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Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis
Published on: September 7, 2022
Infected malnourished children displayed changes in early activation and lymphocyte subpopulations
Oralia Nájera-Medina1, Fernando Valencia-Chavarría2, Consuelo Cortés-Bejar2
1Departamento de Atención a la Salud, CBS, Universidad Autónoma Metropolitana-Xochimilco, Ciudad de México, Mexico.
Insights
Malnutrition impairs immune responses in children, leading to reduced lymphocyte activation and memory cell function during infections. Malnourished children exhibit persistent deficiencies in natural killer (NK) cell activity post-treatment.
Area of Science:
- Immunology
- Pediatrics
- Nutrition Science
Background:
- Malnutrition and infections significantly alter immune system components, specifically lymphocyte subpopulations and their functional capabilities.
- Understanding these immunological changes is crucial for managing pediatric infections in vulnerable populations.
Purpose of the Study:
- To evaluate lymphocyte activation capacity and memory cell function in well-nourished and malnourished infected children.
- To assess these immune parameters before and after therapeutic intervention.
Main Methods:
- Study involved pediatric patients under three years of age in Mexico City.
- Flow cytometry was used to analyze the expression of cluster of differentiation (CD) markers, including CD45RA (naïve) and CD45RO (memory) on CD4 lymphocytes, and CD69 activation marker on all lymphocytes.
- Immune cell analysis was performed before and after treatment.
Main Results:
- Well-nourished infected children displayed increased percentages of activated T lymphocytes (T cells), CD8+, and CD4+ memory cells during infection.
- Malnourished infected children showed diminished percentages of activated and memory T cells.
- While T cell populations normalized in well-nourished children post-infection, their T, B lymphocyte, and natural killer (NK) cell counts remained elevated; malnourished children had low activated NK cell counts both pre- and post-therapy.
Conclusions:
- Malnourished infected children exhibit inadequate NK cell responses during infection resolution, indicating a lasting malnutrition-induced immunological deficit.
- These findings highlight the profound impact of malnutrition on immune recovery and function in children.
Aim:
Malnutrition and infections cause immunological changes in lymphocyte subpopulations and their functionality. We evaluated the activation capacity of lymphocytes and memory cells in 10 well nourished, seven well-nourished infected and eight malnourished infected children before and after treatment.
Methods:
All the children were patients in Mexico City and were less than three years of age. The expression of various cluster of differentiation (CD) cells was assessed by flow cytometry: CD45RA (naïve) and CD45RO (memory) antigens on CD4 lymphocytes and CD69 in all lymphocytes.
Results:
Well-nourished infected children showed a higher percentage of activated T lymphocyte (T cells), CD8+ and CD4+ memory cells during the infectious phase, suggesting that the activation mechanisms were triggered by infection. T cells from malnourished infected children showed a lower percentage of activated and memory cells. The T cell population size returned to baseline during the resolution phase of the infection in well-nourished infected children, but their T, B lymphocyte and natural killer (NK) cell counts remained high. In malnourished infected children, activated NK cells counts were low before and after therapy.
Conclusion:
After therapy, malnourished infected children showed poor NK cell responses during the infection's resolution phase, suggesting a persistent malnutrition-mediated immunological deficiency.
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