John Varga

ORCID: 0000-0001-8400-687X
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About
Contact & Profiles
Research Areas
  • Systemic Sclerosis and Related Diseases
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Dermatologic Treatments and Research
  • Inflammatory Myopathies and Dermatomyositis
  • Connective Tissue Growth Factor Research
  • Mast cells and histamine
  • Eosinophilic Disorders and Syndromes
  • TGF-β signaling in diseases
  • Wnt/β-catenin signaling in development and cancer
  • Skin and Cellular Biology Research
  • Fibroblast Growth Factor Research
  • Eosinophilic Esophagitis
  • Autoimmune Bullous Skin Diseases
  • Dermatological and Skeletal Disorders
  • Pulmonary Hypertension Research and Treatments
  • Dupuytren's Contracture and Treatments
  • Medical Imaging and Pathology Studies
  • Skin Diseases and Diabetes
  • Cell Adhesion Molecules Research
  • Kruppel-like factors research
  • Cytokine Signaling Pathways and Interactions
  • Chronic Myeloid Leukemia Treatments
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • IL-33, ST2, and ILC Pathways
  • Amyloidosis: Diagnosis, Treatment, Outcomes

University of Michigan
2018-2025

Northwestern University
2013-2024

Scleroderma Foundation
2016-2024

Michigan United
2022-2024

Michigan Medicine
2022-2024

Center for Rheumatology
2007-2022

University of Toronto
2021

Northwestern University
2020

Yale University
2019-2020

University of California, Los Angeles
2001-2019

We conducted a double-blind, randomized, placebo-controlled trial to determine the effects of oral cyclophosphamide on lung function and health-related symptoms in patients with evidence active alveolitis scleroderma-related interstitial disease.At 13 clinical centers throughout United States, we enrolled 158 scleroderma, restrictive physiology, dyspnea, inflammatory disease examination bronchoalveolar-lavage fluid, thoracic high-resolution computed tomography, or both. Patients received (<...

10.1056/nejmoa055120 article EN New England Journal of Medicine 2006-06-21

It has been previously shown that transforming growth factor beta (TGF beta) is capable of stimulating fibroblast collagen and fibronectin biosynthesis. The purpose this study was to examine the mechanisms involved in TGF stimulation biosynthetic activity. Our results indicate causes a marked enhancement production types I III collagens by cultured normal human dermal fibroblasts. rate fibroblasts exposed 2-3-fold greater than control cells. These effects were associated with increase...

10.1042/bj2470597 article EN Biochemical Journal 1987-11-01

The Scleroderma Lung Study enrolled 158 patients with scleroderma-related interstitial lung disease in a placebo-controlled trial of oral cyclophosphamide (CYC). Although treatment-related benefits pulmonary function, skin scores, and patient-centered outcomes were demonstrated after 1 year therapy, the duration benefit beyond was unclear.A second follow-up performed to determine if these effects persisted stopping treatment.A detailed analysis data obtained over two years study...

10.1164/rccm.200702-326oc article EN American Journal of Respiratory and Critical Care Medicine 2007-11-05

Systemic sclerosis (SSc) is a complex disease characterized by early microvascular abnormalities, immune dysregulation and chronic inflammation, subsequent fibrosis of the skin internal organs. Excessive fibrosis, distinguishing hallmark SSc, end result series interlinked vascular injury activation, represents maladaptive repair process. Activated vascular, epithelial, cells generate pro-fibrotic cytokines, chemokines, growth factors, lipid mediators, autoantibodies, reactive oxygen species....

10.5301/jsrd.5000249 article EN Journal of Scleroderma and Related Disorders 2017-07-19

Abstract The factors responsible for maintaining persistent organ fibrosis in systemic sclerosis (SSc) are not known but emerging evidence implicates toll-like receptors (TLRs) the pathogenesis of SSc. Here we show expression, mechanism action and pathogenic role endogenous TLR activators skin from patients with SSc, fibroblasts, mouse models fibrosis. Levels tenascin-C elevated SSc biopsy samples, serum fibrotic tissues mice. Exogenous stimulates collagen gene expression myofibroblast...

10.1038/ncomms11703 article EN cc-by Nature Communications 2016-06-03

Because recent studies implicate Toll-like receptors (TLRs) in the pathogenesis of fibrosis, we sought to investigate vitro and vivo role mechanism TLR4-mediated fibroblast responses fibrogenesis. We found that TLR4 was constitutively expressed, accumulation endogenous ligands significantly elevated, lesional skin lung tissues from patients with scleroderma. Activation signaling explanted fibroblasts resulted enhanced collagen synthesis increased expression multiple genes involved tissue...

10.1016/j.ajpath.2012.09.007 article EN cc-by-nc-nd American Journal Of Pathology 2012-11-07
Maureen D. Mayes Lara Bossini‐Castillo Olga Y. Gorlova José-Ezequiel Martín Xiaodong Zhou and 95 more Wei V. Chen Shervin Assassi Binwu Ying Filemon K. Tan Frank C. Arnett John D. Reveille Sandra G. Guerra María Teruel F. David Carmona Peter K. Gregersen Annette T. Lee Elena López‐Isac Eguzkine Ochoa Patrícia Carreira Carmen Pilar Simeón‐Aznar I. Castellví Miguel Á. González‐Gay Alexandra Zhernakova Leonid Padyukov Marta E. Alarcón‐Riquelme Cisca Wijmenga Matthew A. Brown Lorenzo Beretta Gabriela Riemekasten Torsten Witte Nicolas Hunzelmann Alexander Kreuter Jörg H. W. Distler Alexandre E. Voskuyl Annemie J. Schuerwegh Roger Hesselstrand Annica Nordin Paolo Airò Claudio Lunardi Paul G. Shiels Jacob M. van Laar Ariane L. Herrick Jane Worthington Christopher P. Denton Fredrick M. Wigley Laura K. Hummers John Varga Monique Hinchcliff Murray Baron Marie Hudson Janet Pope Daniel E. Furst Dinesh Khanna Kristin Phillips Elena Schiopu Barbara Segal Jerry A. Molitor Richard M. Silver Virginia Steen Robert W. Simms Robert Lafyatis Barri J. Fessler Tracy Frech Firas Alkassab Peter Docherty Elżbieta Kamińska Nader Khalidi Henry Niall Jones Janet Markland David Robinson Jasper Broen Timothy R. D. J. Radstake Carmen Fonseca Bobby P. C. Koeleman Javier Martı́n Norberto Ortego‐Centeno Raquel Ríos José Luis Callejas‐Rubio Nuria Navarrete Navarrete Rosa García Portales María Teresa Camps Antonio Fernández‐Nebro María Francisca González‐Escribano Julio Sánchez-Román Francisco José García Hernández María Jesús Castillo M. Á. Aguirre Inmaculada Gómez-Gracia Benjamín Fernández‐Gutiérrez Luis Rodríguez‐Rodríguez Esther Vicente José Luís Andreu M. Fernández Castro Paloma García de la Peña Francisco Javier López-Longo L. Martínez V Fonollosa Gerard Espinosa Carlos Tolosa A. Pros

10.1016/j.ajhg.2013.12.002 article EN publisher-specific-oa The American Journal of Human Genetics 2014-01-01

Section:ChooseTop of pageAbstract <<PathogenesisGenetics and EpigeneticsRisk Factors for the Deve...Blood Serum BAL Fluid...Comparison with IPFConclusionsReferencesCITING ARTICLES

10.1164/rccm.201903-0563ci article EN cc-by-nc-nd American Journal of Respiratory and Critical Care Medicine 2019-12-16

Objective We provide evidence‐based recommendations regarding screening for interstitial lung disease (ILD) and the monitoring ILD progression in people with systemic autoimmune rheumatic diseases (SARDs), specifically rheumatoid arthritis, sclerosis, idiopathic inflammatory myopathies, mixed connective tissue disease, Sjögren disease. Methods developed clinically relevant population, intervention, comparator, outcomes questions related to patients SARDs. A systematic literature review was...

10.1002/art.42860 article EN cc-by-nc-nd Arthritis & Rheumatology 2024-07-08

Abstract Systemic sclerosis (SSc) is a devastating autoimmune disease characterized by excessive production and accumulation of extracellular matrix, leading to fibrosis skin other internal organs. However, the main cellular participants in SSc remain incompletely understood. Here using differentiation trajectories at single cell level, we demonstrate dual source matrix deposition from both myofibroblasts endothelial-to-mesenchymal-transitioning cells (EndoMT). We further define central role...

10.1038/s41467-023-44645-6 article EN cc-by Nature Communications 2024-01-03

Objective We provide evidence‐based recommendations regarding screening for interstitial lung disease (ILD) and the monitoring ILD progression in people with systemic autoimmune rheumatic diseases (SARDs), specifically rheumatoid arthritis, sclerosis, idiopathic inflammatory myopathies, mixed connective tissue disease, Sjögren disease. Methods developed clinically relevant population, intervention, comparator, outcomes questions related to patients SARDs. A systematic literature review was...

10.1002/acr.25347 article EN cc-by-nc-nd Arthritis Care & Research 2024-07-08

Objective To test the hypothesis that systemic sclerosis (SSc) patients taking high-dose D-penicillamine (D-Pen) would have greater softening of skin, lower frequency renal crisis, and better survival than low-dose D-Pen. Methods Seventeen centers enrolled 134 SSc with early (≤18 months) diffuse cutaneous scleroderma into a 2-year, double-blind, randomized comparison D-Pen (750–1,000 mg/day) versus (125 mg every other day). All were followed up for mean ± SD 4.0 1.1 years to assess...

10.1002/1529-0131(199906)42:6<1194::aid-anr16>3.0.co;2-7 article EN Arthritis & Rheumatism 1999-06-01
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