Evidence map›Paper›PMID 30279688›Full record

ArticleFrontiers in immunology2018

Taurodeoxycholate Increases the Number of Myeloid-Derived Suppressor Cells That Ameliorate Sepsis in Mice.

Sooghee Chang, Youn-Hee Kim, Young-Joo Kim, Young-Woo Kim, Sungyoon Moon, Yong Yook Lee, Jin Sun Jung, Youngsoo Kim, Hi-Eun Jung, Tae-Joo Kim and 14 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 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

24 authors at 3 institutions in 2 countries.

Sooghee ChangDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Youn-Hee KimDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Young-Joo KimDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Young-Woo KimDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Sungyoon MoonWide River Institute of Immunology, Seoul National University, Seoul, South Korea.
Yong Yook LeeWide River Institute of Immunology, Seoul National University, Seoul, South Korea.
Jin Sun JungWide River Institute of Immunology, Seoul National University, Seoul, South Korea.
Youngsoo KimDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Hi-Eun JungDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Tae-Joo KimDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Taek-Chin CheongDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Hye-Jung MoonDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Jung-Ah ChoDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Hang-Rae KimDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Dohyun HanBiomedical Research Institute, Seoul National University Hospital, Seoul, South Korea.
Yirang NaDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Seung-Hyeok SeokDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Nam-Hyuk ChoDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Hai-Chon LeeWide River Institute of Immunology, Seoul National University, Seoul, South Korea.
Eun-Hee NamWide River Institute of Immunology, Seoul National University, Seoul, South Korea.
Hyosuk ChoDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Murim ChoiDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Nagahiro MinatoDepartment of Immunology and Cell Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Seung-Yong SeongDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, South Korea.
Seoul National University · KRSeoul National University Hospital · KRKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bile acids (BAs) control metabolism and inflammation by interacting with several receptors. Here, we report that intravenous infusion of taurodeoxycholate (TDCA) decreases serum pro-inflammatory cytokines, normalizes hypotension, protects against renal injury, and prolongs mouse survival during sepsis. TDCA increases the number of granulocytic myeloid-derived suppressor cells (MDSC

Indexed as

AnimalsCell CountCell ProliferationCells, CulturedDisease Models, AnimalGene Expression RegulationHumansImmune ToleranceLeukocyte ElastaseLipopolysaccharidesMiceMice, Inbred C57BLMice, KnockoutMyeloid-Derived Suppressor CellsOncostatin MSepsisLeukocyte ElastaseLipopolysaccharidesOncostatin MTaurodeoxycholic Acidinflammationmyeloid-derived suppressor cellssepsistaurodeoxycholateTGR5

Identifiers

PMID30279688
PMCPMC6153344
OpenAlexW2889597388

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.