Advancing understanding, diagnosis, and therapies for cutaneous lupus erythematosus within the broader context of systemic lupus erythematosus.
Kristen L ChenRebecca L KrainVictoria P WerthPublished in: F1000Research (2019)
Cutaneous lupus erythematosus (CLE) is an autoimmune disease that can be associated with systemic lupus erythematosus (SLE) symptoms. The pathogenesis of both CLE and SLE is multifactorial, involving genetic susceptibility, environmental factors, and innate and adaptive immune responses. Despite the efficacy of current medications, many patients remain refractory, highlighting the necessity for new treatment options. Unfortunately, owing to challenges related in part to trial design and disease heterogeneity, only one new biologic in the last 50 years has been approved by the US Food and Drug Administration for the treatment of SLE. Thus, although SLE and CLE have a similar pathogenesis, patients with CLE who do not meet criteria for SLE cannot benefit from this advancement. This article discusses the recent trials and emphasizes the need to include patients with single-organ lupus, such as CLE, in SLE trials.
Keyphrases
- systemic lupus erythematosus
- disease activity
- immune response
- drug administration
- end stage renal disease
- rheumatoid arthritis
- newly diagnosed
- multiple sclerosis
- ejection fraction
- clinical trial
- chronic kidney disease
- randomized controlled trial
- dendritic cells
- prognostic factors
- risk assessment
- study protocol
- genome wide
- phase ii
- physical activity
- phase iii
- smoking cessation
- sleep quality
- double blind