TY - JOUR
T1 - Biologics for Treatment of Atopic Dermatitis
T2 - Current Status and Future Prospect
AU - Ratchataswan, Thanaporn
AU - Banzon, Tina M
AU - Thyssen, Jacob P
AU - Weidinger, Stephan
AU - Guttman-Yassky, Emma
AU - Phipatanakul, Wanda
N1 - Copyright © 2020 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
PY - 2021/3
Y1 - 2021/3
N2 - Atopic dermatitis (AD) is a common inflammatory skin disease characterized by intense pruritus and recurrent eczematous lesions that significantly impair quality of life. It is a heterogeneous disease affecting both children and adults. The treatment of moderate-to-severe forms of AD is challenging, as topical corticosteroids are often insufficient to achieve disease control or inappropriate and off-label use of immunosuppressants may have significant undesirable side effects. The development of targeted biologic therapies specifically for AD is thus highly desirable. Dupilumab is the only biologic therapy that is Food and Drug Administration approved for the treatment of moderate-to-severe AD in patients 6 years and older, with consistent long-term efficacy and safety trial data. In this article, we review the mechanisms, safety, and efficacy of dupilumab from recent clinical trials, and we review the current data, mechanism of action, clinical efficacy, and limitations of new biologics currently in phase 2 and 3 clinical trials (lebrikizumab, tralokinumab, nemolizumab, tezepelumab, and ISB 830).
AB - Atopic dermatitis (AD) is a common inflammatory skin disease characterized by intense pruritus and recurrent eczematous lesions that significantly impair quality of life. It is a heterogeneous disease affecting both children and adults. The treatment of moderate-to-severe forms of AD is challenging, as topical corticosteroids are often insufficient to achieve disease control or inappropriate and off-label use of immunosuppressants may have significant undesirable side effects. The development of targeted biologic therapies specifically for AD is thus highly desirable. Dupilumab is the only biologic therapy that is Food and Drug Administration approved for the treatment of moderate-to-severe AD in patients 6 years and older, with consistent long-term efficacy and safety trial data. In this article, we review the mechanisms, safety, and efficacy of dupilumab from recent clinical trials, and we review the current data, mechanism of action, clinical efficacy, and limitations of new biologics currently in phase 2 and 3 clinical trials (lebrikizumab, tralokinumab, nemolizumab, tezepelumab, and ISB 830).
KW - Adult
KW - Biological Products/therapeutic use
KW - Child
KW - Dermatitis, Atopic/drug therapy
KW - Eczema
KW - Humans
KW - Pruritus
KW - Quality of Life
KW - Treatment Outcome
KW - Tezepelumab
KW - Tralokinumab
KW - GBR 830
KW - Lebrikizumab
KW - Nemolizumab
KW - Atopic dermatitis
KW - ISB 830
KW - Dupilumab
KW - Biologic therapy
UR - http://www.scopus.com/inward/record.url?scp=85101654431&partnerID=8YFLogxK
U2 - 10.1016/j.jaip.2020.11.034
DO - 10.1016/j.jaip.2020.11.034
M3 - Review
C2 - 33685604
SN - 2213-2198
VL - 9
SP - 1053
EP - 1065
JO - The journal of allergy and clinical immunology. In practice
JF - The journal of allergy and clinical immunology. In practice
IS - 3
ER -