Managing Atopic Dermatitis with Lebrikizumab - The Evidence to Date.
IL-13
atopic dermatitis
eczema
lebrikizumab
monoclonal antibody inhibitor
Journal
Clinical, cosmetic and investigational dermatology
ISSN: 1178-7015
Titre abrégé: Clin Cosmet Investig Dermatol
Pays: New Zealand
ID NLM: 101543449
Informations de publication
Date de publication:
2022
2022
Historique:
received:
05
04
2022
accepted:
02
06
2022
entrez:
15
6
2022
pubmed:
16
6
2022
medline:
16
6
2022
Statut:
epublish
Résumé
Atopic dermatitis is a prevalent, inflammatory skin disease that presents with an eczematous, itchy rash. As of late, there have been many emerging monoclonal antibody inhibitor and small molecule therapies that have changed the course of eczema treatment. One of the treatments in the pipeline for atopic dermatitis is interleukin 13 monoclonal antibody inhibitor, lebrikizumab. As interleukin 13 has been identified as a pro-inflammatory cytokine in the immunological cascade of eczema, it is thought that lebrikizumab can be a great treatment choice for patients with atopic dermatitis. Lebrikizumab is currently being investigated in several studies. Thus far, lebrikizumab for the treatment of eczema has been found to be efficacious; in particular, a rapid response of pruritus improvement has been demonstrated in as early as 2 days. Additionally, it is well tolerated and has an acceptable safety profile, with reports suggesting that are decreased risks of infection when compared to dupilumab. In this review, we aim to summarize the current understanding of lebrikizumab in terms of the mechanism of action, preclinical pharmacology, pharmacokinetics and metabolism, efficacy and safety, and drug indications.
Identifiants
pubmed: 35702658
doi: 10.2147/CCID.S295672
pii: 295672
pmc: PMC9188775
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
1065-1072Informations de copyright
© 2022 Labib et al.
Déclaration de conflit d'intérêts
Angelina Labib and Teresa Ju state no conflicts of interests. Dr. Gil Yosipovitch has been an investigator and consultant to Galderma, Pfizer, Sanofi Regeneron, Eli Lilly, Bellus, Kiniksa, Leo, Trevi, and Cellcept. The authors report no other conflicts of interest in this work.
Références
J Mol Biol. 2017 Jan 20;429(2):208-219
pubmed: 27956146
Clin Cosmet Investig Dermatol. 2021 Aug 03;14:959-969
pubmed: 34377004
Int J Toxicol. 2008 Sep-Oct;27(5):351-8
pubmed: 19037805
Curr Opin Immunol. 2016 Oct;42:1-8
pubmed: 27206013
J Mol Biol. 2013 Apr 26;425(8):1330-9
pubmed: 23357170
Nat Rev Immunol. 2018 Jul;18(7):454-466
pubmed: 29626211
Lancet. 2020 Aug 1;396(10247):345-360
pubmed: 32738956
Allergy Asthma Proc. 2019 Mar 1;40(2):84-92
pubmed: 30819278
J Am Acad Dermatol. 2018 May;78(5):863-871.e11
pubmed: 29353026
J Invest Dermatol. 2019 Jul;139(7):1480-1489
pubmed: 30641038
J Allergy Clin Immunol. 2013 Sep;132(3):567-574.e12
pubmed: 23726041
Int J Mol Sci. 2020 Jul 29;21(15):
pubmed: 32751111
Pediatr Dermatol. 2008 Jan-Feb;25(1):1-6
pubmed: 18304144
J Allergy Clin Immunol. 2022 Mar 1;:
pubmed: 35240144
Biologics. 2012;6:329-35
pubmed: 23055690
Ann Allergy Asthma Immunol. 2020 Jan;124(1):36-43
pubmed: 31622670
Clin Dermatol. 2018 Sep - Oct;36(5):648-652
pubmed: 30217277
Drugs. 2020 Jul;80(11):1041-1052
pubmed: 32519223
Pediatr Dermatol. 2005 May-Jun;22(3):192-9
pubmed: 15916563
Clin Exp Allergy. 2020 Dec;50(12):1342-1351
pubmed: 32909660
Br J Dermatol. 2021 Feb;184(2):304-309
pubmed: 33006135
Thorax. 2015 Aug;70(8):748-56
pubmed: 26001563
Cytokine. 2004 Dec 21;28(6):224-32
pubmed: 15566951
Int Immunopharmacol. 2009 Feb;9(2):201-6
pubmed: 19041426
J Pharmacol Exp Ther. 2008 Jun;325(3):882-92
pubmed: 18337474
Int J Mol Sci. 2021 Apr 16;22(8):
pubmed: 33923629
Pharmacoeconomics. 2003;21(2):105-13
pubmed: 12515572
Expert Rev Clin Immunol. 2017 May;13(5):425-437
pubmed: 28277826
Lancet. 2016 Mar 12;387(10023):1109-1122
pubmed: 26377142
JAMA Dermatol. 2020 Apr 1;156(4):411-420
pubmed: 32101256
Eur Respir J. 2021 Feb 4;57(2):
pubmed: 33008934
Curr Allergy Asthma Rep. 2008 Jul;8(4):306-11
pubmed: 18606082