相关实验视频
Updated: Jul 20, 2025

07:37
An Adoptive Transfer Model of Rheumatoid Arthritis in Mice
Published on: June 6, 2025
196
作为类风湿性疾病及其他疾病的治疗点的TNF和TNF受体
Daniela Siegmund1, Harald Wajant2
1Division of Molecular Internal Medicine, Department of Internal Medicine II, University Hospital of Würzburg, Würzburg, Germany.
Nature reviews. Rheumatology
|August 4, 2023
概括
瘤坏死因子 (TNF) 在免疫疾病中起着复杂的作用,通过TNFR1和TNFR2起作用. 针对特定受体的新疗法可能为炎症条件提供更好的治疗方法.
科学领域:
- 免疫学 免疫学 免疫学
- 分子生物学分子生物学
- 药理学 药理学 是一个学科.
背景情况:
- 瘤坏死因子 (TNF) 是免疫媒介疾病的关键调解者.
- 目前的TNF中和药物广泛用于炎症疾病,但具有局限性.
- 通过两个受体:TNFR1和TNFR2. TNF通过两个受体发挥多种作用.
研究的目的:
- 探索TNFR1和TNFR2信号在疾病发病过程中的不同作用.
- 研究特定受体生物药物治疗TNF相关疾病的潜力.
- 为了解决当前广泛的TNF抑制剂的局限性.
主要方法:
- 对TNF信号通路的现有文献的审查.
- 对TNFR1和TNFR2激活背后的机制的分析.
- 对新型受体特异性药物的临床前和临床数据的检查.
主要成果:
- TNFR1信号传递可能是细胞毒性和促炎性.
- 在TNFR2信号传递中介抗炎和组织保护作用.
- 选择性调节TNFR1和TNFR2提供了治疗潜力.
结论:
- 针对特定的TNF受体 (TNFR1或TNFR2) 可以克服当前TNF抑制剂的局限性.
- 受体特异性生物药物代表了免疫介导疾病的有前途的新治疗策略.
- 进一步临床开发TNFR1抑制剂和TNFR2激活剂是有必要的.
相关概念视频
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF
173
Tumor Necrosis Factor (TNF), a proinflammatory cytokine, contributes significantly to the inflammation seen in Crohn's disease. It exists as soluble TNF and membrane-bound TNF, with actions mediated through TNF receptors (TNFR). TNFR activation leads to the release of proinflammatory cytokines, T-cell activation, collagen production, and leukocyte migration, all contributing to inflammation in Crohn's disease. Anti-TNF monoclonal antibodies, namely infliximab (Remicade), adalimumab...
173
T Cell Types and Functions
1.1K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
1.1K
Transducer Mechanism: Enzyme-Linked Receptors
2.5K
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
Major types that are helpful drug targets include:
2.5K
NF-κB-dependent Signaling Pathway
7.5K
The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The...
NF-κB-dependent Signaling Mechanism
The...
7.5K
Transducer Mechanism: Nuclear Receptors
1.4K
Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, development, or metabolism. Their ability to be stimulated by small lipophilic ligands and control vital cellular processes makes them ideal drug targets. Nearly 10-15% of currently prescribed drugs target these receptors.
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
1.4K
The JAK-STAT Signaling Pathway
9.0K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
9.0K

