• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

银屑病:全科医生入门指南。

Psoriasis: A Primer for General Physicians.

作者信息

Dasari Shalini, Choudhary Ankita, Madke Bhushan

机构信息

Dermatology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

Dermatology, B.J. Medical College, Ahmedabad, IND.

出版信息

Cureus. 2023 Apr 24;15(4):e38037. doi: 10.7759/cureus.38037. eCollection 2023 Apr.

DOI:10.7759/cureus.38037
PMID:37228538
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10208009/
Abstract

Psoriasis is a multisystem, polygenic, inflammatory condition that typically causes changes in the skin. Although there is a significant genetic component, environmental factors like infections can have a significant impact on triggering the disease. A major part of the pathogenesis of psoriasis is played by the Interleukin (IL) IL23/IL17 axis along with the immune-related cells mainly macrophages and dendritic cells (DCs). Additionally, the role of various cytokines along with the toll-like receptors has also been pointed out in immunopathogenesis. These have been supported by the efficacy of biological therapies including TNF alpha inhibitors and inhibitors of IL17 and IL23. We have summarized the topical as well as systemic therapies for psoriasis including biologics. The article throws light on a few emerging therapeutic options like modulators of sphingosine 1-phosphate receptor 1 and Rho-associated kinase 2 inhibitors.

摘要

银屑病是一种多系统、多基因的炎症性疾病,通常会导致皮肤发生变化。虽然存在显著的遗传因素,但感染等环境因素对触发该疾病会产生重大影响。银屑病发病机制的一个主要部分由白细胞介素(IL)IL23/IL17轴以及主要为巨噬细胞和树突状细胞(DCs)的免疫相关细胞发挥作用。此外,各种细胞因子以及Toll样受体在免疫发病机制中的作用也已得到指出。包括肿瘤坏死因子α抑制剂以及IL17和IL23抑制剂在内的生物疗法的疗效也证实了这些作用。我们总结了银屑病的局部和全身治疗方法,包括生物制剂。本文还介绍了一些新兴的治疗选择,如1-磷酸鞘氨醇受体1调节剂和Rho相关激酶2抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac87/10208009/bed9d48ea0b9/cureus-0015-00000038037-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac87/10208009/001543c3c64c/cureus-0015-00000038037-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac87/10208009/bed9d48ea0b9/cureus-0015-00000038037-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac87/10208009/001543c3c64c/cureus-0015-00000038037-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac87/10208009/bed9d48ea0b9/cureus-0015-00000038037-i02.jpg

相似文献

1
Psoriasis: A Primer for General Physicians.银屑病:全科医生入门指南。
Cureus. 2023 Apr 24;15(4):e38037. doi: 10.7759/cureus.38037. eCollection 2023 Apr.
2
New Treatment Addressing the Pathogenesis of Psoriasis.新型疗法直击银屑病发病根源。
Int J Mol Sci. 2020 Oct 11;21(20):7488. doi: 10.3390/ijms21207488.
3
Major Role of the IL17/23 Axis in Psoriasis Supports the Development of New Targeted Therapies.IL17/23 轴在银屑病中的主要作用支持新靶向治疗的发展。
Front Immunol. 2021 Feb 25;12:621956. doi: 10.3389/fimmu.2021.621956. eCollection 2021.
4
Psoriasis and the TNF/IL23/IL17 axis.银屑病与 TNF/IL23/IL17 轴。
G Ital Dermatol Venereol. 2019 Aug;154(4):418-424. doi: 10.23736/S0392-0488.18.06202-8. Epub 2019 Jan 15.
5
[Actual treatments of psoriasis : from etanercept to anti-IL17 and anti-IL23 antagonists].[银屑病的实际治疗:从依那西普到抗IL17和抗IL23拮抗剂]
Rev Med Liege. 2020 May;75(5-6):376-381.
6
Anti-IL17 and anti-IL23 biologic drugs for scalp psoriasis: A single-center retrospective comparative study.抗白介素 17 和抗白介素 23 生物药物治疗头皮银屑病:单中心回顾性对比研究。
Dermatol Ther. 2022 Feb;35(2):e15228. doi: 10.1111/dth.15228. Epub 2021 Nov 30.
7
[Pathogenesis of psoriasis].[银屑病的发病机制]
Hautarzt. 2016 Jun;67(6):422-31. doi: 10.1007/s00105-016-3800-8.
8
The TNF/IL-23/IL-17 axis-Head-to-head trials comparing different biologics in psoriasis treatment.TNF/IL-23/IL-17 轴——头对头试验比较不同生物制剂治疗银屑病的疗效。
Scand J Immunol. 2020 Oct;92(4):e12946. doi: 10.1111/sji.12946.
9
Inhibition of interleukin-17, interleukin-23 and the TH17 cell pathway in the treatment of psoriatic arthritis and psoriasis.抑制白细胞介素-17、白细胞介素-23及TH17细胞通路在银屑病关节炎和银屑病治疗中的应用
Curr Opin Rheumatol. 2015 Mar;27(2):127-33. doi: 10.1097/BOR.0000000000000147.
10
Bruton's tyrosine kinase inhibitor suppresses imiquimod-induced psoriasis-like inflammation in mice through regulation of IL-23/IL-17A in innate immune cells.布鲁顿酪氨酸激酶抑制剂通过调节固有免疫细胞中的 IL-23/IL-17A 抑制咪喹莫特诱导的小鼠银屑病样炎症。
Int Immunopharmacol. 2020 Mar;80:106215. doi: 10.1016/j.intimp.2020.106215. Epub 2020 Jan 24.

本文引用的文献

1
The Role of Helper T Cells in Psoriasis.辅助性 T 细胞在银屑病中的作用。
Front Immunol. 2021 Dec 15;12:788940. doi: 10.3389/fimmu.2021.788940. eCollection 2021.
2
Role of Janus Kinase Inhibitors in Therapy of Psoriasis.Janus激酶抑制剂在银屑病治疗中的作用。
J Clin Med. 2021 Sep 22;10(19):4307. doi: 10.3390/jcm10194307.
3
The Role of Chemokines in Psoriasis-An Overview.趋化因子在银屑病中的作用——概述。
Medicina (Kaunas). 2021 Jul 26;57(8):754. doi: 10.3390/medicina57080754.
4
Experimental Pharmacological Management of Psoriasis.银屑病的实验性药理治疗
J Exp Pharmacol. 2021 Jul 26;13:725-737. doi: 10.2147/JEP.S265632. eCollection 2021.
5
New Treatment Addressing the Pathogenesis of Psoriasis.新型疗法直击银屑病发病根源。
Int J Mol Sci. 2020 Oct 11;21(20):7488. doi: 10.3390/ijms21207488.
6
Aryl Hydrocarbon Receptor in Cutaneous Vascular Endothelial Cells Restricts Psoriasis Development by Negatively Regulating Neutrophil Recruitment.芳烃受体在皮肤血管内皮细胞中通过负向调节中性粒细胞募集来限制银屑病的发展。
J Invest Dermatol. 2020 Jun;140(6):1233-1243.e9. doi: 10.1016/j.jid.2019.11.022. Epub 2019 Dec 30.
7
Transcription Factor Retinoid-Related Orphan Receptor γt: A Promising Target for the Treatment of Psoriasis.转录因子维 A 酸相关孤儿受体 γt:治疗银屑病的有前途的靶点。
Front Immunol. 2018 May 30;9:1210. doi: 10.3389/fimmu.2018.01210. eCollection 2018.
8
Drug-induced psoriasis: clinical perspectives.药物性银屑病:临床视角
Psoriasis (Auckl). 2017 Dec 7;7:87-94. doi: 10.2147/PTT.S126727. eCollection 2017.
9
Clinical Pattern of Psoriasis in Punjab.旁遮普邦银屑病的临床模式
Indian J Dermatol Venereol. 1966 Jan-Feb;32(1):5-8.
10
Lack of placental transfer of certolizumab pegol during pregnancy: results from CRIB, a prospective, postmarketing, pharmacokinetic study.妊娠期间培塞丽珠(certolizumab pegol)胎盘转移缺失:来自 CRIB 的前瞻性上市后药代动力学研究结果。
Ann Rheum Dis. 2018 Feb;77(2):228-233. doi: 10.1136/annrheumdis-2017-212196. Epub 2017 Oct 13.