Evidence map›Paper›PMID 38660807›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2024

Interactions Between HDL and CD4+ T Cells: A Novel Understanding of HDL Anti-Inflammatory Properties.

Laura Atehortua, W Sean Davidson, Claire A Chougnet

Open access · greenAbstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.3field-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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  15. Dysfunctional high-density lipoprotein: an updated review.Frontiers in cardiovascular medicine · 2025
    Review
  16. Article
  17. 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

3 authors at 2 institutions in 2 countries.

Laura AtehortuaCincinnati Children's Hospital Medical Center, OH (L.A., C.A.C.).ORCID 0000-0002-9981-3225
W Sean DavidsonDivision of Experimental Pathology, Department of Pathology and Laboratory Medicine, University of Cincinnati, OH (W.S.D.).ORCID 0000-0003-2756-2989
Claire A ChougnetCincinnati Children's Hospital Medical Center, OH (L.A., C.A.C.).ORCID 0000-0003-0217-3442
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · US

Funding

Project 3 - HDL Structure/Function in LCAT Deficient HumansP01HL128203 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jere P Segrest · 2016 to 2026
$25.1M
Tissue Repository CoreP30AR070549 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI Leah Claire Kottyan · 2016 to 2026
$7.7M
Xenotransplant and Genome Editing CoreU54DK126108 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Daniel Starczynowski, YI ZHENG · 2021 to 2026
$5.0M
Role of apoE in HDL-mediated enhanced survival of human regulatory T-cellsR01HL167200 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI W Sean Davidson, AMY SANGHAVI SHAH · 2023 to 2026
$2.6M
NHLBI NIH HHS P01 HL128203NHLBI NIH HHS R01 HL167200NIAMS NIH HHS P30 AR070549NIDDK NIH HHS U54 DK126108
6 · The paper itself

Abstract

Several studies in animal models and human cohorts have recently suggested that HDLs (high-density lipoproteins) not only modulate innate immune responses but also adaptative immune responses, particularly CD4+ T cells. CD4+ T cells are central effectors and regulators of the adaptive immune system, and any alterations in their homeostasis contribute to the pathogenesis of cardiovascular diseases, autoimmunity, and inflammatory diseases. In this review, we focus on how HDLs and their components affect CD4+ T-cell homeostasis by modulating cholesterol efflux, immune synapsis, proliferation, differentiation, oxidative stress, and apoptosis. While the effects of apoB-containing lipoproteins on T cells have been relatively well established, this review focuses specifically on new connections between HDL and CD4+ T cells. We present a model where HDL may modulate T cells through both direct and indirect mechanisms.

Indexed as

CD4-Positive T-LymphocytesLipoproteins, HDLAdaptive ImmunityAnimalsAnti-Inflammatory AgentsApoptosisCell ProliferationHomeostasisHumansInflammationOxidative StressSignal TransductionAnti-Inflammatory AgentsLipoproteins, HDLcardiovascular diseaseshomeostasisinflammationlipoproteins, HDLT lymphocytes

Identifiers

PMID38660807
PMCPMC11111342
OpenAlexW4395463674

What OpenQuestion holds

Textmetadata
LicenceTDM
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.