Temat: "DENDRITIC cells" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Lymph node stromal cells support the maturation of pre-DCs into cDC-like cells via colony-stimulating factor 1.
Autorzy:: Wiechers C; Department Experimental Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Pezoldt J; Department Experimental Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.; Laboratory of Systems Biology and Genetics, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Beckstette M; Department Experimental Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.; Department of Computational Biology for Individualised Medicine, Centre for Individualised Infection Medicine, Helmholtz Centre for Infection Research and Hannover Medical School, Hannover, Germany.
Berner J; Institute for Cardiovascular Physiology and Pathophysiology, Biomedical Center, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Germany.; Walter-Brendel-Centre of Experimental Medicine, University Hospital, LMU Munich, Planegg-Martinsried, Germany.
Schraml BU; Institute for Cardiovascular Physiology and Pathophysiology, Biomedical Center, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Germany.; Walter-Brendel-Centre of Experimental Medicine, University Hospital, LMU Munich, Planegg-Martinsried, Germany.
Huehn J; Department Experimental Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.; Pokaż więcej
Źródło:: Immunology [Immunology] 2022 Aug; Vol. 166 (4), pp. 475-491. Date of Electronic Publication: 2022 Jun 02.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Dendritic Cells*/metabolism
Macrophage Colony-Stimulating Factor*/metabolism
Macrophage Colony-Stimulating Factor*/pharmacology
Cell Differentiation ; Cells, Cultured ; Cytokines/metabolism ; Lymph Nodes ; Stromal Cells ; T-Lymphocytes

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Skocz do pozycji: 2.

Tytuł:: Distinct antigen uptake receptors route to the same storage compartments for cross-presentation in dendritic cells.
Autorzy:: Ho NI; Department of Immunology, Leiden University Medical Center, Leiden, The Netherlands.
Camps MG; Department of Immunology, Leiden University Medical Center, Leiden, The Netherlands.
Garcia-Vallejo JJ; Department of Molecular Cell Biology and Immunology, VU University Medical Center, Amsterdam, The Netherlands.
Bos E; Department of Molecular Cell Biology, Section Electron Microscopy, Leiden University Medical Center, Leiden, The Netherlands.
Koster AJ; Department of Molecular Cell Biology, Section Electron Microscopy, Leiden University Medical Center, Leiden, The Netherlands.
Verdoes M; Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
van Kooyk Y; Department of Molecular Cell Biology and Immunology, VU University Medical Center, Amsterdam, The Netherlands.
Ossendorp F; Department of Immunology, Leiden University Medical Center, Leiden, The Netherlands.; Pokaż więcej
Źródło:: Immunology [Immunology] 2021 Nov; Vol. 164 (3), pp. 494-506. Date of Electronic Publication: 2021 Jun 30.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Cross-Priming*
Antigens/*metabolism
Dendritic Cells/*immunology
Lectins, C-Type/*metabolism
Receptors, IgG/*metabolism
Animals ; Antigen Presentation ; Antigens/immunology ; Cathepsins/metabolism ; Dendritic Cells/metabolism ; Dendritic Cells/ultrastructure ; Endosomes/immunology ; Endosomes/metabolism ; Endosomes/ultrastructure ; Histocompatibility Antigens Class I/metabolism ; Histocompatibility Antigens Class II/metabolism ; Lysosomes/immunology ; Lysosomes/metabolism ; Lysosomes/ultrastructure ; Mice ; Microscopy, Electron, Transmission ; Models, Animal ; NIH 3T3 Cells ; Primary Cell Culture

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Skocz do pozycji: 3.

Tytuł:: Immune control of Mycobacterium tuberculosis is dependent on both soluble TNFRp55 and soluble TNFRp75.
Autorzy:: Keeton R; Division of Immunology, Department of Pathology and Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Observatory, South Africa.
du Toit JP; Division of Immunology, Department of Pathology and Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Observatory, South Africa.
Hsu NJ; Division of Immunology, Department of Pathology and Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Observatory, South Africa.
Dube F; Division of Immunology, Department of Pathology and Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Observatory, South Africa.
Jacobs M; Division of Immunology, Department of Pathology and Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Observatory, South Africa.; National Health Laboratory Service, Johannesburg, South Africa.; Immunology of Infectious Disease Research Unit, University of Cape Town, Cape Town, South Africa.; Pokaż więcej
Źródło:: Immunology [Immunology] 2021 Nov; Vol. 164 (3), pp. 524-540. Date of Electronic Publication: 2021 Jul 08.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Dendritic Cells/*immunology
Mycobacterium tuberculosis/*immunology
Receptors, Tumor Necrosis Factor, Type I/*metabolism
Receptors, Tumor Necrosis Factor, Type II/*metabolism
Tuberculosis/*immunology
Animals ; Dendritic Cells/metabolism ; Disease Models, Animal ; Female ; Humans ; Male ; Mice ; Mice, Transgenic ; Receptors, Tumor Necrosis Factor, Type I/genetics ; Receptors, Tumor Necrosis Factor, Type II/genetics ; Tuberculosis/microbiology

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Skocz do pozycji: 4.

Tytuł:: Inducible ablation of CD11c cells to determine their role in skin wound repair.
Autorzy:: Li Z; Department of Biosciences, Biophysical Sciences Institute, Durham University, Durham, UK.; Department of Biology, Centre for Immunology and Infection, Hull York Medical School, York, UK.
Lamb R; Department of Biosciences, Biophysical Sciences Institute, Durham University, Durham, UK.
Coles MC; Department of Biology, Centre for Immunology and Infection, Hull York Medical School, York, UK.; Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Bennett CL; Institute of Immunity and Transplantation, University College London, London, UK.; Division of Cancer Studies, University College London, London, UK.
Ambler CA; Department of Biosciences, Biophysical Sciences Institute, Durham University, Durham, UK.; Pokaż więcej
Źródło:: Immunology [Immunology] 2021 May; Vol. 163 (1), pp. 105-111. Date of Electronic Publication: 2021 Mar 01.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Wound Healing*
CD11 Antigens/*deficiency
Dendritic Cells/*immunology
Skin/*immunology
Wounds and Injuries/*immunology
Animals ; CD11 Antigens/genetics ; Dendritic Cells/metabolism ; Disease Models, Animal ; Kinetics ; Langerhans Cells/immunology ; Langerhans Cells/metabolism ; Mice, Inbred C57BL ; Mice, Transgenic ; Skin/metabolism ; Skin/pathology ; Wounds and Injuries/genetics ; Wounds and Injuries/metabolism ; Wounds and Injuries/pathology ; Mice

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Skocz do pozycji: 5.

Tytuł:: PTBP1 is necessary for dendritic cells to regulate T-cell homeostasis and antitumour immunity.
Autorzy:: Geng G; State Key Laboratory of Experimental Hematology, State Key Laboratory of Medicinal Chemical Biology, College of Life Sciences, Nankai University, Tianjin, China.
Xu C; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Peng N; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Li Y; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Liu J; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Wu J; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Liang J; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Zhu Y; State Key Laboratory of Experimental Hematology, State Key Laboratory of Medicinal Chemical Biology, College of Life Sciences, Nankai University, Tianjin, China.
Shi L; State Key Laboratory of Experimental Hematology, State Key Laboratory of Medicinal Chemical Biology, College of Life Sciences, Nankai University, Tianjin, China.; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.; Pokaż więcej
Źródło:: Immunology [Immunology] 2021 May; Vol. 163 (1), pp. 74-85. Date of Electronic Publication: 2021 Feb 03.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Asthma/*enzymology
Dendritic Cells/*enzymology
Heterogeneous-Nuclear Ribonucleoproteins/*metabolism
Lung/*enzymology
Lymphocytes, Tumor-Infiltrating/*metabolism
Melanoma, Experimental/*enzymology
Polypyrimidine Tract-Binding Protein/*metabolism
Skin Neoplasms/*enzymology
T-Lymphocytes/*metabolism
Alternative Splicing ; Animals ; Asthma/genetics ; Asthma/immunology ; Asthma/pathology ; Cell Line, Tumor ; Cytokines/genetics ; Cytokines/metabolism ; Dendritic Cells/immunology ; Gene Expression Regulation ; Heterogeneous-Nuclear Ribonucleoproteins/genetics ; Histocompatibility Antigens Class II/metabolism ; Homeostasis ; Lung/immunology ; Lung/pathology ; Lymphocyte Activation ; Lymphocytes, Tumor-Infiltrating/immunology ; Melanoma, Experimental/genetics ; Melanoma, Experimental/immunology ; Melanoma, Experimental/metabolism ; Mice, Knockout ; Polypyrimidine Tract-Binding Protein/genetics ; Pyruvate Kinase/genetics ; Pyruvate Kinase/metabolism ; Skin Neoplasms/genetics ; Skin Neoplasms/immunology ; Skin Neoplasms/pathology ; T-Lymphocytes/immunology ; Tumor Escape ; Tumor Microenvironment ; Mice

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Skocz do pozycji: 6.

Tytuł:: Optimal CD8 T-cell memory formation following subcutaneous cytomegalovirus infection requires virus replication but not early dendritic cell responses.
Autorzy:: Dimonte S; Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
Gimeno-Brias S; Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
Marsden M; Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
Chapman L; Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
Sabberwal P; Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
Clement M; Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
Humphreys IR; Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.; Pokaż więcej
Źródło:: Immunology [Immunology] 2021 Oct; Vol. 164 (2), pp. 279-291. Date of Electronic Publication: 2021 Jun 13.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: CD8-Positive T-Lymphocytes/*immunology
Cytomegalovirus/*immunology
Cytomegalovirus Infections/*immunology
Dendritic Cells/*immunology
Immunologic Memory/*immunology
Skin/*immunology
Virus Replication/*immunology
Animals ; Antigens, Viral/immunology ; CD8-Positive T-Lymphocytes/virology ; Cytomegalovirus Infections/virology ; Dendritic Cells/virology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Skin/virology

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Skocz do pozycji: 7.

Tytuł:: Melanoma tumour‐derived glycans hijack dendritic cell subsets through C‐type lectin receptor binding.
Autorzy:: Niveau, Camille (AUTHOR)
Sosa Cuevas, Eleonora (AUTHOR)
Roubinet, Benoît (AUTHOR)
Pezet, Mylène (AUTHOR)
Thépaut, Michel (AUTHOR)
Mouret, Stéphane (AUTHOR)
Charles, Julie (AUTHOR)
Fieschi, Franck (AUTHOR)
Landemarre, Ludovic (AUTHOR)
Chaperot, Laurence (AUTHOR)
Saas, Philippe (AUTHOR)
Aspord, Caroline (AUTHOR); Pokaż więcej
Źródło:: Immunology. Feb2024, Vol. 171 Issue 2, p286-311. 26p.

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Skocz do pozycji: 8.

Tytuł:: Quantitative and qualitative alterations of circulating myeloid cells and plasmacytoid DC in SARS-CoV-2 infection.
Autorzy:: Peruzzi B; Flow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.
Bencini S; Flow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.
Capone M; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Mazzoni A; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Maggi L; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Salvati L; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Vanni A; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Orazzini C; Flow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.
Nozzoli C; Internal Medicine Unit 1, AOU Careggi, Florence, Italy.
Morettini A; Internal Medicine Unit 2, AOU Careggi, Florence, Italy.
Poggesi L; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.; Internal Medicine Unit 3, AOU Careggi, Florence, Italy.
Pieralli F; High Intensity Internal Medicine, AOU Careggi, Florence, Italy.
Peris A; Intensive Care Unit, AOU Careggi, Florence, Italy.
Bartoloni A; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.; Infectious and Tropical Diseases Unit, AOU Careggi, Florence, Italy.
Vannucchi AM; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.; Center for Research and Innovation on Myeloproliferative Neoplasms (CRIMM), SOD Hematology, University of Florence and AOU Careggi, Florence, Italy.
Liotta F; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.; Immunology and Cell Therapy Unit, AOU Careggi, Florence, Italy.
Caporale R; Flow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.
Cosmi L; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.; Immunology and Cell Therapy Unit, AOU Careggi, Florence, Italy.
Annunziato F; Flow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.; Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.; Pokaż więcej
Źródło:: Immunology [Immunology] 2020 Dec; Vol. 161 (4), pp. 345-353. Date of Electronic Publication: 2020 Oct 06.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: COVID-19/*immunology
Dendritic Cells/*immunology
Myeloid Cells/*immunology
Adult ; Aged ; COVID-19/pathology ; Dendritic Cells/pathology ; Female ; Flow Cytometry ; Humans ; Intensive Care Units ; Male ; Myeloid Cells/pathology

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Skocz do pozycji: 9.

Tytuł:: Conditional knockout of oestrogen receptor alpha in CD11c cells impacts female survival and inflammatory cytokine profile in murine lupus.
Autorzy:: Lennard Richard ML; Department of Medicine, Division of Rheumatology & Immunology, Medical University of South Carolina, Charleston, South Carolina, USA.
Wirth JR; Department of Medicine, Division of Rheumatology & Immunology, Medical University of South Carolina, Charleston, South Carolina, USA.
Khatiwada A; Department of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
Chung D; Department of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, Ohio, USA.
Gilkeson GS; Department of Medicine, Division of Rheumatology & Immunology, Medical University of South Carolina, Charleston, South Carolina, USA.; Medical Research Service, Ralph H. Johnson Veterans Affairs Medical Center, Charleston, South Carolina, USA.
Cunningham MA; Department of Medicine, Division of Rheumatology & Immunology, Medical University of South Carolina, Charleston, South Carolina, USA.; Pokaż więcej
Źródło:: Immunology [Immunology] 2022 Nov; Vol. 167 (3), pp. 354-367. Date of Electronic Publication: 2022 Jul 30.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:: Estrogen Receptor alpha*/genetics
Estrogen Receptor alpha*/metabolism
Interleukin-17*/metabolism
Animals ; CD11c Antigen/metabolism ; Dendritic Cells ; Estrogens/metabolism ; Female ; Inflammation/genetics ; Inflammation/metabolism ; Interferons/metabolism ; Mice ; Toll-Like Receptors/metabolism

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Skocz do pozycji: 10.

Tytuł:: Signalling lymphocyte activation molecule family member 9 is found on select subsets of antigen-presenting cells and promotes resistance to Salmonella infection.
Autorzy:: Wilson TJ; Department of Microbiology, Miami University, Oxford, OH, USA.; Department of Medicine, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.
Clare S; Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Mikulin J; Department of Microbiology, Miami University, Oxford, OH, USA.
Johnson CM; MRC Laboratory of Molecular Biology, Cambridge, UK.
Harcourt K; Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Lyons PA; Department of Medicine, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.; Cambridge Institute for Therapeutic Immunology and Infectious Disease, Department of Medicine, University of Cambridge, Cambridge, UK.
Dougan G; Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.; Cambridge Institute for Therapeutic Immunology and Infectious Disease, Department of Medicine, University of Cambridge, Cambridge, UK.
Smith KGC; Department of Medicine, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.; Cambridge Institute for Therapeutic Immunology and Infectious Disease, Department of Medicine, University of Cambridge, Cambridge, UK.; Pokaż więcej
Źródło:: Immunology [Immunology] 2020 Apr; Vol. 159 (4), pp. 393-403. Date of Electronic Publication: 2020 Jan 28.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Dendritic Cells/*immunology
Host-Pathogen Interactions/*immunology
Liver/*immunology
Salmonella Infections/*immunology
Salmonella typhimurium/*immunology
Signaling Lymphocytic Activation Molecule Family/*immunology
Animals ; B-Lymphocytes/immunology ; B-Lymphocytes/microbiology ; Cell Differentiation ; Dendritic Cells/drug effects ; Dendritic Cells/microbiology ; Gene Expression Regulation ; Granulocyte-Macrophage Colony-Stimulating Factor/genetics ; Granulocyte-Macrophage Colony-Stimulating Factor/immunology ; Host-Pathogen Interactions/genetics ; Humans ; Interleukin-1beta/genetics ; Interleukin-1beta/immunology ; Lipopolysaccharides/pharmacology ; Liver/microbiology ; Macrophages/drug effects ; Macrophages/immunology ; Macrophages/microbiology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Monocytes/drug effects ; Monocytes/immunology ; Monocytes/microbiology ; Salmonella Infections/genetics ; Salmonella Infections/microbiology ; Salmonella typhimurium/pathogenicity ; Signal Transduction ; Signaling Lymphocytic Activation Molecule Family/deficiency ; Signaling Lymphocytic Activation Molecule Family/genetics ; THP-1 Cells ; Tumor Necrosis Factor-alpha/genetics ; Tumor Necrosis Factor-alpha/immunology

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Skocz do pozycji: 11.

Tytuł:: Body fluid from the parasitic worm Ascaris suum inhibits broad-acting pro-inflammatory programs in dendritic cells.
Autorzy:: Arora P; Department of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.
Moll JM; Department of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.
Andersen D; Department of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.
Workman CT; Department of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.
Williams AR; Parasitology and Aquatic Pathobiology, University of Copenhagen, Copenhagen, Denmark.
Kristiansen K; Laboratory of Genomics and Molecular Biomedicine, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Brix S; Department of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.; Pokaż więcej
Źródło:: Immunology [Immunology] 2020 Mar; Vol. 159 (3), pp. 322-334. Date of Electronic Publication: 2019 Dec 03.
Typ publikacji:: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Ascaris suum/*immunology
Body Fluids/*immunology
Dendritic Cells/*immunology
Inflammation Mediators/*immunology
Th1 Cells/*immunology
Th17 Cells/*immunology
Animals ; Ascaris suum/metabolism ; Ascaris suum/pathogenicity ; Bacteria/immunology ; Bacteria/metabolism ; Bacteria/pathogenicity ; Body Fluids/metabolism ; Butyrates/pharmacology ; Cell Communication ; Cytokines/metabolism ; Cytokines/pharmacology ; Dendritic Cells/drug effects ; Dendritic Cells/metabolism ; Gastrointestinal Microbiome ; Host-Parasite Interactions ; Humans ; Inflammation Mediators/metabolism ; Lipopolysaccharides/pharmacology ; Myeloid Differentiation Factor 88/metabolism ; Signal Transduction ; Th1 Cells/metabolism ; Th17 Cells/metabolism ; Toll-Like Receptor 4/metabolism

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Skocz do pozycji: 12.

Tytuł:: Protection of Batf3-deficient mice from experimental cerebral malaria correlates with impaired cytotoxic T-cell responses and immune regulation.
Autorzy:: Kuehlwein JM; Institute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Borsche M; Institute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Korir PJ; Institute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Risch F; Institute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Mueller AK; Parasitology Unit, Centre for Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.; DZIF German Center for Infection Research, Partner Site Heidelberg, Heidelberg, Germany.
Hübner MP; Institute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Hildner K; Medical Department 1, University Hospital Erlangen, Erlangen, Germany.
Hoerauf A; Institute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.; DZIF German Center for Infection Research, Partner Site Bonn-Cologne, Bonn, Germany.
Dunay IR; Institute of Inflammation and Neurodegeneration, University of Magdeburg, Magdeburg, Germany.
Schumak B; Institute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.; Pokaż więcej
Źródło:: Immunology [Immunology] 2020 Feb; Vol. 159 (2), pp. 193-204. Date of Electronic Publication: 2019 Nov 13.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Basic-Leucine Zipper Transcription Factors/*deficiency
Brain/*immunology
Dendritic Cells/*immunology
Malaria, Cerebral/*prevention & control
Plasmodium berghei/*pathogenicity
Repressor Proteins/*deficiency
T-Lymphocytes, Cytotoxic/*immunology
Animals ; Basic-Leucine Zipper Transcription Factors/genetics ; Blood-Brain Barrier/immunology ; Blood-Brain Barrier/parasitology ; Brain/metabolism ; Brain/parasitology ; Cells, Cultured ; Dendritic Cells/metabolism ; Dendritic Cells/parasitology ; Disease Models, Animal ; Female ; Granzymes/immunology ; Granzymes/metabolism ; Host-Parasite Interactions ; Interferon-gamma/immunology ; Interferon-gamma/metabolism ; Interleukin-10/immunology ; Interleukin-10/metabolism ; Malaria, Cerebral/immunology ; Malaria, Cerebral/metabolism ; Malaria, Cerebral/parasitology ; Mice, Inbred C57BL ; Mice, Knockout ; Plasmodium berghei/immunology ; Repressor Proteins/genetics ; Spleen/immunology ; Spleen/metabolism ; Spleen/parasitology ; T-Lymphocytes, Cytotoxic/metabolism ; T-Lymphocytes, Cytotoxic/parasitology

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Skocz do pozycji: 13.

Tytuł:: CD8α conventional dendritic cells control Vβ T-cell immunity in response to Staphylococcus aureus infection in mice.
Autorzy:: Zhang W; Shanghai Public Health Clinical Center &, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Xu L; Shanghai Public Health Clinical Center &, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Zhang X; Shanghai Public Health Clinical Center &, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Xu J; Shanghai Public Health Clinical Center &, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Jin JO; Shanghai Public Health Clinical Center &, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.; Department of Medical Biotechnology, Yeungnam University, Gyeongsan, South Korea.; Pokaż więcej
Źródło:: Immunology [Immunology] 2020 Apr; Vol. 159 (4), pp. 404-412. Date of Electronic Publication: 2020 Jan 21.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: CD8 Antigens/*immunology
CD8-Positive T-Lymphocytes/*immunology
Dendritic Cells/*immunology
Receptors, Antigen, T-Cell, alpha-beta/*immunology
Staphylococcal Infections/*immunology
Staphylococcus aureus/*immunology
Animals ; CD4-Positive T-Lymphocytes/immunology ; CD4-Positive T-Lymphocytes/microbiology ; CD4-Positive T-Lymphocytes/pathology ; CD8 Antigens/deficiency ; CD8 Antigens/genetics ; CD8-Positive T-Lymphocytes/microbiology ; CD8-Positive T-Lymphocytes/pathology ; Cell Lineage/immunology ; Dendritic Cells/microbiology ; Gene Expression ; Host-Pathogen Interactions/immunology ; Immunity, Cellular ; Interferon-gamma/genetics ; Interferon-gamma/immunology ; Interleukin-17/genetics ; Interleukin-17/immunology ; Lymphocyte Activation ; Mice ; Mice, Inbred C57BL ; Phagocytosis ; Receptors, Antigen, T-Cell, alpha-beta/genetics ; Spleen/immunology ; Spleen/microbiology ; Spleen/pathology ; Staphylococcal Infections/microbiology ; Staphylococcal Infections/pathology ; Staphylococcus aureus/pathogenicity

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Skocz do pozycji: 14.

Tytuł:: Tissue-resident innate immunity in the lung.
Autorzy:: Ardain A; Africa Health Research Institute, KwaZulu-Natal, South Africa.; College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.
Marakalala MJ; Africa Health Research Institute, KwaZulu-Natal, South Africa.; Department of Infection and Immunity, University College London, London, UK.
Leslie A; Africa Health Research Institute, KwaZulu-Natal, South Africa.; Department of Infection and Immunity, University College London, London, UK.; Pokaż więcej
Źródło:: Immunology [Immunology] 2020 Mar; Vol. 159 (3), pp. 245-256. Date of Electronic Publication: 2019 Nov 21.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:: Immunity, Innate*
Dendritic Cells/*immunology
Lung/*immunology
Lung Diseases/*immunology
Lymphocytes/*immunology
Macrophages/*immunology
Animals ; Cellular Microenvironment ; Dendritic Cells/metabolism ; Dendritic Cells/pathology ; Humans ; Killer Cells, Natural/immunology ; Lung/metabolism ; Lung/pathology ; Lung Diseases/metabolism ; Lung Diseases/pathology ; Lymphocytes/metabolism ; Lymphocytes/pathology ; Macrophages/metabolism ; Macrophages/pathology ; Signal Transduction

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Skocz do pozycji: 15.

Tytuł:: Blockage of immune checkpoint molecules increases T-cell priming potential of dendritic cell vaccine.
Autorzy:: Hassannia H; Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.; Immunogenetic Research Center, Faculty of Medicine and Amol Faculty of Paramedical Sciences, Mazandaran University of Medical Sciences, Sari, Iran.
Ghasemi Chaleshtari M; Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Atyabi F; Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Nosouhian M; Department of Biochemistry, Falavarjan Branch, Islamic Azad University, Isfahan, Iran.
Masjedi A; Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Hojjat-Farsangi M; Bioclinicum, Department of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.; The Persian Gulf Marine Biotechnology Medicine Research Center, Bushehr University of Medical Sciences, Bushehr, Iran.
Namdar A; Department of Dentistry, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
Azizi G; Non-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran.
Mohammadi H; Non-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran.
Ghalamfarsa G; Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.
Sabz G; Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.
Hasanzadeh S; Department of Internal Medicine, Yasuj University of Medical Sciences, Yasuj, Iran.
Yousefi M; Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Jadidi-Niaragh F; Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.; Department of Immunology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.; Pokaż więcej
Źródło:: Immunology [Immunology] 2020 Jan; Vol. 159 (1), pp. 75-87. Date of Electronic Publication: 2019 Oct 24.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Lymphocyte Activation*
RNAi Therapeutics*
B7-H1 Antigen/*immunology
Breast Neoplasms/*therapy
Cancer Vaccines/*immunology
Colonic Neoplasms/*therapy
Dendritic Cells/*transplantation
Lymphocytes, Tumor-Infiltrating/*immunology
Programmed Cell Death 1 Receptor/*immunology
T-Lymphocytes/*immunology
Animals ; Apoptosis ; B7-H1 Antigen/genetics ; B7-H1 Antigen/metabolism ; Breast Neoplasms/genetics ; Breast Neoplasms/immunology ; Breast Neoplasms/metabolism ; Cell Line, Tumor ; Cell Movement ; Coculture Techniques ; Colonic Neoplasms/genetics ; Colonic Neoplasms/immunology ; Colonic Neoplasms/metabolism ; Cytokines/immunology ; Cytokines/metabolism ; Dendritic Cells/immunology ; Dendritic Cells/metabolism ; Female ; Lymphocytes, Tumor-Infiltrating/metabolism ; Mice, Inbred BALB C ; Programmed Cell Death 1 Receptor/genetics ; Programmed Cell Death 1 Receptor/metabolism ; Signal Transduction ; T-Lymphocytes/metabolism

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Skocz do pozycji: 16.

Tytuł:: The immunosuppressive functions of two novel tick serpins, HlSerpin-a and HlSerpin-b, from Haemaphysalis longicornis.
Autorzy:: Wang F; Institutes of Biology and Medical Sciences, Jiangsu Key Laboratory of Infection and Immunity, Soochow University, Suzhou, China.
Song Z; Institutes of Biology and Medical Sciences, Jiangsu Key Laboratory of Infection and Immunity, Soochow University, Suzhou, China.
Chen J; NHC Key Lab of Reproduction Regulation (Shanghai Institute of Planned Parenthood Research), Fudan University, Shanghai, China.
Wu Q; NHC Key Lab of Reproduction Regulation (Shanghai Institute of Planned Parenthood Research), Fudan University, Shanghai, China.
Zhou X; School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
Ni X; NHC Key Lab of Reproduction Regulation (Shanghai Institute of Planned Parenthood Research), Fudan University, Shanghai, China.
Dai J; Institutes of Biology and Medical Sciences, Jiangsu Key Laboratory of Infection and Immunity, Soochow University, Suzhou, China.; Pokaż więcej
Źródło:: Immunology [Immunology] 2020 Jan; Vol. 159 (1), pp. 109-120. Date of Electronic Publication: 2019 Nov 10.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Arthritis, Experimental/*prevention & control
Arthropod Proteins/*pharmacology
Dendritic Cells/*drug effects
Immunosuppressive Agents/*pharmacology
Ixodidae/*metabolism
Joints/*drug effects
Macrophages/*drug effects
Serpins/*pharmacology
Animals ; Arthritis, Experimental/immunology ; Arthritis, Experimental/metabolism ; Arthritis, Experimental/pathology ; Arthropod Proteins/genetics ; Arthropod Proteins/isolation & purification ; Cytokines/metabolism ; Dendritic Cells/immunology ; Dendritic Cells/metabolism ; Immunosuppressive Agents/isolation & purification ; Ixodidae/genetics ; Joints/immunology ; Joints/metabolism ; Joints/pathology ; Macrophages/immunology ; Macrophages/metabolism ; Male ; Mice ; Mice, Inbred DBA ; Protein Conformation ; RAW 264.7 Cells ; Saliva/metabolism ; Serpins/genetics ; Serpins/isolation & purification ; Structure-Activity Relationship

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Skocz do pozycji: 17.

Tytuł:: Tolerogenic dendritic cell transfer ameliorates systemic lupus erythematosus in mice.
Autorzy:: Funes SC; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Ríos M; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Gómez-Santander F; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Fernández-Fierro A; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Altamirano-Lagos MJ; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Rivera-Perez D; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Pulgar-Sepúlveda R; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Jara EL; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Rebolledo-Zelada D; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Villarroel A; Departamento de Anatomía Patológica, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Roa JC; Departamento de Anatomía Patológica, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Mackern-Oberti JP; Instituto de Medicina y Biología Experimental de Cuyo, IMBECU CCT Mendoza- CONICET, Mendoza, Argentina.; Instituto de Fisiología, Facultad de Ciencias Médicas, Universidad Nacional de Cuyo, Mendoza, Argentina.
Kalergis AM; Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.; Departamento de Endocrinología, Escuela de Medicina, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.; Pokaż więcej
Źródło:: Immunology [Immunology] 2019 Dec; Vol. 158 (4), pp. 322-339. Date of Electronic Publication: 2019 Oct 07.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Dendritic Cells/*immunology
Immunotherapy, Adoptive/*methods
Kidney/*pathology
Lupus Erythematosus, Systemic/*therapy
T-Lymphocytes, Regulatory/*immunology
Animals ; Antibodies, Antinuclear/blood ; Cell Differentiation ; Cells, Cultured ; Dendritic Cells/transplantation ; Dexamethasone/metabolism ; Disease Models, Animal ; Humans ; Immune Tolerance ; Lupus Erythematosus, Systemic/immunology ; Lymphocyte Activation ; Mice ; Mice, Inbred MRL lpr ; Pyrazines/metabolism ; Pyrroles/metabolism ; Rosiglitazone/metabolism

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Skocz do pozycji: 18.

Tytuł:: CD38 modulates respiratory syncytial virus-driven proinflammatory processes in human monocyte-derived dendritic cells.
Autorzy:: Schiavoni I; Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Scagnolari C; Department of Molecular Medicine, Laboratory of Virology affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Sapienza University, Rome, Italy.
Horenstein AL; Laboratory of Immunogenetics, Department of Medical Sciences, University of Torino, Torino, Italy.; CERMS, University of Torino, Torino, Italy.
Leone P; Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Pierangeli A; Department of Molecular Medicine, Laboratory of Virology affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Sapienza University, Rome, Italy.
Malavasi F; Laboratory of Immunogenetics, Department of Medical Sciences, University of Torino, Torino, Italy.; CERMS, University of Torino, Torino, Italy.; Transplantation Immunology 'Città della Salute e della Scienza' Hospital, Torino, Italy.
Ausiello CM; Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Fedele G; Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.; Pokaż więcej
Źródło:: Immunology [Immunology] 2018 May; Vol. 154 (1), pp. 122-131. Date of Electronic Publication: 2017 Dec 18.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: ADP-ribosyl Cyclase 1/*metabolism
Dendritic Cells/*enzymology
Dendritic Cells/*virology
Membrane Glycoproteins/*metabolism
Respiratory Syncytial Virus Infections/*enzymology
Respiratory Syncytial Virus Infections/*virology
Respiratory Syncytial Virus, Human/*immunology
ADP-ribosyl Cyclase 1/antagonists & inhibitors ; ADP-ribosyl Cyclase 1/genetics ; ADP-ribosyl Cyclase 1/immunology ; Antiviral Agents/therapeutic use ; Cells, Cultured ; Cyclic ADP-Ribose/metabolism ; Dendritic Cells/drug effects ; Dendritic Cells/immunology ; Enzyme Activation ; Enzyme Inhibitors/therapeutic use ; Host-Pathogen Interactions ; Humans ; Interferon Type I/metabolism ; Membrane Glycoproteins/antagonists & inhibitors ; Membrane Glycoproteins/genetics ; Membrane Glycoproteins/immunology ; Oxidative Stress ; Reactive Oxygen Species/metabolism ; Respiratory Syncytial Virus Infections/drug therapy ; Respiratory Syncytial Virus Infections/immunology ; Signal Transduction

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Skocz do pozycji: 19.

Tytuł:: MicroRNA signature of central nervous system-infiltrating dendritic cells in an animal model of multiple sclerosis.
Autorzy:: Hoye ML; Department of Neurology, Washington University School of Medicine, St Louis, MO, USA.
Archambault AS; Department of Neurology, Washington University School of Medicine, St Louis, MO, USA.
Gordon TM; Department of Neurology, Washington University School of Medicine, St Louis, MO, USA.
Oetjen LK; Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
Cain MD; Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
Klein RS; Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.; The Hope Center for Neurological Disorders, Washington University School of Medicine, St Louis, MO, USA.
Crosby SD; Genome Technology Access Center, Washington University School of Medicine, St Louis, MO, USA.
Kim BS; Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.; Department of Immunology & Pathology, Washington University School of Medicine, St Louis, MO, USA.; Center for the Study of Itch, Washington University School of Medicine, St Louis, MO, USA.
Miller TM; Department of Neurology, Washington University School of Medicine, St Louis, MO, USA.; The Hope Center for Neurological Disorders, Washington University School of Medicine, St Louis, MO, USA.
Wu GF; Department of Neurology, Washington University School of Medicine, St Louis, MO, USA.; The Hope Center for Neurological Disorders, Washington University School of Medicine, St Louis, MO, USA.; Department of Immunology & Pathology, Washington University School of Medicine, St Louis, MO, USA.; Pokaż więcej
Źródło:: Immunology [Immunology] 2018 Sep; Vol. 155 (1), pp. 112-122. Date of Electronic Publication: 2018 May 10.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Central Nervous System/*immunology
Dendritic Cells/*immunology
Dendritic Cells/*metabolism
Encephalomyelitis, Autoimmune, Experimental/*immunology
MicroRNAs/*immunology
Multiple Sclerosis/*immunology
Animals ; Dendritic Cells/cytology ; Disease Models, Animal ; Inflammation/immunology ; Mice ; Mice, Inbred C57BL

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Skocz do pozycji: 20.

Tytuł:: Activation of T cell checkpoint pathways during β-cell antigen presentation by engineered dendritic cells promotes protection from type 1 diabetes.
Autorzy:: Gudi RR; Department of Microbiology and Immunology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
Perez N; Department of Surgery, College of Medicine, University of Illinois, Chicago, Illinois, USA.
Karumuthil-Melethil S; Department of Surgery, College of Medicine, University of Illinois, Chicago, Illinois, USA.
Li G; Department of Surgery, College of Medicine, University of Illinois, Chicago, Illinois, USA.
Vasu C; Department of Microbiology and Immunology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.; Department of Surgery, College of Medicine, University of Illinois, Chicago, Illinois, USA.; Pokaż więcej
Źródło:: Immunology [Immunology] 2022 Jul; Vol. 166 (3), pp. 341-356. Date of Electronic Publication: 2022 Apr 22.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:: Diabetes Mellitus, Experimental*/pathology
Diabetes Mellitus, Type 1*/metabolism
Hyperglycemia*/metabolism
Hyperglycemia*/pathology
Animals ; Antigen Presentation ; CTLA-4 Antigen/metabolism ; Dendritic Cells ; Immune Tolerance ; Ligands ; Mice ; Receptors, Immunologic ; T-Lymphocytes, Regulatory

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