Evidence map›Paper›PMID 31782624›Full record

ArticleEMBO molecular medicine2020

Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection.

Yue-Qing Zhou, Yun Shi, Ling Yang, Yu-Fen Sun, Yu-Fei Han, Zi-Xian Zhao, Yu-Jia Wang, Ying Liu, Yu Ma, Ting Zhang and 7 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
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

23 citing papers in PubMed, 44 citations in OpenAlex.

  1. Autologous transplantation of P63Cell reports. Medicine · 2024
    Trial
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  12. Stem cell-based therapy for pulmonary fibrosis.Stem cell research & therapy · 2022
    Review
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  16. Article
  17. 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

17 authors at 6 institutions in 2 countries.

Yue-Qing ZhouDepartment of Respiratory and Critical Care Medicine, Clinical Translation Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Yun ShiShanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Ling YangDepartment of Respiratory and Critical Care Medicine, Clinical Translation Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Yu-Fen SunDepartment of Respiratory and Critical Care Medicine, Clinical Translation Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Yu-Fei HanDepartment of Respiratory and Critical Care Medicine, Clinical Translation Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Zi-Xian ZhaoDepartment of Respiratory and Critical Care Medicine, Clinical Translation Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Yu-Jia WangDepartment of Respiratory and Critical Care Medicine, Clinical Translation Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Ying LiuShanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Yu MaShanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Ting ZhangRegend Therapeutics Co. Ltd, Zhejiang, China.
Tao RenShanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Tina P DaleGuy Hilton Research Center, School of Pharmacy and Bioengineering, Keele University, Staffordshire, UK.
Nicholas R ForsythGuy Hilton Research Center, School of Pharmacy and Bioengineering, Keele University, Staffordshire, UK.ORCID 0000-0001-5156-4824
Fa-Guang JinDepartment of Respiratory and Critical Care Medicine, Tangdu Hospital, Fourth Military Medical University of PLA, Xi'an, China.
Jie-Ming QuRuijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.ORCID 0000-0003-4517-9473
Wei ZuoDepartment of Respiratory and Critical Care Medicine, Clinical Translation Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.ORCID 0000-0002-4460-0337
Jin-Fu XuDepartment of Respiratory and Critical Care Medicine, Clinical Translation Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.ORCID 0000-0002-8039-8973
Tongji University · CNShanghai East Hospital · CNKeele University · GBAir Force Medical University · CNRegend Therapeutics (China) · CNShanghai Jiao Tong University · CN

Funding

Key Project of Fundamental Research Funds for the Central Universities 2017ZD002National Key Research Program 2017YFA0104600National Science Foundation of China 81570091National Science Foundation of China 81600003National Science Foundation of China 81670006National Science Foundation of China 81770073National Science Foundation of China NSFC81630001Project of the Shanghai Hospital Development Center 16CR3036AShanghai Leading Talent Program 2016036Shanghai Pulmonary Hospital Annual GrantThe National Science Fund for Distinguished Young Scholars 81925001Tongji University Basic Scientific Research-Interdisciplinary Fund and 985 GrantYouth 1000 Talent Plan of China
6 · The paper itself

Abstract

Severe pulmonary infection is a major threat to human health accompanied by substantial medical costs, prolonged inpatient requirements, and high mortality rates. New antimicrobial therapeutic strategies are urgently required to address the emergence of antibiotic resistance and persistent bacterial infections. In this study, we show that the constitutive expression of a native antimicrobial peptide LL-37 in transgenic mice aids in clearing Pseudomonas aeruginosa (PAO1), a major pathogen of clinical pulmonary infection. Orthotopic transplantation of adult mouse distal airway stem cells (DASCs), genetically engineered to express LL-37, into injured mouse lung foci enabled large-scale incorporation of cells and long-term release of the host defense peptide, protecting the mice from bacterial pneumonia and hypoxemia. Further, correlates of DASCs in adult humans were isolated, expanded, and genetically engineered to demonstrate successful construction of an anti-infective artificial lung. Together, our stem cell-based gene delivery therapeutic platform proposes a new strategy for addressing recurrent pulmonary infections with future translational opportunities.

Indexed as

Escherichia coliPseudomonas InfectionsStem Cell TransplantationAnimalsAntimicrobial Cationic PeptidesCathelicidinsFemaleLung DiseasesMaleMiceMice, Inbred C57BLMice, TransgenicPseudomonas aeruginosaRatsRats, Sprague-DawleyAntimicrobial Cationic PeptidesCathelicidinsantimicrobial peptidedistal airway stem cellspulmonary infectiontransplantation

Identifiers

PMID31782624
PMCPMC6949487
OpenAlexW2990637450

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.