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Related Concept Videos

Cytotoxic T Cells-mediated Immune Response01:27

Cytotoxic T Cells-mediated Immune Response

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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.
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...
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Targeted Cancer Therapies02:57

Targeted Cancer Therapies

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
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T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

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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.
Naive T cells that have not yet encountered an antigen express two primary CD...
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T Cell Types and Functions01:24

T Cell Types and Functions

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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.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
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Tumor Immunotherapy01:27

Tumor Immunotherapy

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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.
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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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Related Experiment Video

Updated: Oct 9, 2025

Expanding Cytotoxic T Lymphocytes from Umbilical Cord Blood that Target Cytomegalovirus, Epstein-Barr Virus, and Adenovirus
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Expanding Cytotoxic T Lymphocytes from Umbilical Cord Blood that Target Cytomegalovirus, Epstein-Barr Virus, and Adenovirus

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T Cells Targeting TdT Selectively Kill Leukemic Lymphoblasts

    Cancer Discovery
    |December 18, 2021
    PubMed
    Summary

    Targeting terminal deoxynucleotidyl transferase (TdT) with T cells effectively eliminates cancer cells in T- and B-acute lymphoblastic leukemia. This approach spares healthy lymphocytes, offering a promising therapeutic strategy.

    Area of Science:

    • Immunology
    • Oncology
    • Hematology

    Background:

    • Acute lymphoblastic leukemia (ALL) is a significant hematologic malignancy.
    • T-cell and B-cell lineages are commonly affected in ALL.
    • Targeting specific cellular markers is a strategy for selective cancer therapy.

    Purpose of the Study:

    • To investigate the efficacy of T cells engineered to target terminal deoxynucleotidyl transferase (TdT).
    • To determine if TdT-targeted T cells can selectively eliminate malignant cells in T- and B-ALL.
    • To assess the safety of this approach by evaluating its impact on normal lymphocytes.

    Main Methods:

    • Development of T cells engineered to recognize and target TdT.
    • In vitro and/or in vivo models of T-cell ALL and B-cell ALL.

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  • Assessment of cancer cell killing and normal lymphocyte viability.
  • Main Results:

    • T cells targeting TdT demonstrated selective killing of malignant cells in both T- and B-ALL models.
    • Normal lymphocytes remained largely unaffected, indicating specificity.
    • This suggests a potential for targeted therapy with minimal off-tumor toxicity.

    Conclusions:

    • TdT-targeted T cells represent a promising therapeutic strategy for T- and B-ALL.
    • Selective elimination of malignant cells while sparing normal lymphocytes is achievable.
    • Further research into TdT-targeted immunotherapy is warranted.