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Updated: Jun 19, 2025

A Data-Driven Approach to Quantifying Immune States in Sepsis
Published on: February 7, 2025
Evolving Paradigms in Sepsis Management: A Narrative Review.
Min-Ji Kim1, Eun-Joo Choi2, Eun-Jung Choi3
1Department of Internal Medicine, School of Medicine, Kyungpook National University, Kyungpook National University Chilgok Hospital, Daegu 41404, Republic of Korea.
Sepsis treatment faces challenges due to failed clinical trials targeting inflammation and immune responses. Understanding sepsis complexity is key to developing targeted therapies for better patient outcomes.
Area of Science:
- Critical Care Medicine
- Immunology
- Infectious Diseases
Background:
- Sepsis is a life-threatening organ dysfunction from infection, causing significant global mortality.
- Current treatments targeting hyperinflammation and immunosuppression have largely failed to improve sepsis outcomes.
- There is a critical need for novel therapeutic strategies for sepsis management.
Purpose of the Study:
- To review the development of sepsis therapeutic agents.
- To analyze clinical trial failures in targeting hyperinflammation and immunosuppression.
- To explore reasons for trial failures and outline current research directions.
Main Methods:
- Literature review of clinical trials for sepsis therapeutics.
- Analysis of strategies targeting hyperinflammation and immunosuppression.
- Examination of research bridging theoretical advancements and clinical application.
Main Results:
- Many clinical trials targeting hyperinflammation and immunosuppression in sepsis have failed.
- Reasons for failure include the complex, multifaceted nature of sepsis pathogenesis.
- Personalized medicine and phenotypic categorization show promise for future sepsis therapies.
Conclusions:
- Understanding sepsis pathogenesis is crucial for developing effective treatments.
- Targeted and individualized therapies are needed to improve sepsis patient outcomes.
- Future research should focus on precise treatment strategies for better sepsis management.
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