Assessing the new and emerging treatments for atopic dermatitis

Lawrence F. Eichenfield; Sheila F. Friedlander; Eric Simpson; Alan D. Irvine

doi:10.12788/j.sder.2016.043

Assessing the new and emerging treatments for atopic dermatitis

Lawrence F. Eichenfield, Sheila F. Friedlander, Eric Simpson, Alan D. Irvine

Dermatology

Research output: Contribution to journal › Article › peer-review

16 Scopus citations

Abstract

The newer and emerging treatments for atopic dermatitis (AD) focus on blockade of inflammatory cytokines, especially those that derive from T helper cell type 2 (T_H2) and are associated with a pathway of immunoglobulin E (IgE) sensitization. Among the proinflammatory cytokines that have been identified as promising therapeutic targets are chemoattractant receptor-homologous molecule expressed on T_H2 cells (CRT_H2), IgE, thymic stromal lymphopoietin (TSLP), and several monoclonal antibodies that block key cytokine pathways in the innate immune response. Two agents that have been studied in phase III clinical trials are the boronbased phosphodiesterase-4 (PDE-4) inhibitor, crisaborole, and dupilumab, an antibody that inhibits the interleukin-4/IL-13 receptor α chain.

Original language	English (US)
Pages (from-to)	92S-96S
Journal	Seminars in Cutaneous Medicine and Surgery
Volume	35
DOIs	https://doi.org/10.12788/j.sder.2016.043
State	Published - Jun 1 2016

Keywords

Atopic dermatitis
Crisaborole
Dupilumab
Interleukin inhibitors
Petrolatum
Skin barrier

ASJC Scopus subject areas

Surgery
Medicine(all)
Dermatology

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