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Related Concept Videos

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...
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...
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...
Antigens Involved in Adaptive Immunity01:26

Antigens Involved in Adaptive Immunity

An antigen is any substance the immune system identifies as foreign and potentially harmful to the body, prompting an immune response. Antigens have two functional properties: immunogenicity and reactivity. Immunogenicity is the ability of an antigen to stimulate a specific immune response. At the same time, reactivity describes the antigen's ability to react with the cells and antibodies produced in response to it.
Complete Antigens
Complete antigens possess both immunogenicity and reactivity.
Cell-mediated Immune Responses01:40

Cell-mediated Immune Responses

Overview
Canonical Wnt Signaling Pathway02:54

Canonical Wnt Signaling Pathway

The gene encoding the main signaling molecules of the Wnt signaling pathways (the Wnt proteins) was discovered almost four decades ago by Nüsslein-Volhard and Wieschaus. They identified and originally named the gene "wingless" (wg) after a phenotype discovered during their landmark genetic screen in Drosophila for body pattern defects. At around the same time, another researcher named Harold Varmus found that a murine tumor virus activates the mammalian wg homolog, Int-1, which results in tumor...

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Related Experiment Video

Updated: May 19, 2026

Tailoring In Vivo Cytotoxicity Assays to Study Immunodominance in Tumor-specific CD8+ T Cell Responses
10:13

Tailoring In Vivo Cytotoxicity Assays to Study Immunodominance in Tumor-specific CD8+ T Cell Responses

Published on: May 6, 2019

What T cells see in WT-1.

Jeffrey J Molldrem1

  • 1MD Anderson Cancer Center, USA.

Blood
|August 25, 2012
PubMed
Summary

Wilms tumor protein 1 (WT-1) is a tumor antigen found in leukemia. This study catalogs WT-1 derived peptides recognized by CD8 and CD4 T cells, advancing cancer immunology research.

Area of Science:

  • Immunology
  • Oncology
  • Molecular Biology

Background:

  • Wilms tumor protein 1 (WT-1) is a recognized tumor antigen.
  • Aberrant WT-1 expression is observed in myeloid and lymphoid leukemia.
  • Understanding WT-1's immunogenicity is crucial for cancer immunotherapy.

Purpose of the Study:

  • To create the most extensive catalog to date of human leukocyte antigen (HLA)-restricted immunogenic peptides derived from WT-1.
  • To identify WT-1 peptides recognized by CD8+ and CD4+ T cells.

Main Methods:

  • Peptide identification and characterization.
  • HLA-restriction analysis.
  • T cell recognition assays (CD8 and CD4 T cells).

Main Results:

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Tractable In Vivo Reprogramming of Tumor Cells to Type 1 Conventional Dendritic Cell-like Cells

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Last Updated: May 19, 2026

Tailoring In Vivo Cytotoxicity Assays to Study Immunodominance in Tumor-specific CD8+ T Cell Responses
10:13

Tailoring In Vivo Cytotoxicity Assays to Study Immunodominance in Tumor-specific CD8+ T Cell Responses

Published on: May 6, 2019

Tractable In Vivo Reprogramming of Tumor Cells to Type 1 Conventional Dendritic Cell-like Cells
10:04

Tractable In Vivo Reprogramming of Tumor Cells to Type 1 Conventional Dendritic Cell-like Cells

Published on: August 1, 2025

  • A comprehensive catalog of HLA-restricted immunogenic peptides derived from WT-1 was generated.
  • These peptides were confirmed to be recognized by both CD8+ and CD4+ T cells.
  • The findings provide a detailed map of WT-1 T cell epitopes.

Conclusions:

  • The catalog of WT-1 immunogenic peptides offers valuable targets for developing WT-1-specific cancer immunotherapies.
  • This research enhances the understanding of T cell-mediated immune responses against WT-1 in leukemia.
  • The identified peptides can potentially be used in vaccines or T cell-based therapies for WT-1-associated malignancies.