃label pilot study to evaluate the efficacy of tofacitinib in moderate to severe patch⁃type alopecia areata, totalis, and universalis[J]. J Invest Dermatol, 2018,138(7):1539⁃1545. doi: 10.1016/j.jid.2018.01. 032. |
[31] | Patel NU, Oussedik E, Grammenos A, et al. A case report highlighting the effective treatment of alopecia universalis with tofacitinib in an adolescent and adult patient[J]. J Cutan Med Surg, 2018,22(4):439⁃442. doi: 10.1177/1203475418760 512. |
[32] | Ferreira SB, Scheinberg M, Steiner D, et al. Remarkable improvement of nail changes in alopecia areata universalis with 10 months of treatment with tofacitinib: a case report[J]. Case Rep Dermatol, 2016,8(3):262⁃266. doi: 10.1159/000 450848. |
[33] | Kremer JM, Cohen S, Wilkinson BE, et al. A phase IIb dose⁃ranging study of the oral JAK inhibitor tofacitinib (CP⁃690,550) versus placebo in combination with background methotrexate in patients with active rheumatoid arthritis and an inadequate response to methotrexate alone[J]. Arthritis Rheum, 2012,64(4):970⁃981. doi: 10.1002/art.33419. |
[34] | Scott IC, Hider SL, Scott DL. Thromboembolism with Janus kinase (JAK) inhibitors for rheumatoid arthritis: how real is the risk?[J]. Drug Saf, 2018,41(7):645⁃653. doi: 10.1007/s40264⁃018⁃0651⁃5. |
[35] | Curtis JR, Lee EB, Kaplan IV, et al. Tofacitinib, an oral Janus kinase inhibitor: analysis of malignancies across the rheumatoid arthritis clinical development programme[J]. Ann Rheum Dis, 2016,75(5):831⁃841. doi: 10.1136/annrheumdis⁃2014⁃205847. |
[1] | 梁源 刘玲玲 王珊 赵作涛 马琳 向欣 顾恒 陈崑 王华 易红 陈谨萍 张金桃 姚志荣 郭一峰 陈戟 程颖 朱学骏. 0.03%他克莫司软膏长期间歇维持治疗儿童特应性皮炎的多中心随机对照临床研究[J]. 中华皮肤科杂志, 2019, 52(8): 519-524. |
[2] | 路坦 王珊 王榴慧 李萍 舒虹 申春平 吴瑶 罗珍 缪丽敏 王红兵 焦磊 田晶 彭晓霞 赵牧童 刘盈 聂晓璐 马琳 何黎. 一种含青刺果油等提取物的润肤剂改善儿童特应性皮炎缓解期临床症状的多中心、随机、平行对照临床研究[J]. 中华皮肤科杂志, 2019, 52(8): 537-541. |
[3] | 卢旭亚 徐强 李品川 张朝晖. 下肢痛性溃疡诊疗进展[J]. 中华皮肤科杂志, 2019, 52(7): 510-514. |
[4] | 陈怡雯 苏婷 苏忠兰. 银屑病与STAT3[J]. 中华皮肤科杂志, 2019, 52(7): 502-505. |
[5] | 周园 陈韡 王大光. 钳形甲的治疗进展[J]. 中华皮肤科杂志, 2019, 52(5): 364-367. |
[6] | 罗金成 陈曙光 刘文英 徐艳 宋志强. 自体全血注射对自体血清皮肤试验阳性的难治性慢性自发性荨麻疹患者嗜碱性粒细胞FcεRⅠ与CD63表达的影响[J]. 中华皮肤科杂志, 2019, 52(4): 241-247. |
[7] | 雷杰豪 樊奇敏 陈荣 许爱娥. 白癜风患者窄谱中波紫外线治疗效果与光疗反应的关系及相关因素分析[J]. 中华皮肤科杂志, 2019, 52(4): 259-262. |
[8] | 中华医学会皮肤性病学分会银屑病专业委员会. 中国银屑病诊疗指南(2018简版)[J]. 中华皮肤科杂志, 2019, 52(4): 223-230. |
[9] | 中华医学会皮肤性病学分会红斑狼疮研究中心. 皮肤型红斑狼疮诊疗指南(2019版)[J]. 中华皮肤科杂志, 2019, 52(3): 149-155. |
[10] | 翟寒月 宋益兴. 585 nm脉冲染料激光治疗儿童传染性软疣的临床观察[J]. 中华皮肤科杂志, 2019, 52(3): 195-197. |
[11] | 王刚. 皮肤科生物制剂的主要不良反应及对策[J]. 中华皮肤科杂志, 2019, 52(2): 77-80. |
[12] | 关欣 张春雷. 英夫利西单抗长疗程治疗中重度寻常性银屑病的疗效评价[J]. 中华皮肤科杂志, 2019, 52(2): 86-89. |
[13] | 胡宇晴 张建中. 特应性皮炎治疗药物研究进展[J]. 中华皮肤科杂志, 2019, 52(1): 57-60. |
[14] | 中华医学会皮肤性病学分会荨麻疹研究中心. 中国荨麻疹诊疗指南(2018版)[J]. 中华皮肤科杂志, 2019, 52(1): 1-5. |
[15] | 余艺昕 杨斌. 手湿疹中外诊疗指南概述[J]. 中华皮肤科杂志, 2019, 52(1): 53-56. |
|