TNF-α: a treatment target or cause of sarcoidosis?

J Eur Acad Dermatol Venereol. 2015 Nov;29(11):2104-11. doi: 10.1111/jdv.13246. Epub 2015 Aug 26.

Abstract

Sarcoidosis is a systemic granulomatous disease that affects numerous organs, commonly manifesting at the lungs and skin. While corticosteroids remain the first line of treatment, tumour necrosis factor alpha (TNF-α) inhibitors have been investigated as one potential steroid sparing treatment for sarcoidosis. TNF-α is one of many components involved in the formation of granulomas in sarcoidosis. While there have been larger scale studies of biologic TNF-α inhibition in systemic sarcoidosis, studies in cutaneous disease are limited. Paradoxically, in some patients treated with biologic TNF-α inhibitors for other diseases, treatment can induce the development of sarcoidosis. In the light of this complexity, we discuss the role of TNF-α in granuloma formation, the therapeutic role of TNF-α inhibition and immunologic abnormalities following treatment with these TNF-α inhibitors including drug-specific alterations involving interferon-γ, lymphotoxin-α, TNF receptor 2 (TNFR2) and T-regulatory cells.

Publication types

  • Review

MeSH terms

  • Adalimumab / therapeutic use
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Biological Products / therapeutic use*
  • Etanercept / therapeutic use
  • Granuloma / metabolism
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Infliximab / therapeutic use
  • Lung Diseases / drug therapy*
  • Lung Diseases / etiology
  • Lung Diseases / metabolism
  • Molecular Targeted Therapy
  • Sarcoidosis / drug therapy*
  • Sarcoidosis / etiology
  • Sarcoidosis / metabolism
  • Skin Diseases / drug therapy*
  • Skin Diseases / etiology
  • Skin Diseases / metabolism
  • Thalidomide / therapeutic use
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors*
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Biological Products
  • Immunosuppressive Agents
  • Tumor Necrosis Factor-alpha
  • Thalidomide
  • Infliximab
  • Adalimumab
  • Etanercept