Evidence map›Paper›PMID 25658487›Full record

ArticlePloS one2015

Serpin treatment suppresses inflammatory vascular lesions in temporal artery implants (TAI) from patients with giant cell arteritis.

Hao Chen, Donghang Zheng, Sriram Ambadapadi, Jennifer Davids, Sally Ryden, Hazem Samy, Mee Bartee, Eric Sobel, Erbin Dai, Liying Liu and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  10. [Postoperative changes of Th17/Treg balance in patients with intracranial aneurysm rupture].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2016
    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

15 authors at 3 institutions in 2 countries.

Hao ChenDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America; Department of Molecular Genetics & Microbiology, University of Florida, Gainesville, Florida, United States of America.
Donghang ZhengDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America; Department of Molecular Genetics & Microbiology, University of Florida, Gainesville, Florida, United States of America.
Sriram AmbadapadiDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America.
Jennifer DavidsDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America.
Sally RydenDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America.
Hazem SamyDepartment of Ophthalmology, University of Florida, Gainesville, Florida, United States of America.
Mee BarteeDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America.
Eric SobelDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America.
Erbin DaiDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America.
Liying LiuDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America.
Colin MacaulayViron Therapeutics, London, Ontario, Canada.
Anthony YachnisDepartment of Pathology, University of Florida, Gainesville, Florida, United States of America.
Cornelia WeyandDivision of Immunology and Rheumatology, Stanford University School of Medicine, Stanford, California, United States of America.
Robert ThoburnDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America.
Alexandra LucasDepartment of Medicine, University of Florida, Gainesville, Florida, United States of America; Department of Ophthalmology, University of Florida, Gainesville, Florida, United States of America; Viron Therapeutics, London, Ontario, Canada.
University of Florida · USStanford University · USViron Therapeutics (Canada) · CA

Funding

Vascular specific ACE expression and atherosclerosisP01HL058000 · NHLBI · VANDERBILT UNIVERSITY · PI DIKALOV, SERGEY · 1998 to 2013
$20.7M
The NOTCH Signaling Pathway in Large Vessel VasculitisR01HL117913 · NHLBI · STANFORD UNIVERSITY · PI WEYAND, CORNELIA M. · 2014 to 2025
$5.0M
Serpin Modulation of Inflammatory Vasculitis; Potential for Immunomodulatory TherRC1HL100202 · NHLBI · UNIVERSITY OF FLORIDA · PI LUCAS, ALEXANDRA ROSE · 2009 to 2010
$1.0M
NHLBI NIH HHS 1RC1HL100202NHLBI NIH HHS P01 HL058000NHLBI NIH HHS R01 HL117913NHLBI NIH HHS RC1 HL100202
6 · The paper itself

Abstract

Giant cell arteritis (GCA) and Takayasu's disease are inflammatory vasculitic syndromes (IVS) causing sudden blindness and widespread arterial obstruction and aneurysm formation. Glucocorticoids and aspirin are mainstays of treatment, predominantly targeting T cells. Serp-1, a Myxomavirus-derived serpin, blocks macrophage and T cells in a wide range of animal models. Serp-1 also reduced markers of myocardial injury in a Phase IIa clinical trial for unstable coronary disease. In recent work, we detected improved survival and decreased arterial inflammation in a mouse Herpesvirus model of IVS. Here we examine Serp-1 treatment of human temporal artery (TA) biopsies from patients with suspected TA GCA arteritis after implant (TAI) into the aorta of immunodeficient SCID (severe combined immunodeficiency) mice. TAI positive for arteritis (GCApos) had significantly increased inflammation and plaque when compared to negative TAI (GCAneg). Serp-1 significantly reduced intimal inflammation and CD11b+ cell infiltrates in TAI, with reduced splenocyte Th1, Th17, and Treg. Splenocytes from mice with GCApos grafts had increased gene expression for interleukin-1 beta (IL-1β), IL-17, and CD25 and decreased Factor II. Serp-1 decreased IL-1β expression. In conclusion, GCApos TAI xenografts in mice provide a viable disease model and have increased intimal inflammation as expected and Serp-1 significantly reduces vascular inflammatory lesions with reduced IL-1β.

Indexed as

Giant Cell ArteritisTemporal ArteriesAnimalsDisease Models, AnimalFemaleHeterograftsHumansMaleMiceMice, Inbred NODMice, SCIDSerpinsTakayasu ArteritisViral ProteinsSerpinsViral Proteins

Identifiers

PMID25658487
PMCPMC4319900
OpenAlexW2093937980

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.