Evidence map›Paper›PMID 42324269›Full record

ArticleNature communications2026

Lipopolysaccharide hydrolysis-targeting nano-chimeras detoxify endotoxin through specific adsorption and efficient degradation.

Lulu Jin, Chenyin Zhang, Hongli Yi, Jing Tang, Kexin Yu, Yuanyuan Wang, Feihe Huang, Ketao Jin, Zhengwei Mao, Lidan Hu and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. The two faces of mitochondrial CaJournal of physiology and biochemistry · 2026
    Review
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

11 authors.

Lulu JinCenter for Rehabilitation Medicine, Rehabilitation and Sports Medicine Research Institute of Zhejiang Province, Department of Rehabilitation Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital of Hangzhou Medical College, Hangzhou, China.
Chenyin ZhangMOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, China.
Hongli YiMOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, China.
Jing TangMOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, China.
Kexin YuTranslational Medicine Center, Zhejiang Key Laboratory of Tumor Molecular Diagnosis and Individualized Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital of Hangzhou Medical College, Hangzhou, China.
Yuanyuan WangTranslational Medicine Center, Zhejiang Key Laboratory of Tumor Molecular Diagnosis and Individualized Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital of Hangzhou Medical College, Hangzhou, China.
Feihe HuangStoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou, China.ORCID http://orcid.org/0000-0003-3177-6744
Ketao JinDepartment of Colorectal and Anal Surgery, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, China. jinketao2001@zju.edu.cn.
Zhengwei MaoMOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, China. zwmao@zju.edu.cn.ORCID http://orcid.org/0000-0001-7990-2856
Lidan HuChildren's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, China. hulidan@zju.edu.cn.
Xiaozhou MouCenter for Rehabilitation Medicine, Rehabilitation and Sports Medicine Research Institute of Zhejiang Province, Department of Rehabilitation Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital of Hangzhou Medical College, Hangzhou, China. mouxz@zju.edu.cn.ORCID http://orcid.org/0000-0002-3234-1737

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipopolysaccharide (LPS), a potent immunogenic component of the outer membrane of Gram-negative bacteria, triggers severe inflammation and organ failure even at nanomolar concentrations. However, neutralizing LPS in vivo remains challenging due to the high abundance of other biomolecules in biological fluids, which interfere with LPS detoxification. Brassicaceae species produce a transmembrane protein termed lipooligosaccharide-specific reduced elicitation (LORE) that specifically recognizes and binds LPS. Here, we prepare plant-derived nanovesicles naturally presenting LORE on their surface and integrate them with cerium-based nanozymes exhibiting LPS hydrolysis activity. We show that these hybrid nanostructures (Atv@Ce) neutralize LPS through two coordinated mechanisms: LORE captures LPS specifically, while nanozymes chemically degrade the phosphate groups and glycosidic bonds in the lipid A moiety. This dual strategy effectively attenuates both local and systemic inflammation, offering a biocompatible detoxification strategy with translational potential. Our work provides an insight into nanomaterial-mediated detoxification.

Indexed as

EndotoxinsLipopolysaccharidesNanostructuresAdsorptionAnimalsHydrolysisMiceEndotoxinsLipopolysaccharides

Identifiers

PMID42324269
PMCPMC13438714

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.