Evidence map›Paper›PMID 38658669›Full record

ReviewNature reviews. Nephrology2024

Immune mechanisms in the pathophysiology of hypertension.

Bianca A Nguyen, Matthew R Alexander, David G Harrison

Abstract readReview
In one paragraph

Review in Nature reviews. Nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
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

46 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Unveiling the Immune Mechanisms of Hypertension With Single-Cell Transcriptome-Wide Mendelian Randomization.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  6. Hypertensive mt. tRNARedox biology · 2026
    Article
  7. Article
  8. Article
  9. Salt and chronic kidney disease.Nature reviews. Nephrology · 2026
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

3 authors.

Bianca A NguyenDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA.
Matthew R AlexanderDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA.
David G HarrisonDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA. david.g.harrison@vumc.org.

Funding

Mechanisms of Immune Activation in HypertensionR35HL140016 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HARRISON, DAVID G · 2018 to 2024
$5.3M
Vanderbilt Hypertension and Blood Pressure Regulation ProgramT32HL144446 · NHLBI · VANDERBILT UNIVERSITY · PI HARRISON, DAVID G · 2019 to 2023
$1.7M
The Role of CCR10+ Regulatory T Cells In HypertensionK08HL153786 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALEXANDER, MATTHEW R · 2020 to 2024
$792k
The Role of CCR10 and CCR10+ Tregs in HypertensionF31HL176154 · NHLBI · VANDERBILT UNIVERSITY · PI Bianca Alexandra Nguyen · 2024 to 2026
$70k
NHLBI NIH HHS F31 HL176154NHLBI NIH HHS K08 HL153786NHLBI NIH HHS R35 HL140016NHLBI NIH HHS T32 HL144446
6 · The paper itself

Abstract

Hypertension is a leading risk factor for morbidity and mortality worldwide. Despite current anti-hypertensive therapies, most individuals with hypertension fail to achieve adequate blood pressure control. Moreover, even with adequate control, a residual risk of cardiovascular events and associated organ damage remains. These findings suggest that current treatment modalities are not addressing a key element of the underlying pathology. Emerging evidence implicates immune cells as key mediators in the development and progression of hypertension. In this Review, we discuss our current understanding of the diverse roles of innate and adaptive immune cells in hypertension, highlighting key findings from human and rodent studies. We explore mechanisms by which these immune cells promote hypertensive pathophysiology, shedding light on their multifaceted involvement. In addition, we highlight advances in our understanding of autoimmunity, HIV and immune checkpoints that provide valuable insight into mechanisms of chronic and dysregulated inflammation in hypertension.

Indexed as

Adaptive ImmunityHypertensionAnimalsAutoimmunityHIV InfectionsHumansImmunity, InnateInflammation

Identifiers

PMID38658669
PMCPMC12060254

What Socratic 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 Socratic graph.