Evidence map›Paper›PMID 38408467›Full record

ReviewThe Lancet. Respiratory medicine2024

Reframing sepsis immunobiology for translation: towards informative subtyping and targeted immunomodulatory therapies.

Manu Shankar-Hari, Thierry Calandra, Miguel P Soares, Michael Bauer, W Joost Wiersinga, Hallie C Prescott, Julian C Knight, Kenneth J Baillie, Lieuwe D J Bos, Lennie P G Derde and 11 more

Open access · greenAbstract readReview
In one paragraph

Review in The Lancet. Respiratory medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 2 pooled it
40.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

81 citing papers in PubMed, 2 syntheses or guidelines pooled it, 104 citations in OpenAlex.

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21 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 19 institutions in 10 countries.

Manu Shankar-HariInstitute for Regeneration and Repair, College of Medicine and Veterinary Medicine, The University of Edinburgh, Edinburgh, UK. Electronic address: manu.shankar-hari@ed.ac.uk.
Thierry CalandraService of Immunology and Allergy, Center of Human Immunology Lausanne, Department of Medicine and Department of Laboratory Medicine and Pathology, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.
Miguel P SoaresInstituto Gulbenkian de Ciência, Oeiras, Portugal.
Michael BauerCenter for Sepsis Control and Care, Jena University Hospital, Jena, Germany.
W Joost WiersingaCenter for Experimental and Molecular Medicine and Division of Infectious Diseases, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, Netherlands.
Hallie C PrescottDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Julian C KnightWellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Kenneth J BaillieInstitute for Regeneration and Repair, College of Medicine and Veterinary Medicine, The University of Edinburgh, Edinburgh, UK.
Lieuwe D J BosDepartment of Intensive Care, Academic Medical Center, Amsterdam, Netherlands.
Lennie P G DerdeIntensive Care Center, University Medical Center Utrecht, Utrecht, Netherlands.
Simon FinferCritical Care Division, The George Institute for Global Health, University of New South Wales, Sydney, NSW, Australia.
Richard S HotchkissDepartment of Anesthesiology and Critical Care Medicine, Washington University School of Medicine in St Louis, St Louis, MO, USA.
John MarshallInterdepartmental Division of Critical Care, University of Toronto, Toronto, ON, Canada.
Peter J M OpenshawNational Heart and Lung Institute, Imperial College London, London, UK.
Christopher W SeymourDepartment of Critical Care Medicine, The Clinical Research, Investigation, and Systems Modeling of Acute illness (CRISMA) Center, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Fabienne VenetImmunology Laboratory, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.
Jean-Louis VincentDepartment of Intensive Care, Hôpital Erasme, Brussels, Belgium.
Christophe Le TourneauDepartment of Drug Development and Innovation (D3i), Institut Curie, Paris-Saclay University, Paris, France.
Anke H Maitland-van der ZeeDepartment of Pulmonary Medicine, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, Netherlands.
Iain B McInnesCollege of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Tom van der PollCenter for Experimental and Molecular Medicine and Division of Infectious Diseases, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, Netherlands.
Amsterdam University Medical Centers · NLUniversity of Edinburgh · GBAcademic Medical Center · NLCentre for Human Genetics · GBErasmus Hospital · BEHospices Civils de Lyon · FRImperial College London · GBInstituto Gulbenkian de Ciência · PTJena University Hospital · DEThe George Institute for Global Health · AUUniversité Paris-Saclay · FRUniversity Medical Center Utrecht · NLUniversity of Amsterdam · NLUniversity of Glasgow · GBUniversity of Lausanne · CHUniversity of Michigan–Ann Arbor · USUniversity of Pittsburgh · USUniversity of Toronto · CAWashington University in St. Louis · US

Funding

Sepsis subtypes: biology, treatment, and bedside applicationR35GM119519 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Christopher W. Seymour · 2016 to 2026
$4.9M
Enhancing Innate and Adaptive Immunity to Improve Sepsis SurvivalR35GM126928 · NIGMS · WASHINGTON UNIVERSITY · PI Richard Samuel Hotchkiss · 2018 to 2026
$4.7M
Medical Research Council MR/V002503/1NIGMS NIH HHS R35 GM119519NIGMS NIH HHS R35 GM126928Wellcome Trust
6 · The paper itself

Abstract

Sepsis is a common and deadly condition. Within the current model of sepsis immunobiology, the framing of dysregulated host immune responses into proinflammatory and immunosuppressive responses for the testing of novel treatments has not resulted in successful immunomodulatory therapies. Thus, the recent focus has been to parse observable heterogeneity into subtypes of sepsis to enable personalised immunomodulation. In this Personal View, we highlight that many fundamental immunological concepts such as resistance, disease tolerance, resilience, resolution, and repair are not incorporated into the current sepsis immunobiology model. The focus for addressing heterogeneity in sepsis should be broadened beyond subtyping to encompass the identification of deterministic molecular networks or dominant mechanisms. We explicitly reframe the dysregulated host immune responses in sepsis as altered homoeostasis with pathological disruption of immune-driven resistance, disease tolerance, resilience, and resolution mechanisms. Our proposal highlights opportunities to identify novel treatment targets and could enable successful immunomodulation in the future.

Indexed as

Disease ResistanceSepsisHumansImmunomodulation

Identifiers

PMID38408467
PMCPMC11025021
OpenAlexW4392112563

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.