Diet-induced obesity exacerbates imiquimod-mediated psoriasiform dermatitis in anti-PD-1 antibody-treated mice: Implications for patients being treated with checkpoint inhibitors for cancer

J Dermatol Sci. 2020 Mar;97(3):194-200. doi: 10.1016/j.jdermsci.2020.01.011. Epub 2020 Jan 24.

Abstract

Background: An ever-increasing number of cancer patients are being treated with checkpoint inhibitors such as anti-PD-1 antibodies, and a small percentage of these patients develop a psoriasis-like skin eruption or severe flares of prior psoriasis.

Objective: We investigated the role of obesity in immune checkpoint inhibitors-exacerbated psoriasiform eruption.

Methods: We fed female C57BL/6 mice a so-called Western diet (WD) or a control diet (CD). Imiquimod (IMQ) was applied topically on ears for 5 consecutive days to induce psoriasiform dermatitis (PsD). Psoriasis-related markers were examined by quantitative real-time PCR. Then we induced PsD in WD- and CD-fed mice in the presence or absence of systemic treatment of anti-PD-1 antibodies to examine if obese mice are more susceptible to anti-PD-1 related PsD than lean mice.

Results: WD-fed mice showed higher baseline mRNA expression levels of psoriasis-associated cytokines such as IL-17, S100A8, and S100A9 compared to mice fed with CD. Furthermore, WD-fed mice had more γδ low (GDL) T cells in the whole skin and higher expression of PD-1 on GDL T cells than CD-fed mice. WD-fed mice receiving anti-PD-1 had more prominent ear swelling than lean mice receiving anti-PD-1 during the 5-day IMQ course (2-fold increase, P < 0.0001 on day 5).

Conclusion: WD-induced obesity enhances IMQ-induced psoriasiform inflammation. The finding that WD-fed mice have a more dramatic response to anti-PD-1 than lean mice in terms of IMQ-induced ear swelling suggests that obesity could be a risk factor in the development of psoriasiform eruption during anti-PD-1 therapy.

Keywords: High-fat diet; Immune checkpoint; Psoriasis; Sugar; Western diet.

MeSH terms

  • Animals
  • Diet, Western / adverse effects
  • Disease Models, Animal
  • Female
  • Humans
  • Imiquimod / immunology
  • Immune Checkpoint Inhibitors / adverse effects*
  • Mice
  • Neoplasms / complications
  • Neoplasms / drug therapy*
  • Neoplasms / immunology
  • Obesity / etiology
  • Obesity / immunology*
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Programmed Cell Death 1 Receptor / immunology
  • Psoriasis / immunology*
  • Psoriasis / pathology
  • Risk Factors
  • Skin / immunology
  • Skin / pathology
  • Symptom Flare Up

Substances

  • Immune Checkpoint Inhibitors
  • Pdcd1 protein, mouse
  • Programmed Cell Death 1 Receptor
  • Imiquimod