Evidence map›Paper›PMID 42905373›Full record

ReviewHuman cell2026

Neutrophil plasticity in inflammation resolution: mechanisms and therapeutic potential.

Yan Liao, Yuting Wang, Min Wang, Chenglong Zhu, Lizhou Song, Haoling Zhang, Wangzheqi Zhang, Zui Zou

Abstract readReview
PubMed Publisher
In one paragraph

Review in Human cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yan Liao *School of Anesthesiology, Naval Medical University, Shanghai, China.
Yuting Wang *Department of Cardiology, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China.
Min Wang *Shanghai Sixth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200233, China.
Chenglong ZhuSchool of Anesthesiology, Naval Medical University, Shanghai, China.
Lizhou SongSchool of Anesthesiology, Naval Medical University, Shanghai, China.
Haoling ZhangDepartment of Biomedical Sciences, Cancer Research and Specialist Centre, Universiti Sains Malaysia, 13200, Penang, Malaysia. zhanghaolingedu@163.com.
Wangzheqi ZhangSchool of Anesthesiology, Naval Medical University, Shanghai, China. zwzq001031@smmu.edu.cn.
Zui ZouSchool of Anesthesiology, Naval Medical University, Shanghai, China. zouzui@smmu.edu.cn.ORCID http://orcid.org/0000-0002-8433-8388

Funding

National Natural Science Foundation of China 82572494
6 · The paper itself

Abstract

As primary effector cells of the innate immune response, neutrophils exert pivotal regulatory effects on inflammatory responses at the initiation, amplification and resolution stages. This dynamic nature is apparent in multilayered signaling responses, functional plasticity and their mutual actions within the immune network. During early inflammation, neutrophils are rapidly recruited to sites of injury or infection through chemotactic axes, including the interleukin (IL)-8/C-X-C chemokine receptor (CXCR)1/2 axis and the C-X-C motif chemokine ligand 2/CXCR2 axis, as well as by pro-inflammatory cytokines such as interleukin-1 beta (IL-1β) and tumor necrosis factor alpha (TNF-α). At these sites, they destroy pathogens by phagocytosis, by producing reactive oxygen species (ROS), and through the release of so-called neutrophil extracellular traps (NETs). At the intermediate phase, activation of signaling pathways including nuclear factor kappa B (NF-κB) and mitogen-activated protein kinase (MAPK) leads to neutrophil activation and immunity amplification, while NETs support the equilibrium by regulating macrophage, dendritic cell, and T lymphocyte activities. Neutrophil apoptosis and subsequent macrophage-mediated efferocytosis contribute to limiting inflammatory activity and promoting tissue repair during resolution of inflammation; by contrast neutrophil-associated anti-inflammatory and pro-resolving responses, which vary according to the inflammatory context, exhibit a more complex role. Heterogeneous neutrophil populations and functional states in chronic inflammatory lesions and the tumor microenvironment (TME) may show divergent effects on tissue injury and repair. Neutrophils with primarily pro-inflammatory functions can sustain inflammation and tissue destruction, whereas neutrophils displaying anti-inflammatory or reparative programs may contribute to the repair of damaged tissues and the re-establishment of homeostasis. Together, neutrophils perform stage-specific actions across the inflammatory continuum, and their spatiotemporal fine-tuning and signal redirection could become potential targets for precise treatment of infections, autoimmunity, and tumor-related inflammation.

Indexed as

Cell PlasticityInflammationNeutrophilsAnimalsApoptosisCytokinesEfferocytosisExtracellular TrapsHumansImmunity, InnateMacrophagesMitogen-Activated Protein KinasesNF-kappa BPhagocytosisReactive Oxygen SpeciesSignal TransductionCytokinesMitogen-Activated Protein KinasesNF-kappa BReactive Oxygen SpeciesApoptosisChronic inflammationImmune regulationInflammatory responseNeutrophil extracellular trapsNeutrophilsTissue repair

Identifiers

What OpenQuestion holds

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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.