Evidence map›Paper›PMID 29751831›Full record

ArticleStem cell research & therapy2018

Intravenous injection of allogeneic umbilical cord-derived multipotent mesenchymal stromal cells reduces the infarct area and ameliorates cardiac function in a porcine model of acute myocardial infarction.

Meikuang Lim, Weiqiang Wang, Lu Liang, Zhi-Bo Han, Zongjin Li, Jie Geng, Meng Zhao, Honghong Jia, Jie Feng, Zhe Wei and 10 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 116 citations in OpenAlex.

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  13. Spinal cord injury: molecular mechanisms and therapeutic interventions.Signal transduction and targeted therapy · 2023
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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

20 authors at 5 institutions in 1 country.

Meikuang LimNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China.
Weiqiang WangBeijing Institute of Stem Cells, Health & Biotech Co., Ltd, Beijing, People's Republic of China.
Lu LiangNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China.
Zhi-Bo HanNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China.
Zongjin LiBeijing Institute of Stem Cells, Health & Biotech Co., Ltd, Beijing, People's Republic of China.
Jie GengNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China.
Meng ZhaoNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China.
Honghong JiaNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China.
Jie FengNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China.
Zhe WeiNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China.
Baoquan SongState Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, People's Republic of China.
Jiemin ZhangAnimal Medical Experiment Center, TEDA International Cardiovascular Hospital, Tianjin, People's Republic of China.
Jun LiAnimal Medical Experiment Center, TEDA International Cardiovascular Hospital, Tianjin, People's Republic of China.
Tianwen LiuAnimal Medical Experiment Center, TEDA International Cardiovascular Hospital, Tianjin, People's Republic of China.
Fan WangAnimal Medical Experiment Center, TEDA International Cardiovascular Hospital, Tianjin, People's Republic of China.
Ting LiNuclear Medicine Department, TEDA International Cardiovascular Hospital, Tianjin, People's Republic of China.
Jianming LiNuclear Medicine Department, TEDA International Cardiovascular Hospital, Tianjin, People's Republic of China.
Yihu FangInstitute of Stem Cell, Jiangxi Medical College, ShangRao, Jiangxi, People's Republic of China.
Jianhua GaoInstitute of Stem Cell, Jiangxi Medical College, ShangRao, Jiangxi, People's Republic of China.
Zhongchao HanNational Engineering Research Center of Cell Products, Tianjin AmCellGene Engineering Co., Ltd, Tianjin, People's Republic of China. hanzhongchao@hotmail.com.
TEDA International Cardiovascular Hospital · CNSinovac Biotech · CNFirst Affiliated Hospital of Jiangxi Medical College · CNInstitute of Hematology & Blood Diseases Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

China National Science and Technology Major Projects of Drug Discovery 2014ZX09508002-003National Natural Science Foundation of China 31470951National Natural Science Foundation of China 81330015Natural Science Foundation of Jiangxi, China 20161BAB205281
6 · The paper itself

Abstract

backgroundMultipotent mesenchymal stromal cell (MSC) therapy has been widely recognized as a feasible strategy for regenerating injured myocardial tissue. However, little is known about the efficacy of intravenous injection of allogeneic umbilical cord (UC) MSCs in preclinical models of porcine myocardial infarction.

methodsDifferent dosages of allogeneic UC-MSCs or the vehicle [phosphate-buffered saline (PBS)] were delivered intravenously into an acute myocardial infarction (AMI) porcine model twice after coronary ligation. Echocardiography was performed to examine the cardiac function and single photon emission computed tomography (SPECT) and positron emission tomography (PET)/computed tomography (CT) was performed to detect cardiac perfusion and nonviable myocardium. At the end of the experiment, 2,3,5-triphenyl-tetrazolium chloride (TTC) staining and Masson T staining were performed to determine the infarct area. The protein and gene expression levels associated with cardiac function, inflammation, and angiogenesis were examined by Western blot and real time polymerase chain reaction (PCR). In vivo trafficking of intravenous injection of allogeneic UC-MSCs enhanced green fluorescent protein (eGFP) was detected by real time PCR and immunofluorescence.

resultsAfter systemic delivery, allogeneic UC-MSCs were largely distributed in the lungs and some in the infracted myocardium. At week 8 following AMI, echocardiography demonstrated significantly improved fractional shortening in the high-dose (1.5 × 10

conclusionsIntravenous injection of UC-MSCs is a feasible and effective way to preserve LV function and ameliorate myocardial remodeling in porcine AMI. The cardioprotective effects of UC-MSCs were attributed to paracrine factors that appear to augment angiogenesis, limit inflammation, and preserve Cx43 gap junction.

Indexed as

Acute DiseaseAnimalsDisease Models, AnimalEchocardiographyInjections, IntravenousMesenchymal Stem CellsMyocardial InfarctionPositron Emission Tomography Computed TomographySwineUmbilical CordAcute myocardial infarctionMultipotent mesenchymal stromal cellPorcineUmbilical cord

Identifiers

PMID29751831
PMCPMC5948807
OpenAlexW2805250768

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.