Paradoxical Psoriasis in Patients Receiving Therapy with Tumor Necrosis Factor Inhibitors: Potential Pathogenic Mechanisms and the Role of Genetic Factors

Int J Mol Sci. 2024 Jun 27;25(13):7018. doi: 10.3390/ijms25137018.

Abstract

TNF inhibitors (TNFi) have revolutionized the therapeutic management of various chronic immune-mediated inflammatory diseases. Despite their known benefits, these therapies are related to paradoxical adverse effects (PAEs), including paradoxical psoriasis (PP). Although the underlying mechanism remains somewhat unclear, some theories suggest that genetic factors, particularly certain single-nucleotide polymorphisms (SNPs), may play an important role. The present review aimed to research and analyze recent findings regarding the pathomechanisms involved in the appearance of PP and the association between various genetic factors and PP in individuals treated with TNFi. We performed a literature search and found that certain genes (IL23R, TNF, FBXL19, CTLA4, SLC12A8, TAP1) are strongly associated with the occurrence of PP in pediatric and adult patients during therapy with TNFi. The identification of the specific SNPs involved in the appearance of PP and other PAEs in patients treated with TNFi for various diseases and in different populations may later favor the recognition of those patients at a high risk of developing such adverse effects and could guide personalized therapeutic strategies in future years.

Keywords: gene; genetic polymorphisms; genetic predisposition; paradoxical adverse effects; paradoxical psoriasis; tumor necrosis factor-alpha inhibitors.

Publication types

  • Review

MeSH terms

  • Genetic Predisposition to Disease
  • Humans
  • Polymorphism, Single Nucleotide*
  • Psoriasis* / drug therapy
  • Psoriasis* / genetics
  • Tumor Necrosis Factor Inhibitors* / adverse effects
  • Tumor Necrosis Factor Inhibitors* / therapeutic use
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Tumor Necrosis Factor Inhibitors
  • Tumor Necrosis Factor-alpha

Grants and funding

This research received no external funding.