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Adaptive immune function in critical illness
1Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Critical illness, such as sepsis and acute lung injury, causes adaptive immune system dysfunction, termed immunoparalysis. This T-cell suppression can be reversed, but diagnostic markers are needed for effective therapy.
Area of Science:
- Immunology
- Critical Care Medicine
- Pathophysiology
Background:
- Adaptive immune system function is crucial in critical illnesses like sepsis and acute lung injury.
- Dysregulation of the immune response significantly contributes to morbidity and mortality in these conditions.
Purpose of the Study:
- To review and update the literature on adaptive immune system function in critical illness.
- To specifically focus on the role of T cells in sepsis and acute lung injury.
Main Methods:
- Literature review focusing on T-cell function in sepsis and acute lung injury.
- Analysis of mechanisms contributing to immune dysfunction, including lymphocyte apoptosis and regulatory T-cell expansion.
Main Results:
- Adaptive immune responses are similarly dysfunctional in sepsis and acute lung injury, characterized by 'immunoparalysis'.
- Key mechanisms include T-cell suppression, lymphocyte apoptosis, altered cytokine expression, and increased regulatory T cells.
- Experimental reversal of these abnormalities improves outcomes.
Conclusions:
- Immunoparalysis is a critical factor in sepsis and acute lung injury outcomes.
- Therapeutic strategies targeting inhibited pathways and using immunostimulant cytokines show promise.
- Development of immunomonitoring diagnostics is essential for timely and effective treatment.
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