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Published on: January 27, 2019
Altered immune status of circulating T lymphocytes during sepsis: children also
1Unité Cytokines & Inflammation, Institut Pasteur, 28 Rue Dr. Roux, 75014, Paris, France. jean-marc.cavaillon@pasteur.fr.
Insights
Pediatric septic shock alters immune cells, specifically T helper 1 and T helper 2 lymphocytes. These cells show reduced cytokine production, indicating an impaired immune response in children with this condition.
Area of Science:
- Immunology
- Pediatrics
- Critical Care Medicine
Background:
- Sepsis and septic shock are associated with altered immune cell function in adults.
- Immune dysregulation is a critical factor in the severity and outcomes of pediatric sepsis.
Purpose of the Study:
- To investigate the immune status of T helper 1 (Th1) and T helper 2 (Th2) lymphocytes in children with septic shock.
- To assess ex vivo cytokine production by these lymphocytes upon activation.
Main Methods:
- Analysis of blood leukocytes from pediatric patients diagnosed with septic shock.
- Ex vivo stimulation of lymphocytes using phytohemagglutinin (PHA).
- Measurement of cytokine production from stimulated T helper 1 and T helper 2 cells.
Main Results:
- Children with septic shock exhibit an altered immune status of blood leukocytes.
- Reduced ex vivo cytokine production was observed for both T helper 1 and T helper 2 lymphocytes in pediatric septic shock patients.
- This suggests impaired cellular immune function in pediatric septic shock.
Conclusions:
- Pediatric septic shock is characterized by significant immune cell dysfunction.
- Impaired T helper cell cytokine responses contribute to the pathophysiology of pediatric septic shock.
- Further research into immune modulation strategies may improve outcomes for these critically ill children.
Abstract:
Altered immune status of blood leukocytes is a general phenomenon observed in adult patients with sepsis or septic shock. This is also the case in children with septic shock for both T helper 1 and T helper 2 lymphocytes, as demonstrated by their reduced ex vivo cytokine production upon activation by phytohemagglutinin.
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