TY - JOUR
T1 - Novel treatments for pediatric atopic dermatitis
AU - Scott, Jennifer B.
AU - Paller, Amy S.
N1 - Funding Information:
J.B.S.'s salary was supported in part by a grant from the National Psoriasis Foundation.
Publisher Copyright:
© 2021 Lippincott Williams and Wilkins. All rights reserved.
PY - 2021/8/1
Y1 - 2021/8/1
N2 - Purpose of reviewTo describe new and emerging therapies for pediatric atopic dermatitis (AD).Recent findingsRecent investigations have highlighted the importance of type 2 immunity and interrelationships among the skin immune system, epidermal barrier, and microbiome in the pathogenesis of AD, including in infants and children. These discoveries have translated into more targeted therapy. Crisaborole ointment, a topical phosphodiesterase 4 (PDE4) inhibitor, and dupilumab, a subcutaneously injected interleukin (IL)-4 receptor inhibitor, are now Food and Drug Administration-approved. Topical agents under investigation for use in the pediatric population include Janus kinase (JAK) inhibitors, PDE4 inhibitors, an aryl hydrocarbon receptor agonist, an antimicrobial peptide, and commensal skin bacteria. Emerging systemic agents for pediatric AD include biologics targeting IL-13, the IL-31 receptor, and the IL-5 receptor, as well as oral JAK inhibitors.SummaryIncreased understanding of AD pathogenesis has resulted in the development of new, more targeted therapies that show promising safety and efficacy results in Phase 2 and 3 clinical trials, although long-term safety remains to be evaluated. AD is a heterogeneous disease and having choices of therapies with different mechanisms of action will allow a broader group of children and adolescents with moderate-to-severe disease to achieve disease control.
AB - Purpose of reviewTo describe new and emerging therapies for pediatric atopic dermatitis (AD).Recent findingsRecent investigations have highlighted the importance of type 2 immunity and interrelationships among the skin immune system, epidermal barrier, and microbiome in the pathogenesis of AD, including in infants and children. These discoveries have translated into more targeted therapy. Crisaborole ointment, a topical phosphodiesterase 4 (PDE4) inhibitor, and dupilumab, a subcutaneously injected interleukin (IL)-4 receptor inhibitor, are now Food and Drug Administration-approved. Topical agents under investigation for use in the pediatric population include Janus kinase (JAK) inhibitors, PDE4 inhibitors, an aryl hydrocarbon receptor agonist, an antimicrobial peptide, and commensal skin bacteria. Emerging systemic agents for pediatric AD include biologics targeting IL-13, the IL-31 receptor, and the IL-5 receptor, as well as oral JAK inhibitors.SummaryIncreased understanding of AD pathogenesis has resulted in the development of new, more targeted therapies that show promising safety and efficacy results in Phase 2 and 3 clinical trials, although long-term safety remains to be evaluated. AD is a heterogeneous disease and having choices of therapies with different mechanisms of action will allow a broader group of children and adolescents with moderate-to-severe disease to achieve disease control.
KW - Janus kinase inhibitors
KW - atopic dermatitis
KW - biologics
KW - child
KW - pruritus
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UR - http://www.scopus.com/inward/citedby.url?scp=85112119805&partnerID=8YFLogxK
U2 - 10.1097/MOP.0000000000001027
DO - 10.1097/MOP.0000000000001027
M3 - Review article
C2 - 34001717
AN - SCOPUS:85112119805
SN - 1040-8703
VL - 33
SP - 392
EP - 401
JO - Current Opinion in Pediatrics
JF - Current Opinion in Pediatrics
IS - 4
ER -