Evidence map›Paper›PMID 38474140›Full record

ArticleInternational journal of molecular sciences2024

Single Cell High Dimensional Analysis of Human Peripheral Blood Mononuclear Cells Reveals Unique Intermediate Monocyte Subsets Associated with Sex Differences in Coronary Artery Disease.

Nandini Chatterjee, Ravi K Komaravolu, Christopher P Durant, Runpei Wu, Chantel McSkimming, Fabrizio Drago, Sunil Kumar, Gabriel Valentin-Guillama, Yury I Miller, Coleen A McNamara and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. 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
3.1field-weighted citation impact, top 8% 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.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Single-cell analysis of CD14Frontiers in immunology · 2025
    Article
  6. Article
  7. Article
  8. Article
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

14 authors at 4 institutions in 1 country.

Nandini ChatterjeeLa Jolla Institute of Immunology, La Jolla, CA 92037, USA.
Ravi K KomaravoluDepartment of Medicine, Immunology Center of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-3167-8960
Christopher P DurantLa Jolla Institute of Immunology, La Jolla, CA 92037, USA.
Runpei WuLa Jolla Institute of Immunology, La Jolla, CA 92037, USA.
Chantel McSkimmingBeirne Carter Immunology Center, University of Virginia, Charlottesville, VA 22904, USA.
Fabrizio DragoBeirne Carter Immunology Center, University of Virginia, Charlottesville, VA 22904, USA.
Sunil KumarDepartment of Medicine, Immunology Center of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0003-3139-114X
Gabriel Valentin-GuillamaDepartment of Medicine, Immunology Center of Georgia, Augusta University, Augusta, GA 30912, USA.
Yury I MillerDivision of Endocrinology, University of California San Diego, La Jolla, CA 92093, USA.
Coleen A McNamaraBeirne Carter Immunology Center, University of Virginia, Charlottesville, VA 22904, USA.
Klaus LeyLa Jolla Institute of Immunology, La Jolla, CA 92037, USA.
Angela TaylorBeirne Carter Immunology Center, University of Virginia, Charlottesville, VA 22904, USA.ORCID 0000-0003-4927-4320
Ahmad AlimadadiLa Jolla Institute of Immunology, La Jolla, CA 92037, USA.ORCID 0000-0002-7888-5019
Catherine C HedrickLa Jolla Institute of Immunology, La Jolla, CA 92037, USA.
La Jolla Institute for Immunology · USCarter Center · USAugusta University Health · USUniversity of California San Diego · US

Funding

Project 4: APOB-specific CD4 and CD8 T cells exacerbate atherosclerosisP01HL136275 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Catherine C Hedrick · 2017 to 2026
$25.5M
Vascular macrophages and T cells in atherosclerosisR35HL145241 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI LEY, KLAUS F. · 2019 to 2025
$5.9M
NHLBI NIH HHS P01 HL136275NHLBI NIH HHS R35 HL145241NIH HHS NIH P01 HL136275
6 · The paper itself

Abstract

Monocytes are associated with human cardiovascular disease progression. Monocytes are segregated into three major subsets: classical (cMo), intermediate (iMo), and nonclassical (nMo). Recent studies have identified heterogeneity within each of these main monocyte classes, yet the extent to which these subsets contribute to heart disease progression is not known. Peripheral blood mononuclear cells (PBMC) were obtained from 61 human subjects within the Coronary Assessment of Virginia (CAVA) Cohort. Coronary atherosclerosis severity was quantified using the Gensini Score (GS). We employed high-dimensional single-cell transcriptome and protein methods to define how human monocytes differ in subjects with low to severe coronary artery disease. We analyzed 487 immune-related genes and 49 surface proteins at the single-cell level using Antibody-Seq (Ab-Seq). We identified six subsets of myeloid cells (cMo, iMo, nMo, plasmacytoid DC, classical DC, and DC3) at the single-cell level based on surface proteins, and we associated these subsets with coronary artery disease (CAD) incidence based on Gensini score (GS) in each subject. Only frequencies of iMo were associated with high CAD (GS > 32),

Indexed as

Coronary Artery DiseaseFemaleHLA-DR AntigensHumansLeukocytes, MononuclearMaleMonocytesSex CharacteristicsHLA-DR Antigensantibody-sequencing (Ab-Seq)coronary artery disease (CAD)generalized linear mixed mdel (GLMM)Gensini score (GS)monocytes

Identifiers

PMID38474140
PMCPMC10932111
OpenAlexW4392359597

What Socratic 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 Socratic graph.