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Review
. 2024;16(14-15):925-935.
doi: 10.1080/1750743X.2024.2383554. Epub 2024 Aug 9.

The role of nemolizumab in the treatment of atopic dermatitis for the adult population

Affiliations
Review

The role of nemolizumab in the treatment of atopic dermatitis for the adult population

Stuti Prajapati et al. Immunotherapy. 2024.

Abstract

Atopic dermatitis (AD) often requires long-term treatment that may be associated with adverse effects. This review aims to characterize nemolizumab as a treatment for AD in adults. A literature search was performed to assess nemolizumab's role in moderate-to-severe AD in adults. Currently, clinical trials are being conducted to evaluate the clinical efficacy, safety profile and optimal dosing of nemolizumab for adults with moderate-to-severe AD. The most common adverse effects include nasopharyngitis, AD exacerbation and increased blood creatinine phosphokinase. Recent data from clinical trials suggest nemolizumab may be an acceptable treatment in adults with moderate-to-severe AD.

Keywords: IL-31; atopic dermatitis; eczema; immunotherapy; pruritus; systemic treatment.

Plain language summary

Atopic dermatitis, also known as eczema, is a long-lasting skin condition that is difficult to treat. Symptoms include itching, redness, dryness and pain. Various eczema treatments are available to help patients based on how severe their symptoms are. Nemolizumab is a treatment that blocks immune system pathways involving itching and inflammation. This review describes nemolizumab as a treatment option for moderate-to-severe eczema in adults. We completed a literature search to understand nemolizumab's role in eczema treatment. Nemolizumab has decreased itchiness in adults with moderate-to-severe eczema in clinical trials. The most common side effects of nemolizumab treatment were the common cold, worsening of eczema and an increased muscle marker (creatinine phosphokinase). Nemolizumab appears to be an effective treatment for moderate-to-severe eczema in adults with bearable side effects.

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Conflict of interest statement

The authors have no competing interests or relevant affiliations with any organization or entity with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, stock ownership or options and expert testimony.

Figures

Figure 1.
Figure 1.
Mechanism of action for nemolizumab. AKT: Protein kinase B; IL-31: Interleukin-31; IL-31Rα: Interleukin-31 alpha receptor; JAK/STAT: Janus kinase/signal transducers and activators of transcription; MAPK: Mitogen-activated protein kinase; OSMRB: Oncostatin Mβ receptor; PI3K: Phosphoinositide-3-kinase.

References

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