Inflammatory cytokines and peripheral mediators in the pathophysiology of pruritus in cutaneous T-cell lymphoma

J Eur Acad Dermatol Venereol. 2018 Oct;32(10):1652-1656. doi: 10.1111/jdv.15075. Epub 2018 Jun 8.

Abstract

Cutaneous T-cell lymphoma (CTCL) includes a diverse group of neoplasms, including mycosis fungoides and Sézary syndrome. One of the earliest and most common symptoms of CTCL is pruritus, which affects up to 88% of patients. The severity of pruritus can range from mild to very debilitating, producing tremendous discomfort and a significant decrease in quality of life. Patients with advanced disease, in particular, may experience a more chronic, intractable pruritus. However, the underlying mechanism of pruritus in CTCL remains unknown. Conventional antipruritic agents, such as antihistamines, gamma-aminobutyric acid analogs and antidepressants, are only partially effective in relieving symptoms, suggesting a more complex, unique pathophysiology. In this review, we summarize the current research on cytokines and peripheral mediators implicated in pruritus in CTCL.

Publication types

  • Review

MeSH terms

  • Analgesics, Opioid / metabolism
  • Histamine / metabolism
  • Humans
  • Interleukins / metabolism*
  • Lymphoma, T-Cell, Cutaneous / complications
  • Lymphoma, T-Cell, Cutaneous / metabolism*
  • Nerve Growth Factor / metabolism
  • Nicotinamide Phosphoribosyltransferase / metabolism
  • Pruritus / etiology
  • Pruritus / metabolism*
  • Substance P / metabolism

Substances

  • Analgesics, Opioid
  • Interleukins
  • Substance P
  • Histamine
  • Nerve Growth Factor
  • Nicotinamide Phosphoribosyltransferase