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.
Original language | English |
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Pages (from-to) | 488-491 |
Number of pages | 4 |
Journal | JDDG - Journal of the German Society of Dermatology |
Volume | 17 |
Issue number | 5 |
DOIs | |
Publication status | Published - May 2019 |
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