Evidence map›Paper›PMID 41155215›Full record

ReviewInternational journal of molecular sciences2025

Immunology of Hypertension: Pathophysiological and Therapeutic Aspects.

Alexander Manzano, Heliana Parra, Daniela Ariza, Maria Marquina, Pablo Duran, María J Calvo, Manuel Nava, Omar Ross, Julio César Contreras-Velásquez, Diego Rivera-Porras and 1 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

11 authors.

Alexander ManzanoEndocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0001-6652-8834
Heliana ParraEndocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0002-6604-4212
Daniela ArizaEndocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0002-0123-3629
Maria MarquinaEndocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0002-6203-181X
Pablo DuranEndocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0002-8030-1780
María J CalvoEndocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0002-9569-2796
Manuel NavaEndocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0001-9769-1693
Omar RossEndocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0009-0004-3852-9716
Julio César Contreras-VelásquezUniversidad de la Costa, Departamento de Productividad e Innovación, Barranquilla, Atlántico, Colombia, Barranquilla 080001, Colombia.
Diego Rivera-PorrasUniversidad de la Costa, Departamento de Productividad e Innovación, Barranquilla, Atlántico, Colombia, Barranquilla 080001, Colombia.ORCID 0000-0003-2169-3208
Valmore BermúdezUniversidad Simón Bolívar, Centro de Investigaciones en Ciencias de la Vida, Barranquilla 080001, Colombia.ORCID 0000-0003-1880-8887

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertension affects over 1.39 billion people globally, causing 9.4 million deaths annually. This paper examines the intricate relationship between the immune system and hypertension, highlighting the contributions of both innate and adaptive immune responses. The innate response, involving natural killer (NK) cells, macrophages, toll-like receptors (TLRs), and dendritic cells, contributes to organ damage and inflammatory responses, exacerbating hypertension. Adaptive immunity, particularly T cells, further exacerbates vascular and renal dysfunction through the release of cytokines such as IFN-γ, IL-17A, and TNF-α, ultimately leading to multisystem damage. Therapeutic strategies targeting these immune responses are being explored, including immunosuppressants such as mycophenolate mofetil (MMF) and methotrexate (MTX), as well as monoclonal antibodies against IL-1β and TNF-α. While these strategies show promise, further research is needed to evaluate their efficacy and safety. Furthermore, this paper highlights the potential benefits of immunological approaches in managing the root causes of hypertension, offering an alternative to conventional therapies focused on the renin-angiotensin-aldosterone system. In conclusion, this work highlights the immune mechanisms in the hypertension pathogenesis, identifying them as potential therapeutic targets for enhanced management and improved patient outcomes.

Indexed as

HypertensionAdaptive ImmunityAnimalsCytokinesHumansImmunity, InnateCytokinescytokineshypertensionimmune systeminflammationmonoclonal antibodies

Identifiers

PMID41155215
PMCPMC12563126

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.