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
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

Pagination

295-307

Auteurs

Juliane Medler (J)

a Division for Molecular Internal Medicine, Department of Internal Medicine II , University Hospital Würzburg , Würzburg , Germany.

Harald Wajant (H)

a Division for Molecular Internal Medicine, Department of Internal Medicine II , University Hospital Würzburg , Würzburg , Germany.

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Classifications MeSH