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Dupilumab: A review of its use in the treatment of atopic dermatitis
Abstract
Atopic dermatitis (AD) is a chronic, pruritic immune-mediated inflammatory dermatosis characterized by a T helper 2 (Th2) immune response phenotype and may be associated with systemic inflammation. Dupilumab is an interleukin 4 (IL-4) receptor α-antagonist that inhibits IL-4 and IL-13 signaling through blockade of the shared IL-4α subunit. Blockade of IL-4/13 is effective in reducing Th2 response. Dupilumab has recently been approved in the United States and Europe for the treatment of adult patients with moderate-to-severe AD. Clinical trials have shown that adults with moderate-to-severe AD who receive weekly or biweekly dupilumab injections have significantly improved clinical and patient-reported outcomes, including Eczema Area Severity Index, SCORing Atopic Dermatitis, Dermatology Life Quality Index, and itch Numeric Rating Scale scores. Concomitant use of topical corticosteroids along with dupilumab results in a greater improvement in signs and symptoms of AD than with use of dupilumab alone. Biomarker analyses show that dupilumab modulates the AD molecular signature and other Th2-associated biomarkers. Common adverse events reported in the clinical trials were nasopharyngitis, upper respiratory tract infection, injection site reactions, skin infections, and conjunctivitis. These were mild-to-moderate in nature, and overall rates of adverse events occurred with similar frequency between the treatment and placebo groups. There were no significant serious safety concerns identified in phase III clinical trials. Dupilumab, as monotherapy or with concomitant use of topical corticosteroids, can significantly improve clinical outcomes and quality of life in patients suffering from moderate-to-severe AD. Ongoing studies of dupilumab will help determine the clinical efficacy and safety profile of its long-term use.
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“This dampens the T H 2 inflammatory response, thereby improving the symptoms associated with atopic dermatitis.1,2”
From Dupilumab for Allergic Contact Dermatitis: An Overview of Its Use and Impact on Patch Testing. (2022) · cites this paper as [2]
In the citing paper
“Through inhibition of the IL-4Rα subunit, it prevents activation of the IL-4/IL-13 signaling cascade.”
From Dupilumab for Allergic Contact Dermatitis: An Overview of Its Use and Impact on Patch Testing. (2022) · cites this paper as [2]
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“Clinical trials have shown that adults with moderate-to-severe AD who receive weekly or biweekly dupilumab injections have significantly improved clinical and patient-reported outcomes, including Eczema Area Severity Index, SCORing Atopic Dermatitis, Dermatology Life Quality Index, and Itch Numeric Rating Scale scores…”
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“It is also characterized by a T helper 2 (Th2) immune response phenotype.(1) AD has a substantial physical and psychosocial impact on patients and relatives.”
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“17 Owing to this mechanism of action this drug has emerged as a targeted biologic treatment for AD but also for other suspected type-2 helper T cell mediated in fl am-matory conditions like chronic rhinosinusitis with nasal polyps and uncontrolled persistent asthma.”
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“ment for children 6 to 11 years old prior to recent approval in that age group.(6,7) There are some case reports of dupilumab being used with success in heart transplant recipients older than 18 years of age,”
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“33 In AD patients, circadian rhythm disturbances affect the secretion of cortisol, disrupt melatonin levels and worsen barrier function at night, resulting in an aggravated inflammatory response and the natural rhythm of immune cells and inflammatory cytokines.”
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“Dupilumab, a monoclonal antibody targeting interleukin-4 and interleukin-13 pathways, has demonstrated efficacy in reducing pruritus and inflammation in various chronic skin conditions including PN and AD [75, 76].”
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“[14] Therefore, the investigation for treatment with high efficacy and low side effect profile continues.”
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da Silva, J. O. N., Silva, R. R. E., Ribeiro, P. V. Z., Farah, P. M. E., & Steglich, R. B. (2025) · Anais Brasileiros de Dermatologia · doi:10.1016/j.abd.2024.08.008 · Cited by 7
Genetically engineered drugs for treatment of bronchial asthma: recent achievements
Zyryanov, S. K., & Butranova, O. I. (2018) · PULMONOLOGIYA · doi:10.18093/0869-0189-2018-28-5-584-601 · Cited by 7
Mastorino, L., Ortoncelli, M., Virginia, B., Rolla, G., Avallone, G., Cavaliere, G., Viola, R., Quaglino, P., & Ribero, S. (2021) · Dermatologic Therapy · doi:10.1111/dth.15117 · Cited by 7
“It is a fully human monoclonal antibody that inhibits IL-4 and IL-13 signaling by blocking the shared receptor subunit IL4Rα reducing the T-helper-2 immune response.(2) Ocular surface disease, injection-site reactions, and recurrent oral herpes are well-known side effects of the atopic patient treated with dupilumab.”
BackgroundDupilumab-associated ulcerative keratitis
Wilson, M., & Daniell, M. D. (2022) · International Journal of Ophthalmology · doi:10.18240/ijo.2022.06.23 · Cited by 7
Yan, D., Ramachandran, V., Weston, G. K., Kim, R. H., & Latkowski, J.-A. M. (2023) · International Journal of Dermatology · doi:10.1111/ijd.16641 · Cited by 7
Two cases of dupilumab‐induced vitiligo
Ferreirinha, A., Farinha, P. S., Costa, T. P. E., & Duarte, B. (2024) · JDDG Journal der Deutschen Dermatologischen Gesellschaft · doi:10.1111/ddg.15564 · Cited by 6
Ninomiya, M., Egholm, C., Breu, D., Boyman, O., & Bode, J. W. (2025) · Science Advances · doi:10.1126/sciadv.adw9755 · Cited by 5
“Dupilumab, an anti–IL-4R α monoclonal antibody, blocks IL-4R–mediated signaling and was approved for atopic dermatitis in 2017 and for asthma in 2018 by the Food and Drug Administration ( 18 – 20 ).”
Silverberg, J. I., Ackerman, L., Bagel, J., Gold, L. S., Blauvelt, A., Rosmarin, D. M., Chovatiya, R., Zirwas, M., Yosipovitch, G., Waibel, J. S., et al. (2026) · Dermatology and Therapy · doi:10.1007/s13555-025-01644-3 · Cited by 6
Treatment of Severe Atopic Dermatitis with Dupilumab in Three Patients with Renal Diseases
Foti, C., Romita, P., Ambrogio, F., Manno, C., Filotico, R., Cassano, N., Vena, G. A., MARCO, A. D., Cazzato, G., & Mennuni, B. G. (2022) · Life · doi:10.3390/life12122002 · Cited by 6
“Dupilumab is a human monoclonal antibody that inhibits interleukin (IL)-4 and IL-13 signaling by binding the shared alpha-subunit of the IL-4 receptor, thus reducing the Th2 response [1].”
BackgroundSaeki, H., Fujita, H., Suzuki, K., & Arima, K. (2023) · Journal of Cutaneous Immunology and Allergy · doi:10.1002/cia2.12303 · Cited by 6
Dupilumab in Patients with Atopic Dermatitis: A Multicentric, Long-Term, Real-World Portuguese Study
Torres, T. R., Cruz, M. J., Gonçalo, M., Filipe, P., Duarte, B., Alves, J., Alvarenga, J. M., da Rosa, G. P., Flor, D., Ramos, J. A., et al. (2024) · Dermatology and Therapy · doi:10.1007/s13555-024-01235-8 · Cited by 6
Efficacy and safety of dupilumab in a patient with metastatic clear cell renal cell carcinoma
Ferreira, C., Freitas, E., & Torres, T. R. (2024) · Journal of International Medical Research · doi:10.1177/03000605241297551 · Cited by 6
Oninla, O. A., Akinkugbe, A., Otike-Odibi, B. I., Oripelaye, M. M., & Olanrewaju, F. O. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.97287 · Cited by 6
Wang, B., Pan, S.-X., Yao, Y.-P., Zeng, L.-X., & Zhang, G. (2022) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.13704 · Cited by 7
“Dupilumab, the first biologic approved as a first-line treatment for moderate-to-severe AD, is an interleukin (IL)-4 receptor antagonist that inhibits IL-4 and IL-13 signalling and showed promising efficacy.(7) Janus kinase (JAK) and signal transducer and activator of transcription (STAT) pathway (JAK–STAT pathway) ar…”
BackgroundAnsai, O., Miyauchi, T., Hayashi, R., Katsumi, T., Nishiguchi, T., Hasegawa, A., Shinkuma, S., Natsuga, K., Nomura, T., Shimomura, Y., et al. (2022) · Clinical and Experimental Dermatology · doi:10.1093/ced/llac069 · Cited by 6
Zhao, X.-Q., Zhu, W.-J., Mou, Y., Meng, X., & Xia, J. (2023) · World Journal of Clinical Cases · doi:10.12998/wjcc.v11.i10.2301 · Cited by 6
Therapy of Allergic and Irritant Contact Dermatitis
Ludriksone, L., Antonov, D., Schliemann, S., & Elsner, P. U. (2020) · Springer eBooks · doi:10.1007/978-3-030-36335-2_72 · Cited by 7
Atopic keratoconjunctivitis alleviated with dupilumab
Chen, J., & Bielory, L. (2022) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2022.05.031 · Cited by 6
Serum Mediators in Patients with Both Type 2 Diabetes Mellitus and Pruritus
He, G.-Y., Hsu, T.-Y., Chen, C.-W., Nien, F., Chen, H., Chu, C., & Wang, L. (2023) · Acta Dermato Venereologica · doi:10.2340/actadv.v103.4863 · Cited by 5
“Dupilumab, an IL4Rα antibody targeting IL4 and IL13, has been shown to have a significant effect on itching relief in AD, prurigo nodularis, and many pruritic skin disorders (22, 23).”
BackgroundGajraj, F. A., Zahir, J., Adereti, C. O., & Gajraj, M. H. (2023) · Cureus · doi:10.7759/cureus.41274 · Cited by 5
“Dupilumab is a monoclonal antibody, commonly used to treat severe AD, which targets the interleukin(IL)-4 receptor alpha subunit (4Rα) found on T-helper cells type 2 (TH2); IL4Rα normally interacts with IL-4 and IL-13 [9].”
BackgroundXuan, Z., Chen, X., Zhou, W., Shen, Y., Sun, Z., Zhang, H., & Yao, Z. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1367958 · Cited by 5
“Notably, the approval of dupilumab, an antagonist of IL-4 and IL-13, for treating patients with moderate-to-severe AD exempli fi es this promising approach (41).”
BackgroundGorritz, M., Boytsov, N. N., Goldblum, O. M., Malatestinic, W. N., Wang, X., & Wade, R. L. (2021) · Journal of Dermatological Treatment · doi:10.1080/09546634.2021.1981813 · Cited by 5
Anti‐pruritic effect of isothiocyanates: Potential involvement of toll‐like receptor 3 signaling
Moriyama, M., Konno, M., Serizawa, K., Yuzawa, N., Majima, Y., Hayashi, I., Suzuki, T., & Kainoh, M. (2022) · Pharmacology Research & Perspectives · doi:10.1002/prp2.1038 · Cited by 4
Metadata
- Authors
- Gooderham, M. J., Hong, H. C.-H., Eshtiaghi, P., & Papp, K. A.
- Affiliations
- Queen's University (CA)
- University of British Columbia (CA)
- Probity Medical Research (CA)
- Corresponding author
- Gooderham, Melinda J.
- Venue
- Journal of the American Academy of Dermatology
- Publisher
- Elsevier BV
- Published
- 2018-03
- Volume
- 78
- Issue
- 3
- Pages
- S28-S36
- ISSN
- 0190-9622 (ISSN-L)
- OpenAlex
- W2789024274
- Cited by
- 343
- References
- 17
- Citations by year
- 2026: 30 · 2025: 39 · 2024: 40 · 2023: 41 · 2022: 47 · 2021: 64 · 2020: 43 · 2019: 28 · 2018: 10
- FWCI
- 39.26
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of the American Academy of Dermatology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Bayer
- LEO Pharma
- Sanofi
- Topics
- Health Sciences › Medicine › Dermatology › Dermatology and Skin Diseases
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Asthma and respiratory diseases
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- dupilumab, atopic dermatitis, IL-4 receptor alpha antagonist, IL-4/IL-13 signaling, Th2 immune response, topical corticosteroids, biomarkers, adverse events, quality of life, moderate-to-severe atopic dermatitis
- MeSH terms
- Patient Reported Outcome Measures, Antibodies, Monoclonal, Biological Products, Dermatitis, Atopic, Female, Humans, Male, Quality of Life, Severity of Illness Index, Drug Delivery Systems, Treatment Outcome, Clinical Trials, Phase III as Topic, Risk Assessment, Antibodies, Monoclonal, Humanized
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