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Related Concept Videos

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...
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...

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Updated: Jul 10, 2026

Mouse Naïve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets
07:12

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Published on: April 16, 2015

Analysis of Th1/Th2 T-cell subsets.

Alla Skapenko1, Hendrik Schulze-Koops

  • 1Nikolaus Fiebiger Center for Molecular Medicine, Clinical Research Group III, University of Erlangen-Nuremberg, Erlangen, Germany.

Methods in Molecular Medicine
|November 7, 2007
PubMed
Summary
This summary is machine-generated.

Understanding T-helper (Th) cell subsets, crucial for immune responses, involves analyzing their signature cytokines like interferon-gamma and interleukin-4. This study details flow cytometry for detecting these cytokines in human Th cells.

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Area of Science:

  • Immunology
  • Cellular Biology

Background:

  • Specific immune responses rely on activated CD4+ T-helper (Th) cells.
  • Two main subsets, Th1 and Th2, are defined by their distinct cytokine profiles: interferon-gamma (Th1) and interleukin-4 (Th2).
  • Analyzing these signature cytokines is key to understanding immune responses, both protective and pathogenic.

Purpose of the Study:

  • To review methods for analyzing Th cell subsets based on cytokine production.
  • To present a detailed protocol for intracellular cytokine detection in human Th subsets using flow cytometry.

Main Methods:

  • The study discusses various techniques including reverse transcriptase polymerase chain reaction (RT-PCR), enzyme-linked immunosorbent assay (ELISA), ELISpot, and intracellular flow cytometry.
  • A standard protocol for flow cytometric analysis of cytoplasmic cytokines in human Th subsets is described.

Main Results:

  • Flow cytometry offers a robust method for identifying and quantifying Th1 and Th2 cells based on their cytokine production.
  • The described protocol enables detailed analysis of human Th subsets.

Conclusions:

  • Accurate analysis of Th cell subsets is vital for advancing the understanding of immune mechanisms.
  • Flow cytometry provides a valuable tool for dissecting Th cell-mediated immunity.