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相关概念视频

Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

501
Antigen receptors are essential components of the immune system crucial in defending the body against foreign invaders. These receptors are present on the surface of B and T cells, enabling them to recognize antigens and mount an appropriate immune response.
Before encountering any antigen, lymphocytes express these receptors. On B cells, the antigen receptor is a membrane-bound antibody molecule called BCR; on T cells, it is a T cell receptor or TCR. B and T cell receptors are composed of two...
501
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

647
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...
647
T Cell Types and Functions01:24

T Cell Types and Functions

946
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...
946
Cells of the Adaptive Immune Response01:23

Cells of the Adaptive Immune Response

950
The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
950
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

1.6K
The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
1.6K
Receptor Tyrosine Kinases01:26

Receptor Tyrosine Kinases

12.2K
Receptor tyrosine kinases or RTKs are membrane-bound receptors that phosphorylate specific tyrosine on protein substrates. RTKs regulate cellular growth, differentiation, survival, and migration. They contain an extracellular ligand binding domain, a transmembrane domain, and a cytosolic tail with intrinsic kinase activity. Several extracellular signaling molecules activate RTKs in one or more ways and relay the signal downstream. Ligands such as platelet-derived growth factor (PDGF) or...
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相关实验视频

Updated: Jun 2, 2025

Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens
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Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens

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进化的T细胞受体识别代码:规则更像是指导方针.

George I Gray1, P Chukwunalu Chukwuma1, Bassant Eldaly1

  • 1Department of Chemistry and Biochemistry and the Harper Cancer Research Institute, University of Notre Dame, Notre Dame, Indiana, USA.

Immunological reviews
|January 13, 2025
PubMed
概括
此摘要是机器生成的。

-MHC复合体的T细胞受体 (TCR) 识别是复杂的,新的结构和生物物理研究揭示了早期模型的例外. 了解TCR结合适应性对于免疫学至关重要.

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Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain
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Retroviral Transduction of Bone Marrow Progenitor Cells to Generate T-cell Receptor Retrogenic Mice
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相关实验视频

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Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens
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Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens

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Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain
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Retroviral Transduction of Bone Marrow Progenitor Cells to Generate T-cell Receptor Retrogenic Mice
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科学领域:

  • 免疫学 免疫学 免疫学
  • 结构生物学 结构生物学
  • 生物物理学的生物物理.

背景情况:

  • 阿尔法-β T 细胞受体 (TCR) 识别了-MHC 复合体,这是适应性免疫的一个基本过程.
  • 早期的结构研究为TCR识别,特异性和MHC限制提供了基础模型.
  • 最近的研究揭示了这些初步理解的复杂性和例外.

研究的目的:

  • 探索基于结构和生物物理数据的TCR识别的不断发展的理解.
  • 为了说明新研究如何挑战TCR-/MHC相互作用的现有范式.
  • 讨论对基础,转化和预测免疫学的影响.

主要方法:

  • 分析日益增长的TCR结构数据库.
  • 整合结构和生物物理调查结果.
  • 审查研究检查TCR识别机制的研究.

主要成果:

  • 结构和生物物理研究揭示了挑战简化TCR识别模型的现象.
  • 越来越多地确定了关于TCR结合,特异性和MHC限制的常见假设的例外.
  • TCR的识别涉及固有的适应性,灵活性,有时还涉及"生物物理的疏忽".

结论:

  • 我们对TCR认可的理解正在扩大,超越了早期的简化框架.
  • /MHC复合体的TCR结合和区分的复杂性需要进一步研究.
  • 考虑TCR适应性对于推进基础,转化和预测免疫学至关重要.