Evidence map›Paper›PMID 34888745›Full record

ReviewCurrent hypertension reports2021

T Cell Immunometabolism and Redox Signaling in Hypertension.

David L Mattson, Justine M Abais-Battad

Open access · greenAbstract readReview
In one paragraph

Review in Current hypertension reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Immunosenescence in Aging-Related Vascular Dysfunction.International journal of molecular sciences · 2022
    Article
  5. Article
  6. 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

2 authors at 1 institution in 1 country.

David L MattsonDepartment of Physiology, Medical College of Georgia at Augusta University, Augusta, GA, USA.
Justine M Abais-BattadDepartment of Physiology, Medical College of Georgia at Augusta University, Augusta, GA, USA. jabaisbattad@augusta.edu.ORCID 0000-0001-5252-0903
Augusta University · US

Funding

Therapeutic Effects of mTOR Inhibition in Salt-Sensitive HypertensionP01HL116264 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI MATTSON, DAVID L. · 2013 to 2021
$18.7M
Mechanisms of renal immune cell infiltration in salt-sensitive hypertensionR01HL137748 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI COWLEY, ALLEN W, MATTSON, DAVID L. · 2018 to 2021
$2.3M
American Heart Association 19CDA34660184NHLBI NIH HHS HL116264NHLBI NIH HHS HL137748NHLBI NIH HHS P01 HL116264NHLBI NIH HHS R01 HL137748
6 · The paper itself

Abstract

purpose of reviewIn this article, we summarize the current literature supporting metabolic and redox signaling pathways as important mechanisms underlying T cell activation in the context of hypertension. RECENT

findingsT cell immunometabolism undergoes dramatic remodeling in order to meet the demands of T cell activation, differentiation, and proliferation. Recent evidence demonstrates that the T cell oxidation-reduction (redox) system also undergoes significant changes upon activation, which can itself modulate metabolic processes and T cell function. Dysregulation of these signaling pathways can lead to aberrant T cell activation and inappropriate ROS production, both of which are linked to pathological conditions like hypertension. While the contribution of T cells to the progression of hypertension has been thoroughly investigated, how T cell metabolism and redox signaling changes, both separately and together, is an area of study that remains largely untouched. This review presents evidence from our own laboratory as well as others to highlight the importance of these two mechanisms in the study of hypertension.

Indexed as

HypertensionT-LymphocytesHumansOxidation-ReductionReactive Oxygen SpeciesSignal TransductionReactive Oxygen SpeciesHypertensionImmune cellsImmunometabolismRedox signalingT cells

Identifiers

PMID34888745
PMCPMC9764136
OpenAlexW4200412882

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.