Evidence map›Paper›PMID 28852174›Full record

ArticleScientific reports2017

Activation of invariant natural killer T cells stimulated with microbial α-mannosyl glycolipids.

Michio Shimamura, Masaki Yamamura, Tatsuya Nabeshima, Naoki Kitano, Peter van den Elzen, Hasan Yesilkaya, Peter Andrew, Petr Illarionov

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

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  5. Recognition ofMicroorganisms · 2020
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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

8 authors at 5 institutions in 3 countries.

Michio ShimamuraTsukuba Research Center for Interdisciplinary Materials Science, University of Tsukuba, Tsukuba, 305-8571, Japan. m.shimamura@thu.ac.jp.
Masaki YamamuraTsukuba Research Center for Interdisciplinary Materials Science, University of Tsukuba, Tsukuba, 305-8571, Japan.
Tatsuya NabeshimaTsukuba Research Center for Interdisciplinary Materials Science, University of Tsukuba, Tsukuba, 305-8571, Japan.ORCID 0000-0003-1269-7725
Naoki KitanoChild and Family Research Institute, University of British Columbia, Vancouver, V5Z4H4, BC, Canada.
Peter van den ElzenChild and Family Research Institute, University of British Columbia, Vancouver, V5Z4H4, BC, Canada.
Hasan YesilkayaDepartment of Infection, Immunity and Inflammation, University of Leicester, Leicester, LE1 9HN, United Kingdom.
Peter AndrewDepartment of Infection, Immunity and Inflammation, University of Leicester, Leicester, LE1 9HN, United Kingdom.
Petr IllarionovSchool of Biosciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom. illar@yahoo.com.ORCID 0000-0002-7342-0714
University of British Columbia · CAUniversity of Leicester · GBUniversity of Tsukuba · JPMitsubishi Group (Japan) · JPUniversity of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some synthetic and bacterial glycolipids presented by CD1d specifically activate invariant NKT (iNKT) cells bearing an invariant Vα14-Jα18 (mouse) or Vα24-Jα18 (human) TCR. The antigenic glycolipids identified to date consist of two hydrophobic chains and an α-glycoside in which the 2'-OH group is in the cis orientation toward the anomeric group, namely, either an α-galactoside or an α-glucoside. Several microbial α-mannosyl glycolipids, in which the 2'-OH group is in the trans orientation, were herein examined to establish whether they have potential to activate iNKT cells. We found that α-mannnosyl1-3 (6'-O-acyl α-mannosyl)-1-1 monoacylglycerol and cholesteryl 6'-O-acyl α-mannoside, found in Saccharopolyspora and Candida albicans, respectively, induced the activation of iNKT cells, dependent on CD1d. In contrast, α-mannosyldiacylglycerol found in Streptococcus suis or α-mannosylceramide demonstrated markedly less antigenicity for iNKT cells. The potentially antigenic α-mannosyl glycolipids contributed to the protection of mice against infection with S. pneumoniae in which iNKT cells have previously been found to participate. Furthermore, these glycolipids induced the production of proinflammatory cytokines by macrophages, thereby suggesting their recognition by specific pattern recognition receptors (PRRs). Collectively, these results suggest that these microbial α-mannosyl glycolipids are capable of being recognized by both the invariant TCR and PRRs and inducing immune responses.

Indexed as

AnimalsAntigens, BacterialAntigens, CD1dBiomarkersGlycolipidsHumansImmunophenotypingLymphocyte ActivationMiceMice, KnockoutMolecular StructureNatural Killer T-CellsReceptors, Antigen, T-Cell, alpha-betaAntigens, BacterialAntigens, CD1dBiomarkersGlycolipidsReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID28852174
PMCPMC5574887
OpenAlexW2748646866

What OpenQuestion holds

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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.