Evidence map›Paper›PMID 42509246›Full record

ArticleNature communications2026

Personalized Phage Therapy in an ICU Patient with Polymicrobial Pulmonary Infections: a case from a single-arm trial.

Yongxin Shi, Jie Li, Qian Yang, Jianhui Li, Linlin Li, Jianfang Liu, Jia Dai, Yumeng Shang, Xin Zhou, Lan Yang and 8 more

Abstract readCase Reports
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. 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

18 authors.

Yongxin Shi *Department of Critical Care Medicine, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
Jie Li *Shanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
Qian Yang *CreatiPhage Biotechnology, Co., Ltd., Shanghai, 20030, China.
Jianhui LiShanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.ORCID 0000-0002-3975-9079
Linlin LiShanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
Jianfang LiuCreatiPhage Biotechnology, Co., Ltd., Shanghai, 20030, China.
Jia DaiShanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
Yumeng ShangDepartment of Critical Care Medicine, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
Xin ZhouCreatiPhage Biotechnology, Co., Ltd., Shanghai, 20030, China.
Lan YangShanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
Chuanjiang ChenCreatiPhage Biotechnology, Co., Ltd., Shanghai, 20030, China.
Ziqi ZhaoCreatiPhage Biotechnology, Co., Ltd., Shanghai, 20030, China.
Huiqin ZhangCreatiPhage Biotechnology, Co., Ltd., Shanghai, 20030, China.
Juan BaoShanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
Tongyu ZhuShanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
Mengjun ChengShanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China. 124785048@qq.com.
Nannan WuShanghai Institute of Phage, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China. nannan.wu@cphage.com.ORCID 0000-0003-1244-0030
He WangDepartment of Critical Care Medicine, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China. wanghe@shphc.org.cn.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82070772, 32470145, 32100113
6 · The paper itself

Abstract

Ventilator-associated infections (VAIs) caused by multidrug-resistant (MDR) pathogens poses a significant challenge in intensive care units (ICUs). Phage therapy has emerged as a promising alternative for VAIs, though its efficacy depends on multiple factors. We report a 40-year-old male ICU patient with sequential pulmonary infections of MDR Acinetobacter baumannii, Klebsiella pneumoniae, and Stenotrophomonas maltophilia. Seven rounds of tailored phage therapy-targeting single or dual pathogens-were administered adjunctive to antibiotics. A. baumannii was complete eradication, but K. pneumoniae and S. maltophilia showed cyclical clearance and recurrence due to strain replacement and phage resistance. Phage therapy correlated with reduced bacterial load, fever, procalcitonin, and IL-6 levels, alongside improved pulmonary inflammation, while white blood cell counts and C-reactive protein showed limited response. No severe adverse events occurred. Dynamic shifts in dominant pathogens aligned with clinical progression, with phage therapy providing transient control, extending the window for intervention and reducing high-level antibiotic use. After six months, the patient was weaned from ventilation and discharged. This case underscores the complexity of VAI management and highlights the potential of personalized phage therapy to mitigate MDR infections and minimize antibiotic reliance. This case was enrolled in a single arm trial (ChiCTR2000036801).

Indexed as

CoinfectionPhage TherapyPneumonia, Ventilator-AssociatedAcinetobacter baumanniiAcinetobacter InfectionsAdultAnti-Bacterial AgentsDrug Resistance, Multiple, BacterialHumansIntensive Care UnitsKlebsiella InfectionsKlebsiella pneumoniaeMalePrecision MedicineStenotrophomonas maltophiliaAnti-Bacterial Agents

Identifiers

PMID42509246
PMCPMC13408689

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.