[The expression of some homing and co-receptor molecules on CD4+ T cells in AIDS patients]

Yan Tan1, Ming-Xia Zhang, Ying-Xia Liu

  • 1The Third People's Hospital of Shenzhen, Shenzhen 518020, China.

Insights

In AIDS patients, CD4+ T cell function is impaired, with reduced expression of homing receptors CD49d, CCR9, CD62L, and CCR5. Highly Active Antiretroviral Therapy (HAART) partially restores this function, indicating potential use of these markers for disease progression monitoring.

Area of Science:

  • Immunology
  • Virology
  • Cell Biology

Background:

  • CD4+ T cells play a crucial role in immune response.
  • Acquired Immunodeficiency Syndrome (AIDS) significantly impairs CD4+ T cell function.
  • Understanding immune cell marker expression is vital for assessing disease progression and treatment efficacy.

Purpose of the Study:

  • To evaluate the expression of CD49d, CCR9, CD62L, and CCR5 on CD4+ T cells in AIDS patients before and after Highly Active Antiretroviral Therapy (HAART).
  • To assess the potential of these markers in indicating AIDS progression and immune reconstitution.

Main Methods:

  • Flow cytometry was used to analyze the expression of CD49d, CCR9, CD62L, and CCR5 on CD4+ T cells.
  • The study included 42 AIDS patients and 18 healthy controls.
  • Expression levels were compared between pre-HAART, post-HAART, and HIV-negative groups.

Main Results:

  • AIDS patients pre-HAART showed decreased CD4+ T cell numbers and frequencies of CD4+ T cells expressing CCR9 and CCR5 compared to post-HAART.
  • Expression of CD49d, CCR9, and CD62L on CD4+ T cells was significantly lower in pre-HAART patients.
  • Post-HAART patients still exhibited lower frequencies of CD4+ T cells, CD62L+, and CCR5+ cells compared to HIV-negative controls.

Conclusions:

  • CD4+ T cell number and function are impaired in AIDS patients, evidenced by reduced expression of homing receptors (CD49d, CCR9, CD62L) and coreceptor (CCR5).
  • HAART therapy can partially reverse these pathological changes.
  • CD49d, CCR9, and CD62L expression levels may serve as indicators for AIDS progression and immune recovery following HAART.
Abstract

Related Concept Videos

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...
Antigens Involved in Adaptive Immunity01:26

Antigens Involved in Adaptive Immunity

An antigen is any substance the immune system identifies as foreign and potentially harmful to the body, prompting an immune response. Antigens have two functional properties: immunogenicity and reactivity. Immunogenicity is the ability of an antigen to stimulate a specific immune response. At the same time, reactivity describes the antigen's ability to react with the cells and antibodies produced in response to it.
Complete Antigens
Complete antigens possess both immunogenicity and reactivity.
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...
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...
Immunodeficiency Diseases01:25

Immunodeficiency Diseases

Immunodeficiency disorders are conditions in which the immune system's ability to fight infectious disease and cancer is compromised or entirely absent. The immune system comprises a complex network of cells, tissues, and organs that work together to protect the body from potentially harmful invaders. When this system is deficient or not functioning properly, it leaves the body susceptible to infections, diseases, or other complications.
There are three main causes of immunodeficiency disorders...
Immune Response Against Viral Pathogens01:29

Immune Response Against Viral Pathogens

The immune system's response to viral infections is a complex and coordinated process involving natural killer (NK) cells, T cell-mediated responses, and antibody-mediated responses.
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...