Tumor necrosis factor receptor-2 (TNFR2): an overview of an emerging drug target.
Antibody
Fc-gamma receptors
TNF receptor 1 (TNFR1)
TNF receptor 2 (TNFR2)
antibody fusion proteins
autoimmune disease
cancer treatment
multiple sclerosis
regulatory T-cell (Treg)
rheumatoid arthritis
tumor necrosis factor (TNF)
Journal
Expert opinion on therapeutic targets
ISSN: 1744-7631
Titre abrégé: Expert Opin Ther Targets
Pays: England
ID NLM: 101127833
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
pubmed:
12
3
2019
medline:
7
3
2020
entrez:
12
3
2019
Statut:
ppublish
Résumé
Tumor necrosis factor (TNF) receptor 2 (TNFR2) is one of two receptors of the cytokines, TNF and lymphotoxin-α. TNFR1 is a strong inducer of proinflammatory activities. TNFR2 has proinflammatory effects too, but it also elicits strong anti-inflammatory activities and has protective effects on oligodendrocytes, cardiomyocytes, and keratinocytes. The protective and anti-inflammatory effects of TNFR2 may explain why TNF inhibitors failed to be effective in diseases such as heart failure or multiple sclerosis, where TNF has been strongly implicated as a driving force. Stimulatory and inhibitory TNFR2 targeting hence attracts considerable interest for the treatment of autoimmune diseases and cancer. Areas covered: Based on a brief description of the pathophysiological importance of the TNF-TNFR1/2 system, we discuss the potential applications of TNFR2 targeting therapies. We also debate TNFR2 activation as a way forward in the search for TNFR2-specific agents. Expert opinion: The use of TNFR2 to target regulatory T-cells is attractive, but this approach is just one amongst many suitable targets. With respect to its preference for Treg stimulation and protection of non-immune cells, TNFR2 is more unique and thus offers opportunities for translational success.
Identifiants
pubmed: 30856027
doi: 10.1080/14728222.2019.1586886
doi:
Substances chimiques
Receptors, Tumor Necrosis Factor, Type II
0
TNFRSF1B protein, human
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM