TNFR2 signalling in inflammatory diseases

Richard O. Williams*, Felix IL Clanchy, Yi Shu Huang, Wen Yi Tseng, Trevor W. Stone

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

1 Scopus citations

Abstract

TNF signals via two receptors, TNFR1 and TNFR2, which play contrasting roles in immunity. Most of the pro-inflammatory effects of TNF are mediated by TNFR1, whereas TNFR2 is mainly involved in immune homeostasis and tissue healing, but also contributes to tumour progression. However, all currently available anti-TNF biologics inhibit signalling via both receptors and there is increasing interest in the development of selective inhibitors; TNFR1 inhibitors for autoimmune disease and TNFR2 inhibitors for cancer. It is hypothesised that selective inhibition of TNFR1 in autoimmune disease would alleviate inflammation and promote homeostasis by allowing TNFR2 signalling to proceed unimpeded. Validation of this concept would pave the way for the development and testing of TNF specific antagonists. Another therapeutic approach being explored is the use of TNFR2 specific agonists, which could be administered alone or in combination with a TNFR1 antagonist.

Original languageEnglish
Article number101941
Pages (from-to)101941
JournalBest Practice and Research: Clinical Rheumatology
Volume38
Issue number2
Early online date26 03 2024
DOIs
StatePublished - 05 2024
Externally publishedYes

Bibliographical note

Copyright © 2024 Elsevier Ltd. All rights reserved.

Keywords

  • Autoimmunity
  • Inflammation
  • Rheumatoid arthritis
  • TNF
  • TNF receptors
  • Humans
  • Neoplasms/drug therapy
  • Signal Transduction/drug effects
  • Inflammation/immunology
  • Tumor Necrosis Factor-alpha/antagonists & inhibitors
  • Autoimmune Diseases/immunology
  • Receptors, Tumor Necrosis Factor, Type I/antagonists & inhibitors
  • Receptors, Tumor Necrosis Factor, Type II

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