Cargando…

Emerging Therapies in Cutaneous Lupus Erythematosus

Cutaneous lupus erythematosus (CLE) is an autoimmune disease that can occur with or without underlying systemic lupus erythematosus (SLE) and often has a profoundly negative impact on patient quality of life. There is substantial need for new and more effective therapies to treat CLE. CLE has a mult...

Descripción completa

Detalles Bibliográficos
Autores principales: Sprow, Grant, Dan, Joshua, Merola, Joseph F., Werth, Victoria P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313535/
https://www.ncbi.nlm.nih.gov/pubmed/35899214
http://dx.doi.org/10.3389/fmed.2022.968323
_version_ 1784754102733897728
author Sprow, Grant
Dan, Joshua
Merola, Joseph F.
Werth, Victoria P.
author_facet Sprow, Grant
Dan, Joshua
Merola, Joseph F.
Werth, Victoria P.
author_sort Sprow, Grant
collection PubMed
description Cutaneous lupus erythematosus (CLE) is an autoimmune disease that can occur with or without underlying systemic lupus erythematosus (SLE) and often has a profoundly negative impact on patient quality of life. There is substantial need for new and more effective therapies to treat CLE. CLE has a multifactorial pathogenesis that involves several key immune cells and pathways, including abnormalities in innate (e.g., type 1 interferon pathways) and adaptive immune responses (e.g., B and T cell autoreactivity), presenting multiple opportunities for more targeted therapies that do not require immunosuppression. Here we review several emerging therapies and their efficacy in CLE. Anifrolumab and belimumab have both been approved for the treatment of SLE in recent years, and clinical trial evidence suggests some forms of CLE may improve with these agents. Therapies currently in development that are being evaluated with CLE-specific outcome measures include BIIB059 and VIB7734, which target plasmacytoid dendritic cells (pDCs), and iberdomide, a cereblon modulator. These novel therapies all have previously demonstrated clinical benefit in some forms of CLE. Other therapies which target molecules believed to play a role in CLE pathogenesis, such as Janus kinases (JAKs), spleen tyrosine kinase (SYK), interferon γ (IFNγ), IL-12, and IL-23, have been evaluated in lupus clinical trials with skin-specific outcomes but failed to meet their primary endpoints.
format Online
Article
Text
id pubmed-9313535
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-93135352022-07-26 Emerging Therapies in Cutaneous Lupus Erythematosus Sprow, Grant Dan, Joshua Merola, Joseph F. Werth, Victoria P. Front Med (Lausanne) Medicine Cutaneous lupus erythematosus (CLE) is an autoimmune disease that can occur with or without underlying systemic lupus erythematosus (SLE) and often has a profoundly negative impact on patient quality of life. There is substantial need for new and more effective therapies to treat CLE. CLE has a multifactorial pathogenesis that involves several key immune cells and pathways, including abnormalities in innate (e.g., type 1 interferon pathways) and adaptive immune responses (e.g., B and T cell autoreactivity), presenting multiple opportunities for more targeted therapies that do not require immunosuppression. Here we review several emerging therapies and their efficacy in CLE. Anifrolumab and belimumab have both been approved for the treatment of SLE in recent years, and clinical trial evidence suggests some forms of CLE may improve with these agents. Therapies currently in development that are being evaluated with CLE-specific outcome measures include BIIB059 and VIB7734, which target plasmacytoid dendritic cells (pDCs), and iberdomide, a cereblon modulator. These novel therapies all have previously demonstrated clinical benefit in some forms of CLE. Other therapies which target molecules believed to play a role in CLE pathogenesis, such as Janus kinases (JAKs), spleen tyrosine kinase (SYK), interferon γ (IFNγ), IL-12, and IL-23, have been evaluated in lupus clinical trials with skin-specific outcomes but failed to meet their primary endpoints. Frontiers Media S.A. 2022-07-11 /pmc/articles/PMC9313535/ /pubmed/35899214 http://dx.doi.org/10.3389/fmed.2022.968323 Text en Copyright © 2022 Sprow, Dan, Merola and Werth. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Sprow, Grant
Dan, Joshua
Merola, Joseph F.
Werth, Victoria P.
Emerging Therapies in Cutaneous Lupus Erythematosus
title Emerging Therapies in Cutaneous Lupus Erythematosus
title_full Emerging Therapies in Cutaneous Lupus Erythematosus
title_fullStr Emerging Therapies in Cutaneous Lupus Erythematosus
title_full_unstemmed Emerging Therapies in Cutaneous Lupus Erythematosus
title_short Emerging Therapies in Cutaneous Lupus Erythematosus
title_sort emerging therapies in cutaneous lupus erythematosus
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313535/
https://www.ncbi.nlm.nih.gov/pubmed/35899214
http://dx.doi.org/10.3389/fmed.2022.968323
work_keys_str_mv AT sprowgrant emergingtherapiesincutaneouslupuserythematosus
AT danjoshua emergingtherapiesincutaneouslupuserythematosus
AT merolajosephf emergingtherapiesincutaneouslupuserythematosus
AT werthvictoriap emergingtherapiesincutaneouslupuserythematosus