Evidence map›Paper›PMID 34468107›Full record

ArticleEuropean journal of histochemistry : EJH2021

Swertianolin ameliorates immune dysfunction in sepsis <em>via</em> blocking the immunosuppressive function of myeloid- derived suppressor cells.

Zongfang Ren, Haoren Tang, Linjun Wan, Xing Liu, Ning Tang, Lingling Wang, Zhenhui Guo

Open access · goldAbstract read
In one paragraph

Article in European journal of histochemistry : EJH, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 5 institutions in 1 country.

Zongfang RenThe First School of Clinical Medicine, Southern Medical University, Guangzhou. zfrenkunming@163.com.
Haoren TangDepartment of Gastroenterological Surgery, the Second Affiliated Hospital of Kunming Medical University, Kunming . knigth1190@sina.com.
Linjun WanDepartment of Critical Care Medicine, the Second Affiliated Hospital of Kunming Medical University, Kunming . wanlj2003@163.com.
Xing LiuGraduate School of Guangzhou University of Chinese Medicine, Guangzhou. 1473328067@qq.com.
Ning TangDepartment of Neurology, The First People's Hospital of Yunnan Province, Kunming University of Science and Technology, Kunming. 28580655@qq.com.
Lingling WangDepartment of Medical Intensive Care Unit, General Hospital of Southern Theater Command of PLA, Guangzhou . 317542137@qq.com.
Zhenhui GuoThe First School of Clinical Medicine, Southern Medical University, Guangzhou. micugzh@vip.sina.com.
Kunming Medical University · CNSouthern Medical University · CNGuangzhou University of Chinese Medicine · CNKunming University of Science and Technology · CNThird Affiliated Hospital of Southern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we studied the long-term proliferation trajectory of myeloid-derived suppressor cells (MDSCs) in murine sepsis model and investigated whether swertianolin could modulate the immunosuppressive function of MDSCs. A murine sepsis model was established by cecal ligation and perforation (CLP), according to the Minimum Quality Threshold in Pre-Clinical Sepsis Studies (MQTiPSS) guidelines. The bone marrow and spleen of the mice were collected at 24 h, 72 h, 7 and 15 d after sepsis induction. The proportions of monocytic-MDSCs (M-MDSCs; CD11b+LY6G-LY6Chi) and granulocytic-MDSCs (G-MDSC, CD11b+ Ly6G+ Ly6Clow) were analyzed by flow cytometry. Then, we have investigated whether swertianolin could modulate the immunosuppressive function of MDSCs in in vitro experiments. G-MDSCs and M-MDSCs increased acutely after sepsis with high levels sustained over a long period of time. G-MDSCs were the main subtype identified in the murine model of sepsis with polymicrobial peritonitis. Furthermore, it was found that swertianolin reduced significantly interleukin-10 (IL-10), nitric oxide (NO), reactive oxygen species (ROS), and arginase production in MDSCs, while reducing MDSC proliferation and promoting MDSC differentiation into dendritic cells. Swertianolin also improved T-cell activity by blocking the immunosuppressive effect of MDSCs. Both subsets of MDSCs significantly increased in the bone marrow and spleen of the mice with sepsis, with G-MDSCs being the main subtype identified. Swertianolin effectively regulated the functions of MDSCs and reduced immune suppression.

Indexed as

AnimalsCell DifferentiationCell ProliferationDendritic CellsImmune ToleranceIridoid GlucosidesLegionella pneumophilaLungMiceMice, Inbred C57BLMyeloid-Derived Suppressor CellsPeritonitisSepsisXanthonesIridoid GlucosidesswertianolinXanthones

Identifiers

PMID34468107
PMCPMC8419598
OpenAlexW3198826028

What OpenQuestion holds

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LicenceCC BY-NC
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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.