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

Life (Basel)

Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padova, Italy.

Published: February 2024

AI Article Synopsis

  • IL-4 and IL-13 play significant roles in the development and symptoms of cutaneous T cell lymphomas (CTCL), particularly in relation to itching (pruritus).
  • The transition from a Th1 immune response to a Th2 profile in advanced CTCL may help explain the disease's progression, highlighting the need for early understanding of these interleukins.
  • Targeted treatments aimed at blocking IL-4, IL-13, and IL-31 show promise for managing CTCL symptoms and require further investigation through clinical trials to explore their therapeutic potential.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10889933PMC
http://dx.doi.org/10.3390/life14020245DOI Listing

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