Disease modification in chronic spontaneous urticaria

• Published in: Allergy (Copenhagen) 2024-09, Vol.79 (9), p.2396-2413
• Main Authors: Maurer, Marcus, Kolkhir, Pavel, Pereira, Manuel P., Siebenhaar, Frank, Witte‐Händel, Ellen, Bergmann, Karl‐Christian, Bonnekoh, Hanna, Buttgereit, Thomas, Fluhr, Joachim W., Frischbutter, Stefan, Grekowitz, Eva Maria, Herzog, Leonie, Kiefer, Lea Alice, Krause, Karoline, Magerl, Markus, Muñoz, Melba, Neisinger, Sophia, Nojarov, Nicole, Prins, Samantha, Pyatilova, Polina, Ramanauskaité, Aisté, Scheffel, Jörg, Terhorst‐Molawi, Dorothea, Treudler, Regina, Weller, Karsten, Zuberbier, Torsten, Metz, Martin
• Format: Article
• Language: English
• Subjects: Autoantibodies; Bruton's tyrosine kinase; Cell activation; chronic spontaneous urticaria; Chronic Urticaria - drug therapy; Chronic Urticaria - etiology; Comorbidity; Disease Management; disease modification; Disease Progression; disease‐driving signals; disease‐modifying treatments; Drug therapy; Humans; Immune system; Intestinal microflora; Mast Cells - immunology; Mast Cells - metabolism; Medical treatment; Microbiomes; Remission; Remission (Medicine); Skin diseases; therapy‐free clinical remission; Treatment Outcome; Urticaria
• ISSN: 0105-4538; 1398-9995; 1398-9995
• DOI: 10.1111/all.16243

Chronic spontaneous urticaria (CSU) is a debilitating, inflammatory skin condition characterized by infiltrating immune cells. Available treatments are limited to improving the signs and symptoms. There is an unmet need to develop therapies that target disease‐driving pathways upstream of mast cell activation to inhibit or delay the progression of CSU and associated comorbidities. Here, we aim to define disease modification due to a treatment intervention and criteria that disease‐modifying treatments (DMTs) must meet in CSU. We have defined disease modification in CSU as a favorable treatment‐induced change in the underlying pathophysiology and, therefore, the disease course, which is clinically beneficial and enduring. A DMT must fulfil the following criteria: (1) prevents or delays the progression of CSU, (2) induces long‐term, therapy‐free clinical remission, which is the sustained absence of CSU signs and symptoms without the need for treatment, and (3) affects the underlying mechanism of CSU, as demonstrated by an effect on disease‐driving signals and/or a biomarker. DMTs in CSU should slow disease progression, achieve long‐lasting disease remission, target disease‐driving mechanisms, reduce mast cell‐activating IgE autoantibodies, target cytokine profile polarization, and normalize the gut microbiome and barrier. Treating CSU at the immune system level could provide valuable alternatives to pharmacotherapy in CSU management. Specific DMTs in CSU are yet to be developed, but some show potential benefits, such as inhibitors of Bruton's Tyrosine Kinase, IL‐4 and IL‐13. Future therapies could prevent CSU signs and symptoms, achieve long‐term clinical benefits after discontinuing treatment, and prevent associated concomitant disorders.