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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...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
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...
Cell-mediated Immune Responses01:40

Cell-mediated Immune Responses

Overview
Cells of the Adaptive Immune Response01:23

Cells of the Adaptive Immune Response

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: Jun 4, 2026

Mouse Na&#239;ve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets
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Published on: April 16, 2015

Function of CD27 in helper T cell differentiation.

Sten Libregts1, Ronald W van Olffen, Koenraad F van der Sluijs

  • 1Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

Immunology Letters
|February 1, 2011
PubMed
Summary

CD27 signaling influences T-helper cell differentiation, supporting T(H)1 cell formation but inhibiting T(H)17 cells. This effect is dependent on cytokine environment and genetic background, not providing instructive signals for specific T(H) subsets.

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Area of Science:

  • Immunology
  • Cellular and Molecular Immunology

Background:

  • T-helper (T(H)) cell differentiation into distinct subsets is crucial for adaptive immunity.
  • Both cytokines and costimulatory molecules regulate T(H) cell polarization.
  • The role of CD27 signaling in T(H) cell differentiation remains incompletely understood.

Purpose of the Study:

  • To investigate whether CD27 triggering provides instructive signals for T(H)1 differentiation or broadly supports T(H) cell formation.
  • To determine the influence of CD27 signaling on the differentiation of various T(H) subsets (T(H)1, T(H)2, T(H)17, and regulatory T cells).

Main Methods:

  • Utilized CD70-transgenic (CD70TG) mice on different genetic backgrounds (C57Bl/6J and Balb/c).
  • Performed in vitro differentiation assays with varying cytokine milieus.
  • Assessed T(H) cell subset populations and transcription factor expression levels.
  • Induced allergic airway inflammation model in CD70TG mice.

Main Results:

  • CD70TG mice on a T(H)1-prone background showed increased T(H)1 cells, but this was lost on a T(H)2-prone background without a reciprocal increase in T(H)2 cells.
  • CD70-overexpression did not induce T(H)17 cell formation or affect regulatory T cell generation.
  • In vitro, CD27 triggering supported T(H)1 differentiation and inhibited T(H)17, but not T(H)2, differentiation, depending on cytokine milieu and genetic background.
  • In vivo, CD27 signaling supported T(H)1 differentiation in allergic airway inflammation without affecting T(H)2 responses.

Conclusions:

  • CD27 signaling plays a supportive, rather than instructive, role in T(H) cell differentiation.
  • The influence of CD27 on T(H) cell polarization is highly context-dependent, varying with cytokine environment and host genetic background.
  • CD27 signaling modulates T(H)1 and T(H)17 differentiation, highlighting its nuanced role in immune responses.