Evidence map›Paper›PMID 31511535›Full record

ArticleCell death & disease2019

Efficacy of pulmonary transplantation of engineered macrophages secreting IL-4 on acute lung injury in C57BL/6J mice.

Huiying Liu, Yuan He, Cheng Lu, Pengfei Zhang, Chenchen Zhou, Yanli Ni, Wenkai Niu, Xin Yuan, Puyuan Li, Jing Zheng and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 27 citations in OpenAlex.

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  18. International journal of molecular sciences · 2022
    Article
  19. Article
  20. Engineering of Immune Microenvironment for Enhanced Tissue Remodeling.Tissue engineering and regenerative medicine · 2022
    Review
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

13 authors at 2 institutions in 1 country.

Huiying LiuDepartment of Respiratory and Critical Care Diseases, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China. liuhuiying1982@sina.com.
Yuan HeDepartment of Respiratory and Critical Care Diseases, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Cheng LuDepartment of Biomedical Engineering, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Pengfei ZhangDepartment of Biomedical Engineering, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Chenchen ZhouDepartment of Biomedical Engineering, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Yanli NiLaboratory of Oncology, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Wenkai NiuDepartment of Respiratory and Critical Care Diseases, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Xin YuanDepartment of Respiratory and Critical Care Diseases, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Puyuan LiDepartment of Respiratory and Critical Care Diseases, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Jing ZhengDepartment of Respiratory and Critical Care Diseases, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Yanhong QinDepartment of Respiratory and Critical Care Diseases, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China.
Luo ZhangDepartment of Biomedical Engineering, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China. marbleluo@126.com.
Changqing BaiDepartment of Respiratory and Critical Care Diseases, The Fifth Medical Center of PLA General Hospital, 100071, Beijing, China. baicq307@163.com.
Chinese PLA General Hospital · CNShenzhen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are major causes of respiratory failure, but currently, no effective pharmacotherapy exists for these disorders. Alveolar macrophages play a critical role in both the acute/initial phase and chronic/resolving phase of ALI, rendering them a potential therapeutic target. Interleukin-4 (IL-4), a Th2 cytokine, not only directly inhibits the secretion of pro-inflammatory factors from macrophages but also drives macrophages to the anti-inflammatory and tissue remodeling M2 type. However, the short half-life of IL-4 in vivo hampers its effect on disease treatment. In this study, macrophages secreting IL-4 (M-IL-4) were established and used to treat ALI through pulmonary macrophage transplantation (PMT). The results showed that highly sustained levels of IL-4 and M2 macrophage markers were detected in mice lungs following pulmonary M-IL-4 transplantation. Furthermore, PMT improved the therapeutic effect by reducing lung inflammation, alleviating tissue injury, reducing alveolar macrophages necrotic cell death, and decreasing mortality in mice with ALI. These results suggest an efficient macrophage-based protein drug delivery strategy, and for the first time, prove the feasibility and efficacy of PMT in ALI treatment.

Indexed as

Acute Lung InjuryAnimalsCell EngineeringFemaleInterleukin-4LipopolysaccharidesLungMacrophagesMacrophages, AlveolarMiceMice, Inbred C57BLPneumoniaIl4 protein, mouseInterleukin-4Lipopolysaccharides

Identifiers

PMID31511535
PMCPMC6739369
OpenAlexW2973014799

What OpenQuestion holds

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Registered trials

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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.