Stem Cells International, ISSN 1687-966X, 2016, Volume 2016, pp. 3585362 - 12
Mesenchymal stem cells (MSCs) are recognised as a promising tool to improve renal recovery in experimental models of cisplatin-induced acute kidney injury....
MESENCHYMAL STROMAL CELLS | IN-VITRO | THERAPY | NECROPTOSIS | DISEASE | MECHANISMS | RENAL INJURY | EXPRESSION | T-CELLS | NEPHROTOXICITY | CELL & TISSUE ENGINEERING | Urea | Cell death | Analysis | Stem cells | Transplantation | B cells | Cisplatin | Immunology | Transplants & implants | Lymphocytes | Cloning | Morphology | Colleges & universities | Inflammation | Umbilical cord | Immune system
MESENCHYMAL STROMAL CELLS | IN-VITRO | THERAPY | NECROPTOSIS | DISEASE | MECHANISMS | RENAL INJURY | EXPRESSION | T-CELLS | NEPHROTOXICITY | CELL & TISSUE ENGINEERING | Urea | Cell death | Analysis | Stem cells | Transplantation | B cells | Cisplatin | Immunology | Transplants & implants | Lymphocytes | Cloning | Morphology | Colleges & universities | Inflammation | Umbilical cord | Immune system
Journal Article
Nature Communications, ISSN 2041-1723, 06/2016, Volume 7, Issue 1, p. 11703
The factors responsible for maintaining persistent organ fibrosis in systemic sclerosis (SSc) are not known but emerging evidence implicates toll-like...
ACTIVATION | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | MOUSE | GENE-EXPRESSION | LUNG INJURY | DEFICIENT MICE | SKIN | SYSTEMIC-SCLEROSIS | RECEPTOR 4 | PULMONARY-FIBROSIS | Up-Regulation | Tenascin - genetics | Skin - metabolism | Humans | Middle Aged | Scleroderma, Systemic - pathology | Male | Fibrosis - metabolism | Tenascin - metabolism | Case-Control Studies | Tenascin - pharmacology | Collagen - drug effects | Adult | Female | Cell Differentiation | Collagen - genetics | Skin - pathology | Disease Models, Animal | Fibroblasts - metabolism | Fibrosis - genetics | Lung - pathology | Signal Transduction | Scleroderma, Systemic - metabolism | Cells, Cultured | Gene Expression Regulation | Scleroderma, Systemic - genetics | Myofibroblasts - drug effects | Toll-Like Receptor 4 - metabolism | Animals | Lung - drug effects | Aged | Mice
ACTIVATION | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | MOUSE | GENE-EXPRESSION | LUNG INJURY | DEFICIENT MICE | SKIN | SYSTEMIC-SCLEROSIS | RECEPTOR 4 | PULMONARY-FIBROSIS | Up-Regulation | Tenascin - genetics | Skin - metabolism | Humans | Middle Aged | Scleroderma, Systemic - pathology | Male | Fibrosis - metabolism | Tenascin - metabolism | Case-Control Studies | Tenascin - pharmacology | Collagen - drug effects | Adult | Female | Cell Differentiation | Collagen - genetics | Skin - pathology | Disease Models, Animal | Fibroblasts - metabolism | Fibrosis - genetics | Lung - pathology | Signal Transduction | Scleroderma, Systemic - metabolism | Cells, Cultured | Gene Expression Regulation | Scleroderma, Systemic - genetics | Myofibroblasts - drug effects | Toll-Like Receptor 4 - metabolism | Animals | Lung - drug effects | Aged | Mice
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 08/2019, Volume 78, Issue 8, pp. 1142 - 1142
Correspondence to Dr John Varga, Northwestern Scleroderma Program, Feinberg School of Medicine, Northwestern University, Chicago, USA; j-varga@northwestern.edu...
autoantibodies | systemic sclerosis | pulmonary fibrosis | INTERSTITIAL LUNG-DISEASE | PULMONARY | SCLERODERMA | RHEUMATOLOGY | Flow cytometry | Immunoglobulins | Autoantibodies | Raynaud disease | Lung diseases | Rheumatology | Arthritis | RNA polymerase | Hybridization | DNA-directed RNA polymerase | Studies | Telomeres | Pulmonary fibrosis | Granulocytes | Lymphocytes | Systemic sclerosis | Fibrosis | Mutation | Leukocytes (granulocytic) | Scleroderma | Telomerase | Age | Smoking
autoantibodies | systemic sclerosis | pulmonary fibrosis | INTERSTITIAL LUNG-DISEASE | PULMONARY | SCLERODERMA | RHEUMATOLOGY | Flow cytometry | Immunoglobulins | Autoantibodies | Raynaud disease | Lung diseases | Rheumatology | Arthritis | RNA polymerase | Hybridization | DNA-directed RNA polymerase | Studies | Telomeres | Pulmonary fibrosis | Granulocytes | Lymphocytes | Systemic sclerosis | Fibrosis | Mutation | Leukocytes (granulocytic) | Scleroderma | Telomerase | Age | Smoking
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2018, Volume 13, Issue 4, p. e0195346
Serum amyloid A (SAA) is a sensitive inflammatory marker rapidly increased in response to infection, injury or trauma during the acute phase. Resolution of the...
C-REACTIVE PROTEIN | RHEUMATOID-ARTHRITIS | AUTOANTIBODIES | ACUTE-PHASE PROTEINS | MESSENGER-RNA EXPRESSION | INTRAVENOUS IMMUNOGLOBULIN | MULTIDISCIPLINARY SCIENCES | RECEPTOR ANTIBODY | DISEASE | NECROSIS-FACTOR-ALPHA | AA AMYLOIDOSIS | Viral antibodies | Amyloid beta-protein | Physiological aspects | Antibodies | Genetic aspects | Inflammation | Research | Interleukin-6 | Intravenous administration | Leukocytes (mononuclear) | Blood | Inflammatory diseases | Interleukin 6 | Proteins | Kawasaki disease | Peripheral blood mononuclear cells | Amyloid | Chronic obstructive pulmonary disease | Enzyme-linked immunosorbent assay | Antigens | Immunoglobulins | Autoantibodies | Cytokines | Blood & organ donations | Neutrophils | Rheumatology | Trauma | Blood donors | Rheumatoid arthritis | Avidity | Cancer
C-REACTIVE PROTEIN | RHEUMATOID-ARTHRITIS | AUTOANTIBODIES | ACUTE-PHASE PROTEINS | MESSENGER-RNA EXPRESSION | INTRAVENOUS IMMUNOGLOBULIN | MULTIDISCIPLINARY SCIENCES | RECEPTOR ANTIBODY | DISEASE | NECROSIS-FACTOR-ALPHA | AA AMYLOIDOSIS | Viral antibodies | Amyloid beta-protein | Physiological aspects | Antibodies | Genetic aspects | Inflammation | Research | Interleukin-6 | Intravenous administration | Leukocytes (mononuclear) | Blood | Inflammatory diseases | Interleukin 6 | Proteins | Kawasaki disease | Peripheral blood mononuclear cells | Amyloid | Chronic obstructive pulmonary disease | Enzyme-linked immunosorbent assay | Antigens | Immunoglobulins | Autoantibodies | Cytokines | Blood & organ donations | Neutrophils | Rheumatology | Trauma | Blood donors | Rheumatoid arthritis | Avidity | Cancer
Journal Article
Atherosclerosis, ISSN 0021-9150, 12/2019, Volume 291, pp. 1 - 8
Patients with rheumatic diseases have an increased risk of atherosclerosis with up-regulated serum amyloid A (SAA), tumor necrosis factor-α (TNF-α) and...
Anti-Infliximab antibodies | Infliximab | Atherosclerosis | Rheumatic disease
Anti-Infliximab antibodies | Infliximab | Atherosclerosis | Rheumatic disease
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2015, Volume 10, Issue 1, p. e0110820
Inflammation in systemic sclerosis (SSc) is a prominent, but incompletely characterized feature in early stages of the disease. The goal of these studies was...
INTERSTITIAL LUNG-DISEASE | C-REACTIVE PROTEIN | OVEREXPRESSION | RESPONSES | ACTIVATION | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | SKIN | INTERLEUKIN-6 | CORONARY-ARTERY | VALIDITY | Blood Sedimentation | Lung - pathology | Scleroderma, Systemic - blood | Serum Amyloid A Protein - metabolism | C-Reactive Protein | Humans | Self Report | Scleroderma, Systemic - pathology | Lung - physiopathology | Biomarkers - blood | Patient Outcome Assessment | Scleroderma, Systemic - epidemiology | Case-Control Studies | Lung - metabolism | Respiratory Function Tests | Interleukin-6 - metabolism | Fibroblasts - metabolism | Systemic scleroderma | Inflammation | Scleroderma (Disease) | Multiplexing | Arthritis | Interleukin 6 | Biological effects | Dyspnea | Fibroblasts | Tumor necrosis factor-TNF | Amyloid | Carbon monoxide | Scleroderma | Interleukin 8 | Recombinant | Hypertension | Cytokines | Incubation | Review boards | Pulmonary arteries | Mortality | Lung diseases | Rheumatology | RNA polymerase | Preventive medicine | Patients | Serum levels | Lungs | Systemic sclerosis | Coronary vessels | Proteomics | Biomarkers | Skin | Respiration | Health risk assessment | Chemokines | Veins & arteries
INTERSTITIAL LUNG-DISEASE | C-REACTIVE PROTEIN | OVEREXPRESSION | RESPONSES | ACTIVATION | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | SKIN | INTERLEUKIN-6 | CORONARY-ARTERY | VALIDITY | Blood Sedimentation | Lung - pathology | Scleroderma, Systemic - blood | Serum Amyloid A Protein - metabolism | C-Reactive Protein | Humans | Self Report | Scleroderma, Systemic - pathology | Lung - physiopathology | Biomarkers - blood | Patient Outcome Assessment | Scleroderma, Systemic - epidemiology | Case-Control Studies | Lung - metabolism | Respiratory Function Tests | Interleukin-6 - metabolism | Fibroblasts - metabolism | Systemic scleroderma | Inflammation | Scleroderma (Disease) | Multiplexing | Arthritis | Interleukin 6 | Biological effects | Dyspnea | Fibroblasts | Tumor necrosis factor-TNF | Amyloid | Carbon monoxide | Scleroderma | Interleukin 8 | Recombinant | Hypertension | Cytokines | Incubation | Review boards | Pulmonary arteries | Mortality | Lung diseases | Rheumatology | RNA polymerase | Preventive medicine | Patients | Serum levels | Lungs | Systemic sclerosis | Coronary vessels | Proteomics | Biomarkers | Skin | Respiration | Health risk assessment | Chemokines | Veins & arteries
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 11843 - 14
The hallmarks of systemic sclerosis (SSc) are autoimmunity, microangiopathy and fibrosis. Skin fibrosis is accompanied by attrition of the dermal white adipose...
INTERSTITIAL LUNG-DISEASE | CELLS | GROWTH-FACTOR-BETA | SCLERODERMA | ENDOTHELIAL-MESENCHYMAL TRANSITION | MULTIDISCIPLINARY SCIENCES | DERMAL FIBROBLASTS | SKIN SCLEROSIS | PULMONARY VASCULAR INVOLVEMENT | EXPRESSION | CLINICAL-SIGNIFICANCE | Phenotypes | Animal models | Adipose tissue | Immune response | Mesenchyme | Helper cells | Lymphocytes T | Adiponectin | Bleomycin | Systemic sclerosis | Fibrosis | Fibroblasts | Skin diseases | Microvasculature
INTERSTITIAL LUNG-DISEASE | CELLS | GROWTH-FACTOR-BETA | SCLERODERMA | ENDOTHELIAL-MESENCHYMAL TRANSITION | MULTIDISCIPLINARY SCIENCES | DERMAL FIBROBLASTS | SKIN SCLEROSIS | PULMONARY VASCULAR INVOLVEMENT | EXPRESSION | CLINICAL-SIGNIFICANCE | Phenotypes | Animal models | Adipose tissue | Immune response | Mesenchyme | Helper cells | Lymphocytes T | Adiponectin | Bleomycin | Systemic sclerosis | Fibrosis | Fibroblasts | Skin diseases | Microvasculature
Journal Article
Clinical Rheumatology, ISSN 0770-3198, 2/2019, Volume 38, Issue 2, pp. 361 - 370
Therapeutic drug monitoring of TNF-alpha inhibitors is crucial for evaluating patients with inflammatory diseases on a personalized level. It has been...
Reporter gene assay | Anti-infliximab antibodies | Medicine & Public Health | Anti-adalimumab antibodies | Competitive ELISA | Rheumatology | RHEUMATOID-ARTHRITIS | ASSAY | ADALIMUMAB | INFLIXIMAB ANTIBODY | GENERATION | RHEUMATOLOGY | BIOPHARMACEUTICALS | HARMONIZATION | Viral antibodies | Analysis | Resveratrol | Antibodies | Medical records | Rankings | Enzyme-linked immunosorbent assay | Biopharmaceutics | Immunoglobulins | Reporter gene | Infliximab | Monoclonal antibodies | TNF inhibitors | Tumor necrosis factor-α | Patients | Inflammatory diseases
Reporter gene assay | Anti-infliximab antibodies | Medicine & Public Health | Anti-adalimumab antibodies | Competitive ELISA | Rheumatology | RHEUMATOID-ARTHRITIS | ASSAY | ADALIMUMAB | INFLIXIMAB ANTIBODY | GENERATION | RHEUMATOLOGY | BIOPHARMACEUTICALS | HARMONIZATION | Viral antibodies | Analysis | Resveratrol | Antibodies | Medical records | Rankings | Enzyme-linked immunosorbent assay | Biopharmaceutics | Immunoglobulins | Reporter gene | Infliximab | Monoclonal antibodies | TNF inhibitors | Tumor necrosis factor-α | Patients | Inflammatory diseases
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 4397 - 12
Skin fibrosis in systemic sclerosis (SSc) is accompanied by attrition of dermal white adipose tissue (dWAT) and reduced levels of circulating adiponectin....
SCLERODERMA | PROFIBROTIC RESPONSES | MULTIDISCIPLINARY SCIENCES | ACTIVATED-RECEPTOR-GAMMA | GENE-EXPRESSION | DERMAL ADIPOCYTES | SKIN FIBROSIS | SYSTEMIC-SCLEROSIS | CIRCULATING ADIPONECTIN | ADIPOSE-TISSUE | BETA | Adiponectin - pharmacology | Fibrosis - drug therapy | Skin - metabolism | Humans | Scleroderma, Systemic - metabolism | Scleroderma, Systemic - pathology | Receptors, Adiponectin - metabolism | Mice, Transgenic | Fibrosis - metabolism | Mice, Knockout | Animals | Scleroderma, Systemic - etiology | Signal Transduction - drug effects | Biopsy | Fibroblasts - drug effects | Fluorescent Antibody Technique | Adiponectin - metabolism | Mice | Fibrosis - pathology | Oligopeptides - pharmacology | Skin - pathology | Disease Models, Animal | Fibroblasts - metabolism | Signal transduction | Adipose tissue | Medical innovations | Systemic sclerosis | Fibrosis | Transgenic mice | Fibroblasts | Skin | Adiponectin | Peritoneum
SCLERODERMA | PROFIBROTIC RESPONSES | MULTIDISCIPLINARY SCIENCES | ACTIVATED-RECEPTOR-GAMMA | GENE-EXPRESSION | DERMAL ADIPOCYTES | SKIN FIBROSIS | SYSTEMIC-SCLEROSIS | CIRCULATING ADIPONECTIN | ADIPOSE-TISSUE | BETA | Adiponectin - pharmacology | Fibrosis - drug therapy | Skin - metabolism | Humans | Scleroderma, Systemic - metabolism | Scleroderma, Systemic - pathology | Receptors, Adiponectin - metabolism | Mice, Transgenic | Fibrosis - metabolism | Mice, Knockout | Animals | Scleroderma, Systemic - etiology | Signal Transduction - drug effects | Biopsy | Fibroblasts - drug effects | Fluorescent Antibody Technique | Adiponectin - metabolism | Mice | Fibrosis - pathology | Oligopeptides - pharmacology | Skin - pathology | Disease Models, Animal | Fibroblasts - metabolism | Signal transduction | Adipose tissue | Medical innovations | Systemic sclerosis | Fibrosis | Transgenic mice | Fibroblasts | Skin | Adiponectin | Peritoneum
Journal Article
Inflammation, ISSN 0360-3997, 8/2019, Volume 42, Issue 4, pp. 1413 - 1425
Serum amyloid A (SAA) is an acute-phase protein with important, pathogenic role in the development of atherosclerosis. Since dysfunctional endothelium...
atherosclerosis | Pathology | Biomedicine | Immunology | intercellular transport | serum amyloid A | Rheumatology | Internal Medicine | Pharmacology/Toxicology | IL-1β | human coronary artery endothelial cells | C-REACTIVE PROTEIN | ACTIVATION | IL-1 beta | INDUCTION | IMMUNOLOGY | IL-6 | CELL BIOLOGY | ACUTE-PHASE | MESSENGER-RNA | ISOTYPE | DISEASE | GENE-EXPRESSION | SAA1 | Flow cytometry | Atherogenesis | Intercellular signalling | Dexamethasone | Coronary artery | Nanotubes | Inflammation | Gene expression | Endothelial cells | Western blotting | Endothelium | Interleukin 6 | Acute phase substances | Arteriosclerosis | Coronary vessels | Atherosclerosis | Amyloid | Intracellular | Enzyme-linked immunosorbent assay
atherosclerosis | Pathology | Biomedicine | Immunology | intercellular transport | serum amyloid A | Rheumatology | Internal Medicine | Pharmacology/Toxicology | IL-1β | human coronary artery endothelial cells | C-REACTIVE PROTEIN | ACTIVATION | IL-1 beta | INDUCTION | IMMUNOLOGY | IL-6 | CELL BIOLOGY | ACUTE-PHASE | MESSENGER-RNA | ISOTYPE | DISEASE | GENE-EXPRESSION | SAA1 | Flow cytometry | Atherogenesis | Intercellular signalling | Dexamethasone | Coronary artery | Nanotubes | Inflammation | Gene expression | Endothelial cells | Western blotting | Endothelium | Interleukin 6 | Acute phase substances | Arteriosclerosis | Coronary vessels | Atherosclerosis | Amyloid | Intracellular | Enzyme-linked immunosorbent assay
Journal Article
Clinical Rheumatology, ISSN 0770-3198, 2/2019, Volume 38, Issue 2, pp. 307 - 316
Giant cell arteritis (GCA) is a systemic vasculitis in individuals older than 50 years, characterized by headaches, visual disturbances, painful scalp, jaw...
Vasculitis | Medicine & Public Health | Temporal artery biopsy | Rheumatology | miRNA | Giant cell arteritis | mRNA expression | WALL | INFLAMED ARTERIES | POLYMYALGIA-RHEUMATICA | TISSUE | MARKERS | RHEUMATOLOGY | BIOMARKERS | EPIGENETICS | TEMPORAL ARTERIES | INFLAMMATION | ASSOCIATION | Occlusion | Headache | Jaw | MiRNA | Stenosis | Systematic review | Arteries | Arteritis | Biopsy | Scalp | Epigenetics | Cardiovascular diseases | Systemic vasculitis
Vasculitis | Medicine & Public Health | Temporal artery biopsy | Rheumatology | miRNA | Giant cell arteritis | mRNA expression | WALL | INFLAMED ARTERIES | POLYMYALGIA-RHEUMATICA | TISSUE | MARKERS | RHEUMATOLOGY | BIOMARKERS | EPIGENETICS | TEMPORAL ARTERIES | INFLAMMATION | ASSOCIATION | Occlusion | Headache | Jaw | MiRNA | Stenosis | Systematic review | Arteries | Arteritis | Biopsy | Scalp | Epigenetics | Cardiovascular diseases | Systemic vasculitis
Journal Article
Clinical Rheumatology, ISSN 0770-3198, 2/2019, Volume 38, Issue 2, pp. 317 - 329
Early diagnosis and treatment of giant cell arteritis (GCA) is crucial for preventing ischemic complications. Multiple serological markers have been...
Relapse | Prognosis | Medicine & Public Health | Complications | Rheumatology | Biomarkers | Giant cell arteritis | Clustering | RISK | RHEUMATOLOGY | DISEASE-ACTIVITY | TOCILIZUMAB | INFLAMMATION | SERUM MARKERS | ASSOCIATION | Medical research | Care and treatment | Haptoglobin | Analysis | Medicine, Experimental | Protein C | Biological markers | Blood donors | Immunoglobulin G | Macrophage colony-stimulating factor | Principal components analysis | Interleukin 23 | Matrix metalloproteinase | Tumor necrosis factor-α | a-fetoprotein | Patients | Interleukin 18 | Arteritis | Gelatinase A | Nephelometry | Interleukin 6 | Acute phase substances | Ischemia | Interstitial collagenase | Enzyme-linked immunosorbent assay
Relapse | Prognosis | Medicine & Public Health | Complications | Rheumatology | Biomarkers | Giant cell arteritis | Clustering | RISK | RHEUMATOLOGY | DISEASE-ACTIVITY | TOCILIZUMAB | INFLAMMATION | SERUM MARKERS | ASSOCIATION | Medical research | Care and treatment | Haptoglobin | Analysis | Medicine, Experimental | Protein C | Biological markers | Blood donors | Immunoglobulin G | Macrophage colony-stimulating factor | Principal components analysis | Interleukin 23 | Matrix metalloproteinase | Tumor necrosis factor-α | a-fetoprotein | Patients | Interleukin 18 | Arteritis | Gelatinase A | Nephelometry | Interleukin 6 | Acute phase substances | Ischemia | Interstitial collagenase | Enzyme-linked immunosorbent assay
Journal Article