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Immunotherapy in sepsis - brake or accelerate?

  1. Author:
    Steinhagen, Folkert
    Schmidt, Susanne
    Schewe, Jens-Christian
    Peukert, Konrad
    Klinman,Dennis
    Bode, Christian
  2. Author Address

    Univ Bonn, Dept Anesthesiol & Crit Care Med, Venusberg Campus 1, D-53127 Bonn, Germany.Univ Bonn, Inst Innate Immun, Bonn, Germany.NCI, Canc & Inflammat Program, Ctr Canc Res, Frederick, MD 21701 USA.
    1. Year: 2020
    2. Date: APR
    3. Epub Date: 2020 01 10
  1. Journal: Pharmacology & therapeutics
  2. PERGAMON-ELSEVIER SCIENCE LTD,
    1. 208
  3. Type of Article: Review
  4. Article Number: 107476
  5. ISSN: 0163-7258
  1. Abstract:

    Sepsis, a life threating syndrome characterized by organ failure alter infection, is the most common cause of death in hospitalized patients. The treatment of sepsis is generally supportive in nature, involving the administration of intravenous fluids, vasoactive substances and oxygen plus antibiotics to eliminate the pathogen. No drugs have been approved specifically for the treatment of sepsis, and clinical trials of potential therapies have failed to reduce mortality - suggesting that new approaches are needed. Abnormalities in the immune response elicited by the pathogen, ranging from excessive inflammation to immunosuppression, contribute to disease pathogenesis. Although hundreds of immunomodulatory agents are potentially available, it remains unclear which patient benefits from which immune therapy at a given time point. Results indicate the importance of personalized therapy, specifically the need to identify the type of intervention required by each individual patient at a given point in the disease process. To address this issue will require using biomarkers to stratify patients based on their individual immune status. This article reviews recent and ongoing clinical investigations using immunostimulatory or immunosuppressive therapies against sepsis including non-pharmacological and novel preclinical approaches. (C) 2020 The Author(s). Published by Elsevier Inc.

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External Sources

  1. DOI: 10.1016/j.pharmthera.2020.107476
  2. PMID: 31931100
  3. WOS: 000522634400006

Library Notes

  1. Fiscal Year: FY2019-2020
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