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Wyszukujesz frazę ""Chemokine CXCL9"" wg kryterium: Temat


Tytuł :
CXCL9, CXCL10, and CXCL11; biomarkers of pulmonary inflammation associated with autoimmunity in patients with collagen vascular diseases-associated interstitial lung disease and interstitial pneumonia with autoimmune features.
Autorzy :
Kameda M; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Otsuka M; Department of Respiratory Medicine, Sapporo-Kosei General Hospital, Sapporo, Hokkaido, Japan.
Chiba H; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Kuronuma K; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Hasegawa T; Sysmex Corporation, Kobe, Japan.
Takahashi H; Department of Rheumatology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Takahashi H; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
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Źródło :
PloS one [PLoS One] 2020 Nov 02; Vol. 15 (11), pp. e0241719. Date of Electronic Publication: 2020 Nov 02 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Biomarkers/*blood
Chemokine CXCL10/*blood
Chemokine CXCL11/*blood
Chemokine CXCL9/*blood
Lung Diseases, Interstitial/*diagnosis
Vascular Diseases/*complications
Aged ; Autoimmunity ; Biomarkers/analysis ; Bronchoalveolar Lavage Fluid/chemistry ; Bronchoalveolar Lavage Fluid/cytology ; Bronchoalveolar Lavage Fluid/immunology ; C-Reactive Protein/analysis ; Chemokine CXCL10/analysis ; Chemokine CXCL11/analysis ; Chemokine CXCL9/analysis ; Collagen/metabolism ; Female ; Humans ; Idiopathic Pulmonary Fibrosis/diagnosis ; Lung Diseases, Interstitial/etiology ; Lymphocytes/cytology ; Lymphocytes/metabolism ; Macrophages/cytology ; Macrophages/metabolism ; Male ; Middle Aged ; Retrospective Studies ; Vascular Diseases/pathology ; Vital Capacity
Czasopismo naukowe
Tytuł :
Hepatectomy leads to loss of TRAIL-expressing liver NK cells via downregulation of the CXCL9-CXCR3 axis in mice.
Autorzy :
Yano T; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Ohira M; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Nakano R; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Tanaka Y; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Ohdan H; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
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Źródło :
PloS one [PLoS One] 2017 Oct 31; Vol. 12 (10), pp. e0186997. Date of Electronic Publication: 2017 Oct 31 (Print Publication: 2017).
Typ publikacji :
Journal Article
MeSH Terms :
Chemokine CXCL9/*genetics
Hepatectomy/*methods
Killer Cells, Natural/*metabolism
Liver/*metabolism
Receptors, CXCR3/*genetics
TNF-Related Apoptosis-Inducing Ligand/*genetics
Animals ; Chemokine CXCL9/metabolism ; Down-Regulation ; Female ; Flow Cytometry ; Gene Expression ; Male ; Mice, Inbred C57BL ; Mice, Knockout ; Perioperative Period ; Receptors, CXCR3/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; TNF-Related Apoptosis-Inducing Ligand/metabolism
Czasopismo naukowe
Tytuł :
The interferon-gamma pathway is selectively up-regulated in the liver of patients with secondary hemophagocytic lymphohistiocytosis.
Autorzy :
Prencipe G; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Bracaglia C; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Caiello I; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Pascarella A; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Francalanci P; Department of Pathology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Pardeo M; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Meneghel A; Department of Woman and Child Health, University of Padua, Padua, Italy.
Martini G; Department of Woman and Child Health, University of Padua, Padua, Italy.
Rossi MN; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Insalaco A; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Marucci G; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Nobili V; Hepatology Gastroenterology and Nutrition Disease Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Spada M; Division of Abdominal Transplantation and Hepatobiliopancreatic Surgery, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Zulian F; Department of Woman and Child Health, University of Padua, Padua, Italy.
De Benedetti F; Division of Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
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Źródło :
PloS one [PLoS One] 2019 Dec 17; Vol. 14 (12), pp. e0226043. Date of Electronic Publication: 2019 Dec 17 (Print Publication: 2019).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Interferon-gamma/*metabolism
Liver/*metabolism
Lymphohistiocytosis, Hemophagocytic/*pathology
Adolescent ; Chemokine CXCL9/blood ; Child, Preschool ; Female ; Humans ; Interferon-gamma/genetics ; Leukocytes, Mononuclear/cytology ; Leukocytes, Mononuclear/metabolism ; Liver/pathology ; Lymphohistiocytosis, Hemophagocytic/blood ; Lymphohistiocytosis, Hemophagocytic/metabolism ; Male ; Phosphorylation ; RNA, Messenger/metabolism ; STAT1 Transcription Factor/genetics ; STAT1 Transcription Factor/metabolism ; Signal Transduction/genetics ; Up-Regulation ; Young Adult
Czasopismo naukowe
Tytuł :
Serum CXCL9 and CCL17 as biomarkers of declining pulmonary function in chronic bird-related hypersensitivity pneumonitis.
Autorzy :
Nukui Y; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Yamana T; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Masuo M; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Tateishi T; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Kishino M; Department of Diagnostic Radiology, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Tateishi U; Department of Diagnostic Radiology, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Tomita M; Department of Clinical Research Center, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Hasegawa T; Sysmex Corporation, Nishi-Ku, Kobe, Japan.
Aritsu T; Sysmex Corporation, Nishi-Ku, Kobe, Japan.
Miyazaki Y; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
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Źródło :
PloS one [PLoS One] 2019 Aug 01; Vol. 14 (8), pp. e0220462. Date of Electronic Publication: 2019 Aug 01 (Print Publication: 2019).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Allergens*/immunology
Birds*/immunology
Alveolitis, Extrinsic Allergic/*blood
Chemokine CCL17/*blood
Chemokine CXCL9/*blood
Lung/*physiopathology
Adult ; Aged ; Alveolitis, Extrinsic Allergic/diagnosis ; Alveolitis, Extrinsic Allergic/etiology ; Alveolitis, Extrinsic Allergic/physiopathology ; Animals ; Biomarkers/blood ; Bronchoalveolar Lavage Fluid/chemistry ; Bronchoalveolar Lavage Fluid/cytology ; Female ; Humans ; Male ; Middle Aged ; Mucin-1/blood ; Respiratory Function Tests ; Vital Capacity
Czasopismo naukowe
Tytuł :
Extracellular Histones Induce Chemokine Production in Whole Blood Ex Vivo and Leukocyte Recruitment In Vivo.
Autorzy :
Westman J; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Papareddy P; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Dahlgren MW; Department of Experimental Medical Science, Adaptive Immunity, Biomedical Center, Lund, Sweden.
Chakrakodi B; Department of Medicine, Center for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Norrby-Teglund A; Department of Medicine, Center for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Smeds E; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Linder A; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Mörgelin M; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Johansson-Lindbom B; Department of Experimental Medical Science, Adaptive Immunity, Biomedical Center, Lund, Sweden.
Egesten A; Department of Clinical Sciences, Respiratory Medicine & Allergy, Biomedical Center, Lund, Sweden.
Herwald H; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
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Źródło :
PLoS pathogens [PLoS Pathog] 2015 Dec 08; Vol. 11 (12), pp. e1005319. Date of Electronic Publication: 2015 Dec 08 (Print Publication: 2015).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chemokine CXCL10/*biosynthesis
Chemokine CXCL9/*biosynthesis
Chemotaxis, Leukocyte/*immunology
Histones/*immunology
Leukocytes/*immunology
Animals ; Chemokine CXCL10/immunology ; Chemokine CXCL9/immunology ; Chemokines/biosynthesis ; Enzyme-Linked Immunosorbent Assay ; Female ; Humans ; Leukocytes/metabolism ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Microscopy, Immunoelectron ; Monocytes/immunology ; Surface Plasmon Resonance
Czasopismo naukowe
Tytuł :
Left Ventricular Dysfunction and CXCR3 Ligands in Hypertension: From Animal Experiments to a Population-Based Pilot Study.
Autorzy :
Altara R; Department of Pharmacology and Toxicology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.
Gu YM; Studies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.
Struijker-Boudier HA; Department of Pharmacology and Toxicology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.
Thijs L; Studies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.
Staessen JA; Studies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium; VitaK Research and Development, Maastricht University, Maastricht, The Netherlands.
Blankesteijn WM; Department of Pharmacology and Toxicology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.
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Źródło :
PloS one [PLoS One] 2015 Oct 27; Vol. 10 (10), pp. e0141394. Date of Electronic Publication: 2015 Oct 27 (Print Publication: 2015).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chemokine CXCL10/*blood
Chemokine CXCL11/*blood
Chemokine CXCL9/*blood
Hypertension/*blood
Ventricular Dysfunction, Left/*blood
Animals ; Blood Pressure ; Chemokine CXCL9/genetics ; Female ; Humans ; Hypertension/genetics ; Hypertension/physiopathology ; Inflammation/blood ; Inflammation/genetics ; Inflammation/physiopathology ; Ligands ; Male ; Mice ; Natriuretic Peptide, Brain/blood ; Peptide Fragments/blood ; Receptors, CXCR3/blood ; Receptors, CXCR3/genetics ; Ventricular Dysfunction, Left/genetics ; Ventricular Dysfunction, Left/physiopathology
Czasopismo naukowe
Tytuł :
Effect of JAK Inhibitors on Release of CXCL9, CXCL10 and CXCL11 from Human Airway Epithelial Cells.
Autorzy :
Fenwick PS; Airway Disease, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Macedo P; Airway Disease, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Kilty IC; Pfizer Inc, Cambridge, Massachusetts, United States of America.
Barnes PJ; Airway Disease, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Donnelly LE; Airway Disease, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
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Źródło :
PloS one [PLoS One] 2015 Jun 19; Vol. 10 (6), pp. e0128757. Date of Electronic Publication: 2015 Jun 19 (Print Publication: 2015).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chemokine CXCL10/*metabolism
Chemokine CXCL11/*metabolism
Chemokine CXCL9/*metabolism
Epithelial Cells/*drug effects
Epithelial Cells/*metabolism
Protein Kinase Inhibitors/*pharmacology
Respiratory Mucosa/*metabolism
Aged ; Cell Line ; Chemokine CXCL10/genetics ; Chemokine CXCL11/genetics ; Chemokine CXCL9/genetics ; Female ; Gene Expression Regulation/drug effects ; Humans ; Inhibitory Concentration 50 ; Janus Kinases/antagonists & inhibitors ; Male ; Middle Aged ; Receptors, CXCR3/metabolism ; STAT1 Transcription Factor/metabolism ; Transcription, Genetic
Czasopismo naukowe
Tytuł :
CXCL9 associated with sustained virological response in chronic hepatitis B patients receiving peginterferon alfa-2a therapy: a pilot study.
Autorzy :
Lee IC; Division of Gastroenterology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan ; Institute of Clinical Medicine, National Yang-Ming University School of Medicine, Taipei, Taiwan ; Department of Medicine, National Yang-Ming University Hospital, I-Lan, Taiwan.
Huang YH
Su CW
Wang YJ
Huo TI
Lee KC
Lin HC
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Źródło :
PloS one [PLoS One] 2013 Oct 04; Vol. 8 (10), pp. e76798. Date of Electronic Publication: 2013 Oct 04 (Print Publication: 2013).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Hepatitis B virus*/genetics
Hepatitis B virus*/immunology
Chemokine CXCL9/*metabolism
Hepatitis B, Chronic/*metabolism
Hepatitis B, Chronic/*virology
Adult ; Alanine Transaminase/blood ; Alanine Transaminase/metabolism ; Antiviral Agents/therapeutic use ; Chemokine CXCL9/blood ; Cytokines/blood ; Cytokines/metabolism ; Female ; Genotype ; Hepatitis B e Antigens/immunology ; Hepatitis B, Chronic/drug therapy ; Humans ; Interferon-alpha/therapeutic use ; Male ; Middle Aged ; Pilot Projects ; Polyethylene Glycols/therapeutic use ; Prognosis ; Recombinant Proteins/therapeutic use ; Time Factors ; Treatment Outcome ; Viral Load
Czasopismo naukowe
Tytuł :
The prognostic importance of CXCR3 chemokine during organizing pneumonia on the risk of chronic lung allograft dysfunction after lung transplantation.
Autorzy :
Shino MY; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Weigt SS; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Li N; Department of Biomathematics, University of California at Los Angeles, Los Angeles, California, United States of America.
Palchevskiy V; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Derhovanessian A; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Saggar R; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Sayah DM; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Huynh RH; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Gregson AL; Division of Infectious Diseases, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Fishbein MC; Department of Pathology, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Ardehali A; Division of Cardiothoracic Surgery, Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Ross DJ; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Lynch JP 3rd; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.
Elashoff RM; Department of Biomathematics, University of California at Los Angeles, Los Angeles, California, United States of America.
Belperio JA; Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America.; Department of Biomathematics, University of California at Los Angeles, Los Angeles, California, United States of America.
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Źródło :
PloS one [PLoS One] 2017 Jul 07; Vol. 12 (7), pp. e0180281. Date of Electronic Publication: 2017 Jul 07 (Print Publication: 2017).
Typ publikacji :
Journal Article
MeSH Terms :
Lung Transplantation*
Lung/*diagnostic imaging
Lung/*physiopathology
Pneumonia/*diagnostic imaging
Pneumonia/*physiopathology
Receptors, CXCR3/*immunology
Adult ; Biomarkers/chemistry ; Biomarkers/metabolism ; Biopsy ; Bronchoalveolar Lavage Fluid/chemistry ; Bronchoalveolar Lavage Fluid/immunology ; Bronchoscopy ; Chemokine CXCL10/genetics ; Chemokine CXCL10/immunology ; Chemokine CXCL11/genetics ; Chemokine CXCL11/immunology ; Chemokine CXCL9/genetics ; Chemokine CXCL9/immunology ; Female ; Gene Expression ; Humans ; Ligands ; Lung/immunology ; Male ; Middle Aged ; Pneumonia/genetics ; Pneumonia/immunology ; Proportional Hazards Models ; Receptors, CXCR3/genetics ; Respiratory Function Tests ; Retrospective Studies ; Risk ; Transplantation, Homologous
Czasopismo naukowe
Tytuł :
Tissue-specific regulation of CXCL9/10/11 chemokines in keratinocytes: Implications for oral inflammatory disease.
Autorzy :
Marshall A; University College London, UCL Eastman Dental Institute, London, United Kingdom.
Celentano A; Department of Neurosciences, Reproductive and Odontostomatological Sciences, University Federico II of Naples, Naples, Italy.; Melbourne Dental School and Oral Health CRC, The University of Melbourne, Victoria, Australia.
Cirillo N; Melbourne Dental School and Oral Health CRC, The University of Melbourne, Victoria, Australia.
McCullough M; Melbourne Dental School and Oral Health CRC, The University of Melbourne, Victoria, Australia.
Porter S; University College London, UCL Eastman Dental Institute, London, United Kingdom.
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Źródło :
PloS one [PLoS One] 2017 Mar 02; Vol. 12 (3), pp. e0172821. Date of Electronic Publication: 2017 Mar 02 (Print Publication: 2017).
Typ publikacji :
Journal Article
MeSH Terms :
Chemokines, CXC/*metabolism
Keratinocytes/*metabolism
Lichen Planus, Oral/*metabolism
Lichen Planus, Oral/*pathology
Cell Line, Tumor ; Cell Movement/drug effects ; Chemokine CXCL10/genetics ; Chemokine CXCL10/metabolism ; Chemokine CXCL11/genetics ; Chemokine CXCL11/metabolism ; Chemokine CXCL9/genetics ; Chemokine CXCL9/metabolism ; Chemokines, CXC/genetics ; Gene Expression Regulation/drug effects ; Humans ; Interferon-gamma/pharmacology ; Keratinocytes/drug effects ; Keratinocytes/immunology ; Lichen Planus, Oral/genetics ; Lichen Planus, Oral/immunology ; Mouth Mucosa/pathology ; Organ Specificity ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Receptors, CXCR3/metabolism ; T-Lymphocytes/cytology ; T-Lymphocytes/drug effects
Czasopismo naukowe
Tytuł :
Characteristics of Allergic Pulmonary Inflammation in CXCR3Knockout Mice Sensitized and Challenged with House Dust Mite Protein.
Autorzy :
Liu Z; Department of Laboratory Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Chen H; Department of Respiratory Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Chen X; Department of Respiratory Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Gao J; Department of Respiratory Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Guo Z; Department of Laboratory Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
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Źródło :
PloS one [PLoS One] 2016 Oct 11; Vol. 11 (10), pp. e0162905. Date of Electronic Publication: 2016 Oct 11 (Print Publication: 2016).
Typ publikacji :
Journal Article
MeSH Terms :
Arthropod Proteins/*immunology
Asthma/*physiopathology
Bronchial Hyperreactivity/*pathology
Pyroglyphidae/*metabolism
Receptors, CXCR3/*genetics
Animals ; Bronchial Hyperreactivity/immunology ; Bronchoalveolar Lavage Fluid/chemistry ; Bronchoalveolar Lavage Fluid/cytology ; CD4-Positive T-Lymphocytes/cytology ; CD4-Positive T-Lymphocytes/metabolism ; CD8-Positive T-Lymphocytes/cytology ; CD8-Positive T-Lymphocytes/metabolism ; Cells, Cultured ; Chemokine CXCL10/genetics ; Chemokine CXCL10/metabolism ; Chemokine CXCL9/genetics ; Chemokine CXCL9/metabolism ; Disease Models, Animal ; Interferon-gamma/analysis ; Interleukin-4/analysis ; Lung/cytology ; Lung/metabolism ; Lung/pathology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Receptors, CXCR3/deficiency ; Spleen/cytology ; Spleen/metabolism ; Spleen/pathology
Czasopismo naukowe
Tytuł :
Myocardial chemokine expression and intensity of myocarditis in Chagas cardiomyopathy are controlled by polymorphisms in CXCL9 and CXCL10.
Autorzy :
Nogueira LG; Laboratory of Immunology, Heart Institute (InCor), School of Medicine, University of São Paulo, São Paulo, Brazil.
Santos RH
Ianni BM
Fiorelli AI
Mairena EC
Benvenuti LA
Frade A
Donadi E
Dias F
Saba B
Wang HT
Fragata A
Sampaio M
Hirata MH
Buck P
Mady C
Bocchi EA
Stolf NA
Kalil J
Cunha-Neto E
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Źródło :
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2012; Vol. 6 (10), pp. e1867. Date of Electronic Publication: 2012 Oct 25.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Polymorphism, Genetic*
Chagas Cardiomyopathy/*genetics
Chagas Cardiomyopathy/*pathology
Chemokine CXCL10/*biosynthesis
Chemokine CXCL9/*biosynthesis
Trypanosoma cruzi/*pathogenicity
Adolescent ; Adult ; Chemokine CXCL10/genetics ; Chemokine CXCL9/genetics ; Disease Resistance ; Female ; Gene Expression Profiling ; Humans ; Male ; Middle Aged ; Young Adult
Czasopismo naukowe
Tytuł :
CXCL10/IP-10 Neutralization Can Ameliorate Lipopolysaccharide-Induced Acute Respiratory Distress Syndrome in Rats.
Autorzy :
Lang S; Department of Respiratory Diseases, Chinese PLA General Hospital, Beijing, China.
Li L; Department of Cardiovascular Surgery, Chinese PLA General Hospital, Beijing, China.
Wang X; Department of Surgical Oncology, Chinese PLA General Hospital, Beijing, China.
Sun J; Department of Respiratory Diseases, Chinese PLA General Hospital, Beijing, China.
Xue X; Department of Respiratory Diseases, Chinese PLA General Hospital, Beijing, China.
Xiao Y; Department of Respiratory Diseases, Chinese PLA General Hospital, Beijing, China.
Zhang M; Department of Respiratory Diseases, Chinese PLA General Hospital, Beijing, China.
Ao T; Department of Respiratory Diseases, Chinese PLA General Hospital, Beijing, China.
Wang J; Department of Respiratory Diseases, Chinese PLA General Hospital, Beijing, China.
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Źródło :
PloS one [PLoS One] 2017 Jan 03; Vol. 12 (1), pp. e0169100. Date of Electronic Publication: 2017 Jan 03 (Print Publication: 2017).
Typ publikacji :
Journal Article
MeSH Terms :
Chemokine CXCL10/*antagonists & inhibitors
Chemokine CXCL10/*chemistry
Respiratory Distress Syndrome/*drug therapy
Animals ; Blood Gas Analysis ; Bronchoalveolar Lavage Fluid ; CD8-Positive T-Lymphocytes/metabolism ; Chemokine CXCL11/metabolism ; Chemokine CXCL9/metabolism ; Disease Models, Animal ; Inflammation ; Intercellular Adhesion Molecule-1/metabolism ; Interferon-gamma/metabolism ; Interleukin-6/metabolism ; Ligands ; Lipopolysaccharides ; Male ; Rats ; Rats, Wistar ; Receptors, CXCR3/metabolism ; Respiratory Distress Syndrome/chemically induced
Czasopismo naukowe
Tytuł :
MIG and the regulatory cytokines IL-10 and TGF-β1 correlate with malaria vaccine immunogenicity and efficacy.
Autorzy :
Dunachie SJ; Centre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, University of Oxford, Oxford, United Kingdom. />Berthoud T
Keating SM
Hill AV
Fletcher HA
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Źródło :
PloS one [PLoS One] 2010 Sep 03; Vol. 5 (9), pp. e12557. Date of Electronic Publication: 2010 Sep 03.
Typ publikacji :
Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation*
Chemokine CXCL9/*immunology
Interleukin-10/*immunology
Malaria Vaccines/*immunology
Malaria, Falciparum/*immunology
Transforming Growth Factor beta1/*immunology
Antibodies, Protozoan/immunology ; Chemokine CXCL9/genetics ; Humans ; Interferon-gamma/genetics ; Interferon-gamma/immunology ; Interleukin-10/genetics ; Malaria Vaccines/administration & dosage ; Malaria, Falciparum/parasitology ; Malaria, Falciparum/prevention & control ; Plasmodium falciparum/immunology ; Protozoan Proteins/administration & dosage ; Protozoan Proteins/immunology ; Transforming Growth Factor beta1/genetics
Czasopismo naukowe
Tytuł :
Post-Exercise Heart Rate Recovery Independently Predicts Clinical Outcome in Patients with Acute Decompensated Heart Failure.
Autorzy :
Youn JC; Division of Cardiology, Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Republic of Korea.; Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Lee HS; Department of Biostatistics, Yonsei University College of Medicine, Seoul, Republic of Korea.
Choi SW; Division of Cardiology, Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Republic of Korea.
Han SW; Division of Cardiology, Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Republic of Korea.
Ryu KH; Division of Cardiology, Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Republic of Korea.
Shin EC; Laboratory of Immunology and Infectious Diseases, Graduate School of Medical Science and Engineering, KAIST, Daejeon, Republic of Korea.
Kang SM; Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Źródło :
PloS one [PLoS One] 2016 May 02; Vol. 11 (5), pp. e0154534. Date of Electronic Publication: 2016 May 02 (Print Publication: 2016).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Heart Failure/*blood
Heart Failure/*physiopathology
Heart Rate/*physiology
Acute Disease ; Aged ; Chemokine CXCL9/blood ; Echocardiography ; Exercise Test ; Female ; Heart Failure/pathology ; Humans ; Immunoassay ; Male ; Middle Aged ; Proportional Hazards Models ; Prospective Studies
Czasopismo naukowe
Tytuł :
Natural Killer Cells Improve Hematopoietic Stem Cell Engraftment by Increasing Stem Cell Clonogenicity In Vitro and in a Humanized Mouse Model.
Autorzy :
Escobedo-Cousin M; University College London, Cancer Institute, London, United Kingdom; Anthony Nolan Research Institute, Royal Free Campus, London, United Kingdom.
Jackson N; Anthony Nolan Research Institute, Royal Free Campus, London, United Kingdom.
Laza-Briviesca R; Anthony Nolan Research Institute, Royal Free Campus, London, United Kingdom.
Ariza-McNaughton L; Cancer Research UK, London Research Institute, London, United Kingdom.
Luevano M; University College London, Cancer Institute, London, United Kingdom; Anthony Nolan Research Institute, Royal Free Campus, London, United Kingdom.
Derniame S; University College London, Cancer Institute, London, United Kingdom; Anthony Nolan Research Institute, Royal Free Campus, London, United Kingdom.
Querol S; Programa Concordia Banc de Sang i Teixits, Barcelona, Spain.
Blundell M; University College London, Institute of Child Health, London, United Kingdom.
Thrasher A; University College London, Institute of Child Health, London, United Kingdom.
Soria B; Andalusian Center for Molecular Biology and Regenerative Medicine (CABIMER), Fundación Progreso y Salud, Seville, Spain; Biomedical Research Network on Diabetes and Related Metabolic Diseases (CIBERDEM), Instituto de Salud Carlos III, Madrid, Spain.
Cooper N; Haematology Department, Hammersmith Hospital, London, United Kingdom.
Bonnet D; Cancer Research UK, London Research Institute, London, United Kingdom.
Madrigal A; University College London, Cancer Institute, London, United Kingdom; Anthony Nolan Research Institute, Royal Free Campus, London, United Kingdom.
Saudemont A; University College London, Cancer Institute, London, United Kingdom; Anthony Nolan Research Institute, Royal Free Campus, London, United Kingdom.
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Źródło :
PloS one [PLoS One] 2015 Oct 14; Vol. 10 (10), pp. e0138623. Date of Electronic Publication: 2015 Oct 14 (Print Publication: 2015).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Cord Blood Stem Cell Transplantation/*methods
Hematopoietic Stem Cell Transplantation/*methods
Hematopoietic Stem Cells/*cytology
Killer Cells, Natural/*cytology
Stem Cells/*cytology
Animals ; Cell Movement ; Chemokine CXCL9/metabolism ; Cytokines/metabolism ; Female ; Fetal Blood/cytology ; Gene Expression Regulation ; Graft vs Host Disease/physiopathology ; Graft vs Leukemia Effect ; Humans ; Interleukin-15/metabolism ; Leukocytes, Mononuclear/cytology ; Male ; Mice ; Mice, Inbred NOD ; Mice, SCID ; Oligonucleotide Array Sequence Analysis ; Recombinant Proteins/metabolism
Czasopismo naukowe
Tytuł :
The Orphan Nuclear Receptor TLX Is an Enhancer of STAT1-Mediated Transcription and Immunity to Toxoplasma gondii.
Autorzy :
Beiting DP; Department of Pathobiology, University of Pennsylvania, Philadelphia, Pennsylvania, Philadelphia, United States of America.
Hidano S; Department of Pathobiology, University of Pennsylvania, Philadelphia, Pennsylvania, Philadelphia, United States of America.
Baggs JE; Department of Pharmacology and the Institute for Translational Medicine and Therapeutics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, United States of America.
Geskes JM; Department of Pharmacology and the Institute for Translational Medicine and Therapeutics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, United States of America.
Fang Q; Department of Pathobiology, University of Pennsylvania, Philadelphia, Pennsylvania, Philadelphia, United States of America.
Wherry EJ; Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, United States of America.
Hunter CA; Department of Pathobiology, University of Pennsylvania, Philadelphia, Pennsylvania, Philadelphia, United States of America.
Roos DS; Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Cherry S; Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, United States of America.
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Źródło :
PLoS biology [PLoS Biol] 2015 Jul 21; Vol. 13 (7), pp. e1002200. Date of Electronic Publication: 2015 Jul 21 (Print Publication: 2015).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation*
Host-Pathogen Interactions*
Receptors, Cytoplasmic and Nuclear/*metabolism
STAT1 Transcription Factor/*metabolism
Toxoplasma/*immunology
Animals ; Brain/metabolism ; Central Nervous System Infections/metabolism ; Chemokine CXCL10/metabolism ; Chemokine CXCL9/metabolism ; Chronic Disease ; Interferon-gamma/metabolism ; Mice, Inbred CBA
Czasopismo naukowe
Tytuł :
IL-21 promotes late activator APC-mediated T follicular helper cell differentiation in experimental pulmonary virus infection.
Autorzy :
Yoo JK; Inflammation Research, Amgen Inc., Seattle, Washington, United States of America; Beirne B. Carter Center for Immunology Research, University of Virginia, Charlottesville, Virginia, United States of America.
Braciale TJ; Beirne B. Carter Center for Immunology Research, University of Virginia, Charlottesville, Virginia, United States of America; Department of Microbiology, University of Virginia, Charlottesville, Virginia, United States of America; Department of Pathology, University of Virginia, Charlottesville, Virginia, United States of America.
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Źródło :
PloS one [PLoS One] 2014 Sep 24; Vol. 9 (9), pp. e105872. Date of Electronic Publication: 2014 Sep 24 (Print Publication: 2014).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Antigen-Presenting Cells/*immunology
Cell Differentiation/*immunology
Interleukins/*immunology
Lung Diseases/*immunology
Orthomyxoviridae Infections/*immunology
T-Lymphocytes, Helper-Inducer/*immunology
Animals ; Antigen-Presenting Cells/metabolism ; CD4-Positive T-Lymphocytes/immunology ; CD4-Positive T-Lymphocytes/metabolism ; Cell Differentiation/genetics ; Cell Movement/genetics ; Cell Movement/immunology ; Chemokine CXCL9/genetics ; Chemokine CXCL9/immunology ; Chemokine CXCL9/metabolism ; Dendritic Cells/immunology ; Dendritic Cells/metabolism ; Flow Cytometry ; Host-Pathogen Interactions/immunology ; Influenza A virus/immunology ; Influenza A virus/physiology ; Interleukin-21 Receptor alpha Subunit/deficiency ; Interleukin-21 Receptor alpha Subunit/genetics ; Interleukin-21 Receptor alpha Subunit/immunology ; Interleukins/deficiency ; Interleukins/genetics ; Lung Diseases/genetics ; Lung Diseases/virology ; Lymph Nodes/immunology ; Lymph Nodes/metabolism ; Mice, Inbred C57BL ; Mice, Knockout ; Orthomyxoviridae Infections/genetics ; Orthomyxoviridae Infections/virology ; Receptors, CXCR3/genetics ; Receptors, CXCR3/immunology ; Receptors, CXCR3/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; T-Lymphocytes, Helper-Inducer/metabolism ; Tumor Necrosis Factor-alpha/deficiency ; Tumor Necrosis Factor-alpha/genetics ; Tumor Necrosis Factor-alpha/immunology
Czasopismo naukowe
Tytuł :
Chemokine Transfer by Liver Sinusoidal Endothelial Cells Contributes to the Recruitment of CD4+ T Cells into the Murine Liver.
Autorzy :
Neumann K; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany; Research Center Immunosciences, Charité-Universitätsmedizin, Berlin, Germany; Department of Cellular Immunology, Clinic for Rheumatology and Clinical Immunology, Charité-Universitätsmedizin, Berlin, Germany.
Erben U; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany; Research Center Immunosciences, Charité-Universitätsmedizin, Berlin, Germany.
Kruse N; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Wechsung K; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Schumann M; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Klugewitz K; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Scheffold A; Department of Cellular Immunology, Clinic for Rheumatology and Clinical Immunology, Charité-Universitätsmedizin, Berlin, Germany; German Rheumatism Research Centre Berlin, an Institute of the Leibniz-Association, Berlin, Germany.
Kühl AA; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany; Research Center Immunosciences, Charité-Universitätsmedizin, Berlin, Germany.
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Źródło :
PloS one [PLoS One] 2015 Jun 08; Vol. 10 (6), pp. e0123867. Date of Electronic Publication: 2015 Jun 08 (Print Publication: 2015).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chemokine CXCL10/*metabolism
Chemokine CXCL12/*metabolism
Chemokine CXCL9/*metabolism
Endothelial Cells/*metabolism
Liver/*pathology
Animals ; CD4-Positive T-Lymphocytes/immunology ; Caveolae/drug effects ; Caveolae/metabolism ; Chlorpromazine/pharmacology ; Clathrin/metabolism ; Clathrin-Coated Vesicles/drug effects ; Clathrin-Coated Vesicles/metabolism ; Endocytosis/drug effects ; Endosomes/drug effects ; Endosomes/metabolism ; Endothelial Cells/drug effects ; Hepatitis/immunology ; Hepatitis/pathology ; Homeostasis/drug effects ; Inflammation/pathology ; Inflammation Mediators/metabolism ; Liver/drug effects ; Liver/immunology ; Lysosomes/drug effects ; Lysosomes/metabolism ; Mice, Inbred C57BL
Czasopismo naukowe
Tytuł :
Th1-Like ICOS+ Foxp3+ Treg Cells Preferentially Express CXCR3 and Home to β-Islets during Pre-Diabetes in BDC2.5 NOD Mice.
Autorzy :
Kornete M; Department of Microbiology and Immunology, McGill University, Montréal, QC, Canada, H3A 2B4.
Mason ES; Department of Microbiology and Immunology, McGill University, Montréal, QC, Canada, H3A 2B4.
Girouard J; Department of Microbiology and Immunology, McGill University, Montréal, QC, Canada, H3A 2B4.
Lafferty EI; Division of Experimental Medicine, McGill University, Montreal, QC, Canada.
Qureshi S; Department of Medicine, McGill University, Montreal, QC, Canada.
Piccirillo CA; Department of Microbiology and Immunology, McGill University, Montréal, QC, Canada, H3A 2B4; Microbiome and Disease Tolerance Centre, McGill University, Montreal, QC, Canada, H3A 2B4; FOCIS Center of Excellence in Translational Immunology, Research Institute of the McGill University Health Centre, Montreal, QC, Canada, H3G 1A4.
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Źródło :
PloS one [PLoS One] 2015 May 06; Vol. 10 (5), pp. e0126311. Date of Electronic Publication: 2015 May 06 (Print Publication: 2015).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Diabetes Mellitus, Type 1/*immunology
Inducible T-Cell Co-Stimulator Protein/*metabolism
Receptors, CXCR3/*biosynthesis
T-Lymphocytes, Regulatory/*immunology
Th1 Cells/*immunology
Adoptive Transfer ; Animals ; Autoimmunity/immunology ; Cell Movement/immunology ; Chemokine CXCL10/metabolism ; Chemokine CXCL11/metabolism ; Chemokine CXCL9/metabolism ; Insulin-Secreting Cells/immunology ; Interferon-gamma/biosynthesis ; Interferon-gamma/immunology ; Interleukin-2/deficiency ; Interleukin-2/immunology ; Mice ; Mice, Inbred NOD ; Mice, Transgenic ; Prediabetic State/immunology ; T-Lymphocytes, Regulatory/transplantation ; Th1 Cells/transplantation
Czasopismo naukowe

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