TNFR2 signalling in inflammatory diseases

被引:1
|
作者
Williams, Richard O. [1 ]
Clanchy, Felix IL. [1 ]
Huang, Yi-Shu [1 ]
Tseng, Wen-Yi [1 ]
Stone, Trevor W. [1 ]
机构
[1] Univ Oxford, Kennedy Inst Rheumatol, Roosevelt Dr, Oxford OX3 7FY, England
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2024年 / 38卷 / 02期
关键词
TNF; TNF receptors; Inflammation; Rheumatoid arthritis; Autoimmunity; TUMOR-NECROSIS-FACTOR; REGULATORY T-CELLS; MESENCHYMAL STEM-CELLS; RHEUMATOID-ARTHRITIS; FOXP3; EXPRESSION; INFLIXIMAB; ALPHA; INDUCTION; ETANERCEPT; ACTIVATION;
D O I
10.1016/j.berh.2024.101941
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:7
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