Evidence map›Paper›PMID 21629707›Full record

ReviewJournal of biomedicine & biotechnology2011

The role of natural killer cells in sepsis.

Laurent Chiche, Jean-Marie Forel, Guillemette Thomas, Catherine Farnarier, Fréderic Vely, Mathieu Bléry, Laurent Papazian, Eric Vivier

Abstract readReview
In one paragraph

Review in Journal of biomedicine & biotechnology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
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

46 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Cytokine Storm and Sepsis-Induced Multiple Organ Dysfunction Syndrome.Advances in experimental medicine and biology · 2024
    Review
  7. Article
  8. Redox regulation of the immune response.Cellular & molecular immunology · 2022
    Review
  9. Article
  10. NK Cell-Derived IL-10 Supports Host Survival during Sepsis.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  11. Article
  12. Observational
  13. Increased percentage of PD-L1Critical care (London, England) · 2020
    Observational
  14. Review
  15. Review
  16. Article
  17. IL-33 attenuates mortality by promoting IFN-γ production in sepsis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2018
    Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Laurent ChicheCentre d'Immunologie de Marseille-Luminy, Université de la Méditerranée UM 631, Campus de Luminy, 13288 Marseille, France. laurent.chiche@ap-hm.fr
Jean-Marie Forel
Guillemette Thomas
Catherine Farnarier
Fréderic Vely
Mathieu Bléry
Laurent Papazian
Eric Vivier

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe sepsis and septic shock are still deadly conditions urging to develop novel therapies. A better understanding of the complex modifications of the immune system of septic patients is needed for the development of innovative immunointerventions. Natural killer (NK) cells are characterized as CD3(-)NKp46(+)CD56(+) cells that can be cytotoxic and/or produce high amounts of cytokines such as IFN-γ. NK cells are also engaged in crosstalks with other immune cells, such as dendritic cells, macrophages, and neutrophils. During the early stage of septic shock, NK cells may play a key role in the promotion of the systemic inflammation, as suggested in mice models. Alternatively, at a later stage, NK cells-acquired dysfunction could favor nosocomial infections and mortality. Standardized biological tools defining patients' NK cell status during the different stages of sepsis are mandatory to guide potential immuno-interventions. Herein, we review the potential role of NK cells during severe sepsis and septic shock.

Indexed as

Models, ImmunologicalAnimalsHumansKiller Cells, NaturalMiceSepsisSystemic Inflammatory Response Syndrome

Identifiers

PMID21629707
PMCPMC3100670

What OpenQuestion holds

Textmetadata
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.