Monoclonal antibodies against interleukin 13 and interleukin 31RA in development for atopic dermatitis - 21/02/18
Abstract |
The interleukin 13 (IL-13) and IL-31 cytokines and inflammatory pathways have been identified as important for the pathophysiology of atopic dermatitis (AD). Monoclonal antibodies against IL-13 have been studied for the treatment of asthma since 2011. More recently, 2 phase 2 trials have been completed with these antibodies in AD treatment. In both trials, significant reductions of Eczema Area and Severity Index scores were seen. IL-31 is thought to play a role transmitting itch sensation to the central nervous system, and blocking IL-31 activity reduces itch in patients with AD. One phase 2 trial has been completed for a humanized antibody against IL-31 receptor alpha, which is 1 subunit of the IL-31 receptor complex. This study showed significant dose-dependent reductions in pruritus, Eczema Area and Severity Index scores, and markers of sleep quality. Initial clinical trials for monoclonal antibodies against IL-13 and IL-31 receptor A all show promise, although long-term safety and efficacy data are lacking. Nevertheless, these medications will likely play a role in the treatment of moderate-to-severe AD.
Le texte complet de cet article est disponible en PDF.Key words : atopic dermatitis, dipeptidyl peptidase-4, Eczema Area and Severity Index, interleukin, IL-31RA, Investigator's Global Assessment, Janus kinase, c-Jun N-terminal kinase, mitogen-activated protein kinase, oncostatin M receptor β, STAT signal transducer and activator of transcription, T helper, topical corticosteroids, Visual Analogue Scale
Abbreviations used : AD, EASI, IGA, IL, JAK, STAT, TCS, Th2
Plan
Publication of this article was supported by Leo Pharma, Bayer, and Sanofi/Regeneron. |
|
Funding sources: Supported by Bayer (grant #19670), LEO Pharma, and Sanofi Genzyme (grant #IME-2017-11043). |
|
Disclosure: Dr Thyssen is supported by an unrestricted grant from the Lundbeck Foundation; he has attended advisory boards for Roche and Sanofi-Genzyme and received speaker honoraria from LEO Pharma and Sanofi-Genzyme, and he is an investigator for LEO Pharma on their phase 3 tralokinumab study. Dr Hamann disclosed no conflicts of interest. |
Vol 78 - N° 3S1
P. S37-S42 - mars 2018 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.
Déjà abonné à cette revue ?