Evidence map›Paper›PMID 38651687›Full record

ReviewJournal of cellular physiology2024

B cells and atherosclerosis: A HIV perspective.

Laventa M Obare, Rachel H Bonami, Amanda C Doran, Celestine N Wanjalla

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of cellular physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Targeted drug delivery systems for atherosclerosis.Journal of nanobiotechnology · 2025
    Review
  5. Mouse Models of HIV-Associated Atherosclerosis.International journal of molecular sciences · 2025
    Review
  6. Review
  7. 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

4 authors at 1 institution in 1 country.

Laventa M ObareDivision of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Rachel H BonamiDivision of Rheumatology and Immunology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Amanda C DoranDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Celestine N WanjallaDivision of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0001-9159-5414
Vanderbilt University Medical Center · US

Funding

Selection &Regulation of B Lymphocytes in IDDMR01AI051448 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BONAMI, RACHEL H · 2003 to 2022
$7.3M
Critical Mediators of Inflammation Resolution and Immune Memory in AtherosclerosisR01HL159487 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DORAN, AMANDA C · 2021 to 2025
$3.2M
The Origins of Human Anti-Insulin B Lymphocytes in Type 1 DiabetesR01DK131070 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Rachel H Bonami · 2022 to 2026
$2.2M
Anti-cytomegalovirus Immune Responses in Atherosclerotic Cardiovascular Disease in Persons Living with HIVK23HL156759 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WANJALLA, CELESTINE N · 2021 to 2025
$860k
Molecular Characterization of Autoreactive B Cells in Immune Checkpoint Inhibitor-Induced Autoimmune SiccaR03AI163835 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BONAMI, RACHEL H · 2021 to 2022
$173k
NHLBI NIH HHS K23 HL156759NHLBI NIH HHS R01 HL159487NIAID NIH HHS R01 AI051448NIAID NIH HHS R03 AI163835NIDDK NIH HHS R01 DK131070
6 · The paper itself

Abstract

Atherosclerosis remains a leading cause of cardiovascular disease (CVD) globally, with the complex interplay of inflammation and lipid metabolism at its core. Recent evidence suggests a role of B cells in the pathogenesis of atherosclerosis; however, this relationship remains poorly understood, particularly in the context of HIV. We review the multifaceted functions of B cells in atherosclerosis, with a specific focus on HIV. Unique to atherosclerosis is the pivotal role of natural antibodies, particularly those targeting oxidized epitopes abundant in modified lipoproteins and cellular debris. B cells can exert control over cellular immune responses within atherosclerotic arteries through antigen presentation, chemokine production, cytokine production, and cell-cell interactions, actively participating in local and systemic immune responses. We explore how HIV, characterized by chronic immune activation and dysregulation, influences B cells in the context of atherosclerosis, potentially exacerbating CVD risk in persons with HIV. By examining the proatherogenic and antiatherogenic properties of B cells, we aim to deepen our understanding of how B cells influence atherosclerotic plaque development, especially within the framework of HIV. This research provides a foundation for novel B cell-targeted interventions, with the potential to mitigate inflammation-driven cardiovascular events, offering new perspectives on CVD risk management in PLWH.

Indexed as

AtherosclerosisB-LymphocytesHIV InfectionsAnimalsCell DifferentiationHumansInflammationPlaque, AtheroscleroticatherosclerosisB cellscardiovascular diseaseHIVinflammation

Identifiers

PMID38651687
PMCPMC11209796
OpenAlexW4395049062

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.