Search Results - "T-Lymphocytes metabolism"

1

T cell reconstitution after lymphocyte depletion features a different pattern of inhibitory receptor expression in ABO‐ versus HLA‐incompatible kidney transplant recipients

Authors: Del Bello, A., Kamar, N., Treiner, E.

Contributors: Centre de Physiopathologie Toulouse Purpan (CPTP), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Département de Néphrologie et Transplantation d'organes, Hôpital de Rangueil, CHU Toulouse [Toulouse]-CHU Toulouse [Toulouse], CHU Toulouse [Toulouse]

Source: Clinical and Experimental Immunology
Clinical and Experimental Immunology, Wiley, 2020, 200 (1), pp.89-104. ⟨10.1111/cei.13412⟩
Clin Exp Immunol

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::224fd1281567a921d5b700e491fdcbe5
https://hal-univ-tlse3.archives-ouvertes.fr/hal-03155080

2

IL13-Mediated Dectin-1 and Mannose Receptor Overexpression Promotes Macrophage Antitumor Activities through Recognition of Sialylated Tumor Cells

Authors: Alaeddine, Mohamad, Prat, Mélissa, Poinsot, Véréna, Gouazé-Andersson, Valérie, Authier, Hélène, Meunier, Etienne, Lefèvre, Lise, Alric, Camille, Dardenne, Christophe, Bernad, José, Alric, Laurent, Segui, Bruno, Balard, Patricia, Couderc, François, Couderc, Bettina, Pipy, Bernard, Coste, Agnès

Contributors: Interactions moléculaires et réactivité chimique et photochimique (IMRCP), Centre National de la Recherche Scientifique (CNRS)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Institut de Recherche pour le Développement (IRD)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées, Polarisation des Macrophages et Récepteurs Nucléaires dans les Pathologies Inflammatoires et Infectieuses, Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-IFR50, Infections Parasitaires : Transmission, Physiopathologie et Thérapeutiques (IP-TPT), Service de Santé des Armées-Assistance Publique - Hôpitaux de Marseille (APHM)-Aix Marseille Université (AMU)-Institut de Recherche pour le Développement (IRD), Institut de Recherche en Santé Digestive (IRSD ), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Vétérinaire de Toulouse (ENVT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut de médecine moléculaire de Rangueil (I2MR), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-IFR150-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire d'Astrophysique de Marseille (LAM), Centre National de la Recherche Scientifique (CNRS)-Institut national des sciences de l'Univers (INSU - CNRS)-Aix Marseille Université (AMU)-Centre National d'Études Spatiales [Toulouse] (CNES), Institut Claudius Regaud, CRLCC Institut Claudius Regaud, Institut de Recherche pour le Développement (IRD)-Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Service de Santé des Armées, Institut National de la Recherche Agronomique (INRA)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Ecole Nationale Vétérinaire de Toulouse (ENVT), Aix Marseille Université (AMU)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS), Pharmacochimie et Biologie pour le Développement (PHARMA-DEV), Institut de Recherche pour le Développement (IRD)-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut de Recherche pour le Développement (IRD)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Université Toulouse III - Paul Sabatier (UT3), Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS), Centre de Recherches en Cancérologie de Toulouse (CRCT), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Laboratoire Nutergia, This research was supported by a grant from CIFRE-Association Nationale de la Recherche et de la Technologie (ANRT) awarded to M. Alaeddine (2012/1416) and from the Nutergia Laboratory (to A. Coste and B. Pipy)

Source: Cancer Immunology Research
Cancer Immunology Research, American Association for Cancer Research, 2019, ⟨10.1158/2326-6066.CIR-18-0213⟩

Subject Terms: [CHIM]Chemical Sciences, Animals, Arginase / metabolism, Cell Line, Tumor, Gene Expression, Humans, Interleukin-13 / genetics, Interleukin-13 / metabolism, Lectins, C-Type / genetics, C-Type / metabolism, Macrophages / immunology, Macrophages / metabolism, Mannose-Binding Lectins / genetics, Mannose-Binding Lectins / metabolism, Mice, Mice Knockout, N-Acetylneuraminic Acid / metabolism, Necrosis / genetics, Necrosis / immunology, Neoplasms / etiology, Neoplasms / metabolism, Neoplasms / mortality, Neoplasms / pathology, Prognosis, Reactive Oxygen Species / metabolism, Receptors, Cell Surface / genetics, Cell Surface / metabolism, Signal Transduction, T-Lymphocytes / immunology, T-Lymphocytes / metabolism, Cancer Research, Immunology, Cytotoxic T cell, Receptor, Cancer research, Chemistry, Lectin, biology.protein, biology, Receptor expression, Mannose receptor, Glycan, Cytotoxicity, Effector

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::597fe2b756836ba339dd007adcd2a9c5
https://hal.archives-ouvertes.fr/hal-02194445

3

Modulation of CD4 T cell function via CD6-targeting

Authors: Freitas, Raquel Filipa, Basto, Afonso, Almeida, Silvia C.P., Santos, Rita F., Gonçalves, Carine M., Corria-Osorio, Jesus, Carvalho, Tânia, Carmo, Alexandre M., Oliveira, Vanessa G., Leon, Kalet, Graca, Luis

Contributors: Instituto de Investigação e Inovação em Saúde

Source: EBioMedicine

Subject Terms: General Biochemistry, Genetics and Molecular Biology, General Medicine, Antibody, biology.protein, biology, T cell, medicine.anatomical_structure, medicine, In vivo, FOXP3, Cd4 t cell, Immune modulation, In vitro, Cell biology, Immunological synapse, Research paper, CD6, CD4 T cells, Treg cells, Foxp3, EAE, T-cell polarization, Animals, Antigens, CD / metabolism, Antigens, Differentiation, T-Lymphocyte / metabolism, Biomarkers, CD4-Positive T-Lymphocytes / cytology, CD4-Positive T-Lymphocytes / immunology, CD4-Positive T-Lymphocytes / metabolism, Cell Adhesion Molecules, Neuronal / metabolism, Cell Differentiation, Fetal Proteins / metabolism, Humans, Lymphocyte Activation, Mice, Mice, Transgenic, T-Lymphocyte Subsets / immunology, T-Lymphocyte Subsets / metabolism

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4

Melanoma cell lysosome secretory burst neutralizes the CTL-mediated cytotoxicity at the lytic synapse

Authors: Nicolas Gaudenzio, Salvatore Valitutti, Roxana Khazen, Marie-Pierre Puissegur, Sabina Müller, Eric Espinosa

Contributors: Centre de Physiopathologie Toulouse Purpan (CPTP), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Department of Pathology [Stanford], Stanford Medicine, Stanford University-Stanford University, Institut Universitaire du Cancer de Toulouse - Oncopole (IUCT Oncopole - UMR 1037), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-CHU Toulouse [Toulouse]-Institut National de la Santé et de la Recherche Médicale (INSERM), Fondation ARC pour la Recherche sur le Cancer (EML2012090493), Institut National du Cancer (INCa PBLIO11-130 et INCa/DGOS 2012-054), ANR-11-LABX-0068,TOUCAN,Analyse intégrée de la résistance dans les cancers hématologiques(2011)

Source: Nature Communications, Vol 7, Iss 1, Pp 1-15 (2016)
Nature Communications
Nature Communications, Nature Publishing Group, 2016, 7 (1), pp.1-15. ⟨10.1038/ncomms10823⟩
ResearcherID

Subject Terms: Science, MESH: CD8-Positive T-Lymphocytes / metabolism, MESH: CD8-Positive T-Lymphocytes / physiology, MESH: Hydrogen-Ion Concentration, MESH: Lymphocyte Activation, MESH: Lysosomes / metabolism, MESH: Melanoma / metabolism, MESH: Perforin / genetics, MESH: Perforin / metabolism, MESH: Protein Transport, MESH: Qb-SNARE Proteins / genetics, MESH: Qb-SNARE Proteins / metabolism, MESH: Qc-SNARE Proteins / genetics, MESH: Qc-SNARE Proteins / metabolism, MESH: Cathepsins / metabolism, MESH: Cell Line, MESH: Cytotoxicity, Immunologic / physiology, MESH: Endosomes / physiology, MESH: Gene Expression Regulation, Neoplastic / physiology, MESH: Humans, [SDV.IMM]Life Sciences [q-bio]/Immunology, Article, General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry, Perforin, biology.protein, biology, Late endosome, CTL-mediated cytotoxicity, CTL, Granzyme B, Lysosome, medicine.anatomical_structure, medicine, Cell biology, Lytic cycle, Cytotoxic T cell, chemical and pharmacologic phenomena, hemic and immune systems

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27bf2ad43f626283ba18819fec6ab184
https://doaj.org/article/6d7abd7b4f83446997c996c983b66c0d

5

Modified tumour antigen-encoding mRNA facilitates the analysis of naturally occurring and vaccine-induced CD4 and CD8 T cells in cancer patients

Authors: Jean-Marie Tiercy, Elke Jäger, Alfred Zippelius, Olga de la Rosa, Maries van den Broek, Steve Pascolo, Natko Nuber, Alexander Knuth, Christopher W. Thomson, Ashley Knights

Source: Cancer Immunology, Immunotherapy, Vol. 58, No 3 (2009) pp. 325-338
Knights, A J; Nuber, N; Thomson, C W; de la Rosa, O; Jäger, E; Tiercy, J M; van den Broek, Maries; Pascolo, S; Knuth, A; Zippelius, A (2009). Modified tumour antigen-encoding mRNA facilitates the analysis of naturally occurring and vaccine-induced CD4 and CD8 T cells in cancer patients. Cancer Immunology, Immunotherapy, 58(3):325-338.

Subject Terms: Cancer Research, Oncology, Immunology, Immunology and Allergy, Major histocompatibility complex, biology.protein, biology, Cytotoxic T cell, Cancer research, Streptamer, Antigen-presenting cell, CD28, T cell, medicine.anatomical_structure, medicine, Epitope, Antigen, ddc:616, Antibodies, Monoclonal/chemistry, Antigens, Neoplasm/chemistry/*metabolism, CD4-Positive T-Lymphocytes/*metabolism, CD8-Positive T-Lymphocytes/*metabolism, Cancer Vaccines, Carcinoma, Non-Small-Cell Lung/metabolism, Cell Line, Tumor, Epitopes/chemistry, Humans, Interferon-gamma/metabolism, Lung Neoplasms/metabolism, Models, Genetic, Neoplasms/*blood/*metabolism, Peptides/chemistry, RNA, Messenger/*metabolism, Clinic for Oncology and Hematology, 610 Medicine & health

File Description: application/pdf

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http://link.springer.com/content/pdf/10.1007/s00262-008-0556-8.pdf

6

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

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http://europepmc.org/articles/PMC2626680

7

Critical Influence of Natural Regulatory CD25+ T Cells on the Fate of Allografts in the Absence of Immunosuppression

Authors: Véronique Flamand, Herman Waldmann, Michel Goldman, Michel Y Braun, Luis Graca, Alain Le Moine, Fleur Samantha Benghiat, Sofia Buonocore, Sophie Detienne, Fabrice Moore

Source: Transplantation, 79 (6

Subject Terms: Transplantation, Immune system, Major histocompatibility complex, biology.protein, biology, T lymphocyte, Receptor, Immunosuppression, medicine.medical_treatment, medicine, IL-2 receptor, Interleukin, Immunology, Lymphocyte, medicine.anatomical_structure, Sciences bio-médicales et agricoles, Animals, Cytokines -- immunology, Cytokines -- metabolism, Female, Graft Rejection -- immunology, Graft Survival -- immunology, Heart Transplantation -- immunology, Heart Transplantation -- pathology, Lymphocyte Culture Test, Mixed, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Rats, Receptors, Antigen, T-Cell -- genetics, Receptors, Antigen, T-Cell -- immunology, Receptors, Interleukin-2 -- immunology, Receptors, Interleukin-2 -- metabolism, Skin Transplantation -- immunology, Skin Transplantation -- pathology, T-Lymphocytes -- immunology, T-Lymphocytes -- metabolism, Th1 Cells -- immunology, Th1 Cells -- metabolism, Th2 Cells -- immunology, Th2 Cells -- metabolism, Transplantation, Homologous -- immunology, Allograft, Regulatory T cell, Tolerance, hemic and immune systems, chemical and pharmacologic phenomena

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

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http://journals.lww.com/00007632-200503151-00005

8

Differential control of CD22 ligand expression on B and T lymphocytes, and enhanced expression in murine systemic lupus

Authors: Che-Leung Law, Thomas Moll, Shuichi Kikuchi, Akinori Ida, Liliane Fossati-Jimack, Frédéric Lajaunias, Shozo Izui, Eduardo Martinez-Soria

Source: Arthritis and Rheumatism, Vol. 48, No 6 (2003) pp. 1612-1621

Subject Terms: Pharmacology (medical), Immunology, Rheumatology, Immunology and Allergy, Antigen, ZAP70, Molecular biology, T lymphocyte, CD40, biology.protein, biology, Cytotoxic T cell, CD22, B-1 cell, Antigen-presenting cell, ddc:616.07, Animals, Antigens, CD/ metabolism, Antigens, CD22, Antigens, Differentiation, B-Lymphocyte/ metabolism, B-Lymphocytes/ metabolism, Cell Adhesion Molecules, Cells, Cultured, Disease Models, Animal, Female, Flow Cytometry, Lectins/ metabolism, Ligands, Lupus Erythematosus, Systemic/ metabolism/mortality/pathology, Lupus Nephritis/metabolism/mortality/pathology, Lymphocyte Activation, Male, Mice, Mice, Inbred BALB C, Mice, Transgenic, Receptors, Antigen, B-Cell/ metabolism, Recombinant Proteins, Spleen/cytology/immunology, Survival Rate, T-Lymphocytes/ metabolism, Up-Regulation, immune system diseases, skin and connective tissue diseases

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c194b4631f3c59e888afe34942391d8a
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fart.11021

9

Progressive loss of CD3 expression after HTLV-I infection results from chromatin remodeling affecting all the CD3 genes and persists despite early viral genes silencing

Authors: Gratiela Dobirta, Maria Moschitta, Makram Merimi, Philippe Martiat, Germain Manfouo-Foutsop, Arsène Burny, Karen Willard-Gallo, Haidar Akl, Bassam Badran

Source: Virology Journal, Vol 4, Iss 1, p 85 (2007)
Virology Journal, 4 (85
Virology Journal

Subject Terms: lcsh:Infectious and parasitic diseases, lcsh:RC109-216, Cancérologie, Antigens, CD3 -- genetics, Antigens, CD3 -- metabolism, CD4-Positive T-Lymphocytes -- metabolism, CD4-Positive T-Lymphocytes -- virology, Cell Line, Chromatin Assembly and Disassembly, Deoxyribonuclease I -- metabolism, Gene Expression, Gene Silencing, Genes, Viral, Human T-lymphotropic virus 1 -- genetics, Human T-lymphotropic virus 1 -- physiology, Humans, Promoter Regions, Genetic, T-Lymphocytes -- metabolism, T-Lymphocytes -- physiology, T-Lymphocytes -- virology, Transcription Factors -- metabolism, Transcription, Genetic, Virology, Infectious Diseases, Research, Gene expression, Gene, Chromatin remodeling, Promoter, Enhancer, Gene silencing, Epigenetics, Transcription factor, Biology, Molecular biology

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http://www.virologyj.com/content/4/1/85

10

Differentiation associated regulation of microRNA expression in vivo in human CD8+ T cell subsets

Authors: Petra Baumgaertner, Philippe Martiat, Yasuko Tsunetsugu-Yokota, Hussein Fayyad-Kazan, Brigitte Autran, Bassam Badran, Estelle Devevre, Anirudh Ramesh, Lukas Baitsch, Redouane Rouas, Marion Braun, Bruno Salaun, Antoine Roux, Daniel E. Speiser, Takuya Yamamoto, Pedro Romero, Victor Appay

Contributors: Division of Clinical Onco-Immunology, Université de Lausanne (UNIL)-Ludwig Center for Cancer Research, Department of Immunology, National Institute of Infectious Diseases, Shinjuku-ku, Laboratory of Experimental Hematology, Université libre de Bruxelles (ULB)-Institut Jules Bordet [Bruxelles], Faculté de Médecine [Bruxelles] (ULB), Université libre de Bruxelles (ULB)-Université libre de Bruxelles (ULB)-Faculté de Médecine [Bruxelles] (ULB), Université libre de Bruxelles (ULB), Laboratory of immunology, Department of Biochemistry, Lebanese University [Beirut] (LU)-Laboratory of Immunology, Immunité et Infection, Université Pierre et Marie Curie - Paris 6 (UPMC)-IFR113-Institut National de la Santé et de la Recherche Médicale (INSERM), Université de Lausanne (UNIL), Department of Biological Sciences, Cornell University [New York], This work was supported by grants from the Fondation MEDIC and the European Framework Program FP6 'Cancer immunotherapy' to B.S. and P. R.

Source: Journal of Translational Medicine, vol. 9, pp. 44
Journal of Translational Medicine
Journal of Translational Medicine, BioMed Central, 2011, 9 (1), pp.44. ⟨10.1186/1479-5876-9-44⟩
Journal of translational medicine, 9

Subject Terms: CD8-Positive T-Lymphocytes/metabolism, Cell Differentiation, Gene Expression Regulation, Humans, MicroRNAs/genetics, T-Lymphocyte Subsets, Research, MESH: CD8-Positive T-Lymphocytes, MESH: Cell Differentiation, MESH: Gene Expression Regulation, MESH: Humans, MESH: MicroRNAs, MESH: T-Lymphocyte Subsets, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, [SDV.IMM]Life Sciences [q-bio]/Immunology, General Biochemistry, Genetics and Molecular Biology, General Medicine, T cell differentiation, Cell biology, Biology, Immunology, Cytotoxic T cell, Cellular differentiation, CD8, Haematopoiesis, Regulation of gene expression, Lymphocyte differentiation, T cell, medicine.anatomical_structure, medicine, Cancérologie, CD8-Positive T-Lymphocytes -- metabolism, MicroRNAs -- genetics, Biochemistry, Genetics and Molecular Biology(all), Medicine(all)

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https://serval.unil.ch/notice/serval:BIB_CD67A5ADF46E

11

HDL interfere with the binding of T cell microparticles to human monocytes to inhibit pro-inflammatory cytokine production

Authors: Anna Scanu, Valery Combes, Danielle Burger, Rakel Carpintero, Lyssia Gruaz, Georges E. Grau, Karim J. Brandt, Dorothée Faille

Source: PLoS ONE, Vol 5, Iss 7, p e11869 (2010)
PLoS ONE
PLOS ONE, Vol. 5, No 7 (2010) P. e11869

Subject Terms: Medicine, Science, Multidisciplinary, CCL4, Flow cytometry, medicine.diagnostic_test, medicine, Chemokine, biology.protein, biology, Molecular biology, Cytokine, medicine.medical_treatment, CCL2, T cell, medicine.anatomical_structure, Monocyte, Tumor necrosis factor alpha, Immunology, Research Article, Cell Biology/Leukocyte Signaling and Gene Expression, Immunology/Autoimmunity, Immunology/Innate Immunity, Neurological Disorders/Multiple Sclerosis and Related Disorders, Rheumatology/Rheumatoid Arthritis, General Science & Technology, T-Lymphocytes, Monocytes, Cells, Cultured, Cell Line, Humans, Lipoproteins, HDL, Cytokines, Microscopy, Electron, Scanning, Interleukin 1 Receptor Antagonist Protein, Interleukin-1beta, Cell-Derived Microparticles, ddc:616, Cell-Derived Microparticles/*metabolism/ultrastructure, Cytokines/*metabolism, Interleukin 1 Receptor Antagonist Protein/metabolism, Interleukin-1beta/metabolism, Lipoproteins, HDL/*pharmacology, Monocytes/*drug effects/*metabolism/ultrastructure, T-Lymphocytes/*metabolism/ultrastructure

File Description: application/pdf

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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20686620/?tool=EBI

PDF Full Text

12

Tracing thymic output in older individuals

Authors: Wayne A. Mitchell, Richard Aspinall, Pierre Olivier Lang

Source: Clinical and Experimental Immunology, Vol. 161, No 3 (2010) pp. 497-503

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca750bb761cc551a6488f2c9bc649e7f
https://archive-ouverte.unige.ch/unige:21148

13

Inhibition of T cell-dependent and RANKL-dependent osteoclastogenic processes associated with high levels of bone mass in interleukin-15 receptor-deficient mice

Authors: Sylvie Ferrari-Lacraz, Souad Djaafar, Rachel Chicheportiche, Dominique D. Pierroz, S. Ferrari, Xin Xiao Zheng

Source: Arthritis and Rheumatism, Vol. 62, No 11 (2010) pp. 3300-3310

Subject Terms: ddc:610, ddc:616, ddc:618.97, Animals, Blotting, Western, Bone Density, Bone Resorption/*metabolism, Bone and Bones/*metabolism, Cell Differentiation, Cells, Cultured, Female, Mice, Mice, Knockout, Osteoclasts/*metabolism, RANK Ligand/genetics/*metabolism, Receptors, Interleukin-15/genetics/*metabolism, Reverse Transcriptase Polymerase Chain Reaction, Signal Transduction, Spleen/metabolism, T-Lymphocytes/*metabolism, Pharmacology (medical), Immunology, Rheumatology, Immunology and Allergy, Internal medicine, medicine.medical_specialty, medicine, RANKL, biology.protein, biology, Dendritic cell, Bone remodeling, Osteoclast, medicine.anatomical_structure, Interleukin 15, Bone resorption, Chemistry, Endocrinology, T cell, Bone mineral, musculoskeletal diseases

Access URL: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ddaccb1c4ab59a185d33edb19ef9f1a
https://archive-ouverte.unige.ch/unige:20904

14

Reviving function in CD4+ T cells adapted to persistent systemic antigen

Authors: Kathleen Weatherly, Sarah Dremier, Benoît Vokaer, Florence Gaudray, Isabelle Salmon, Magali Noval Rivas, Michel Goldman, Michel Y Braun, Marc Hazzan

Source: The Journal of immunology, 183 (7

Subject Terms: Sciences bio-médicales et agricoles, Amino Acid Sequence, Animals, Antigen Presentation -- immunology, CD4-Positive T-Lymphocytes -- immunology, CD4-Positive T-Lymphocytes -- metabolism, CD4-Positive T-Lymphocytes -- transplantation, Cells, Cultured, Female, H-Y Antigen -- immunology, Immune Tolerance, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Minor Histocompatibility Antigens -- immunology, Molecular Sequence Data, Skin Transplantation -- immunology, Immunology, Immunology and Allergy, ZAP70, IL-2 receptor, Cytotoxic T cell, Natural killer T cell, T cell, medicine.anatomical_structure, medicine, Biology, Antigen-presenting cell, Interleukin 21, CD28, CD4-Positive T-Lymphocytes -- immunology -- metabolism -- transplantation

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http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/50329

15

Hetero-oligomerization of CCR2, CCR5, and CXCR4 and the Protean Effects of 'Selective' Antagonists*

Authors: Marc Parmentier, Denis Sohy, Eneko Urizar, Jonathan A. Javitch, Patricia de Nadai, Hideaki Yano, Jean-Yves Springael, Aude Guillabert

Source: The Journal of biological chemistry, 284 (45

Subject Terms: Mechanisms of Signal Transduction, Cell Biology, Molecular Biology, Biochemistry, CC chemokine receptors, Chemokine receptor, XCL2, CCL15, Biology, CXC chemokine receptors, Cell biology, CCL21, CCR1, CCL13, Sciences bio-médicales et agricoles, Amides -- pharmacology, Animals, Cell Line, Cells, Cultured, Heterocyclic Compounds -- pharmacology, Humans, Mice, Mice, Inbred BALB C, Monocytes -- chemistry, Monocytes -- metabolism, Protein Multimerization -- drug effects, Quaternary Ammonium Compounds -- pharmacology, Receptors, CCR2 -- antagonists & inhibitors, Receptors, CCR2 -- chemistry, Receptors, CCR5 -- antagonists & inhibitors, Receptors, CCR5 -- chemistry, Receptors, CXCR4 -- antagonists & inhibitors, Receptors, CXCR4 -- chemistry, T-Lymphocytes -- chemistry, T-Lymphocytes -- metabolism

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https://europepmc.org/articles/PMC2781525/

16

Anti-leukemia activity of MS-275 histone deacetylase inhibitor implicates 4-1BBL/4-1BB immunomodulatory functions

Authors: Daniel Olive, Stéphane de Walque, Berengere Vire, Audrey Restouin, Carine Van Lint, Yves Collette

Source: PLoS ONE, Vol 4, Iss 9, p e7085 (2009)
PLoS ONE
PloS one, 4 (9

Subject Terms: lcsh:Medicine, lcsh:R, lcsh:Science, lcsh:Q, Research Article, Biochemistry/Chemical Biology of the Cell, Biochemistry/Transcription and Translation, Oncology/Hematological Malignancies, Sciences bio-médicales et agricoles, 4-1BB Ligand -- metabolism, Antigens, CD137 -- metabolism, Antineoplastic Agents -- pharmacology, Benzamides -- pharmacology, Cell Proliferation, Gene Expression Regulation, Leukemic, Humans, Hydroxamic Acids -- pharmacology, Immune System -- drug effects, Jurkat Cells, Leukemia -- drug therapy, Mutagenesis, Site-Directed, Pyridines -- pharmacology, Reverse Transcriptase Polymerase Chain Reaction, T-Lymphocytes -- metabolism, U937 Cells, Multidisciplinary, Vorinostat, medicine.drug, medicine, 4-1BB ligand, chemistry.chemical_compound, chemistry, Histone deacetylase, Jurkat cells, Biology, Molecular biology, Raji cell, Chromatin remodeling, Trichostatin A, Histone deacetylase inhibitor, medicine.drug_class

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http://europepmc.org/articles/PMC2738963?pdf=render

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17

CpG Methylation Controls Reactivation of HIV from Latency

Authors: Blazkova, Jana, Trejbalova, Katerina, Gondois-Rey, Françoise, Halfon, Philippe, Philibert, Patrick, Guiguen, Allan, Verdin, Eric, Olive, Daniel, Van Lint, Carine, Hejnar, Jiri, Hirsch, Ivan

Source: PLoS Pathogens, Vol 5, Iss 8, p e1000554 (2009)
PLoS Pathogens
PLoS pathogens, vol 5, iss 8
PLoS pathogens, 5 (8

Subject Terms: Virology, Genetics, Molecular Biology, Immunology, Microbiology, Parasitology, Provirus, Cancer research, HIV Long Terminal Repeat, DNA methylation, CpG site, Chromatin, Epigenetics, Biology, Virus latency, medicine.disease, medicine, Methylation, lcsh:Immunologic diseases. Allergy, lcsh:RC581-607, lcsh:Biology (General), lcsh:QH301-705.5, Research Article, Genetics and Genomics/Epigenetics, Molecular Biology/Chromatin Structure, Molecular Biology/DNA Methylation, Virology/Immune Evasion, Virology/Immunodeficiency Viruses, CD4-Positive T-Lymphocytes, Jurkat Cells, Clone Cells, Humans, Proviruses, HIV-1, Viremia, HIV Infections, Cloning, Molecular, Virus Latency, HIV Seronegativity, DNA Methylation, CpG Islands, Adult, Aged, Middle Aged, Female, Male, Promoter Regions, Genetic, Medical Microbiology, Sciences bio-médicales et agricoles, CD4-Positive T-Lymphocytes -- metabolism, Chromatin -- physiology, Cloning, Molecular, HIV Infections -- metabolism, HIV-1 -- genetics, HIV-1 -- physiology, Promoter Regions, Genetic, Proviruses -- genetics, Proviruses -- metabolism, Viremia -- genetics, Viremia -- metabolism, Virus Latency -- physiology, virus diseases

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18

Synergistic activation of HIV-1 expression by deacetylase inhibitors and prostratin: implications for treatment of latent infection

Contributors: Unité de Recherche en Biologie Moléculaire, Facultés Universitaires Notre Dame de la Paix (FUNDP) - Namur, Institut de Biologie de Lille, Institut Pasteur de Lille, Réseau International des Instituts Pasteur ( RIIP ) -Réseau International des Instituts Pasteur ( RIIP ) -Centre National de la Recherche Scientifique ( CNRS ), Laboratoire de Virologie [CHU Necker], Assistance publique - Hôpitaux de Paris (AP-HP)-CHU Necker - Enfants Malades [AP-HP], Agents pathogènes et inflammation - UFC (EA 4266) ( API ), Université de Franche-Comté ( UFC ), Service de médecine interne et maladies infectieuses, Université Paris-Sud - Paris 11 ( UP11 ) -Assistance publique - Hôpitaux de Paris (AP-HP)-Hôpital Bicêtre, Division of Infectious Diseases, CHR La réunion, Facultés Universitaires Notre Dame de la Paix (FUNDP), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Centre National de la Recherche Scientifique (CNRS), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Agents pathogènes et inflammation - UFC (EA 4266) (API), Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC), Hôpital Bicêtre-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)

Source: PloS one, 4 (6
PLoS ONE
PLoS ONE, Public Library of Science, 2009, 4 (6), pp.e6093. 〈10.1371/journal.pone.0006093〉
PLoS ONE, Public Library of Science, 2009, 4 (6), pp.e6093. ⟨10.1371/journal.pone.0006093⟩
PLoS ONE, Vol 4, Iss 6, p e6093 (2009)
Synergistic activation of HIV-1 expression by deacetylase inhibitors and prostratin: implications for treatment of latent infection. PLoS ONE, 4(6), 6093.San Franscisco, United StatesPublic Library of Science. (2009).

Subject Terms: Sciences bio-médicales et agricoles, Adult, Aged, Anti-HIV Agents -- pharmacology, CD8-Positive T-Lymphocytes -- metabolism, Cell Nucleus -- metabolism, Cytoplasm -- metabolism, Drug Synergism, Enzyme Inhibitors -- pharmacology, HIV Infections -- drug therapy, HIV-1 -- enzymology, HIV-1 -- metabolism, Humans, I-kappa B Proteins -- metabolism, Middle Aged, Monocytes -- virology, NF-kappa B -- antagonists & inhibitors, Nucleosomes -- metabolism, Phorbol Esters -- pharmacology, Virus Latency -- drug effects, MESH : Adult, MESH : Aged, MESH : Humans, MESH : I-kappa B Proteins, MESH : Middle Aged, MESH : Monocytes, MESH : NF-kappa B, MESH : Nucleosomes, MESH : Phorbol Esters, MESH : Virus Latency, MESH : Anti-HIV Agents, MESH : CD8-Positive T-Lymphocytes, MESH : Cell Nucleus, MESH : Cytoplasm, MESH : Drug Synergism, MESH : Enzyme Inhibitors, MESH : HIV Infections, MESH : HIV-1, [ SDV.MP.VIR ] Life Sciences [q-bio]/Microbiology and Parasitology/Virology, MESH: Adult, MESH: Aged, MESH: Humans, MESH: I-kappa B Proteins, MESH: Middle Aged, MESH: Monocytes, MESH: NF-kappa B, MESH: Nucleosomes, MESH: Phorbol Esters, MESH: Virus Latency, MESH: Anti-HIV Agents, MESH: CD8-Positive T-Lymphocytes, MESH: Cell Nucleus, MESH: Cytoplasm, MESH: Drug Synergism, MESH: Enzyme Inhibitors, MESH: HIV Infections, MESH: HIV-1, [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology, Research Article, Molecular Biology/Transcription Initiation and Activation, Virology/Persistence and Latency, Virology/Viral Replication and Gene Regulation, Infectious Diseases/HIV Infection and AIDS, Multidisciplinary, Molecular biology, Biology, Cancer research, Population, education.field_of_study, education, Viral replication, Prostratin, chemistry.chemical_compound, chemistry, IκBα, Virus latency, medicine.disease, medicine, Viral load, Histone deacetylase, Cell culture, lcsh:Medicine, lcsh:R, lcsh:Science, lcsh:Q, Anti-HIV Agents/pharmacology, CD8-Positive T-Lymphocytes/metabolism, Cell Nucleus/metabolism, Cytoplasm/metabolism, Enzyme Inhibitors/pharmacology, HIV Infections/drug therapy, HIV-1/enzymology/metabolism, I-kappa B Proteins/metabolism, Monocytes/virology, NF-kappa B/antagonists & inhibitors, Nucleosomes/metabolism, Phorbol Esters/pharmacology, Virus Latency/drug effects, Biochemistry, biophysics & molecular biology [Life sciences], Biochimie, biophysique & biologie moléculaire [Sciences du vivant]