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系统评价度普利尤单抗治疗瘢痕疙瘩的安全性和有效性。

Systematic review of dupilumab safety and efficacy for treatment of keloid scars.

机构信息

Dermatology Service, Veterans Affairs New York Harbor Healthcare System, Brooklyn Campus, Brooklyn, NY, USA.

New York Medical College, Valhalla, NY, USA.

出版信息

Arch Dermatol Res. 2024 Aug 23;316(8):560. doi: 10.1007/s00403-024-03277-6.

DOI:10.1007/s00403-024-03277-6
PMID:39177869
Abstract

Keloids, characterized by excessive scar formation following dermal inflammation, pose a therapeutic challenge due to high recurrence rates. Radiation therapy, contraindicated in children, can minimize recurrence post-surgical removal. Dupilumab, which inhibits the pro-fibrotic interleukin-4/interleukin-13 axis, may effectively manage keloids when intralesional corticosteroid injections are unsuccessful. It may also prevent recurrence post-surgery in pediatric patients. This systematic review assesses the efficacy and safety of dupilumab for the treatment of keloids. Through a systematic search adhering to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, we identified and analyzed outcomes from three case reports and three case series studies, totaling 15 patients. Results indicate variable responses to treatment, including significant improvements, no clinical change, and worsening of keloid symptoms. Additional research is needed to recommend using dupilumab to treat keloids (Grade D). Treatment response variability may be linked to differences in interleukin-4/interleukin-13 activity between active and inactive keloids. Additionally, the unintended promotion of T helper 17 cell differentiation by dupilumab may worsen keloids.

摘要

瘢痕疙瘩是一种皮肤炎症后过度形成瘢痕的疾病,由于复发率高,治疗具有挑战性。放射治疗不适用于儿童,可在手术后切除后最大限度地减少复发。当局部皮质类固醇注射无效时,抑制致纤维化白细胞介素-4/白细胞介素-13 轴的度普利尤单抗可能有效地治疗瘢痕疙瘩。它也可能预防小儿患者手术后的复发。本系统评价评估了度普利尤单抗治疗瘢痕疙瘩的疗效和安全性。通过遵循系统评价和荟萃分析的首选报告项目进行系统搜索,我们确定并分析了来自 3 份病例报告和 3 份病例系列研究的结果,共有 15 名患者。结果表明,治疗反应存在差异,包括显著改善、无临床变化和瘢痕疙瘩症状恶化。需要进一步研究来推荐使用度普利尤单抗治疗瘢痕疙瘩(D 级)。治疗反应的可变性可能与活性和非活性瘢痕疙瘩中白细胞介素-4/白细胞介素-13 活性的差异有关。此外,度普利尤单抗意外促进 T 辅助 17 细胞分化可能会使瘢痕疙瘩恶化。

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Clin Cosmet Investig Dermatol. 2023 Dec 29;16:3775-3783. doi: 10.2147/CCID.S446018. eCollection 2023.
2
Successful Treatment of Keloids and Hypertrophic Scars With Systemic and Intralesional Dupilumab.系统和皮损内注射度普利尤单抗治疗瘢痕疙瘩和增生性瘢痕的疗效。
J Drugs Dermatol. 2023 Dec 1;22(12):1220-1222. doi: 10.36849/JDD.6385.
3
Effects of dupilumab on keloid stabilization and prevention.度普利尤单抗对瘢痕疙瘩稳定和预防的作用。
JAAD Case Rep. 2023 May 12;37:103-105. doi: 10.1016/j.jdcr.2023.05.001. eCollection 2023 Jul.
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An updated review of the immunological mechanisms of keloid scars.瘢痕疙瘩免疫发病机制的最新研究进展
Front Immunol. 2023 Mar 22;14:1117630. doi: 10.3389/fimmu.2023.1117630. eCollection 2023.
5
Intralesional Corticosteroid Administration in the Treatment of Keloids: A Scoping Review on Injection Methods.瘢痕内皮质类固醇注射治疗:注射方法的范围综述。
Dermatology. 2023;239(3):462-477. doi: 10.1159/000529220. Epub 2023 Jan 19.
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The JAK-STAT pathway in keloid pathogenesis: a systematic review with qualitative synthesis.瘢痕疙瘩发病机制中的JAK-STAT信号通路:一项定性综合的系统评价
Exp Dermatol. 2023 May;32(5):588-598. doi: 10.1111/exd.14747. Epub 2023 Feb 9.
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WNT5A drives interleukin-6-dependent epithelial-mesenchymal transition via the JAK/STAT pathway in keloid pathogenesis.在瘢痕疙瘩发病机制中,WNT5A通过JAK/STAT途径驱动白细胞介素-6依赖性上皮-间质转化。
Burns Trauma. 2022 Oct 7;10:tkac023. doi: 10.1093/burnst/tkac023. eCollection 2022.
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IL-17 Induces Autophagy Dysfunction to Promote Inflammatory Cell Death and Fibrosis in Keloid Fibroblasts the STAT3 and HIF-1α Dependent Signaling Pathways.IL-17 通过 STAT3 和 HIF-1α 依赖性信号通路诱导成纤维细胞自噬功能障碍,促进炎症细胞死亡和纤维化。
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