Evidence map›Paper›PMID 26190499›Full record

ArticleActa pharmacologica Sinica2015

IL-37b gene transfer enhances the therapeutic efficacy of mesenchumal stromal cells in DSS-induced colitis mice.

Wei-qiang Wang, Kui Dong, Lu Zhou, Guo-hui Jiao, Cong-zhong Zhu, Wen-wen Li, Gang Yu, Wan-tong Wu, Song Chen, Zhi-na Sun and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 57 citations in OpenAlex.

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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

15 authors at 3 institutions in 1 country.

Wei-qiang WangDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Kui DongDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Lu ZhouDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Guo-hui JiaoDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Cong-zhong ZhuDepartments of Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Wen-wen LiDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Gang YuState Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Sciences, Tianjin 300020, China.
Wan-tong WuState Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Sciences, Tianjin 300020, China.
Song ChenState Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Sciences, Tianjin 300020, China.
Zhi-na SunState Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Sciences, Tianjin 300020, China.
Yu-ming WangDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Wen-tian LiuDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Jie ZhangDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Bang-mao WangDepartments of Gastroenterology and Hepatology and Gynecology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Xiao-ming FengState Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Sciences, Tianjin 300020, China.
Tianjin Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNInstitute of Hematology & Blood Diseases Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate whether the transfer of the IL-37b gene, a newly identified inhibitor of both innate and adaptive immunity, could improve the therapeutic efficacy of mesenchumal stromal cells (MSCs) in inflammatory bowel disease (IBD).

methodsThe expression of IL-37 in biopsied specimens of the patients with active ulcerative colitis (UC) was detected using RT-PCR and immunohistochemistry. Mice were treated with 3% dextran sulfate sodium (DSS) for 8 days to induce colitis. Before DSS treatment, the mice were injected with MSCs, MSC-eGFP or MSC-IL37b. Their body weight was measured each day, and the colons and spleens were harvested on d 10 for pathological and biochemical analyses.

resultsIn biopsied specimens of the patients with active UC, the expression of IL-37 was dramatically elevated in inflamed mucosa, mainly in epithelial cells and infiltrating immune cells. Compared to MSC-eGFP or MSCs, MSC-IL37b administration significantly attenuated the body weight and colon length reduction, and decreased the histological score in DSS-induced colitis mice. Furthermore, MSC-IL37b administration increased the percentage of myeloid-derived suppressor cells (MDSCs) among total splenic mononuclear cells as well as the percentage of regulatory T cells (Tregs) among splenic CD4+ T cells in the mice. Moreover, MSC-IL37b administration increased the IL-2+ cells and decreased the IFN-γ+ cells among splenic CD4+ T cells.

conclusionIL-37 is involved in the pathophysiology of UC. IL-37b gene transfer enhances the therapeutic efficacy of MSCs in DSS-induced colitis mice by inducing Tregs and MDSCs and regulating cytokine production.

Indexed as

Gene Transfer TechniquesMesenchymal Stem Cell TransplantationAnimalsCytokinesDextran SulfateDisease Models, AnimalFemaleGenetic TherapyHumansInflammatory Bowel DiseasesInterleukin-1MiceMice, Inbred C57BLCytokinesDextran SulfateIL37 protein, humanInterleukin-1

Identifiers

PMID26190499
PMCPMC4635324
OpenAlexW1951659592

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.