Evidence map›Paper›PMID 36059483›Full record

ReviewFrontiers in immunology2022

Dysregulation of neutrophil death in sepsis.

Cheng-Long Zhu, Yi Wang, Qiang Liu, Hui-Ru Li, Chang-Meng Yu, Peng Li, Xiao-Ming Deng, Jia-Feng Wang

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 2 pooled it
8.7field-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

68 citing papers in PubMed, 2 syntheses or guidelines pooled it, 106 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
  7. Immunology of Sepsis.Clinics in chest medicine · 2026
    Review
  8. Article
  9. Review
  10. Acta pharmaceutica Sinica. B · 2026
    Article
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  12. Article
  13. Article
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  16. Review
  17. Observational
  18. Review
  19. Article
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8 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Cheng-Long ZhuFaculty of Anesthesiology, Changhai Hospital, The Naval Medical University, Shanghai, China.
Yi WangFaculty of Anesthesiology, Changhai Hospital, The Naval Medical University, Shanghai, China.
Qiang LiuFaculty of Anesthesiology, Changhai Hospital, The Naval Medical University, Shanghai, China.
Hui-Ru LiFaculty of Anesthesiology, Changhai Hospital, The Naval Medical University, Shanghai, China.
Chang-Meng YuFaculty of Anesthesiology, Changhai Hospital, The Naval Medical University, Shanghai, China.
Peng LiFaculty of Anesthesiology, Changhai Hospital, The Naval Medical University, Shanghai, China.
Xiao-Ming DengFaculty of Anesthesiology, Changhai Hospital, The Naval Medical University, Shanghai, China.
Jia-Feng WangFaculty of Anesthesiology, Changhai Hospital, The Naval Medical University, Shanghai, China.
Changhai Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is a prevalent disease that has alarmingly high mortality rates and, for several survivors, long-term morbidity. The modern definition of sepsis is an aberrant host response to infection followed by a life-threatening organ dysfunction. Sepsis has a complicated pathophysiology and involves multiple immune and non-immune mediators. It is now believed that in the initial stages of sepsis, excessive immune system activation and cascading inflammation are usually accompanied by immunosuppression. During the pathophysiology of severe sepsis, neutrophils are crucial. Recent researches have demonstrated a clear link between the process of neutrophil cell death and the emergence of organ dysfunction in sepsis. During sepsis, spontaneous apoptosis of neutrophils is inhibited and neutrophils may undergo some other types of cell death. In this review, we describe various types of neutrophil cell death, including necrosis, apoptosis, necroptosis, pyroptosis, NETosis, and autophagy, to reveal their known effects in the development and progression of sepsis. However, the exact role and mechanisms of neutrophil cell death in sepsis have not been fully elucidated, and this remains a major challenge for future neutrophil research. We hope that this review will provide hints for researches regarding neutrophil cell death in sepsis and provide insights for clinical practitioners.

Indexed as

NeutrophilsSepsisHumansInflammationMultiple Organ FailurePyroptosisapoptosisautophagycell deathnecroptosisNETsneutrophilpyroptosissepsis

Identifiers

PMID36059483
PMCPMC9434116
OpenAlexW4292482612

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.