Evidence map›Paper›PMID 39953528›Full record

ReviewCell communication and signaling : CCS2025

Dysregulation of neutrophil in sepsis: recent insights and advances.

Ji Zhang, Yuwen Shao, Jingyi Wu, Jing Zhang, Xiangsheng Xiong, Jingjing Mao, Yunwei Wei, Changhong Miao, Hao Zhang

Abstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 2 pooled it
–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

51 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  11. Coordinated expansion of CD163bioRxiv : the preprint server for biology · 2026
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  18. Immune interplay between sepsis and haematological malignancies.Intensive care medicine experimental · 2026
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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

9 authors.

Ji Zhang *Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yuwen Shao *Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jingyi Wu *Department of Anesthesiology, Zhongshan Hospital(Xiamen), Fudan University, Xiamen, China.
Jing ZhangDepartment of Anesthesiology, Hebei General Hospital, Shijiazhuang, China.
Xiangsheng XiongDepartment of Anesthesiology, Huai'an hospital affiliated to Yangzhou University (The fifth People's Hospital of Huai'an), Huai'an, Jiangsu, China.
Jingjing MaoDepartment of Anesthesiology, Huai'an hospital affiliated to Yangzhou University (The fifth People's Hospital of Huai'an), Huai'an, Jiangsu, China.
Yunwei WeiDepartment of Anesthesiology, Women's Health Center of Shanxi, Children's Hospital of Shanxi, Taiyuan, Shanxi, China.
Changhong MiaoDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, China. miaochanghong_zs@163.com.
Hao ZhangDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, China. zhang.hao@zs-hospital.sh.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis remains the leading cause of death in intensive care units. Despite newer antimicrobial and supportive therapies, specific treatments are still lacking. Neutrophils are pivotal components of the effector phase of the host immune defense against pathogens and play a crucial role in the control of infections under normal circumstances. In addition to its anti-infective effects, the dysregulation and overactivation of neutrophils may lead to severe inflammation or tissue damage and are potential mechanisms for poor prognosis in sepsis. This review focuses on recent advancements in the understanding of the functional status of neutrophils across various pathological stages of sepsis to explore the mechanisms by which neutrophils participate in sepsis progression and provide insights for the treatment of sepsis by targeting neutrophils.

Indexed as

NeutrophilsSepsisAnimalsHumansNeutrophilNeutrophil extracellular trapsOrgan injuryOxidative stressSepsis

Identifiers

PMID39953528
PMCPMC11827254

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.