Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Jun 12;19(1):8.
doi: 10.1186/s12948-021-00148-7.

IL-31, itch and hematological malignancies

Affiliations
Review

IL-31, itch and hematological malignancies

Eleonora Di Salvo et al. Clin Mol Allergy. .

Abstract

Pruritus is one of the most common symptoms experienced by neoplastic patients. The pathogenesis of neoplastic itch is complex and multifactorial and could be due to an unbalanced production of humoral mediators by altered immune effector cells. IL-31 is a pro-inflammatory cytokine produced by CD4 + T helper cells. The aim of this review was to evaluate the role of this Th2 cytokine and its receptor IL-31RA, in the onset of neoplastic pruritus. We analysed scientific literature looking for the most relevant original articles linking IL-31to itch in oncologic diseases. Interleukin-31 seems to be a main itch mediator in several hematologic disease such as Cutaneous T cells lymphomas. In these patients IL-31 was positively linked to itch level, and IL-31 matched with disease stage. IL-31 seems to play an important role in the signalling pathway involved in pruritus, but it is also suggested to play a proinflammatory and immunomodulatory role which could play a part in the progression of the neoplastic disease. Further studies will be fundamental in facing pruritus in oncologic patients, since this problem compromise their quality of life worsening an already critic picture.

Keywords: Cancer; Cytokines; IL-31; IL-33; Itch; Malignancies; Pruritus; Skin.

PubMed Disclaimer

Conflict of interest statement

None of the author have any conflict of interests to declare.

Figures

Fig. 1
Fig. 1
Etiopathogenesis of itch in malignancies linked IL-31

Similar articles

Cited by

References

    1. Polat M, Öztas P, \.Ilhan N, Yalçin M, Alli B. Generalized pruritus. Am J Clin Dermatol. 2008;9:39–44. doi: 10.2165/00128071-200809010-00004. - DOI - PubMed
    1. Weisshaar E, Weiss M, Mettang T, Yosipovitch G, Zylicz Z. Paraneoplastic itch: an expert position statement from the special interest group (SIG) of the International Forum on the Study of Itch (IFSI) Acta Derm Venereol. 2015;95:261–5. doi: 10.2340/00015555-1959. - DOI - PubMed
    1. Yosipovitch G. Chronic pruritus: a paraneoplastic sign. Dermatol Ther. 2010;23:590–6. doi: 10.1111/j.1529-8019.2010.01366.x. - DOI - PMC - PubMed
    1. Rowe B, Yosipovitch G. Malignancy-associated pruritus. Eur J Pain. 2015;20:19–23. doi: 10.1002/ejp.760. - DOI - PubMed
    1. Bilsborough J, Leung DYM, Maurer M, Howell M, Boguniewcz M, Yao L, Storey H, LeCiel C, Harder B, Gross JA. IL-31 is associated with cutaneous lymphocyte antigen–positive skin homing T cells in patients with atopic dermatitis. J Allergy Clin Immunol. 2006;117:418–25. doi: 10.1016/j.jaci.2005.10.046. - DOI - PubMed