Management of dupilumab-associated conjunctivitis in atopic dermatitis
Publication date
2019-05
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taverne
Abstract
Since September 2017, the monoclonal antibody dupilumab (Dupixent® ) has been approved in the EU for the treatment of moderate-to-severe atopic dermatitis. By blocking IL-4 and IL-13 signaling pathways, dupilumab improves both objective signs and subjective symptoms of the disease. Blocking of the IL-4aRα subunit leads to improvement of the skin's barrier function and reduction in Th2-mediated inflammation. While the rate of adverse events on dupilumab is generally low, mild-to-moderate conjunctivitis associated with redness as well as a burning and foreign body sensation has been reported in up to 28 % of patients. Treatment options include topical corticosteroids and topical calcineurin inhibitors. The present review highlights the clinical presentation of dupilumab-associated conjunctivitis and addresses pharmacological and non-pharmacological options available for the treatment of this clinically highly relevant condition.
Keywords
Adrenal Cortex Hormones/therapeutic use, Antibodies, Monoclonal, Humanized/adverse effects, Calcineurin Inhibitors/therapeutic use, Clinical Trials, Phase III as Topic, Conjunctivitis/chemically induced, Dermatitis, Atopic/drug therapy, Dermatologic Agents/adverse effects, Humans, Ophthalmic Solutions/therapeutic use, Taverne, Journal Article, Review
Citation
Aszodi, N, Thurau, S, Seegräber, M, de Bruin-Weller, M & Wollenberg, A 2019, 'Management of dupilumab-associated conjunctivitis in atopic dermatitis', JDDG - Journal of the German Society of Dermatology, vol. 17, no. 5, pp. 488-491. https://doi.org/10.1111/ddg.13809