Cited by 2,772Sepsis Diagnosis and TreatmentInflammation biomarkers and pathwaysImmune Response and Inflammation

The DOI matches its Crossref record; 174 of the 174 references it cites were found in a registry or an index.

Sepsis-induced immunosuppression: from cellular dysfunctions to immunotherapy

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Hotchkiss, Richard S., Monneret, Guillaume, Payen, Didier·2013·Nature Reviews Immunology

Abstract

Sepsis - which is a severe life-threatening infection with organ dysfunction - initiates a complex interplay of host pro-inflammatory and anti-inflammatory processes. Sepsis can be considered a race to the death between the pathogens and the host immune system, and it is the proper balance between the often competing pro- and anti-inflammatory pathways that determines the fate of the individual. Although the field of sepsis research has witnessed the failure of many highly touted clinical trials, a better understanding of the pathophysiological basis of the disorder and the mechanisms responsible for the associated pro- and anti-inflammatory responses provides a novel approach for treating this highly lethal condition. Biomarker-guided immunotherapy that is administered to patients at the proper immune phase of sepsis is potentially a major advance in the treatment of sepsis and in the field of infectious disease.

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Metadata

Authors
Hotchkiss, R. S., Monneret, G., & Payen, D.
Affiliations
  • Washington University in St. Louis (US)
  • Hospices Civils de Lyon (FR)
  • Assistance Publique – Hôpitaux de Paris (FR)
Corresponding author
Hotchkiss, Richard S.
Venue
Nature Reviews Immunology
Published
2013-11-15
Volume
13
Issue
12
Pages
862-874
ISSN
  • 1474-1733 (ISSN-L)
  • 1474-1741
OpenAlex
W2083513831
Cited by
2,772
References
174
Citations by year
2026: 364 · 2025: 277 · 2024: 241 · 2023: 227 · 2022: 239 · 2021: 286 · 2020: 227 · 2019: 220 · 2018: 178 · 2017: 199 · 2016: 147 · 2015: 101 · 2014: 62 · 2013: 1
FWCI
12.16
Type
journal article
Language
en
Open access
Locations
  • Nature reviews. Immunology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • University of Washington
  • Hospices Civils de Lyon
  • National Institutes of Health (GM44118)
  • National Cancer Institute (P30CA091842)
  • National Institute of General Medical Sciences (GM55194, R01GM055194, R37GM044118, R01GM098391, R01GM044118, GM 44118)
Topics
  • Health Sciences › Medicine › Critical Care and Intensive Care Medicine › Sepsis Diagnosis and Treatment
  • Life Sciences › Immunology and Microbiology › Immunology › Inflammation biomarkers and pathways
  • Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
Keywords
sepsis, sepsis-induced immunosuppression, immunotherapy, cellular dysfunction, hyperinflammation, biomarker-guided therapy, host immune response, organ dysfunction, intensive care
MeSH terms
Animals, Humans, Immune Tolerance, Immunity, Cellular, Immunity, Innate, Immunotherapy, Inflammation, Sepsis, Models, Animal, Mice

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