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Related Concept Videos

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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Functional Groups02:45

Functional Groups

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Functional groups are a group of atoms with characteristic properties, which when linked to the carbon skeleton of a molecule, alter the properties of that molecule. For example, the presence of certain functional groups on a molecule will make them hydrophilic, whereas others will make them hydrophobic. These functional groups are an indispensable part of organic chemistry and important components of biological molecules, such as carbohydrates, proteins, lipids, and nucleic acids. Each...
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Cell Adhesion Molecules - Types and Functions01:20

Cell Adhesion Molecules - Types and Functions

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Cell adhesion molecules (CAMs) are pivotal to multicellularity and the coordinated functioning of tissues and organ systems. They enable physical interactions between cells and provide mechanical strength to tissues. They also function as receptors for signal transmission across the plasma membrane. The CAMs are broadly classified into four families - integrins, cadherins, selectins, and immunoglobulin-like CAMs (IgCAMs).
CAM Families
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Structural Protein Function01:56

Structural Protein Function

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Structural proteins are a category of proteins responsible for functions ranging from cell shape and movement to providing support to major structures such as bones, cartilage, hair, and muscles. This group includes proteins such as collagen, actin, myosin, and keratin.
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Mechanical Protein Functions01:58

Mechanical Protein Functions

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Proteins perform many mechanical functions in a cell. These proteins can be classified into two general categories- proteins that generate mechanical forces and proteins that are subjected to mechanical forces. Proteins providing mechanical support to the structure of the cell, such as keratin, are subjected to mechanical force, whereas proteins involved in cell movement and transport of molecules across cell membranes, such as an ion pump, are examples of generating mechanical force. 
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Related Experiment Video

Updated: Jan 23, 2026

Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy
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Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy

Published on: December 17, 2019

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The making and function of CAR cells.

Maja Zabel1, Peter A Tauber1, Winfried F Pickl1

  • 1Institute of Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.

Immunology Letters
|June 11, 2019
PubMed
Summary
This summary is machine-generated.

Chimeric antigen receptor (CAR) T cell therapy shows promise for cancer but has side effects. Optimizing CAR signaling domains is crucial for enhanced efficacy, safety, and long-term tumor surveillance.

Keywords:
Adoptive cell therapyCancer immunotherapyChimeric antigen receptorTumor microenvironment

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Area of Science:

  • Immunology
  • Oncology
  • Biomedical Engineering

Background:

  • Chimeric antigen receptor (CAR) T cell therapy offers a novel treatment for cancers, with high response rates in B cell leukemia.
  • However, CAR T cell therapy faces challenges including severe side effects like cytokine release syndrome and the development of target cell resistance.

Purpose of the Study:

  • To explore strategies for optimizing CAR T cell therapy by adjusting intracellular signaling domains.
  • To enhance long-term efficacy and safety, focusing on improved target cell cytotoxicity and sustained tumor surveillance.

Main Methods:

  • Investigating modifications to CAR intracellular signaling domains.
  • Discussing methods to control on-tumor off-target effects and introduce cytokine responsiveness (Signal 3).
  • Exploring strategies for efficient CAR T cell elimination post-remission and developing universal 'off-the-shelf' CAR T cell preparations.

Main Results:

  • Adjusting CAR signaling domains aims to achieve high target cell cytotoxicity and prolonged CAR-expressing cell longevity for extended tumor surveillance.
  • Controlling off-target effects, incorporating cytokine responsiveness, and enabling efficient CAR cell elimination are key areas of development.
  • Universal, 'off-the-shelf' CAR T cell therapies independent of patient HLA type and cell availability are proposed.

Conclusions:

  • Optimizing CAR T cell therapy through intracellular domain adjustments is essential for improving efficacy and safety.
  • Future directions include developing universal CAR T cell systems and exploring applications beyond cancer, such as autoimmune diseases.
  • CAR T cell therapy represents a significant advancement in cellular therapies, comparable to blood transfusions and bone marrow transplantation.