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Related Concept Videos

Special Features of Adaptive Immunity01:20

Special Features of Adaptive Immunity

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The adaptive immune system, a crucial component of the overall immune response, offers a highly specialized defense against pathogens. It involves specific cell types and features, enabling it to combat infections effectively and efficiently.
The primary cell types involved in adaptive immunity are T cells and B cells. Each type has a unique role in defending the body against pathogens. T cells are responsible for cell-mediated immunity. They identify and eliminate infected cells directly,...
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T Cell Activation and Clonal Selection01:22

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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.
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Cytotoxic T Cells-mediated Immune Response01:27

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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.
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T Cell Types and Functions01:24

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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.
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Cells of the Adaptive Immune Response01:23

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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...
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Related Experiment Video

Updated: Nov 7, 2025

In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
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CD8+ T cell self-tolerance permits responsiveness but limits tissue damage.

Emily N Truckenbrod1, Kristina S Burrack1, Todd P Knutson2

  • 1Center for Immunology, University of Minnesota, Saint Paul, United States.

Elife
|April 30, 2021
PubMed
Summary

Self-reactive CD8+ T cells specific for tyrosinase-related protein 2 (Trp2) exhibit functional tolerance. These cells show reduced expansion and impaired differentiation, leading to less efficient autoimmune responses like vitiligo.

Keywords:
T cellautoimmune response/diseaseimmunologyinflammationmousetolerance

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Examination of Thymic Positive and Negative Selection by Flow Cytometry
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Area of Science:

  • Immunology
  • T cell biology
  • Autoimmunity

Background:

  • Self-specific CD8+ T cells can evade deletion, but their behavior in vivo remains poorly understood.
  • Understanding these cells is crucial for managing autoimmune diseases.

Purpose of the Study:

  • To characterize the properties and capabilities of self-specific CD8+ T cells in a physiological context.
  • To investigate the mechanisms underlying functional self-tolerance in CD8+ T cells.

Main Methods:

  • Characterization of polyclonal CD8+ T cells specific for tyrosinase-related protein 2 (Trp2) in wild-type and Dct-deficient mice.
  • Analysis of phenotypic and gene expression profiles, cell expansion, differentiation, and immunopathology mediation.

Main Results:

  • Pre-immune Trp2/K(b)-specific CD8+ T cells showed similar phenotypes and frequencies in wild-type and Dct-deficient mice.
  • Despite comparable initial responses, wild-type cells exhibited blunted expansion and less CD25+ differentiation.
  • Adoptively transferred wild-type cells mediated vitiligo less efficiently, indicating functional self-tolerance.

Conclusions:

  • CD8+ T cell self-specificity is not reliably predicted by precursor frequency, phenotype, or initial responsiveness.
  • Deficient activation-induced CD25 expression and specific gene expression patterns may identify functionally tolerant self-reactive CD8+ T cells.