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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.
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页数:12
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