系统性红斑狼中调节的细胞死亡:关键途径和向疗法
Siying Deng1, Ziwei Hu1, Shaozhe Cai2
1Department of Rheumatology and Immunology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Autoimmunity reviews
|November 20, 2025
概括
调节细胞死亡 (RCD) 途径功能障碍通过促进自身抗原暴露和免疫失调驱动全身性红斑狼 (SLE). 准RCD为SLE提供了新的精确治疗策略.
科学领域:
- 免疫学 免疫学 免疫学
- 病理学 病理学 病理学
- 自免疫性疾病 自免疫性疾病
背景情况:
- 系统性红斑狼 (SLE) 是一种由自身抗体和免疫失调标志的自身免疫性疾病.
- 调节细胞死亡 (RCD) 途径的功能障碍是SLE发展的关键因素.
- 损坏的RCD和碎片清除导致自身抗原的积累和免疫系统的激活.
研究的目的:
- 系统地审查 RCD 途径在 SLE 发病过程中的作用.
- 将SLE中的RCD失调与其他自身免疫性疾病进行比较.
- 评估针对SLE的新型RCD向治疗方法.
主要方法:
- 对SLE中RCD途径的文献进行系统审查.
- 在自身免疫性疾病中对RCD失调的比较分析.
- 评估新兴的RCD向治疗策略.
主要成果:
- RCD通路的异常是SLE病变的核心.
- 特定的RCD失调与其他自身免疫性疾病共同存在,并且与之不同.
- 干扰素I型 (IFN-I) 反应被异常的RCD放大.
结论:
- 异常的RCD对SLE病理和免疫微环境障碍有显著的贡献.
- 了解RCD机制为SLE病原体提供了洞察力.
- 准RCD途径为精确的SLE治疗提供了一个有希望的途径.
相关概念视频
The Extrinsic Apoptotic Pathway
8.0K
The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
8.0K
The Intrinsic Apoptotic Pathway
8.2K
Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
8.2K
Overview of Cell Death
9.3K
Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
9.3K
Regulation of Hematopoietic Stem Cells
3.9K
All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
3.9K
Regulation of the Unfolded Protein Response
2.9K
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.9K
The JAK-STAT Signaling Pathway
11.8K
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...
11.8K


