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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.
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Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies01:22

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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
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Decrease in CD4+CD25+ and CD8+CD28+ T cells in interstitial pneumonitis associated with rheumatic disease.

Akira Katagiri1, Shinji Morimoto, Yutaka Nakiri

  • 1Department of Internal Medicine and Rheumatology, School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.

Modern Rheumatology
|June 20, 2008
PubMed
Summary
This summary is machine-generated.

Patients with interstitial pneumonitis (IP) linked to rheumatic diseases show fewer CD4+CD25+ regulatory T cells and more CD8+CD28- suppressor T cells. These T cell imbalances may contribute to IP development in rheumatic conditions.

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Characterization of Immune Cells and Proinflammatory Mediators in the Pulmonary Environment
09:00

Characterization of Immune Cells and Proinflammatory Mediators in the Pulmonary Environment

Published on: June 24, 2020

Area of Science:

  • Immunology
  • Rheumatology
  • Pulmonology

Background:

  • Interstitial pneumonitis (IP) is a serious complication in rheumatic diseases.
  • The roles of regulatory T cells (CD4+CD25+) and suppressor T cells (CD8+CD28-) in IP pathogenesis are not fully understood.

Purpose of the Study:

  • To investigate the levels of CD4+CD25+ regulatory T cells and CD8+CD28- suppressor T cells in patients with rheumatic diseases and interstitial pneumonitis.
  • To explore the relationship between these T cell populations and the development of IP.

Main Methods:

  • Flow cytometry was used to analyze T cell subsets.
  • Fifty-five patients with rheumatic diseases (with or without IP) and 23 healthy controls were studied.

Main Results:

  • Patients with IP had significantly lower CD4+CD25+ T cell counts compared to non-IP patients.
  • The ratio of CD8+CD28- T cells was significantly higher in IP patients versus non-IP patients and controls.
  • Decreased CD8+CD28+ T cells were observed, potentially linked to activation-induced cell death.

Conclusions:

  • Abnormalities in CD4+CD25+ regulatory T cells may play a role in the pathogenesis of IP in rheumatic diseases.
  • Altered survival and activation of CD8+ T cells, specifically the CD8+CD28- subset, are associated with IP.