蕈样真菌病
医学
杜皮鲁玛
疾病
皮肤T细胞淋巴瘤
发病机制
特应性皮炎
免疫学
临床试验
淋巴瘤
T细胞
皮肤病科
免疫系统
病理
作者
Roberto Mazzetto,Paola Miceli,Jacopo Tartaglia,Christian Ciolfi,Alvise Sernicola,Mauro Alaibac
出处
期刊:Life
[Multidisciplinary Digital Publishing Institute]
日期:2024-02-09
卷期号:14 (2): 245-245
被引量:8
摘要
The interleukins IL-4 and IL-13 are increasingly recognized contributors to the pathogenesis of cutaneous T cell lymphomas (CTCLs), and their role in disease-associated pruritus is accepted. The prevailing Th2 profile in advanced CTCL underscores the significance of understanding IL-4/IL-13 expression dynamics from the early stages of disease, as a shift from Th1 to Th2 may explain CTCL progression. Targeted agents blocking key cytokines of type 2 immunity are established therapeutics in atopic disorders and have a promising therapeutic potential in CTCL, given their involvement in cutaneous symptoms and their contribution to the pathogenesis of disease. IL-4, IL-13, and IL-31 are implicated in pruritus, offering therapeutic targets with dupilumab, tralokinumab, lebrikizumab, and nemolizumab. This review analyzes current knowledge on the IL-4/IL-13 axis in mycosis fungoides and Sezary syndrome, the most common types of CTCL, examining existing literature on the pathogenetic implications with a focus on investigational treatments. Clinical trials and case reports are required to shed light on novel uses of medications in various diseases, and ongoing research into the role of IL-4/IL-13 axis blockers in CTCL therapy might not only improve the management of disease-related pruritus but also provide in-depth insights on the pathophysiologic mechanisms of CTCL.
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