Obese Patients With Nonalcoholic Fatty Liver Disease Have an Increase in Soluble Plasma CD163 and a Concurrent Decrease in Hepatic Expression of CD163
暂无分享,去创建一个
B. Blagoev | S. Moestrup | S. Mandacaru | S. Detlefsen | A. Krag | J. Graversen | C. Wernberg | M. Lauridsen | V. Chandran | Tina Di Caterino | M. K. Skytthe | Felix B. Pedersen
[1] F. Tacke,et al. Mapping the hepatic immune landscape identifies monocytic macrophages as key drivers of steatohepatitis and cholangiopathy progression , 2023, Hepatology.
[2] F. Avolio,et al. Stellate cell expression of SPARC-related modular calcium-binding protein 2 is associated with human non-alcoholic fatty liver disease severity , 2022, JHEP reports : innovation in hepatology.
[3] P. Casciato,et al. The performance of soluble CD163 as a non-invasive biomarker of liver damage in chronically HCV and HCV/HIV infected subjects , 2022, PloS one.
[4] S. Moestrup,et al. Circulating TREM2 as a noninvasive diagnostic biomarker for NASH in patients with elevated liver stiffness , 2022, Hepatology.
[5] M. Krawczyk,et al. Soluble TREM2 levels reflect the recruitment and expansion of TREM2+ macrophages that localize to fibrotic areas and limit NASH. , 2022, Journal of hepatology.
[6] S. Spiegel,et al. A new preclinical model of western diet‐induced progression of non‐alcoholic steatohepatitis to hepatocellular carcinoma , 2022, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[7] H. Grønbæk,et al. Clinical Progression of Metabolic-Associated Fatty Liver Disease Is Rare in a Danish Tertiary Liver Center , 2022, Journal of clinical medicine.
[8] A. Feuchtinger,et al. Liver-fibrosis-activated transcriptional networks govern hepatocyte reprogramming and intra-hepatic communication. , 2021, Cell metabolism.
[9] A. Hanley,et al. The association of soluble CD163, a novel biomarker of macrophage activation, with type 2 diabetes mellitus and its underlying physiological disorders: A systematic review , 2021, Obesity reviews : an official journal of the International Association for the Study of Obesity.
[10] A. Adimora,et al. Decreases in markers of monocyte/macrophage activation after hepatitis C eradication in HIV/hepatitis C virus coinfected women , 2021, AIDS.
[11] T. Karlsen,et al. Circulating Macrophage Activation Markers Predict Transplant-Free Survival in Patients With Primary Sclerosing Cholangitis , 2021, Clinical and translational gastroenterology.
[12] S. Klein,et al. Dynamic Shifts in the Composition of Resident and Recruited Macrophages Influence Tissue Remodeling in NASH , 2021, Cell reports.
[13] H. Ragab,et al. Performance of serum CD163 as a marker of fibrosis in patients with NAFLD. , 2020, Diabetes & metabolic syndrome.
[14] Y. Rotman,et al. Immunological mechanisms and therapeutic targets of fatty liver diseases , 2020, Cellular & molecular immunology.
[15] Y. Saeys,et al. Osteopontin Expression Identifies a Subset of Recruited Macrophages Distinct from Kupffer Cells in the Fatty Liver , 2020, Immunity.
[16] S. Moestrup,et al. Targeting of CD163+ Macrophages in Inflammatory and Malignant Diseases , 2020, International journal of molecular sciences.
[17] H. Møller,et al. Improved prediction of mortality by combinations of inflammatory markers and standard clinical scores in patients with acute‐on‐chronic liver failure and acute decompensation , 2020, Journal of gastroenterology and hepatology.
[18] H. Møller,et al. Macrophage Activation Markers, CD163 and CD206, in Acute-on-Chronic Liver Failure , 2020, Cells.
[19] H. El‐Serag,et al. Women have Lower Risk of Nonalcoholic Fatty Liver Disease but Higher Risk of Progression vs Men: A Systematic Review and Meta-analysis. , 2020, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[20] C. Glass,et al. Niche-Specific Reprogramming of Epigenetic Landscapes Drives Myeloid Cell Diversity in Nonalcoholic Steatohepatitis. , 2020, Immunity.
[21] H. Møller,et al. Soluble CD163 and mannose receptor as markers of liver disease severity and prognosis in patients with primary biliary cholangitis , 2020, Liver international : official journal of the International Association for the Study of the Liver.
[22] K. Natarajan,et al. Transcriptional Dynamics of Hepatic Sinusoid‐Associated Cells After Liver Injury , 2020, Hepatology.
[23] B. Blagoev,et al. Multi-omics characterization of a diet-induced obese model of non-alcoholic steatohepatitis , 2020, Scientific Reports.
[24] H. Malhi,et al. Pathogenesis of Nonalcoholic Steatohepatitis: An Overview , 2020, Hepatology communications.
[25] R. Weiskirchen,et al. Therapeutic Targeting of Hepatic Macrophages for the Treatment of Liver Diseases , 2019, Front. Immunol..
[26] Jiandie D. Lin,et al. Landscape of Intercellular Crosstalk in Healthy and NASH Liver Revealed by Single-Cell Secretome Gene Analysis. , 2019, Molecular cell.
[27] J. Jelsing,et al. Hepatic transcriptome signatures in patients with varying degrees of nonalcoholic fatty liver disease compared with healthy normal-weight individuals. , 2019, American journal of physiology. Gastrointestinal and liver physiology.
[28] H. Møller,et al. Macrophage Markers Are Poorly Associated With Liver Histology in Children With Nonalcoholic Fatty Liver Disease , 2018, Journal of pediatric gastroenterology and nutrition.
[29] Tanveer S. Batth,et al. Protein Aggregation Capture on Microparticles Enables Multipurpose Proteomics Sample Preparation , 2018, Molecular & Cellular Proteomics.
[30] D. Schuppan,et al. The role of macrophages in nonalcoholic fatty liver disease and nonalcoholic steatohepatitis , 2018, Nature Reviews Gastroenterology & Hepatology.
[31] Ludovic C. Gillet,et al. Data‐independent acquisition‐based SWATH‐MS for quantitative proteomics: a tutorial , 2018, Molecular systems biology.
[32] H. Møller,et al. Rapid and persistent decline in soluble CD163 with successful direct-acting antiviral therapy and associations with chronic hepatitis C histology , 2018, Scandinavian journal of gastroenterology.
[33] S. Sarin,et al. Iron-Overload triggers ADAM-17 mediated inflammation in Severe Alcoholic Hepatitis , 2018, Scientific Reports.
[34] S. Hamilton-Dutoit,et al. Soluble CD163 and mannose receptor associate with chronic hepatitis B activity and fibrosis and decline with treatment , 2018, Journal of gastroenterology and hepatology.
[35] B. A. David,et al. Differential Location and Distribution of Hepatic Immune Cells , 2017, Cells.
[36] A. Geerts,et al. Non-alcoholic steatohepatitis induces transient changes within the liver macrophage pool. , 2017, Cellular immunology.
[37] A. Bauman,et al. Effects of lifestyle intervention on soluble CD163, a macrophage activation marker, in patients with non-alcoholic fatty liver disease , 2017, Scandinavian journal of clinical and laboratory investigation.
[38] A. Kaykas,et al. ADAM17 is the main sheddase for the generation of human triggering receptor expressed in myeloid cells (hTREM2) ectodomain and cleaves TREM2 after Histidine 157 , 2017, Neuroscience Letters.
[39] Peter Bankhead,et al. QuPath: Open source software for digital pathology image analysis , 2017, Scientific Reports.
[40] S. Moestrup,et al. Antibody-Directed Glucocorticoid Targeting to CD163 in M2-type Macrophages Attenuates Fructose-Induced Liver Inflammatory Changes , 2016, Molecular therapy. Methods & clinical development.
[41] B. Bibby,et al. The macrophage activation marker sCD163 is associated with morphological disease stages in patients with non‐alcoholic fatty liver disease , 2016, Liver international : official journal of the International Association for the Study of the Liver.
[42] H. Møller,et al. Macrophage activation marker soluble CD163 may predict disease progression in hepatocellular carcinoma , 2016, Scandinavian journal of clinical and laboratory investigation.
[43] R. Chung,et al. Circulating Soluble CD163 is Associated with Steatohepatitis and Advanced Fibrosis in Nonalcoholic Fatty Liver Disease , 2015, Clinical and Translational Gastroenterology.
[44] K. Clément,et al. Macrophage activation marker soluble CD163 and non‐alcoholic fatty liver disease in morbidly obese patients undergoing bariatric surgery , 2015, Journal of gastroenterology and hepatology.
[45] H. Møller,et al. The macrophage activation marker sCD163 is associated with changes in NAFLD and metabolic profile during lifestyle intervention in obese children , 2015, Pediatric obesity.
[46] S. Horgan,et al. Benefits of bariatric surgery do not reach obese men. , 2014, Journal of laparoendoscopic & advanced surgical techniques. Part A.
[47] S. Hamilton-Dutoit,et al. Hepatic Macrophage Activation and the LPS Pathway in Patients With Alcoholic Hepatitis: A Prospective Cohort Study , 2014, The American Journal of Gastroenterology.
[48] B. Bibby,et al. Soluble CD163, a macrophage activation marker, is independently associated with fibrosis in patients with chronic viral hepatitis B and C , 2014, Hepatology.
[49] P. Bedossa. Utility and appropriateness of the fatty liver inhibition of progression (FLIP) algorithm and steatosis, activity, and fibrosis (SAF) score in the evaluation of biopsies of nonalcoholic fatty liver disease , 2014, Hepatology.
[50] H. Randeva,et al. Elevated Soluble CD163 in Gestational Diabetes Mellitus: Secretion from Human Placenta and Adipose Tissue , 2014, PloS one.
[51] Z. Kováčová,et al. Soluble CD163 is associated with CD163 mRNA expression in adipose tissue and with insulin sensitivity in steady-state condition but not in response to calorie restriction. , 2014, The Journal of clinical endocrinology and metabolism.
[52] S. Terai,et al. Hepatic Crown-Like Structure: A Unique Histological Feature in Non-Alcoholic Steatohepatitis in Mice and Humans , 2013, PloS one.
[53] Wei Shi,et al. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features , 2013, Bioinform..
[54] G. Ioannou,et al. Hepatic cholesterol crystals and crown-like structures distinguish NASH from simple steatosis[S] , 2013, Journal of Lipid Research.
[55] Joan Tordjman,et al. Histopathological algorithm and scoring system for evaluation of liver lesions in morbidly obese patients , 2012, Hepatology.
[56] T. Burdo,et al. Relationship between monocyte/macrophage activation marker soluble CD163 and insulin resistance in obese and normal‐weight subjects , 2012, Clinical endocrinology.
[57] B. Bibby,et al. Soluble CD163: a biomarker linking macrophages and insulin resistance , 2012, Diabetologia.
[58] H. Møller. Soluble CD163 , 2012, Scandinavian journal of clinical and laboratory investigation.
[59] Xavier Robin,et al. pROC: an open-source package for R and S+ to analyze and compare ROC curves , 2011, BMC Bioinformatics.
[60] B. Nordestgaard,et al. Serum soluble CD163 predicts risk of type 2 diabetes in the general population. , 2011, Clinical chemistry.
[61] O. Cummings,et al. Design and validation of a histological scoring system for nonalcoholic fatty liver disease , 2005, Hepatology.
[62] S. Moestrup,et al. Characterization of an enzyme-linked immunosorbent assay for soluble CD163 , 2002, Scandinavian journal of clinical and laboratory investigation.
[63] S. Moestrup,et al. Identification of the haemoglobin scavenger receptor , 2001, Nature.
[64] R. Turner,et al. Homeostasis model assessment: insulin resistance and β-cell function from fasting plasma glucose and insulin concentrations in man , 1985, Diabetologia.
[65] S. Moestrup,et al. Tumor necrosis factor -converting enzyme (TACE/ADAM17) mediates ectodomain shedding of the scavenger receptor CD163 , 2010 .
[66] R. Engle,et al. Corresponding author. , 2004 .