Evidence map›Paper›PMID 40473640›Full record

ArticleNature communications2025

Bacterial membrane nanovesicles encapsulating prodrug assemblies combine chemical and immunological therapies for chronic bacterial infection.

Yuanfeng Li, Wei He, Yinzi Piao, Yumeng Wang, Mengna Peng, Huaping Li, Rongdang Hu, Dongdong Li, Linqi Shi, Yong Liu

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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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

10 authors.

Yuanfeng Li *Translational Medicine Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.ORCID http://orcid.org/0009-0002-9139-3139
Wei He *Department of Orthodontics School and Hospital of Stomatology, Wenzhou Medical University Wenzhou, Wenzhou, Zhejiang, China.
Yinzi Piao *Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, Zhejiang, China.
Yumeng WangTranslational Medicine Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Mengna PengWenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, Zhejiang, China.
Huaping LiWenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, Zhejiang, China.
Rongdang HuDepartment of Orthodontics School and Hospital of Stomatology, Wenzhou Medical University Wenzhou, Wenzhou, Zhejiang, China. hurongdang@hotmail.com.
Dongdong LiWenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, Zhejiang, China. ldd@ucas.ac.cn.
Linqi ShiState Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin, China.
Yong LiuTranslational Medicine Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China. y.liu@nankai.edu.cn.ORCID http://orcid.org/0000-0003-1738-7857

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22275043National Natural Science Foundation of China (National Science Foundation of China) 52203184National Natural Science Foundation of China (National Science Foundation of China) 52293383National Natural Science Foundation of China (National Science Foundation of China) 52422307Natural Science Foundation of Zhejiang Province (Zhejiang Provincial Natural Science Foundation) LR24H180001
6 · The paper itself

Abstract

Overcoming challenges in drug targeting and modulating the immunosuppressive microenvironment are critical for treating chronic bacterial infections, which are often characterized by intracellular bacteria and biofilms. To overcome these barriers, we report a multifunctional nanomedicine (CpE@BMV). The prodrug conjugate (CpE), composed of two phenylboronic acid-modified ciprofloxacin (Cip-pba) molecules and ellagic acid (Ea), self-assembles due to its hydrophobic nature and π-π stacking. Bacterial membrane vesicles (BMVs) derived from Escherichia coli aid in CpE assembly and structural stabilization. Upon administration, pathogen-associated molecular patterns on CpE@BMV engage toll-like receptors on macrophages, activating these cells and enhancing their phagocytic response. Once internalized, CpE responds to elevated intracellular H₂O₂ levels, releasing Cip to eliminate intracellular bacteria. Additionally, Ea scavenges excess reactive oxygen species in inflamed macrophages and modulates the expression of inflammatory factors, preventing an exaggerated inflammatory response. The CpE@BMV formulation also penetrates biofilms, eliminating bacteria and releasing antigens. These antigens are transported to draining lymph nodes, where they induce dendritic cell maturation and trigger a robust T and B cell-mediated immune response, helping restore immune balance and combat pathogens effectively in female mouse models. Therefore, our CpE@BMV provide an efficient strategy combining chemical and immunological therapies for chronic bacterial infection management.

Indexed as

Anti-Bacterial AgentsBacterial InfectionsProdrugsAnimalsBiofilmsBoronic AcidsChronic DiseaseCiprofloxacinEscherichia coliFemaleHumansMacrophagesMiceMice, Inbred C57BLAnti-Bacterial Agentsbenzeneboronic acidBoronic AcidsCiprofloxacinProdrugs

Identifiers

PMID40473640
PMCPMC12141615

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.