Role of IL-4 and IL-13 in Cutaneous T Cell Lymphoma

被引:5
|
作者
Mazzetto, Roberto [1 ]
Miceli, Paola [1 ]
Tartaglia, Jacopo [1 ]
Ciolfi, Christian [1 ]
Sernicola, Alvise [1 ]
Alaibac, Mauro [1 ]
机构
[1] Univ Padua, Dept Med DIMED, Dermatol Unit, I-35121 Padua, Italy
来源
LIFE-BASEL | 2024年 / 14卷 / 02期
关键词
interleukin; 4; 13; cutaneous T cell lymphoma; mycosis fungoides; Sezary syndrome; dupilumab; nemolizumab; tralokinumab; lebrikizumab; tezepelumab; THYMIC STROMAL LYMPHOPOIETIN; MYCOSIS-FUNGOIDES; INTERLEUKIN-13; RECEPTOR; ATOPIC-DERMATITIS; SEZARY-SYNDROME; UP-REGULATION; CYTOKINE; PATHOGENESIS; PROGRESSION; ACTIVATION;
D O I
10.3390/life14020245
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
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页数:12
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