Towards understanding the role of nanomedicine in targeting TNFR2 in rheumatoid arthritis

Immunology. 2024 Dec;173(4):622-633. doi: 10.1111/imm.13855. Epub 2024 Aug 27.

Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by inflammation of the synovium and progressive joint destruction which significantly affects both quality of life and socioeconomic status. Admittedly, various treatments are available, but they are usually accompanied by various side effects, from mild to severe, and potentially with adverse events. Tumour necrosis factor-alpha (TNF-α) plays a crucial role in the pathophysiology of RA. It promotes inflammatory, apoptosis and necroptosis via TNF receptor-1 (TNFR1) but elicit anti-inflammatory effects via TNFR2. Herein, targeting TNFR2 has gained attention in RA studies. Understanding the role of nanomedicine in modulating TNFR2 signalling may be the instrument in development of RA therapies. Nanotechnology has made a significant progress in treating various conditions of diseases since its inception. Due to this, nanomedicine has emerged as a promising therapeutics approach for RA. Recent studies have demonstrated the potential of nanomedicine in RA theranostics, combining therapy and diagnostics for improved treatment outcomes. Owing to the challenges and advancements in the field of nanotechnology, nanoparticles are seen as an applicable candidate in the treatment of RA. In this review, we provide an overview of the role of nanomedicine in targeting TNFR2 for the treatment of RA and highlight the limitations of current therapies as well as the potential of nanocarriers with controlled drug release and active targeting abilities.

Keywords: autoimmune disease; nanoparticles; rheumatoid arthritis; tumour necrosis factor receptor 2 (TNFR2); tumour necrosis factor‐alpha (TNF‐α).

Publication types

  • Review

MeSH terms

  • Animals
  • Antirheumatic Agents / therapeutic use
  • Arthritis, Rheumatoid* / drug therapy
  • Humans
  • Molecular Targeted Therapy
  • Nanomedicine* / methods
  • Nanoparticles / therapeutic use
  • Receptors, Tumor Necrosis Factor, Type II* / antagonists & inhibitors
  • Receptors, Tumor Necrosis Factor, Type II* / metabolism
  • Signal Transduction / drug effects
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Receptors, Tumor Necrosis Factor, Type II
  • Antirheumatic Agents
  • Tumor Necrosis Factor-alpha