Evidence map›Paper›PMID 30586716›Full record

ArticleCirculation2019

Dysfunctional and Proinflammatory Regulatory T-Lymphocytes Are Essential for Adverse Cardiac Remodeling in Ischemic Cardiomyopathy.

Shyam S Bansal, Mohamed Ameen Ismahil, Mehak Goel, Guihua Zhou, Gregg Rokosh, Tariq Hamid, Sumanth D Prabhu

Abstract read
In one paragraph

Article in Circulation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 208 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
208citing papers in PubMed, 4 pooled it
20.6field-weighted citation impact, top 1% 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

208 citing papers in PubMed, 4 syntheses or guidelines pooled it, 281 citations in OpenAlex.

  1. Pooled it
  2. Myocardial Immune Cells: The Basis of Cardiac Immunology.Journal of immunology (Baltimore, Md. : 1950) · 2023
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148 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Shyam S BansalDivision of Cardiovascular Disease and Comprehensive Cardiovascular Center, University of Alabama at Birmingham (S.S.B., M.A.I., M.G., G.Z., G.R., T.H., S.D.P.).
Mohamed Ameen IsmahilDivision of Cardiovascular Disease and Comprehensive Cardiovascular Center, University of Alabama at Birmingham (S.S.B., M.A.I., M.G., G.Z., G.R., T.H., S.D.P.).
Mehak GoelDivision of Cardiovascular Disease and Comprehensive Cardiovascular Center, University of Alabama at Birmingham (S.S.B., M.A.I., M.G., G.Z., G.R., T.H., S.D.P.).
Guihua ZhouDivision of Cardiovascular Disease and Comprehensive Cardiovascular Center, University of Alabama at Birmingham (S.S.B., M.A.I., M.G., G.Z., G.R., T.H., S.D.P.).
Gregg RokoshDivision of Cardiovascular Disease and Comprehensive Cardiovascular Center, University of Alabama at Birmingham (S.S.B., M.A.I., M.G., G.Z., G.R., T.H., S.D.P.).
Tariq HamidDivision of Cardiovascular Disease and Comprehensive Cardiovascular Center, University of Alabama at Birmingham (S.S.B., M.A.I., M.G., G.Z., G.R., T.H., S.D.P.).
Sumanth D PrabhuDivision of Cardiovascular Disease and Comprehensive Cardiovascular Center, University of Alabama at Birmingham (S.S.B., M.A.I., M.G., G.Z., G.R., T.H., S.D.P.).
University of Alabama at Birmingham · USCardiovascular Institute of the South · USThe Ohio State University Wexner Medical Center · US

Funding

UAB Statistical Genetics Post-Doctoral Training ProgramT32HL072757 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI TIWARI, HEMANT K. · 2003 to 2016
$3.8M
Splenic Marginal Zone Macrophages in Chronic Ischemic Heart FailureR01HL125735 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PRABHU, SUMANTH D · 2015 to 2018
$1.5M
Pathological TNFR1 Expressing CD4+ T-cells are Critical for HF progressionR00HL132123 · NHLBI · OHIO STATE UNIVERSITY · PI BANSAL, SHYAM SUNDER · 2018 to 2020
$738k
Pathological TNFR1 expressing CD4+ T-cells are critical for HF progressionK99HL132123 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BANSAL, SHYAM SUNDER · 2016 to 2017
$243k
Role of Regulatory T-Lymphocytes in Chronic Heart FailureI01BX002706 · VA · BIRMINGHAM VA MEDICAL CENTER · PI PRABHU, SUMANTH D · 2015 to 2018
–
BLRD VA I01 BX002706NHLBI NIH HHS K99 HL132123NHLBI NIH HHS R00 HL132123NHLBI NIH HHS R01 HL125735NHLBI NIH HHS T32 HL072757
6 · The paper itself

Abstract

backgroundHeart failure (HF) is a state of inappropriately sustained inflammation, suggesting the loss of normal immunosuppressive mechanisms. Regulatory T-lymphocytes (Tregs) are considered key suppressors of immune responses; however, their role in HF is unknown. We hypothesized that Tregs are dysfunctional in ischemic cardiomyopathy and HF, and they promote immune activation and left ventricular (LV) remodeling.

methodsAdult male wild-type C57BL/6 mice, Foxp3-diphtheria toxin receptor transgenic mice, and tumor necrosis factor (TNF) α receptor-1 (TNFR1)

resultsCompared with wild-type sham mice, CD4

conclusionsProinflammatory and antiangiogenic Tregs play an essential pathogenetic role in chronic ischemic HF to promote immune activation and pathological LV remodeling. The restoration of normal Treg function may be a viable approach to therapeutic immunomodulation in this disease.

Indexed as

Ventricular Function, LeftVentricular RemodelingAngiogenic ProteinsAnimalsCardiomyopathiesCells, CulturedCoculture TechniquesDisease Models, AnimalEndothelial CellsFibrosisInflammation MediatorsMaleMice, Inbred C57BLMice, KnockoutMyocardial InfarctionMyocardiumAngiogenic ProteinsInflammation MediatorsReceptors, Tumor Necrosis Factor, Type ITnfrsf1a protein, mouseangiogenic cellsheart failureinflammationneovascularizationregulatory T cells

Identifiers

PMID30586716
PMCPMC6322956
OpenAlexW2890916368

What OpenQuestion holds

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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.