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Design of Cecal Ligation and Puncture and Intranasal Infection Dual Model of Sepsis-Induced Immunosuppression
Published on: June 15, 2019
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Potential Immunotherapeutics for Immunosuppression in Sepsis
1Department of Microbiology, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Biomolecules & Therapeutics
|October 31, 2017
Summary
Sepsis survivors face late-phase mortality due to immune suppression, increasing vulnerability to infections. Therapies now focus on immune-enhancing strategies to combat this persistent threat.
Area of Science:
- Immunology
- Critical Care Medicine
- Infectious Diseases
Background:
- Sepsis, a severe infection response, initially causes hyper-inflammation leading to organ dysfunction.
- Improved early interventions have reduced acute sepsis mortality.
- Late-phase sepsis mortality remains high due to sepsis-induced immunosuppression.
Purpose of the Study:
- To investigate the mechanisms of late-phase sepsis mortality.
- To explore therapeutic strategies targeting immune system recovery in sepsis survivors.
- To address the challenge of long-term mortality in sepsis.
Main Methods:
- Review of current literature on sepsis pathophysiology and treatment.
- Analysis of immune status in sepsis survivors.
- Evaluation of immune-enhancing molecules and strategies.
Main Results:
- Sepsis survivors often exhibit immunosuppression (tolerance, exhaustion, apoptosis).
- This compromised immune state increases susceptibility to nosocomial and opportunistic infections.
- These secondary infections are a major cause of late-phase mortality.
Conclusions:
- Late-phase mortality in sepsis is driven by immune dysfunction, not initial inflammation.
- Therapeutic approaches are shifting towards reversing immunosuppression.
- Targeting immune enhancement offers a promising strategy to reduce long-term sepsis mortality.
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