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相关概念视频

Cell-mediated Immune Responses01:40

Cell-mediated Immune Responses

Overview
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

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...
T Cell Types and Functions01:24

T Cell Types and Functions

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...
Cytotoxic T Cells-mediated Immune Response01:27

Cytotoxic T Cells-mediated Immune Response

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...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

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...

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相关实验视频

Updated: May 12, 2026

Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
14:23

Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells

Published on: April 16, 2012

用CD3和CD46激活人类CD4+细胞诱导T调节细胞1表型.

Claudia Kemper1, Andrew C Chan, Jonathan M Green

  • 1Division of Rheumatology, Washington University School of Medicine, St Louis, Missouri 63110, USA.

Nature
|January 24, 2003
PubMed
概括

新的研究揭示了T调节1 (Tr1) 细胞如何分化. 与IL-2同时参与CD3和CD46诱导Tr1细胞,这对免疫耐受性至关重要,并防止自我破坏性反应.

科学领域:

  • 免疫学 免疫学 免疫学
  • 细胞生物学 细胞生物学
  • 补充系统 补充系统

背景情况:

  • 免疫系统需要对无害的抗原产生耐受性,以预防自身免疫性疾病.
  • 调节T细胞1 (Tr1) 细胞对于通过介质白素-10 (IL-10) 产生和抑制T辅助细胞的免疫耐受性至关重要.
  • 对于Tr1细胞分化的生理触发因素在很大程度上是未知的.

研究的目的:

  • 确定诱导T调节1 (Tr1) 细胞分化的条件.
  • 阐明补充系统在免疫耐受性中的作用.

主要方法:

  • 人类CD4+ T细胞通过CD3和CD46在IL-2存在的同时参与刺激.
  • 进行了对细胞因子生产,增殖和T细胞抑制的分析.
  • 在刺激细胞中评估记忆表型的获取.

主要成果:

  • CD3和CD46与IL-2的同时接触在人类CD4+T细胞中诱导了Tr1特异性细胞因子表型.
  • 刺激的产生IL-10的CD4+T细胞表现出强烈的增殖和抑制旁观者T细胞激活.
  • 这些细胞获得了记忆表型,表明持续的免疫调节.

结论:

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Last Updated: May 12, 2026

Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
14:23

Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells

Published on: April 16, 2012

Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation
15:33

Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation

Published on: August 13, 2013

Generation of Human Chimeric Antigen Receptor Regulatory T Cells
10:29

Generation of Human Chimeric Antigen Receptor Regulatory T Cells

Published on: January 3, 2025

  • 在IL-2的存在下CD3/CD46共同刺激是Tr1细胞分化的一个生理触发因素.
  • 补体系统通过CD46在启动T细胞介导免疫和耐受性方面发挥着重要作用.
  • 这一发现突出了控制免疫反应和预防自身免疫的新机制.