{"title":"New approaches to the management of cutaneous lupus.","authors":"Kathie Velez, Grace A Osborne, Allison C Billi","doi":"10.1097/BOR.0000000000001175","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose of review: </strong>Cutaneous lupus erythematosus (CLE) is a heterogeneous inflammatory skin disease that can be disfiguring and profoundly affect patient quality of life. CLE is frequently challenging to manage and may remain refractory even when systemic disease is well controlled. Currently, no therapies are FDA-approved specifically for isolated CLE. This review summarizes established treatment approaches and highlights emerging targeted therapies informed by recent advances in disease pathogenesis.</p><p><strong>Recent findings: </strong>Recent studies expand the role of biologics and highlight the promise of additional interferon (IFN)-targeted therapies for the treatment of refractory CLE. Therapies targeting B cells, plasmacytoid dendritic cells, the type I IFN receptor, and downstream pathways - including JAK, TYK2, TLR7/8, and IRAK4 inhibitors - continue to broaden therapeutic options. Importantly, the incorporation of skin-specific outcome measures into systemic lupus erythematosus (SLE) clinical trials has supported the evaluation of cutaneous responses within broader SLE programs, which in turn has expanded the use of newer SLE therapies for CLE. This evolution in trial design may also facilitate future FDA approval pathways for treatments aimed at isolated CLE, an area currently lacking approved therapies.</p><p><strong>Summary: </strong>A deepening understanding of CLE pathogenesis has yielded multiple promising new treatments for CLE, with targeting of type I IFN and downstream signaling proving especially fruitful.</p>","PeriodicalId":11145,"journal":{"name":"Current opinion in rheumatology","volume":" ","pages":"349-357"},"PeriodicalIF":5.4000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current opinion in rheumatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/BOR.0000000000001175","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/20 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose of review: Cutaneous lupus erythematosus (CLE) is a heterogeneous inflammatory skin disease that can be disfiguring and profoundly affect patient quality of life. CLE is frequently challenging to manage and may remain refractory even when systemic disease is well controlled. Currently, no therapies are FDA-approved specifically for isolated CLE. This review summarizes established treatment approaches and highlights emerging targeted therapies informed by recent advances in disease pathogenesis.
Recent findings: Recent studies expand the role of biologics and highlight the promise of additional interferon (IFN)-targeted therapies for the treatment of refractory CLE. Therapies targeting B cells, plasmacytoid dendritic cells, the type I IFN receptor, and downstream pathways - including JAK, TYK2, TLR7/8, and IRAK4 inhibitors - continue to broaden therapeutic options. Importantly, the incorporation of skin-specific outcome measures into systemic lupus erythematosus (SLE) clinical trials has supported the evaluation of cutaneous responses within broader SLE programs, which in turn has expanded the use of newer SLE therapies for CLE. This evolution in trial design may also facilitate future FDA approval pathways for treatments aimed at isolated CLE, an area currently lacking approved therapies.
Summary: A deepening understanding of CLE pathogenesis has yielded multiple promising new treatments for CLE, with targeting of type I IFN and downstream signaling proving especially fruitful.
期刊介绍:
A high impact review journal which boasts an international readership, Current Opinion in Rheumatology offers a broad-based perspective on the most recent and exciting developments within the field of rheumatology. Published bimonthly, each issue features insightful editorials and high quality invited reviews covering two or three key disciplines which include vasculitis syndromes, medical physiology and rheumatic diseases, crystal deposition diseases and rheumatoid arthritis. Each discipline introduces world renowned guest editors to ensure the journal is at the forefront of knowledge development and delivers balanced, expert assessments of advances from the previous year.