Evidence map›Paper›PMID 42501393›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2026

Pollen-Based Artificial Enzyme With Efficient Biocatalysis and Immune-Priming to Prevent Primary and Secondary Wound Infection.

Jiangge Li, Mao Wang, Heng Yang, Minjia Yuan, Ting Wang, Mohsen Adeli, Wei Geng, Weifeng Zhao, Chong Cheng, Changsheng Zhao

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 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

10 authors.

Jiangge LiCollege of Biomedical Engineering, National Engineering Research Center for Biomaterials, Sichuan University, Chengdu, China.
Mao WangCollege of Polymer Science and Engineering, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0001-7583-1683
Heng YangCollege of Polymer Science and Engineering, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, China.
Minjia YuanCollege of Polymer Science and Engineering, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, China.
Ting WangCollege of Polymer Science and Engineering, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, China.
Mohsen AdeliDepartment of Endodontics, Department of Orthodontics, State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0001-6895-8491
Wei GengCollege of Polymer Science and Engineering, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, China.
Weifeng ZhaoCollege of Polymer Science and Engineering, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, China.
Chong ChengCollege of Polymer Science and Engineering, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0002-6872-2240
Changsheng ZhaoCollege of Biomedical Engineering, National Engineering Research Center for Biomaterials, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0002-4619-3499

Funding

National Key R&D Program of China 2024YFE0201200National Natural Science Foundation of China 52373148National Natural Science Foundation of China 52403195National Natural Science Foundation of China 52525311National Natural Science Foundation of China 82561160101Open Research Fund of Suzhou Laboratory SZLAB-1308-2025-TS018Sichuan Science and Technology Program 2024YFHZ0263State Key Laboratory of Synergistic Chem-Bio Synthesis sklscbs202576
6 · The paper itself

Abstract

Bacterial infection poses a significant threat to clinical treatment due to the emergence of drug resistance and the high risk of recurrence. Here, we report the de novo design of a spiky pollen-based vanadium artificial enzyme particle (VAE-Pollen) that integrates potent reactive oxygen species (ROS)-catalytic activity with immune priming to prevent both primary and secondary bacterial infections. Experimental and theoretical analyses confirm that bacteria are efficiently captured by the micro-structured surface of VAE-Pollen, and the introduction of oxygen vacancies modulates the electronic configuration of vanadium catalytic sites, significantly enhancing their versatile ROS-catalytic performance. Meanwhile, VAE-Pollen enhances bacterial capture and ROS-triggered release of bacterial antigens, which mimics the sustained allergen exposure characteristic of natural pollen, thereby potently activating systemic defensive responses and providing sustained anti-infective surveillance to prevent secondary wound infection. Notably, the VAE-Pollen demonstrates significant efficacy in treating methicillin-resistant Staphylococcus aureus (MRSA) and preventing its recurrence, offering a potent and intelligent antibacterial alternative that may circumvent the limitations of conventional antibiotics.

Indexed as

Anti-Bacterial AgentsBiocatalysisBiomimetic MaterialsPollenWound InfectionMethicillin-Resistant Staphylococcus aureusReactive Oxygen SpeciesAnti-Bacterial AgentsReactive Oxygen Speciesartificial enzymebacterial disinfectionbiocatalysisreactive oxygen speciestissue regeneration

Identifiers

PMID42501393
PMCPMC13579178

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.