Evidence map›Paper›PMID 27942751›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2017

A sphingosine 1-phosphate receptor agonist ameliorates animal model of vasculitis.

Chie Miyabe, Yoshishige Miyabe, Takaki Komiya, Hiroki Shioya, Noriko N Miura, Kei Takahashi, Naohito Ohno, Ryoji Tsuboi, Andrew D Luster, Shinichi Kawai and 2 more

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 13 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

12 authors at 7 institutions in 2 countries.

Chie MiyabeDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.
Yoshishige MiyabeDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.
Takaki KomiyaDepartment of Biology and Pharmacology, Ono Pharmaceutical Co. Ltd, 3-1-1, Sakurai, Shimamoto-cho, Mishima-gun, Osaka, 618-8585, Japan.
Hiroki ShioyaDepartment of Biology and Pharmacology, Ono Pharmaceutical Co. Ltd, 3-1-1, Sakurai, Shimamoto-cho, Mishima-gun, Osaka, 618-8585, Japan.
Noriko N MiuraDepartment of Immunopharmacology of Microbial Products, Tokyo University of Pharmacy and Life Science School of Pharmacy, 1432-1 Horinouchi, Hachioji, Tokyo, 192-0392, Japan.
Kei TakahashiDepartment of Pathology, Toho University, 2-17-6 Ohashi, Meguro, Tokyo, 153-8515, Japan.
Naohito OhnoDepartment of Immunopharmacology of Microbial Products, Tokyo University of Pharmacy and Life Science School of Pharmacy, 1432-1 Horinouchi, Hachioji, Tokyo, 192-0392, Japan.
Ryoji TsuboiDepartment of Dermatology, Tokyo Medical University, 6-7-1, Nishi-Shinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.
Andrew D LusterCenter for Immunology and Inflammatory Disease, Department of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, CNY149-8 13th St, Boston, MA, 02129, USA.
Shinichi KawaiDivision of Rheumatology, Department of Internal Medicine, Toho University School of Medicine, 6-11-1 Omori-Nishi, Ota-ku, Tokyo, 143-8541, Japan.
Nobuyuki MiyasakaDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.
Toshihiro NankiDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan. toshihiro.nanki@med.toho-u.ac.jp.
Toho University · JPHarvard University · USOno Pharmaceutical (Japan) · JPTokyo University of Pharmacy and Life Sciences · JPMassachusetts General Hospital · USTokyo Medical and Dental University · JPTokyo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSphingosine 1-phosphate (S1P) is a bioactive lipid that binds to cell surface receptors (S1P

methodsMice were administered ONO-W061, and the number of peripheral blood cells was counted. Vasculitis was induced by an intraperitoneal injection of CAWS. Expression of S1P receptors and CXCL1 was analyzed by quantitative RT-PCR. ONO-W061 was orally administered, and vasculitis was evaluated histologically. Number of neutrophils, macrophages and T cells in the vasculitis tissue was counted using flow cytometry. Production of chemokines from S1P-stimulated human umbilical vein endothelial cells (HUVECs) was measured by ELISA.

resultsNumber of peripheral blood lymphocytes was decreased by ONO-W061. Expression of CXCL1 and S1P

conclusionsONO-W061 significantly improved CAWS-induced vasculitis. This effect may be partly exerted through the inhibited production of chemokines by endothelial cells, which in turn could induce neutrophil recruitment into inflamed vessels.

Indexed as

AnimalsCandida albicansChemokine CXCL1Disease Models, AnimalHuman Umbilical Vein Endothelial CellsInterleukin-8Leukocyte CountLysophospholipidsMaleMice, Inbred BALB CReceptors, LysosphingolipidSphingosineVasculitisChemokine CXCL1CXCL8 protein, humanInterleukin-8LysophospholipidsReceptors, LysosphingolipidSphingosinesphingosine 1-phosphateChemokineSphingosine 1-phosphateSphingosine 1-phosphate receptor 1Vasculitis

Identifiers

PMID27942751
OpenAlexW2560723418

What OpenQuestion holds

Textmetadata
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.