Evidence map›Paper›PMID 28584011›Full record

ArticleHypertension (Dallas, Tex. : 1979)2017

Regulatory T-Cell Augmentation or Interleukin-17 Inhibition Prevents Calcineurin Inhibitor-Induced Hypertension in Mice.

Valorie L Chiasson, Abhinandan R Pakanati, Marcos Hernandez, Kristina J Young, Kelsey R Bounds, Brett M Mitchell

Open access · bronzeAbstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Contribution of Th17 cells to tissue injury in hypertension.Current opinion in nephrology and hypertension · 2021
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. 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

6 authors at 1 institution in 1 country.

Valorie L ChiassonFrom the Department of Internal Medicine (V.L.C., A.R.P., M.H., K.J.Y., K.R.B., B.M.M.) and Department of Medical Physiology (B.M.M.), Texas A&M University Health Science Center, College of Medicine, Baylor Scott & White Health, Temple.
Abhinandan R PakanatiFrom the Department of Internal Medicine (V.L.C., A.R.P., M.H., K.J.Y., K.R.B., B.M.M.) and Department of Medical Physiology (B.M.M.), Texas A&M University Health Science Center, College of Medicine, Baylor Scott & White Health, Temple.
Marcos HernandezFrom the Department of Internal Medicine (V.L.C., A.R.P., M.H., K.J.Y., K.R.B., B.M.M.) and Department of Medical Physiology (B.M.M.), Texas A&M University Health Science Center, College of Medicine, Baylor Scott & White Health, Temple.
Kristina J YoungFrom the Department of Internal Medicine (V.L.C., A.R.P., M.H., K.J.Y., K.R.B., B.M.M.) and Department of Medical Physiology (B.M.M.), Texas A&M University Health Science Center, College of Medicine, Baylor Scott & White Health, Temple.
Kelsey R BoundsFrom the Department of Internal Medicine (V.L.C., A.R.P., M.H., K.J.Y., K.R.B., B.M.M.) and Department of Medical Physiology (B.M.M.), Texas A&M University Health Science Center, College of Medicine, Baylor Scott & White Health, Temple.
Brett M MitchellFrom the Department of Internal Medicine (V.L.C., A.R.P., M.H., K.J.Y., K.R.B., B.M.M.) and Department of Medical Physiology (B.M.M.), Texas A&M University Health Science Center, College of Medicine, Baylor Scott & White Health, Temple. bmitchell@tamhsc.edu.
Texas A&M University System · US

Funding

Role of FKBP12/12.6 in Endothelial FunctionR01HL084299 · NHLBI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI MITCHELL, BRETT M · 2007 to 2011
$1.3M
Role of Immune Cells in Immunosuppressive Drug-Induced HypertensionR56HL084299 · NHLBI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI MITCHELL, BRETT M · 2013 to 2013
$364k
NHLBI NIH HHS R01 HL084299NHLBI NIH HHS R56 HL084299
6 · The paper itself

Abstract

The immunosuppressive calcineurin inhibitors cyclosporine A and tacrolimus alter T-cell subsets and can cause hypertension, vascular dysfunction, and renal toxicity. We and others have reported that cyclosporine A and tacrolimus decrease anti-inflammatory regulatory T cells and increase proinflammatory interleukin-17-producing T cells; therefore, we hypothesized that inhibition of these effects using noncellular therapies would prevent the hypertension, endothelial dysfunction, and renal glomerular injury induced by calcineurin inhibitor therapy. Daily treatment of mice with cyclosporine A or tacrolimus for 1 week significantly decreased CD4

Indexed as

Drug-Related Side Effects and Adverse ReactionsHypertensionRenal InsufficiencyAnimalsCalcineurin InhibitorsCyclosporineEndothelium, VascularGlomerular MesangiumImmunosuppressive AgentsInflammationInterleukin-17MiceSignal TransductionTacrolimusT-Lymphocytes, RegulatoryCalcineurin InhibitorsCyclosporineImmunosuppressive AgentsInterleukin-17Tacrolimusantibodies, neutralizingcalcineurin inhibitorshypertensioninflammationlymphocytes

Identifiers

PMID28584011
PMCPMC5501301
OpenAlexW2622568901

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.