Showing 1 - 20 results of 49 for search '"Chemokines metabolism"', query time: 1.18s Refine Results
2
Progressive Control of Streptococcus agalactiae-Induced Innate Inflammatory Response Is Associated with Time Course Expression of MicroRNA-223 by Neutrophils

Authors: Georges Casimir, Mustapha Chamekh, Maud Deny, Olivier Denis, Marta Romano

Source: Infect Immun
Infection and immunity, 88 (12

Subject Terms: Host Response and Inflammation, Sciences bio-médicales et agricoles, Animals, Chemokine CXCL1 -- genetics -- metabolism, Chemokine CXCL2 -- genetics -- metabolism, Chemokines -- metabolism, Cytokines -- metabolism, Inflammation -- metabolism, Interleukin-1beta, Lung -- cytology -- immunology -- pathology, Macrophages -- metabolism, Male, Mice, Mice, Inbred C57BL, MicroRNAs -- genetics -- metabolism, Monocytes -- metabolism, Neutrophils -- metabolism, Pneumonia -- genetics -- immunology -- metabolism, Streptococcus agalactiae -- immunology -- pathogenicity, Tumor Necrosis Factor-alpha -- metabolism, group B streptococcus, inflammation, innate immunity, miR-223, Infectious Diseases, Immunology, Microbiology, Parasitology, CXCL2, Inflammation, medicine.symptom, medicine, Chemokine, biology.protein, biology, Innate immune system, microRNA, Proinflammatory cytokine, mir-223, Monocyte, medicine.anatomical_structure

File Description: 1 full-text file(s): application/pdf

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::497d47715aae5e5f3127dfeabce4eb56
https://europepmc.org/articles/PMC7671897/

3
Inhibition of RANK signaling in breast cancer induces an anti-tumor immune response orchestrated by CD8+ T cells

Authors: Denis Larsimont, Roberto Salgado, Sherene Loi, Laura Polastro, Thierry Walzer, Karen Willard-Gallo, Josef M. Penninger, David Venet, C. Velghe, Marion Maetens, Peter Vuylsteke, Alexandra Barranco, Purificación Muñoz, Geoffrey J. Lindeman, Lourdes Planelles, Enrique Hernández-Jiménez, Clara Gómez-Aleza, Soizic Garaud, Hatem A. Azim, Guillermo Yoldi, Bastien Nguyen, Eva M. Trinidad, Philippe Simon, Pasquale Pellegrini, Françoise Rothé, Maria Zafeiroglou, Marina Ciscar, Gert Van den Eynden, Christos Sotiriou, Eva González-Suárez, Martine Piccart, Hans Wildiers, Sandra Benítez, Stefan Michiels

Contributors: Jules Bordet Institute, European Regional Development Fund (ERDF/FEDER), European Research Council (ERC), Fundacio La Marato de TV3, National Fund for Research (FNRS), Breast Cancer Research Foundation (BCRF)

Source: Nature communications, 11 (1
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)

Subject Terms: Cancérologie, Sciences bio-médicales et agricoles, Médecine pathologie humaine, Adult, Animals, Breast Neoplasms -- blood -- drug therapy -- immunology -- pathology, CD8-Positive T-Lymphocytes -- immunology, Cell Line, Tumor, Chemokines -- metabolism, Denosumab -- pharmacology -- therapeutic use, Female, Humans, Immunity, Immunosuppression, Immunotherapy, Inflammation Mediators -- metabolism, Lymphocytes, Tumor-Infiltrating -- immunology, Mice, Inbred C57BL, Middle Aged, Models, Biological, Myeloid Cells -- immunology, Neoplasm Staging, Neutrophils -- immunology, RANK Ligand -- blood -- metabolism, Receptor Activator of Nuclear Factor-kappa B -- metabolism, Signal Transduction, Article, Cancer immunotherapy, Breast cancer, Breast Neoplasms, CD8-Positive T-Lymphocytes, Chemokines, Denosumab, Inflammation Mediators, Lymphocytes, Tumor-Infiltrating, Myeloid Cells, Neutrophils, RANK Ligand, Receptor Activator of Nuclear Factor-kappa B, lcsh:Science, lcsh:Q, General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry, Tumor-infiltrating lymphocytes, Cancer research, RANKL, biology.protein, biology, Medicine, business.industry, business, CD8, Cytotoxic T cell, Signal transduction, Immune system, medicine.disease, medicine.medical_treatment

File Description: 2 full-text file(s): application/pdf; application/pdf; Electronic

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaab5273f7d1563d1814cb86c4091fe2
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/317452

4
The time-of-day of myocardial infarction onset affects healing through oscillations in cardiac neutrophil recruitment

Authors: Schloss, Maximilian J, Horckmans, Michael, Nitz, Katrin, Duchene, Johan, Drechsler, Maik, Bidzhekov, Kiril, Scheiermann, Christoph, Weber, Christian, Soehnlein, Oliver, Steffens, Sabine

Contributors: Biochemie, RS: CARIM - R3.07 - Structure-function analysis of the chemokine interactome for therapeutic targeting and imaging in atherosclerosis, Pathologie, RS: CARIM - R1.01 - Blood proteins & engineering, Pathology

Source: Embo Molecular Medicine
EMBO Molecular Medicine, Vol. 8, No 8 (2016) pp. 937-48
EMBO molecular medicine, 8 (8
EMBO Molecular Medicine
EMBO Molecular Medicine, 8(8), 937-948. Wiley-Blackwell
EMBO molecular medicine, 8(8), 937-948. Wiley-Blackwell

Subject Terms: circadian rhythm, fibrosis, myocardial infarction healing, neutrophils, progenitors, ddc:610, Institut für Kardiovaskuläre Physiologie und Pathophysiologie, ddc:616.07, Animals, Chemokines/metabolism, Circadian Rhythm, Disease Models, Animal, Female, Mice, Inbred C57BL, Myocardial Infarction/pathology/physiopathology, Neutrophil Infiltration, Molecular Medicine, Cardiology, medicine.medical_specialty, medicine, Cause of death, Cardiac function curve, Immunology, Fibrosis, medicine.disease, Progenitor cell, Internal medicine, business.industry, business, Myocardial infarction, Chemokine, biology.protein, biology, Myeloid, medicine.anatomical_structure, CXC chemokine receptors, Sciences bio-médicales et agricoles, Chemokines -- metabolism, Disease Models, Animal, Mice, Inbred C57BL, Myocardial Infarction -- pathology -- physiopathology, Cardiovascular and Metabolic Diseases, Research Article, Research Articles, Cardiovascular System, cardiovascular system

File Description: application/pdf; 1 full-text file(s): application/pdf

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97098bb226dc7068f13e1d7dc1021fc5

6
The Proteolytic Activation of (H3N2) Influenza A Virus Hemagglutinin Is Facilitated by Different Type II Transmembrane Serine Proteases

Authors: Kühn, Nora, Bergmann, Silke, Kösterke, Nadine, Lambertz, Ruth L. O., Keppner, Anna, van den Brand, Judith M. A., Pöhlmann, Stefan, Weiß, Siegfried, Hummler, Edith, Hatesuer, Bastian, Schughart, Klaus

Contributors: Department of Virology, Helmholtz Centre for infection research, Inhoffenstr. 7, 38124 Braunschweig, Germany.

Source: Journal of Virology
Journal of Virology, vol. 90, no. 9, pp. 4298-4307
Journal of Virology, 90(9), 4298-4307

Subject Terms: Pathogenesis and Immunity, Virology, Insect Science, Immunology, Microbiology, NS2-3 protease, Viral replication, Virus, Protease, medicine.medical_treatment, medicine, Viral load, Proteases, Influenza A virus, medicine.disease_cause, Biology, Hemagglutinin (influenza), biology.protein, Animals, Bronchi/metabolism, Bronchi/virology, Chemokines/metabolism, Cytokines/metabolism, Disease Models, Animal, Disease Susceptibility, Enzyme Activation, Female, Gene Deletion, Gene Expression, Hemagglutinin Glycoproteins, Influenza Virus/metabolism, Host-Pathogen Interactions, Influenza A Virus, H3N2 Subtype/physiology, Membrane Proteins/genetics, Membrane Proteins/metabolism, Mice, Mice, Knockout, Orthomyxoviridae Infections/genetics, Orthomyxoviridae Infections/immunology, %22">Orthomyxoviridae Infections/ , Proteolysis, Pulmonary Alveoli/metabolism, Pulmonary Alveoli/virology, Serine Endopeptidases/genetics, Serine Endopeptidases/metabolism, Viral Load, Virus Replication, viruses

File Description: application/pdf

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f72d355cb06ecd632206fb18ca74c31e
http://europepmc.org/articles/PMC4836353

7
Statins inhibit C-reactive protein-induced chemokine secretion, ICAM-1 upregulation and chemotaxis in adherent human monocytes

Authors: C. Berlier, François Mach, Nana Kwabena Poku, Fabienne Burger, Sabine Steffens, Fabrizio Montecucco, Graziano Pelli

Source: Rheumatology, Vol. 48, No 3 (2009) pp. 233-242

Subject Terms: Pharmacology (medical), Rheumatology, Chemokine secretion, CCL3, Monocyte, medicine.anatomical_structure, medicine, business.industry, business, CCL2, Pharmacology, Intercellular Adhesion Molecule-1, Intercellular adhesion molecule, Chemokine, biology.protein, biology, CCL4, Endocrinology, medicine.medical_specialty, Internal medicine, ddc:616, C-Reactive Protein/*antagonists & inhibitors/pharmacology, Cell Adhesion/physiology, Cells, Cultured, Chemokines/*metabolism, Chemotaxis, Leukocyte/*drug effects, Dose-Response Relationship, Drug, Enzyme Activation/physiology, Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors/*pharmacology, Intercellular Adhesion Molecule-1/*biosynthesis, Mitogen-Activated Protein Kinase 1/metabolism, Mitogen-Activated Protein Kinase 3/metabolism, Monocytes/drug effects/physiology, Receptors, Immunologic/drug effects/metabolism, Recombinant Proteins/pharmacology, Up-Regulation/drug effects

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cecc75d5b87828e11caa1cb153cfa345
http://doc.rero.ch/record/303115/files/ken466.pdf

8
TGFBR2-dependent alterations of exosomal cargo and functions in DNA mismatch repair-deficient HCT116 colorectal cancer cells

Authors: Fricke, Fabia, Lee, Jennifer, Michalak, Malwina, Warnken, Uwe, Haußer, Ingrid, Suarez-Carmona, Meggy, Halama, Niels, Schnölzer, Martina, Kopitz, Jürgen, Gebert, Johannes

Source: Cell Communication and Signaling : CCS
Cell Communication and Signaling, Vol 15, Iss 1, Pp 1-14 (2017)
TGFBR2-dependent alterations of exosomal cargo and functions in DNA mismatch repair-deficient HCT116 colorectal cancer cells. Cell Communication and Signaling, 15(1), 14., United Kingdom. (2017).

Subject Terms: Cell Biology, Molecular Biology, Biochemistry, Phenotype, Cancer research, Transforming growth factor beta, biology.protein, biology, Microsatellite instability, medicine.disease, medicine, Frameshift mutation, DNA mismatch repair, Suppressor, law.invention, law, Microvesicles, Platelet-derived growth factor, chemistry.chemical_compound, chemistry, Research, Exosomes, Intercellular communication, Proteomics, Transforming Growth Factor Beta Receptor Type 2, DNA mismatch repair deficiency, Colorectal cancer, lcsh:Medicine, lcsh:R, lcsh:Cytology, lcsh:QH573-671, Chemokines/metabolism, Colorectal Neoplasms/metabolism, DNA Mismatch Repair, Enzyme-Linked Immunosorbent Assay, Exosomes/metabolism/ultrastructure, Frameshift Mutation/genetics, HCT116 Cells, Hep G2 Cells, Humans, Microsatellite Instability, Platelet-Derived Growth Factor/metabolism, Protein-Serine-Threonine Kinases/metabolism, Proteome/metabolism, Receptor, Transforming Growth Factor-beta Type II, Receptors, Transforming Growth Factor beta/metabolism, Reproducibility of Results, Oncology [Human health sciences], Oncologie [Sciences de la santé humaine], 610 Medical sciences Medicine, digestive system diseases

File Description: application/pdf

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a08cc4807dec0f27b46b9fc65e487d0

PDF Full Text
9
Global analyses revealed age-related alterations in innate immune responses after stimulation of pathogen recognition receptors

Authors: Metcalf, Talibah U, Cubas, Rafael A, Ghneim, Khader, Cartwright, Michael J, Grevenynghe, Julien Van, Richner, Justin M, Olagnier, David P, Wilkinson, Peter A, Cameron, Mark J, Park, Byung S, Hiscott, John B, Diamond, Michael S, Wertheimer, Anne M, Nikolich-Zugich, Janko, Haddad, Elias K

Source: Aging Cell
Metcalf, T U, Cubas, R A, Ghneim, K, Cartwright, M J, Grevenynghe, J V, Richner, J M, Olagnier, D P, Wilkinson, P A, Cameron, M J, Park, B S, Hiscott, J B, Diamond, M S, Wertheimer, A M, Nikolich-Zugich, J & Haddad, E K 2015, ' Global analyses revealed age-related alterations in innate immune responses after stimulation of pathogen recognition receptors ' Aging Cell, vol. 14, no. 3, pp. 421-32 . https://doi.org/10.1111/acel.12320

Subject Terms: Original Articles, immunosenescence, innate immune agonists, innate immunity, interferon signaling, pattern recognition receptors, peripheral blood mononuclear cells, Cell Biology, Ageing, Pattern recognition receptor, Acquired immune system, CCL18, Immune system, Monocyte, medicine.anatomical_structure, medicine, Dendritic cell, Innate lymphoid cell, Biology, Innate immune system, Immunology, Adaptive Immunity/genetics, Adult, Aged, Aged, 80 and over, Aging, B-Lymphocytes/immunology, Chemokines/metabolism, Cytokines/metabolism, Dendritic Cells/immunology, Humans, Immunity, Innate/immunology, Leukocytes, Mononuclear/metabolism, Lymphocyte Activation/genetics, Monocytes/immunology, T-Lymphocytes/immunology, Young Adult

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4de33171427cc1b7eb231e6e19436446
http://europepmc.org/articles/PMC4406671

PDF Full Text
10
Pathophysiological role of neutrophils in acute myocardial infarction

Authors: Federico Carbone, Alessio Nencioni, Fabrizio Montecucco, François Mach, N. Vuilleumier

Source: Thrombosis and Haemostasis
Thrombosis and Haemostasis, Vol. 110, No 3 (2013) pp. 501-514
Thrombosis and Haemostasis; Vol 110

Subject Terms: Hematology, Medicine, business.industry, business, Neointima, Pathogenesis, Pathophysiology, Angioplasty, medicine.medical_treatment, Inflammation, medicine.symptom, Myocardial infarction, medicine.disease, Percutaneous coronary intervention, Pathology, medicine.medical_specialty, Immune system, ddc:616, ddc:576, Acute Coronary Syndrome/metabolism, Animals, Atherosclerosis/metabolism, Chemokines/metabolism, Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use, Inflammation/pathology, Ischemia/pathology, Lipoproteins, HDL/chemistry, Multivariate Analysis, Myocardial Infarction/blood, Myocardial Reperfusion Injury/pathology, Neutrophil Infiltration, Neutrophils/cytology/metabolism, Percutaneous Coronary Intervention, Plaque, Atherosclerotic/metabolism, Reactive Oxygen Species/metabolism

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::507094509d060708f62681a11f03f2d3
http://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH13-03-0211.pdf

11
Dipeptidylpeptidase 4 inhibition enhances lymphocyte trafficking, improving both naturally occurring tumor immunity and immunotherapy

Authors: Barreira da Silva, Rosa, Laird, Melissa E, Yatim, Nader, Fiette, Laurence, Ingersoll, Molly A, Albert, Matthew L

Contributors: Immunobiologie des Cellules Dendritiques, Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM), Histopathologie humaine et Modèles animaux, Institut Pasteur [Paris], Funding was provided by the Institut Pasteur (Pasteur-Roux post-doctoral fellowship to R.B.d.S.), the Pasteur Foundation (fellowship to M.E.L.), the Ligue Contre le Cancer (M.L.A.), the Fondation ARC pour la recherche sur le cancer (M.L.A.) and the French government's Invest in the Future Program, managed by the Agence Nationale de la Recherche (LabEx Immuno-Onco (R.B.d.S., M.E.L., N.Y., M.A.I. and M.L.A.))., ANR-11-IDEX-0005,USPC,Université Sorbonne Paris Cité(2011)

Source: Nature Immunology
Nature Immunology, Nature Publishing Group, 2015, 16 (8), pp.850-858. ⟨10.1038/ni.3201⟩

Subject Terms: Cancer immunotherapy, Protein transport, MESH: Adoptive Transfer, MESH: Animals, MESH: Dipeptidyl Peptidase 4/immunology, MESH: Dipeptidyl Peptidase 4/metabolism, MESH: Dipeptidyl-Peptidase IV Inhibitors/pharmacology, MESH: Female, MESH: Flow Cytometry, MESH: Immunotherapy/methods, MESH: Lymphocytes/immunology, MESH: Lymphocytes/metabolism, MESH: Male, MESH: Mice, Inbred BALB C, MESH: Cell Line, Tumor, MESH: Mice, Inbred C57BL, MESH: Mice, Knockout, MESH: Mice, Transgenic, MESH: Neoplasms, Experimental/genetics, MESH: Neoplasms, Experimental/immunology, MESH: Neoplasms, Experimental/therapy, MESH: Pyrazines/pharmacology, MESH: Receptors, CXCR3/immunology, MESH: Receptors, CXCR3/metabolism, MESH: Sitagliptin Phosphate, MESH: Cell Movement/drug effects, MESH: Triazoles/pharmacology, MESH: Cell Movement/immunology, MESH: Chemokine CXCL10/immunology, MESH: Chemokine CXCL10/metabolism, MESH: Chemokines/immunology, MESH: Chemokines/metabolism, MESH: Dipeptidyl Peptidase 4/genetics, [SDV.IMM]Life Sciences [q-bio]/Immunology, Immunology, Immunology and Allergy, medicine.medical_treatment, medicine, CXCR3, CXCL10, T cell, medicine.anatomical_structure, Adoptive cell transfer, Lymphocyte, Immunotherapy, Immune system, Chemistry

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49e2ab8828a29afd88e17c54fdc280cd
https://hal-pasteur.archives-ouvertes.fr/pasteur-01380810

12
Characterization of nitrotyrosine as a biomarker for arthritis and joint injury

Authors: D. Roman, O. Friese, M.-P. Hellio Le Graverand, Candace Bramson, Melissa R. Radabaugh, L.S. Lohmander, Thomas P. Misko, R. Gallavan, M. Abrams, Maureen K. Highkin

Source: Osteoarthritis and Cartilage; 21(1), pp 151-156 (2013)
Misko, T P, Radabaugh, M R, Highkin, M, Abrams, M, Friese, O, Gallavan, R, Bramson, C, Hellio Le Graverand, M P, Lohmander, S & Roman, D 2013, ' Characterization of nitrotyrosine as a biomarker for arthritis and joint injury ', Osteoarthritis and Cartilage, vol. 21, no. 1, pp. 151-156 . https://doi.org/10.1016/j.joca.2012.09.005

Subject Terms: Rheumatology, Orthopedics and Sports Medicine, Biomedical Engineering, Nitric oxide, Nitrotyrosine, Biomarkers, Arthritis, Joint injury, Rheumatology and Autoimmunity, Internal medicine, medicine.medical_specialty, medicine, Tumor necrosis factor alpha, Biomarker (medicine), Pathology, business.industry, business, medicine.disease, Osteoarthritis, Synovial fluid, Rheumatoid arthritis, chemistry.chemical_compound, chemistry, Gastroenterology, Necrosis, medicine.symptom, Nitrates/metabolism, Matrix Metalloproteinases, Secreted/metabolism, Synovial Fluid/metabolism, Anterior Cruciate Ligament Injuries, Humans, Male, Menisci, Tibial/metabolism, Chemokines/metabolism, Osteoarthritis, Knee/metabolism, Case-Control Studies, Tyrosine/analogs & derivatives, Female, Anterior Cruciate Ligament/metabolism, Cytokines/metabolism, Tibial Meniscus Injuries, Arthritis, Rheumatoid/metabolism, Chondrocalcinosis/metabolism

File Description: application/pdf

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9bb06451dd20cbef6c5c4d01efabe29

13
The Ovarian Cancer Chemokine Landscape is Conducive to Homing of Vaccine-primed and CD3/CD28 Costimulated T cells Prepared for Adoptive Therapy

Authors: Lin Zhang, Lana E. Kandalaft, Thomas Garrabrant, Michael Feldman, Davide Bedognetti, Ian S. Hagemann, Hongzhe Li, Daniel J. Powell, Bruce L. Levine, George Coukos, Priyanka Duttagupta, Francesco M. Marincola, Renee Frank, Carl H. June, Ena Wang, Emese Zsiros, Denarda Dangaj, Janos L. Tanyi

Source: Clinical Cancer Research, vol. 21, no. 12, pp. 2840-2850

Subject Terms: Article, Cancer Research, Oncology, CCL17, CXCL10, CCL5, Biology, CXCL16, CXC chemokine receptors, Chemokine receptor CCR5, biology.protein, Immunology, CC chemokine receptors, Chemokine receptor, Antigens, CD28/metabolism, Antigens, CD3/metabolism, Biomarkers, Cancer Vaccines/immunology, Chemokines/genetics, Chemokines/metabolism, Chemotaxis, Leukocyte, Cluster Analysis, Dendritic Cells/immunology, Dendritic Cells/metabolism, Female, Gene Expression Profiling, Gene Expression Regulation, Neoplastic, Humans, Immunohistochemistry, Immunotherapy, Adoptive, Neoplasm Grading, Neoplasm Staging, Ovarian Neoplasms/diagnosis, Ovarian Neoplasms/genetics, T-Cell Antigen Receptor Specificity/immunology, T-Lymphocyte Subsets/immunology, T-Lymphocyte Subsets/metabolism

File Description: application/pdf

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed0080014a9788b518e2b39aae8b14b6
https://europepmc.org/articles/PMC4987088/

15
Leishmania RNA virus controls the severity of mucocutaneous leishmaniasis

Authors: Ives Annette, Ronet Catherine, Prevel Florence, Ruzzante Giulia, Fuertes-Marraco Silvia, Schutz Frederic, Zangger Haroun, Revaz-Breton Melanie, Lye Lon-Fye, Hickerson Suzanne M, Beverley Stephen M, Acha-Orbea Hans, Launois Pascal, Fasel Nicolas, Masina Slavica

Source: Science (New York N.Y.)
Science, vol. 331, no. 6018, pp. 775-778

Subject Terms: Article, Animals, Chemokines/metabolism, Cytokines/metabolism, Inflammation Mediators/metabolism, Leishmania guyanensis/pathogenicity, Leishmania guyanensis/virology, Leishmaniasis, Mucocutaneous/immunology, Leishmaniasis, Mucocutaneous/parasitology, Leishmaniavirus/immunology, Leishmaniavirus/physiology, Macrophages/immunology, Macrophages/parasitology, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Parasitemia, Phagosomes/parasitology, RNA, Double-Stranded/immunology, RNA, Viral/immunology, Toll-Like Receptor 3/immunology, Toll-Like Receptors/immunology, Multidisciplinary, Leishmaniavirus, Leishmania guyanensis, Intracellular parasite, Immune system, Virology, TLR3, Immunology, Leishmania, biology.organism_classification, biology, medicine.disease, medicine, Proinflammatory cytokine, parasitic diseases, chemical and pharmacologic phenomena

File Description: application/pdf

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b798ff98dc10c23a73df16225357c2b5
http://www.unil.ch/ib/page9490.html#2

16
Chemokines and Antimicrobial Peptides Have a cag -Dependent Early Response to Helicobacter pylori Infection in Primary Human Gastric Epithelial Cells

Authors: Franck Morel, Martine Garnier, Isabelle Paris, Magali Garcia, Cong Tri Tran, Jean-Claude Lecron, Julie Cremniter, Thierry Barthes, Jean-Pierre Faure, Ivo G. Boneca, Pascale Mustapha, Christophe Burucoa, Charles Bodet

Contributors: Laboratoire Inflammation, Tissus épithéliaux et Cytokines (LITEC), Université de Poitiers, Centre hospitalier universitaire de Poitiers (CHU Poitiers), Polyclinique de Poitiers, Biologie et Génétique de la Paroi bactérienne - Biology and Genetics of Bacterial Cell Wall (BGPB), Institut Pasteur [Paris], Equipe Avenir, Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de Bactériologie, CHU de Poitiers, This study was supported in part by a grant from the French Ministry of Health (PHRC Pylorikine). Work in the Ivo G. Boneca laboratory was supported by an ERC Starting Grant (PGNfromSHAPEtoVIR no.202283).

Source: Infection and Immunity
Infection and Immunity, American Society for Microbiology, 2014, 82 (7), pp.2881-2889. ⟨10.1128/IAI.01517-13⟩

Subject Terms: MESH: Antigens, Bacterial/immunology, MESH: Antimicrobial Cationic Peptides/genetics, MESH: Helicobacter pylori/immunology, MESH: Helicobacter pylori/metabolism, MESH: Humans, MESH: Stomach/cytology, MESH: Antimicrobial Cationic Peptides/metabolism, MESH: Bacterial Proteins/immunology, MESH: Cells, Cultured, MESH: Chemokines/genetics, MESH: Chemokines/metabolism, MESH: Epithelial Cells/metabolism, MESH: Epithelial Cells/microbiology, MESH: Genomic Islands, [SDV.IMM.II]Life Sciences [q-bio]/Immunology/Innate immunity, [SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology, Infectious Diseases, Immunology, Microbiology, Parasitology, Tumor necrosis factor alpha, CagA, Inflammation, medicine.symptom, medicine, CXCL1, Chemokine, biology.protein, biology, Interleukin 8, CCL20, Antimicrobial peptides, Host Response and Inflammation

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad5920ece2a5fe7f54b675a642922707
https://hal.archives-ouvertes.fr/hal-01699819

17
Chemerin expression marks early psoriatic skin lesions and correlates with plasmacytoid dendritic cell recruitment

Authors: Albanesi, C., Scarponi, C., Pallotta, S., Daniele, R., Bosisio, D., Madonna, S., Fortugno, P., Gonzalvo-Feo, S., Franssen, J.-D., Parmentier, M., De Pita, O., Girolomoni, G., Sozzani, S.

Source: The Journal of Experimental Medicine
The Journal of experimental medicine, 206 (1
Journal of Experimental Medicine; Vol 206

Subject Terms: Articles, Article, Sciences bio-médicales et agricoles, Adult, Antibodies, Monoclonal -- immunology, Antibodies, Monoclonal -- pharmacology, Antigens, CD -- metabolism, Blotting, Western, CD8-Positive T-Lymphocytes -- cytology, CD8-Positive T-Lymphocytes -- drug effects, CD8-Positive T-Lymphocytes -- metabolism, Calcitriol -- pharmacology, Cells, Cultured, Chemokine CXCL10 -- genetics, Chemokine CXCL10 -- metabolism, Chemokines -- genetics, Chemokines -- metabolism, Chemotaxis, Leukocyte -- drug effects, Chemotaxis, Leukocyte -- physiology, Culture Media, Conditioned -- pharmacology, Dendritic Cells -- cytology, Dendritic Cells -- metabolism, Dermatitis, Atopic -- genetics, Dermatitis, Atopic -- metabolism, Dermatitis, Atopic -- pathology, Extracellular Signal-Regulated MAP Kinases -- metabolism, Fibroblasts -- cytology, Fibroblasts -- drug effects, Fibroblasts -- metabolism, Gene Expression -- drug effects, Humans -- metabolism, Intercellular Adhesion Molecule-1 -- metabolism, Lectins, C-Type -- genetics, Lectins, C-Type -- metabolism, Membrane Glycoproteins -- genetics, Membrane Glycoproteins -- metabolism, Neutrophils -- cytology, Neutrophils -- drug effects, Neutrophils -- metabolism, Psoriasis -- genetics, Psoriasis -- metabolism, Psoriasis -- pathology, Receptors, Chemokine -- genetics, Receptors, Chemokine -- immunology, Receptors, Chemokine -- metabolism, Receptors, Immunologic -- genetics, Receptors, Immunologic -- metabolism, Reverse Transcriptase Polymerase Chain Reaction, Skin -- metabolism, Skin -- pathology, Tretinoin -- pharmacology, Immunology, Immunology and Allergy, Plasmacytoid dendritic cell, Chemerin, biology.protein, biology, Chemokine, Dermis, medicine.anatomical_structure, medicine, Psoriasis, medicine.disease, Calcitriol, medicine.drug, Pathology, medicine.medical_specialty, CD15, CMKLR1, hemic and immune systems, macromolecular substances, integumentary system

File Description: 1 full-text file(s): application/pdf

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::385b592e1216bca1362e6ad027821b85
http://europepmc.org/articles/PMC2626680

18
Epstein-Barr virus infection induces an increase of T regulatory type 1 cells in Hodgkin lymphoma patients

Authors: Moralès, Olivier, Mrizak, Dhafer, François, Violaine, Mustapha, Rami, Miroux, Céline, Depil, Stephane, Decouvelaere, Anne-Valérie, Lionne-Huyghe, Pauline, Auriault, Claude, de Launoit, Yvan, Pancré, Véronique, Delhem, Nadira

Contributors: Institut de biologie de Lille - IBL (IBLI), Université de Lille, Sciences et Technologies-Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Centre National de la Recherche Scientifique (CNRS)-Université de Lille, Droit et Santé, Université libre de Bruxelles (ULB), Service des Maladies du Sang [CHRU Lille], Hôpital Claude Huriez [Lille], CHU Lille-CHU Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Département d'hématologie [Gustave Roussy], Institut Gustave Roussy (IGR), Institut de Pathologie [CHU Lille], Pôle de Biologie Pathologie Génétique [CHU Lille], Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Unité Fonctionnelle d’Anatomie et de Cytologie Pathologiques [Lyon], Département d'anatomopathologie, biopathologie, Centre Léon Bérard [Lyon]-Centre Léon Bérard [Lyon], Groupe Hospitalier Artois-Ternois Centre Hospitalier d’Arras, Institut de pharmacologie moléculaire et cellulaire (IPMC), Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015 - 2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015 - 2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS), Université de Lille, Sciences et Technologies, This work received financial supports from the ‘Association de Recherche contre le Cancer’, the ‘Fondation de Recherche Médical’, OSEO and the Nord‐Pas‐de Calais Region. This work was also supported by SIRIC ONCOLille., The authors would like to thank Han VORNG for his technical assistance.

Source: British Journal of Haematology
British Journal of Haematology, Wiley, 2014, 166 (6), pp.875-890. ⟨10.1111/bjh.12980⟩

Subject Terms: Hematology, Chemokine, biology.protein, biology, Immune system, Immunology, LAG3, Epstein–Barr virus, medicine.disease_cause, medicine, CTL, Epstein–Barr virus infection, medicine.disease, Peripheral blood mononuclear cell, Interleukin 10, Epstein-Barr Virus, Hodgkin lymphoma, IL10, Tr1, chemokines, MESH: Adolescent, MESH: Adult, MESH: Th2 Cells/immunology, MESH: Th2 Cells/virology, MESH: Aged, MESH: Up-Regulation, MESH: Young Adult, MESH: Biomarkers/metabolism, MESH: Chemokines/metabolism, MESH: Child, MESH: Cytokines/metabolism, MESH: Epstein-Barr Virus Infections/immunology, MESH: Hodgkin Disease/immunology, MESH: Female, MESH: Gene Expression Regulation, Neoplastic, MESH: Hodgkin Disease/virology, MESH: Humans, MESH: Male, MESH: Middle Aged, MESH: Phenotype, MESH: T-Lymphocytes, Regulatory/immunology, MESH: T-Lymphocytes, Regulatory/virology, [SDV]Life Sciences [q-bio]

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b1379756aab8bae4f2a0ec70d388160

19
HIV-1 exploits CCR5 conformational heterogeneity to escape inhibition by chemokines

Authors: Yann Benureau, Yongjin Wang, Nuria González, Oliver Hartley, Isabelle Staropoli, Philippe Colin, José Alcamí, Fernando Arenzana-Seisdedos, Bernard Lagane, Anne Brelot

Contributors: Cellule Pasteur UPMC, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Pasteur [Paris], Pathogénie Virale, Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM), Instituto de Salud Carlos III [Madrid] (ISC), Department of Pathology and Immunology, University of Geneva [Switzerland], This work was supported by Agence Nationale de Recherches sur le SIDA (ANRS), SIDACTION, Institut National de la Santé et de la Recherche Médicale, Institut Pasteur, the French Government's Investissement d'Avenir program, Laboratoire d'Excellence 'Integrative Biology of Emerging Infectious Diseases' (Grant ANR-10-LABX-62-IBEID), and the Spanish Ministry of Economy and Competitiveness (FIS PI 080752). O.H. acknowledges support from the Swiss National Science Foundation. Y.B., Y.W., and N.G. were supported by fellowships from SIDACTION, ANRS, and the Spanish AIDS Research Network (ISCIII-RETIC RD06/0006), respectively.

Source: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2013, 110 (23), pp.9475-9480. ⟨10.1073/pnas.1222205110⟩
Proceedings of the National Academy of Sciences, Vol. 110, No 23 (2013) pp. 9475-80

Subject Terms: Biological Sciences, Multidisciplinary, CCR1, G protein, CCL7, CC chemokine receptors, Endocytosis, Biology, Molecular biology, CX3CL1, CCR3, Chemokine, biology.protein, HIV coreceptor, AIDS pathogenesis, β chemokines, [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology, ddc:616.07, CD4-Positive T-Lymphocytes/metabolism, Cell Line, Chemokines/metabolism, Endocytosis/physiology, HIV Infections/metabolism/physiopathology, HIV-1/metabolism/physiology, Humans, Protein Conformation, Radioligand Assay, Receptors, CCR5/chemistry/metabolism, Virus Internalization, virus diseases, viruses

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e378a5be9ae74ef9ead105ed40ebb1a9
https://europepmc.org/articles/PMC3677469/

Search Tools: Get RSS Feed — Email this Search