Evidence map›Paper›PMID 29449556›Full record

ArticleNature communications2018

CD1d-dependent immune suppression mediated by regulatory B cells through modulations of iNKT cells.

K Oleinika, E C Rosser, D E Matei, K Nistala, A Bosma, I Drozdov, C Mauri

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Review
  5. Can we cure autoimmunity?Current opinion in immunology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

K OleinikaCentre for Rheumatology, Division of Medicine, University College London, London, WC1E 6JF, UK.
E C RosserCentre for Rheumatology, Division of Medicine, University College London, London, WC1E 6JF, UK.
D E MateiCentre for Rheumatology, Division of Medicine, University College London, London, WC1E 6JF, UK.
K NistalaCentre for Rheumatology, Division of Medicine, University College London, London, WC1E 6JF, UK.
A BosmaCentre for Rheumatology, Division of Medicine, University College London, London, WC1E 6JF, UK.
I DrozdovBering Limited, London, TW2 6EA, UK.
C MauriCentre for Rheumatology, Division of Medicine, University College London, London, WC1E 6JF, UK. c.mauri@ucl.ac.uk.ORCID http://orcid.org/0000-0001-9761-2625
University College London · GBInstitute of Infection and Immunity · CA

Funding

Medical Research Council G0900950Versus Arthritis 21141Wellcome Trust
6 · The paper itself

Abstract

Regulatory B cells (Breg) express high levels of CD1d that presents lipid antigens to invariant natural killer T (iNKT) cells. The function of CD1d in Breg biology and iNKT cell activity during inflammation remains unclear. Here we show, using chimeric mice, cell depletion and adoptive cell transfer, that CD1d-lipid presentation by Bregs induces iNKT cells to secrete interferon (IFN)-γ to contribute, partially, to the downregulation of T helper (Th)1 and Th17-adaptive immune responses and ameliorate experimental arthritis. Mice lacking CD1d-expressing B cells develop exacerbated disease compared to wild-type mice, and fail to respond to treatment with the prototypical iNKT cell agonist α-galactosylceramide. The absence of lipid presentation by B cells alters iNKT cell activation with disruption of metabolism regulation and cytokine responses. Thus, we identify a mechanism by which Bregs restrain excessive inflammation via lipid presentation.

Indexed as

Adoptive TransferAnimalsAntigens, CD1dArthritis, ExperimentalB-LymphocytesB-Lymphocytes, RegulatoryCells, CulturedGalactosylceramidesInterferon-gammaMaleMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsTh17 CellsTh1 Cellsalpha-galactosylceramideAntigens, CD1dCd1d1 protein, mouseGalactosylceramidesInterferon-gamma

Identifiers

PMID29449556
PMCPMC5814456
OpenAlexW2802757660

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.