Evidence map›Paper›PMID 39221206›Full record

ArticleMaterials today. Bio2024

A biomimic anti-neuroinflammatory nanoplatform for active neutrophil extracellular traps targeting and spinal cord injury therapy.

Chunming Tang, Yaoyao Jin, Min Wu, Feng Jia, Xiaowei Lu, Jinyu Li, Jie Wu, Senlin Zhu, Zhiji Wang, Di An and 4 more

Abstract read
In one paragraph

Article in Materials today. Bio, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Macrophage Extracellular Traps in Immunity and Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 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

14 authors.

Chunming TangDepartment of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China.
Yaoyao JinDepartment of Emergency, The Affiliated Huai'an Hospital of Xuzhou Medical University and The Second People's Hospital of Huai'an, Huai'an, 223022, China.
Min WuDepartment of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China.
Feng JiaDepartment of Neurosurgery, Yancheng NO.1 People's Hospital, The Affiliated Yancheng First Hospital of Nanjing University Medical School, Yancheng, 224008, China.
Xiaowei LuDepartment of Geriatric Neurology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Jinyu LiDepartment of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China.
Jie WuDepartment of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China.
Senlin ZhuDepartment of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China.
Zhiji WangDepartment of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China.
Di AnDepartment of Emergency Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Wu XiongDepartment of Human Anatomy, Nanjing Medical University, Nanjing, 211166, China.
Yongjie ZhangDepartment of Human Anatomy, Nanjing Medical University, Nanjing, 211166, China.
Huae XuDepartment of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China.
Xufeng ChenDepartment of Emergency Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traumatic spinal cord injury (SCI) always leads to severe neurological deficits and permanent damage. Neuroinflammation is a vital process of SCI and have become a promising target for SCI treatment. However, the neuroinflammation-targeted therapy would hinder the functional recovery of spinal cord and lead to the treatment failure. Herein, a biomimic anti-neuroinflammatory nanoplatform (DHCNPs) was developed for active neutrophil extracellular traps (NETs) targeting and SCI treatment. The curcumin-loaded liposome with the anti-inflammatory property acted as the core of the DHCNPs. Platelet membrane and neutrophil membrane were fused to form the biomimic hybrid membrane of the DHCNPs for hijacking neutrophils and neutralizing the elevated neutrophil-related proinflammatory cytokines, respectively. DNAse I modification on the hybrid membrane could achieve NETs degradation, blood spinal cord barrier, and neuron repair. Further studies proved that the DHCNPs could reprogram the multifaceted neuroinflammation and reverse the SCI process via nuclear factor kappa-B (NF-κB) pathway. We believe that the current study provides a new perspective for neuroinflammation inhibition and may shed new light on the treatment of SCI.

Indexed as

DNAse I conjugatingHybrid cell membraneNeutrophil extracellular trapsNeutrophil hijackingNF-κBSpinal cord injury

Identifiers

PMID39221206
PMCPMC11364920

What OpenQuestion holds

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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.