Evidence map›Paper›PMID 39468354›Full record

ArticleNature nanotechnology2025

Filamentous phages as tumour-targeting immunotherapeutic bionanofibres.

Hui Yue, Yan Li, Tao Yang, Yecheng Wang, Qing Bao, Yajing Xu, Xiangyu Liu, Yao Miao, Mingying Yang, Chuanbin Mao

Abstract read
PubMed Publisher
In one paragraph

Article in Nature nanotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  11. Cryo-Inactivated Cancer Cells Derived Magnetic Micromotors for Tumor Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  12. Article
  13. Review
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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.

Hui YueSchool of Materials Science and Engineering, Zhejiang University, Hangzhou, P. R. China.
Yan LiInstitute of Applied Bioresource Research, College of Animal Science, Zhejiang University, Hangzhou, P. R. China.ORCID http://orcid.org/0000-0001-9637-2308
Tao YangDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Sha Tin, P. R. China.
Yecheng WangDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Sha Tin, P. R. China.
Qing BaoSchool of Materials Science and Engineering, Zhejiang University, Hangzhou, P. R. China.
Yajing XuDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Sha Tin, P. R. China.
Xiangyu LiuDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Sha Tin, P. R. China.
Yao MiaoSchool of Materials Science and Engineering, Zhejiang University, Hangzhou, P. R. China.
Mingying YangInstitute of Applied Bioresource Research, College of Animal Science, Zhejiang University, Hangzhou, P. R. China.ORCID http://orcid.org/0000-0003-1256-6514
Chuanbin MaoDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Sha Tin, P. R. China. cmao@cuhk.edu.hk.ORCID http://orcid.org/0000-0002-8142-3659

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81871499
6 · The paper itself

Abstract

Programmed cell death-ligand 1 (PD-L1) blockers have advanced immunotherapy, but their lack of tumour homing capability represents a substantial challenge. Here we show that genetically engineered filamentous phages can be used as tumour-targeting immunotherapeutic agents that reduce the side effects caused by untargeted delivery of PD-L1 blockers. Specifically, we improved biopanning to discover a peptide binding the extracellular domain of PD-L1 and another targeting both melanoma tissues and cancer cells. The two peptides were genetically fused to the sidewall protein and tip protein of fd phages, respectively. The intravenously injected phages homed to tumours and bound PD-L1 on cancer cells, effectively blocking PD-1/PD-L1 recognition to trigger targeted immunotherapy without body weight loss, organ abnormalities and haematological aberrations. The phages, cost-effectively replicated by bacteria, are cancer-targeting immunotherapeutic nanofibres that can be flexibly designed to target different cancer types and immune checkpoints.

Indexed as

B7-H1 AntigenImmunotherapyInovirusMelanomaNeoplasmsAnimalsCell Line, TumorHumansMiceNanofibersPeptidesB7-H1 AntigenCD274 protein, humanPeptides

Identifiers

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.