免疫学隐藏和寻找:表观遗传重新编程的癌细胞和CD8+ T细胞的动态
Jie-Ting Low1,2,3, Michael W Y Chan4,5,6,7, Cheng-Huang Shen8
1Department of Biomedical Sciences, National Chung Cheng University, Min-Hsiung, Chiayi, Taiwan.
Molecular biology reports
|September 4, 2024
概括
癌细胞的表观遗传变化有助于它们在免疫系统中生存并抵抗治疗. 了解这种相互作用是开发新的癌症免疫疗法的关键.
科学领域:
- 在瘤学瘤学.
- 免疫学 免疫学 免疫学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
背景情况:
- 癌症的发展涉及遗传突变和表观遗传失调.
- 表观遗传变化对于瘤发生,免疫反应和治疗耐药性至关重要.
研究的目的:
- 审查表观遗传修饰癌细胞与瘤微环境 (TME) 之间的复杂关系.
- 探索癌细胞如何逃避免疫监测并发展免疫疗法耐药性.
- 为了检查TME内的CD8+T细胞功能障碍.
主要方法:
- 文献综述侧重于癌症免疫学中的表观遗传机制.
- 分析免疫编辑概念 (消除,平衡,逃避).
- 讨论免疫逃避策略和T细胞功能障碍.
主要成果:
- 表观遗传重编程显著影响TME内的癌细胞存活率.
- 瘤细胞使用各种机制来逃避CD8+ T细胞介导的免疫力.
- 功能障碍的CD8+ T细胞是TME复杂动态的结果.
结论:
- 表观遗传机制对于癌细胞对抗免疫攻击的生存至关重要.
- 向表观遗传修饰可能会提高癌症免疫疗法的疗效.
- 进一步研究癌细胞-TME-免疫系统交叉通话是有必要的.
相关概念视频
Tumor Immunotherapy
493
Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
493
Cytotoxic T Cells-mediated Immune Response
861
Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
861
T Cell Activation and Clonal Selection
691
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
Naive T cells that have not yet encountered an antigen express two primary CD...
691
Mitogens and the Cell Cycle
6.4K
Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
6.4K
The Tumor Microenvironment
6.6K
Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
6.6K
T Cell Types and Functions
963
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...
963


