Related Experiment Video
Updated: Aug 11, 2026

08:17
Flow Cytometry-based Assay for the Monitoring of NK Cell Functions
Published on: October 30, 2016
Hormone replacement therapy affects various immune cell subsets and natural cytotoxicity
R Brunelli1, D Frasca, G Perrone
1First Obstetrics and Gynecology Clinic, University, La Sapienza, Rome, Italy.
Gynecologic and Obstetric Investigation
|January 1, 1996
Summary
Hormone replacement therapy (HRT) impacts immune cells, reducing specific lymphocyte subsets and altering granulocyte membrane antigens. These changes highlight HRT's selective influence on immune cell function in menopausal women.
Area of Science:
- Immunology
- Endocrinology
- Women's Health
Background:
- The detailed effects of hormone replacement therapy (HRT) on lymphocytes and granulocytes remain largely undetermined.
- Menopausal women undergoing HRT require a comprehensive understanding of its immunological consequences.
Purpose of the Study:
- To investigate the specific effects of a combined transdermal estradiol and oral medroxyprogesterone acetate regimen on immune cell subsets.
- To analyze the impact of HRT on lymphocyte and granulocyte populations and functions in healthy menopausal women.
Main Methods:
- Ten healthy menopausal women received HRT (transdermal estradiol and oral medroxyprogesterone acetate) for six months.
- Immune cell subsets (CD4+CD45RO+, CD56+, CD8+CD11b+) and natural killer cell function were assessed at multiple time points (days 0, 8, 21, 28) during the first and last month of treatment.
- Granulocyte membrane antigen expression (Leu8, CD11b) was evaluated during the initial month of HRT.
Main Results:
- HRT significantly reduced CD4+CD45RO+ cells by day 8.
- CD56+ and CD8+CD11b+ cells decreased by day 21, returning to baseline by day 28.
- Natural killer cell function showed transient increase on day 8, followed by a significant reduction on day 21.
- Granulocyte membrane antigen expression was notably affected by HRT during the first month.
Conclusions:
- Hormone replacement therapy selectively modulates various immune cell subsets in menopausal women.
- The observed alterations in lymphocytes and granulocytes suggest a significant impact of HRT on the immune system's composition and function.
Related Concept Videos
Cell-mediated Immune Responses
Overview
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...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
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...
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...
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...
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...
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...
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...
Tumor Immunotherapy
Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.

