New and Emerging Systemic Treatments for Atopic Dermatitis.

Drugs

Department of Dermatology, Center for Dermatology Research, Medical Center Boulevard, Wake Forest School of Medicine, Winston-Salem, North Carolina, 27157-1071, USA.

Published: July 2020

AI Article Synopsis

  • * New targeted treatments for AD are being developed due to an improved understanding of its causes, focusing on specific pathways, especially related to proteins like IL-13, IL-31, OX40, and Janus kinases.
  • * The article reviews data on several new therapies, including dupilumab and baricitinib, and discusses the potential benefits and drawbacks of narrower-targeted treatments compared to broader-acting agents like JAK inhibitors.

Article Abstract

Atopic dermatitis (AD) is a prevalent inflammatory skin condition that, depending on its severity, can cause enormous morbidity. Corticosteroids and systemic immunosuppression, traditionally standard of care for difficult-to-treat disease, have many undesirable side effects. The desire for targeted treatments along with an improved understanding of the pathophysiology of AD has spurred the development of novel treatments. In this article, we review promising new treatments and discuss how their targets-IL-13, IL-31, OX40 (CD134), and the Janus kinase family of proteins-participate in the pathogenesis of AD. We review the published phase II and III data for dupilumab, tralokinumab, lebrikizumab, nemolizumab, anti-OX40 antibody, baricitinib, abrocitinib, and upadacitinib. The introduction of new agents may offer new options, but it remains to be seen how narrow-acting agents, like single interleukin inhibitors, will compare in safety and efficacy to broad-acting agents such as JAK inhibitors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281689PMC
http://dx.doi.org/10.1007/s40265-020-01335-7DOI Listing

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