Concurrent Nemolizumab-Induced Cutaneous Adverse Events and Asthma Exacerbation in a Patient With Prurigo Nodularis With Resolution of Both Conditions After Switching to Dupilumab

Prurigo nodularis (PN) is a chronic pruritic inflammatory disease driven by Th2-dominant immune dysregulation and neural hyperactivity. Conventional therapies often fail, while biologics such as dupilumab and nemolizumab have shown efficacy. However, nemolizumab can cause cutaneous adverse events (cAEs) and occasional asthma exacerbation. An 82-year-old woman with long-standing PN and well-controlled asthma developed cAEs and asthma exacerbation one month after initiating nemolizumab, an IL-31 receptor antagonist. Although nemolizumab markedly improved pruritus and PN lesions, acute eczematous eruptions and erythematous papules appeared on previously unaffected skin, accompanied by worsening asthma symptoms. After switching to dupilumab (IL-4/IL-13 inhibitor), both cAEs and asthma improved, with complete resolution within two months. The mechanism underlying nemolizumab-induced cAEs and asthma remains unclear, but activation of Th2-driven inflammation following IL-31 blockade has been proposed. To our knowledge, this is the first reported case of concurrent nemolizumab-induced cAEs and asthma exacerbation in a patient with PN, successfully managed with dupilumab. Given that asthma exacerbations have occurred only in patients with preexisting asthma, careful monitoring is warranted when administering nemolizumab. Further studies are needed to clarify its mechanism and management strategies.

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Publication Details

Journal
Cureus
Published
2025-11-11
DOI
https://doi.org/10.7759/cureus.96605
Citations
2
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
4.01
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article

Concurrent Nemolizumab-Induced Cutaneous Adverse Events and Asthma Exacerbation in a Patient With Prurigo Nodularis With Resolution of Both Conditions After Switching to Dupilumab

Yoshihito Mima, Masako Yamamoto, Ken Iozumi
2 citations
Cureus
Dermatology and Skin Diseases
4.01
article

Concurrent Nemolizumab-Induced Cutaneous Adverse Events and Asthma Exacerbation in a Patient With Prurigo Nodularis With Resolution of Both Conditions After Switching to Dupilumab

Yoshihito Mima, Masako Yamamoto, Ken Iozumi
article en
2 citations

Abstract

Prurigo nodularis (PN) is a chronic pruritic inflammatory disease driven by Th2-dominant immune dysregulation and neural hyperactivity. Conventional therapies often fail, while biologics such as dupilumab and nemolizumab have shown efficacy. However, nemolizumab can cause cutaneous adverse events (cAEs) and occasional asthma exacerbation. An 82-year-old woman with long-standing PN and well-controlled asthma developed cAEs and asthma exacerbation one month after initiating nemolizumab, an IL-31 receptor antagonist. Although nemolizumab markedly improved pruritus and PN lesions, acute eczematous eruptions and erythematous papules appeared on previously unaffected skin, accompanied by worsening asthma symptoms. After switching to dupilumab (IL-4/IL-13 inhibitor), both cAEs and asthma improved, with complete resolution within two months. The mechanism underlying nemolizumab-induced cAEs and asthma remains unclear, but activation of Th2-driven inflammation following IL-31 blockade has been proposed. To our knowledge, this is the first reported case of concurrent nemolizumab-induced cAEs and asthma exacerbation in a patient with PN, successfully managed with dupilumab. Given that asthma exacerbations have occurred only in patients with preexisting asthma, careful monitoring is warranted when administering nemolizumab. Further studies are needed to clarify its mechanism and management strategies.

CureusVol. 17(11)
Tokyo Metropolitan Police Hospital (JP)
Openalex Percentile: Top 6%
Dermatology and Skin Diseases
4.01
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Concurrent Nemolizumab-Induced Cutaneous Adverse Events and Asthma Exacerbation in a Patient With Prurigo Nodularis With Resolution of Both Conditions After Switching to Dupilumab — Yoshihito Mima, Masako Yamamoto, et al. · Cureus (2025) | TGRS Research Map | TGRS