Evidence map›Paper›PMID 36976644›Full record

ArticleJCI insight2023

Lipoproteins act as vehicles for lipid antigen delivery and activation of invariant natural killer T cells.

Suzanne E Engelen, Francesca A Ververs, Angela Markovska, B Christoffer Lagerholm, Jordan M Kraaijenhof, Laura Ie Yousif, Yasemin-Xiomara Zurke, Can Mc Gulersonmez, Sander Kooijman, Michael Goddard and 15 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

25 authors at 6 institutions in 3 countries.

Suzanne E EngelenKennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
Francesca A VerversCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Angela MarkovskaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
B Christoffer LagerholmWolfson Imaging Centre, Medical Research Council (MRC) Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
Jordan M KraaijenhofDepartment of Vascular Medicine, Amsterdam Medical Center, Amsterdam, Netherlands.
Laura Ie YousifKennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
Yasemin-Xiomara ZurkeKennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
Can Mc GulersonmezCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, Netherlands.
Sander KooijmanDivision of Endocrinology and Einthoven Laboratory for Vascular and Regenerative Medicine, Department of Medicine, Leiden University Medical Center, Leiden, Netherlands.
Michael GoddardKennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
Robert J van EijkerenCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, Netherlands.
Peter J JervisInstitute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.
Gurdyal S BesraInstitute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.
Saskia HaitjemaCentral Diagnostic Laboratory and.
Folkert W AsselbergsDivision of Heart & Lungs, Department of Cardiology, University Medical Center Utrecht, Utrecht, Netherlands.
Eric KalkhovenCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, Netherlands.
Hidde L PloeghBoston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Marianne BoesCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Vincenzo CerundoloMRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
G K HovinghDepartment of Vascular Medicine, Amsterdam Medical Center, Amsterdam, Netherlands.
Mariolina SalioMRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
Edwin Ca StigterCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, Netherlands.
Patrick Cn RensenDivision of Endocrinology and Einthoven Laboratory for Vascular and Regenerative Medicine, Department of Medicine, Leiden University Medical Center, Leiden, Netherlands.
Claudia MonacoKennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
Henk S SchipperKennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
University Medical Center Utrecht · NLUniversity of Oxford · GBLeiden University Medical Center · NLUniversity of Birmingham · GBBoston Children's Hospital · USUniversity of London · GB

Funding

Cancer Research UK C399/A2291Medical Research Council MC_UU_12009Medical Research Council MC_UU_12010Medical Research Council MR/S000542/1
6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells act at the interface between lipid metabolism and immunity because of their restriction to lipid antigens presented on CD1d by antigen-presenting cells (APCs). How foreign lipid antigens are delivered to APCs remains elusive. Since lipoproteins routinely bind glycosylceramides structurally similar to lipid antigens, we hypothesized that circulating lipoproteins form complexes with foreign lipid antigens. In this study, we used 2-color fluorescence correlation spectroscopy to show, for the first time to our knowledge, stable complex formation of lipid antigens α-galactosylceramide (αGalCer), isoglobotrihexosylceramide, and OCH, a sphingosine-truncated analog of αGalCer, with VLDL and/or LDL in vitro and in vivo. We demonstrate LDL receptor-mediated (LDLR-mediated) uptake of lipoprotein-αGalCer complexes by APCs, leading to potent complex-mediated activation of iNKT cells in vitro and in vivo. Finally, LDLR-mutant PBMCs of patients with familial hypercholesterolemia showed impaired activation and proliferation of iNKT cells upon stimulation, underscoring the relevance of lipoproteins as a lipid antigen delivery system in humans. Taken together, circulating lipoproteins form complexes with lipid antigens to facilitate their transport and uptake by APCs, leading to enhanced iNKT cell activation. This study thereby reveals a potentially novel mechanism of lipid antigen delivery to APCs and provides further insight into the immunological capacities of circulating lipoproteins.

Indexed as

Natural Killer T-CellsAntigen-Presenting CellsHumansLipoproteinsLipoproteinsImmunologyLipoproteinsNKT cells

Identifiers

PMID36976644
PMCPMC10243825
OpenAlexW4361190957

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.