TY - JOUR
T1 - Treatment of cutaneous lupus erythematosus
T2 - Current approaches and future strategies
AU - Shi, Hong
AU - Gudjonsson, Johann E.
AU - Kahlenberg, J. Michelle
N1 - Funding Information:
The work was supported by the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) of the National Institutes of Health under Award Numbers R01AR071384 to J.M.K. and R01AR069071 to J.E.G. Additional support was provided by the A. Alfred Taubman Medical Research Institute Parfet Emerging Scholar Award (J.M.K.), the Rheumatology Research Foundation Innovative Research Grant (to J.M.K.) and by the Doris Duke Charitable Foundation (to J.M.K.). H.S. received support from the US Department of Veterans Affairs.
Funding Information:
J.M.K. has served on advisory boards for AstraZeneca, Eli Lilly and Bristol-Myers Squibb. J.M.K. and J.E.G. have grant funding from Celgene. J.E.G. has served on advisory boards for Novartis and MiRagen, and he has received additional research support from AbbVie, SunPharma and Genentech. No industry funds were used to complete this study. H.S. has no relevant conflicts.
Publisher Copyright:
© 2020 Lippincott Williams and Wilkins. All rights reserved.
PY - 2020/5/1
Y1 - 2020/5/1
N2 - Purpose of reviewCutaneous lupus erythematosus (CLE) is a highly heterogeneous autoimmune disease. No specific Federal Drug Administration-approved therapies for CLE-alone are available, and resistance to conventional treatments is common. This review will summarize current treatment approaches and pending treatment strategies.Recent findingsResearch into the pathogenesis of CLE is accelerating. A skewed type I interferon production and response contribute to CLE lesions. The pathophysiology of lesions may be similar among the lesional subtypes, and patients with a more TLR9-driven disease mechanism may have more benefit from hydroxychloroquine. Case reports continue to support the use of dapsone for CLE, especially bullous lupus erythematosus. Rituximab and Belimumab have efficacy in patients with systemic lupus erythematosus and severe active CLE. The significant role for type I interferons in CLE and encouraging clinical data suggest anifrolumab as a very promising agent for CLE. Dapirolizumab, BIIB059, Ustekinumab and Janus kinase inhibitors also have supportive early data as promising new strategies for CLE treatment.SummaryContinued research to understand the mechanisms driving CLE will facilitate the development and approval of new targets. The pipeline for new treatments is rich.
AB - Purpose of reviewCutaneous lupus erythematosus (CLE) is a highly heterogeneous autoimmune disease. No specific Federal Drug Administration-approved therapies for CLE-alone are available, and resistance to conventional treatments is common. This review will summarize current treatment approaches and pending treatment strategies.Recent findingsResearch into the pathogenesis of CLE is accelerating. A skewed type I interferon production and response contribute to CLE lesions. The pathophysiology of lesions may be similar among the lesional subtypes, and patients with a more TLR9-driven disease mechanism may have more benefit from hydroxychloroquine. Case reports continue to support the use of dapsone for CLE, especially bullous lupus erythematosus. Rituximab and Belimumab have efficacy in patients with systemic lupus erythematosus and severe active CLE. The significant role for type I interferons in CLE and encouraging clinical data suggest anifrolumab as a very promising agent for CLE. Dapirolizumab, BIIB059, Ustekinumab and Janus kinase inhibitors also have supportive early data as promising new strategies for CLE treatment.SummaryContinued research to understand the mechanisms driving CLE will facilitate the development and approval of new targets. The pipeline for new treatments is rich.
KW - antimalarials
KW - biologic therapies
KW - cutaneous lupus
KW - interferon
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U2 - 10.1097/BOR.0000000000000704
DO - 10.1097/BOR.0000000000000704
M3 - Review article
C2 - 32141953
AN - SCOPUS:85082561246
SN - 1040-8711
VL - 32
SP - 208
EP - 214
JO - Current Opinion in Rheumatology
JF - Current Opinion in Rheumatology
IS - 3
ER -