Nature Immunology, ISSN 1529-2908, 02/2011, Volume 12, Issue 2, pp. 151 - 159
Plasma cells are of crucial importance for long-term immune protection. It is thought that long-lived plasma cells survive in specialized niches in the bone...
SURVIVAL | IMMUNE-RESPONSE | MEMORY B-CELLS | IN-VIVO | CXCR4 | CHEMOKINE | IMMUNOLOGY | STROMAL CELLS | MATURATION | EXPRESSION | APRIL | Tumor Necrosis Factor Ligand Superfamily Member 13 - immunology | Eosinophils - metabolism | Bone Marrow - immunology | Cells, Cultured | Adoptive Transfer | Blood Component Removal | Cell Survival - immunology | Eosinophils - immunology | Tumor Necrosis Factor Ligand Superfamily Member 13 - metabolism | Antigens, Differentiation - biosynthesis | Animals | Apoptosis - immunology | Bone Marrow - pathology | Interleukin-6 - immunology | Immunologic Memory | Plasma Cells - metabolism | Eosinophils - pathology | Mice | Mice, Inbred BALB C | Interleukin-6 - metabolism | Plasma Cells - cytology | Plasma Cells - immunology | Physiological aspects | Bone marrow | Plasma cells | Research | Eosinophils
SURVIVAL | IMMUNE-RESPONSE | MEMORY B-CELLS | IN-VIVO | CXCR4 | CHEMOKINE | IMMUNOLOGY | STROMAL CELLS | MATURATION | EXPRESSION | APRIL | Tumor Necrosis Factor Ligand Superfamily Member 13 - immunology | Eosinophils - metabolism | Bone Marrow - immunology | Cells, Cultured | Adoptive Transfer | Blood Component Removal | Cell Survival - immunology | Eosinophils - immunology | Tumor Necrosis Factor Ligand Superfamily Member 13 - metabolism | Antigens, Differentiation - biosynthesis | Animals | Apoptosis - immunology | Bone Marrow - pathology | Interleukin-6 - immunology | Immunologic Memory | Plasma Cells - metabolism | Eosinophils - pathology | Mice | Mice, Inbred BALB C | Interleukin-6 - metabolism | Plasma Cells - cytology | Plasma Cells - immunology | Physiological aspects | Bone marrow | Plasma cells | Research | Eosinophils
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 513, Issue 7519, pp. 564 - 568
FOXP3+ regulatory T cells (T-reg cells) are abundant in the intestine, where they prevent dysregulated inflammatory responses to self and environmental...
DEPENDENT COLITIS | RESPONSES | COMPLEX | INFLAMMATORY-BOWEL-DISEASE | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION FACTOR FOXP3 | ULCERATIVE-COLITIS | AMELIORATES EXPERIMENTAL COLITIS | CYTOKINE | MICE | SOLUBLE ST2 | Colon - cytology | Inflammation - pathology | Immunity, Mucosal | Colitis - pathology | Colon - immunology | Male | Interleukins - metabolism | Intestines - immunology | T-Lymphocytes, Regulatory - immunology | Receptors, Interleukin - metabolism | Signal Transduction - immunology | Inflammation - metabolism | Interleukins - immunology | T-Lymphocytes, Regulatory - cytology | Female | Colitis - immunology | Disease Models, Animal | Intestines - pathology | Colon - pathology | Interleukin-33 | Mice, Inbred C57BL | Thymus Gland - cytology | Inflammation - immunology | Interleukin-23 - immunology | Interleukins - antagonists & inhibitors | Animals | Mice | Transforming Growth Factor beta - metabolism | Intestines - cytology | Immune response | Interleukins | Gastrointestinal diseases | Physiological aspects | Genetic aspects | Research | T cells | Proteins | Signal transduction | Phosphorylation | Transcription factors | Rodents | T cell receptors | Colon | RNA polymerase | Gene expression | Binding sites
DEPENDENT COLITIS | RESPONSES | COMPLEX | INFLAMMATORY-BOWEL-DISEASE | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION FACTOR FOXP3 | ULCERATIVE-COLITIS | AMELIORATES EXPERIMENTAL COLITIS | CYTOKINE | MICE | SOLUBLE ST2 | Colon - cytology | Inflammation - pathology | Immunity, Mucosal | Colitis - pathology | Colon - immunology | Male | Interleukins - metabolism | Intestines - immunology | T-Lymphocytes, Regulatory - immunology | Receptors, Interleukin - metabolism | Signal Transduction - immunology | Inflammation - metabolism | Interleukins - immunology | T-Lymphocytes, Regulatory - cytology | Female | Colitis - immunology | Disease Models, Animal | Intestines - pathology | Colon - pathology | Interleukin-33 | Mice, Inbred C57BL | Thymus Gland - cytology | Inflammation - immunology | Interleukin-23 - immunology | Interleukins - antagonists & inhibitors | Animals | Mice | Transforming Growth Factor beta - metabolism | Intestines - cytology | Immune response | Interleukins | Gastrointestinal diseases | Physiological aspects | Genetic aspects | Research | T cells | Proteins | Signal transduction | Phosphorylation | Transcription factors | Rodents | T cell receptors | Colon | RNA polymerase | Gene expression | Binding sites
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2015, Volume 112, Issue 13, pp. 4056 - 4061
During infection, the release of damage-associated molecular patterns, so-called “alarmins,” orchestrates the immune response. The alarmin IL-33 plays a role...
ST2 | CD4 T cell | Virus infection | Th1 cell | IL-33 | IFN-GAMMA PRODUCTION | MULTIDISCIPLINARY SCIENCES | EFFECTOR FUNCTION | CHORIOMENINGITIS VIRUS-INFECTION | CYTOKINE | virus infection | SELECTIVE EXPRESSION | NK CELLS | IMMUNE-RESPONSES | MICE | DIFFERENTIATION | TRANSCRIPTION FACTOR | CD8-Positive T-Lymphocytes - cytology | Cell Separation | Interleukin-33 | Mice, Inbred C57BL | Gene Expression Regulation | STAT4 Transcription Factor - metabolism | Gene Expression Profiling | Interferon-gamma - metabolism | Th1 Cells - immunology | T-Box Domain Proteins - metabolism | L-Selectin - metabolism | Animals | Flow Cytometry | Lymphocytic choriomeningitis virus | T-Lymphocytes - cytology | Interleukins - immunology | Hyaluronan Receptors - metabolism | Cell Differentiation | Mice | Th1 Cells - cytology | CD8-Positive T-Lymphocytes - immunology | Arenaviridae Infections - immunology | Gene expression | Immune response | Research | Biological Sciences
ST2 | CD4 T cell | Virus infection | Th1 cell | IL-33 | IFN-GAMMA PRODUCTION | MULTIDISCIPLINARY SCIENCES | EFFECTOR FUNCTION | CHORIOMENINGITIS VIRUS-INFECTION | CYTOKINE | virus infection | SELECTIVE EXPRESSION | NK CELLS | IMMUNE-RESPONSES | MICE | DIFFERENTIATION | TRANSCRIPTION FACTOR | CD8-Positive T-Lymphocytes - cytology | Cell Separation | Interleukin-33 | Mice, Inbred C57BL | Gene Expression Regulation | STAT4 Transcription Factor - metabolism | Gene Expression Profiling | Interferon-gamma - metabolism | Th1 Cells - immunology | T-Box Domain Proteins - metabolism | L-Selectin - metabolism | Animals | Flow Cytometry | Lymphocytic choriomeningitis virus | T-Lymphocytes - cytology | Interleukins - immunology | Hyaluronan Receptors - metabolism | Cell Differentiation | Mice | Th1 Cells - cytology | CD8-Positive T-Lymphocytes - immunology | Arenaviridae Infections - immunology | Gene expression | Immune response | Research | Biological Sciences
Journal Article
Trends in Immunology, ISSN 1471-4906, 2016, Volume 37, Issue 5, pp. 321 - 333
Recent studies have highlighted a role for the alarmin interleukin (IL)-33 in CD4+ and CD8+ T cell activation and function, and have also revealed important...
Allergy and Immunology | STAT4/STAT5 | alarmin IL-33 | T-bet/GATA-3/Foxp3 | ST2/T1/IL-1RL1 | Th1/Th2/Treg/CTL | CD4+ and CD8+ T cell subsets | Alarmin IL-33 | CD4 | and CD8 | T cell subsets | IL-1-LIKE CYTOKINE IL-33 | TH2 CELLS | ADAPTER MOLECULE MYD88 | IFN-GAMMA | MAST-CELLS | CHORIOMENINGITIS VIRUS-INFECTION | INTERFERON-GAMMA PRODUCTION | INNATE LYMPHOID-CELLS | INTERLEUKIN-1 RECEPTOR | IMMUNOLOGY | TRANSCRIPTION FACTOR GATA-3 | T-Lymphocyte Subsets - immunology | Gene Expression Regulation - immunology | Lymphocyte Activation | Humans | Homeostasis | Interleukin-33 - immunology | T-Lymphocytes, Regulatory - immunology | Feedback, Physiological | Animals | Cell Differentiation | Interleukin-1 Receptor-Like 1 Protein - metabolism | GATA3 Transcription Factor - metabolism | Interleukin-1 Receptor-Like 1 Protein - genetics | Interleukins | T cells | Cell differentiation | Osteoarthritis | Antigens | Signal transduction | Transcription factors | Cytokines | Lymphocytes | Cytotoxicity | T cell receptors | Gene expression
Allergy and Immunology | STAT4/STAT5 | alarmin IL-33 | T-bet/GATA-3/Foxp3 | ST2/T1/IL-1RL1 | Th1/Th2/Treg/CTL | CD4+ and CD8+ T cell subsets | Alarmin IL-33 | CD4 | and CD8 | T cell subsets | IL-1-LIKE CYTOKINE IL-33 | TH2 CELLS | ADAPTER MOLECULE MYD88 | IFN-GAMMA | MAST-CELLS | CHORIOMENINGITIS VIRUS-INFECTION | INTERFERON-GAMMA PRODUCTION | INNATE LYMPHOID-CELLS | INTERLEUKIN-1 RECEPTOR | IMMUNOLOGY | TRANSCRIPTION FACTOR GATA-3 | T-Lymphocyte Subsets - immunology | Gene Expression Regulation - immunology | Lymphocyte Activation | Humans | Homeostasis | Interleukin-33 - immunology | T-Lymphocytes, Regulatory - immunology | Feedback, Physiological | Animals | Cell Differentiation | Interleukin-1 Receptor-Like 1 Protein - metabolism | GATA3 Transcription Factor - metabolism | Interleukin-1 Receptor-Like 1 Protein - genetics | Interleukins | T cells | Cell differentiation | Osteoarthritis | Antigens | Signal transduction | Transcription factors | Cytokines | Lymphocytes | Cytotoxicity | T cell receptors | Gene expression
Journal Article
Immunity, ISSN 1074-7613, 06/2014, Volume 40, Issue 6, pp. 949 - 960
Despite development of new antiviral drugs, viral infections are still a major health problem. The most potent antiviral defense mechanism is the innate...
PLASMACYTOID DENDRITIC CELLS | EFFECTOR | NATURAL-KILLER-CELLS | VIRUS | THERAPY | IMMUNE-RESPONSES | CHRONIC HEPATITIS-C | INNATE | RECEPTOR | IMMUNOLOGY | TRANSGENIC MICE | Lymphocytic choriomeningitis virus - immunology | Lymphocytic Choriomeningitis - virology | Mice, Inbred C57BL | Cells, Cultured | Virus Replication - immunology | Basic-Leucine Zipper Transcription Factors - genetics | Immunity, Innate | Interferon Type I - immunology | Lymphocytic Choriomeningitis - immunology | Mice, Knockout | Signal Transduction - immunology | Animals | Receptor, Interferon alpha-beta - immunology | Killer Cells, Natural - immunology | Mice | Receptor, Interferon alpha-beta - genetics | CD8-Positive T-Lymphocytes - immunology | Cytotoxicity, Immunologic | Perforin - biosynthesis | Cytokines | Lymphocytes | Cytotoxicity | Infections | Gene expression | Experiments | Viral infections | Immune system | Chronic illnesses
PLASMACYTOID DENDRITIC CELLS | EFFECTOR | NATURAL-KILLER-CELLS | VIRUS | THERAPY | IMMUNE-RESPONSES | CHRONIC HEPATITIS-C | INNATE | RECEPTOR | IMMUNOLOGY | TRANSGENIC MICE | Lymphocytic choriomeningitis virus - immunology | Lymphocytic Choriomeningitis - virology | Mice, Inbred C57BL | Cells, Cultured | Virus Replication - immunology | Basic-Leucine Zipper Transcription Factors - genetics | Immunity, Innate | Interferon Type I - immunology | Lymphocytic Choriomeningitis - immunology | Mice, Knockout | Signal Transduction - immunology | Animals | Receptor, Interferon alpha-beta - immunology | Killer Cells, Natural - immunology | Mice | Receptor, Interferon alpha-beta - genetics | CD8-Positive T-Lymphocytes - immunology | Cytotoxicity, Immunologic | Perforin - biosynthesis | Cytokines | Lymphocytes | Cytotoxicity | Infections | Gene expression | Experiments | Viral infections | Immune system | Chronic illnesses
Journal Article
6.
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Professional Memory CD4 + T Lymphocytes Preferentially Reside and Rest in the Bone Marrow
Immunity, ISSN 1074-7613, 2009, Volume 30, Issue 5, pp. 721 - 730
CD4 T lymphocytes are key to immunological memory. Here we show that in the memory phase of specific immune responses, most of the memory CD4 T lymphocytes had...
CELLIMMUNO | SURVIVAL | CELL MEMORY | CD8(+) | LYMPHOID HOMEOSTASIS | CD8-T-CELL MEMORY | CD4-T-CELL HELP | ANTIBODY | IMMUNOLOGY | HOMEOSTATIC PROLIFERATION | EXPRESSION | ACUTE INFECTION | Gene Expression | Bone Marrow - immunology | Oligonucleotide Array Sequence Analysis | Stromal Cells - metabolism | CD4-Positive T-Lymphocytes - metabolism | Stromal Cells - immunology | CD4-Positive T-Lymphocytes - immunology | Animals | B-Lymphocytes - immunology | Interleukin-7 - immunology | Antigens, Ly - immunology | Down-Regulation - immunology | Integrin alpha2 - immunology | Immunologic Memory | Mice | Interleukin-7 - metabolism | Spleen | Competition | Antigens | Plasma | Microscopy | Lymphocytes | Homeostasis | T cell receptors | Gene expression | Immune system
CELLIMMUNO | SURVIVAL | CELL MEMORY | CD8(+) | LYMPHOID HOMEOSTASIS | CD8-T-CELL MEMORY | CD4-T-CELL HELP | ANTIBODY | IMMUNOLOGY | HOMEOSTATIC PROLIFERATION | EXPRESSION | ACUTE INFECTION | Gene Expression | Bone Marrow - immunology | Oligonucleotide Array Sequence Analysis | Stromal Cells - metabolism | CD4-Positive T-Lymphocytes - metabolism | Stromal Cells - immunology | CD4-Positive T-Lymphocytes - immunology | Animals | B-Lymphocytes - immunology | Interleukin-7 - immunology | Antigens, Ly - immunology | Down-Regulation - immunology | Integrin alpha2 - immunology | Immunologic Memory | Mice | Interleukin-7 - metabolism | Spleen | Competition | Antigens | Plasma | Microscopy | Lymphocytes | Homeostasis | T cell receptors | Gene expression | Immune system
Journal Article
Immunity, ISSN 1074-7613, 2010, Volume 32, Issue 1, pp. 116 - 128
Current T cell differentiation models invoke separate T helper 2 (Th2) and Th1 cell lineages governed by the lineage-specifying transcription factors GATA-3...
CELLIMMUNO | LINEAGE COMMITMENT | CD4(+) T-CELLS | FATE DETERMINATION | IMMUNOLOGY | TRANSCRIPTION FACTOR GATA-3 | LYMPHOCYTIC CHORIOMENINGITIS VIRUS | T(H)1 CELLS | VIRAL-INFECTION | HELPER LYMPHOCYTES | STAT4 ACTIVATION | IFN-ALPHA | Lymphocytic choriomeningitis virus - immunology | T-Lymphocyte Subsets - immunology | T-Lymphocyte Subsets - cytology | GATA3 Transcription Factor - immunology | T-Box Domain Proteins - immunology | Th2 Cells - immunology | Adoptive Transfer | Interferon-gamma - metabolism | Th1 Cells - immunology | Th1 Cells - metabolism | Lymphocyte Activation - immunology | Flow Cytometry | GATA3 Transcription Factor - metabolism | Cytokines - immunology | Cell Separation | Mice, Inbred C57BL | Th2 Cells - cytology | Th2 Cells - metabolism | T-Box Domain Proteins - metabolism | Mice, Knockout | Cell Differentiation - immunology | Animals | T-Lymphocyte Subsets - metabolism | Interferon-gamma - immunology | Mice | Th1 Cells - cytology | Proteins | Transcription factors | Cytokines | Protein expression | T cell receptors | Infections | Viral infections | Immune system
CELLIMMUNO | LINEAGE COMMITMENT | CD4(+) T-CELLS | FATE DETERMINATION | IMMUNOLOGY | TRANSCRIPTION FACTOR GATA-3 | LYMPHOCYTIC CHORIOMENINGITIS VIRUS | T(H)1 CELLS | VIRAL-INFECTION | HELPER LYMPHOCYTES | STAT4 ACTIVATION | IFN-ALPHA | Lymphocytic choriomeningitis virus - immunology | T-Lymphocyte Subsets - immunology | T-Lymphocyte Subsets - cytology | GATA3 Transcription Factor - immunology | T-Box Domain Proteins - immunology | Th2 Cells - immunology | Adoptive Transfer | Interferon-gamma - metabolism | Th1 Cells - immunology | Th1 Cells - metabolism | Lymphocyte Activation - immunology | Flow Cytometry | GATA3 Transcription Factor - metabolism | Cytokines - immunology | Cell Separation | Mice, Inbred C57BL | Th2 Cells - cytology | Th2 Cells - metabolism | T-Box Domain Proteins - metabolism | Mice, Knockout | Cell Differentiation - immunology | Animals | T-Lymphocyte Subsets - metabolism | Interferon-gamma - immunology | Mice | Th1 Cells - cytology | Proteins | Transcription factors | Cytokines | Protein expression | T cell receptors | Infections | Viral infections | Immune system
Journal Article
Nature Immunology, ISSN 1529-2908, 11/2010, Volume 11, Issue 11, pp. 1057 - 1062
After being activated by antigen, helper T lymphocytes switch from a resting state to clonal expansion. This switch requires inactivation of the transcription...
FORKHEAD TRANSCRIPTION FACTOR | CELLS | IN-VIVO | EFFECTOR FUNCTION | FACTOR FKHR-L1 | PROLIFERATION | DIFFERENTIATION | IMMUNOLOGY | EXPRESSION | INTERLEUKIN-7 RECEPTOR | FOXO1 | Cell Proliferation | Humans | Mice, Inbred C57BL | Cells, Cultured | MicroRNAs - immunology | Animals | Interleukin-2 - immunology | T-Lymphocytes, Helper-Inducer - immunology | T-Lymphocytes, Helper-Inducer - cytology | Arthritis - immunology | Mice | Mice, Inbred BALB C | Disease Models, Animal | Antigens | MicroRNA | Interleukins | Analysis | Physiological aspects | T cells | Health aspects
FORKHEAD TRANSCRIPTION FACTOR | CELLS | IN-VIVO | EFFECTOR FUNCTION | FACTOR FKHR-L1 | PROLIFERATION | DIFFERENTIATION | IMMUNOLOGY | EXPRESSION | INTERLEUKIN-7 RECEPTOR | FOXO1 | Cell Proliferation | Humans | Mice, Inbred C57BL | Cells, Cultured | MicroRNAs - immunology | Animals | Interleukin-2 - immunology | T-Lymphocytes, Helper-Inducer - immunology | T-Lymphocytes, Helper-Inducer - cytology | Arthritis - immunology | Mice | Mice, Inbred BALB C | Disease Models, Animal | Antigens | MicroRNA | Interleukins | Analysis | Physiological aspects | T cells | Health aspects
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2010, Volume 107, Issue 50, pp. 21641 - 21646
The Clone 13 (Cl13) strain of lymphocytic choriomeningitis virus is widely studied as a model of chronic systemic viral infection. Here, we used reverse...
T lymphocytes | Immunosuppression | Lymphocytic choriomeningitis virus | RNA | Dendritic cells | Exhaustion | Cell lines | Viruses | Infections | Genetic mutation | Viral polymerase | Viral tropism | Persistent viral infections | Plasmacytoid dendritic cell | Acquired immunodeficiency syndrome | CHRONIC INFECTION | RNA ANALOGS | MULTIDISCIPLINARY SCIENCES | EFFECTOR FUNCTION | TRANSCRIPTION | plasmacytoid dendritic cell | POLYMERASE | CD8(+) T-CELLS | acquired immunodeficiency syndrome | PLASMACYTOID DENDRITIC CELLS | persistent viral infections | viral tropism | viral polymerase | HEPATITIS-C VIRUS | IN-VIVO | MICE | Lymphocytic choriomeningitis virus - immunology | Genome, Viral | Viremia | Mice, Inbred C57BL | Viral Proteins - genetics | Viral Proteins - metabolism | Point Mutation | Animals | Virus Replication | Lymphocytic choriomeningitis virus - genetics | Lymphocytic choriomeningitis virus - physiology | Mice | CD8-Positive T-Lymphocytes - immunology | Viral meningitis | Physiological aspects | Research | Properties | Immunotherapy | Biological Sciences
T lymphocytes | Immunosuppression | Lymphocytic choriomeningitis virus | RNA | Dendritic cells | Exhaustion | Cell lines | Viruses | Infections | Genetic mutation | Viral polymerase | Viral tropism | Persistent viral infections | Plasmacytoid dendritic cell | Acquired immunodeficiency syndrome | CHRONIC INFECTION | RNA ANALOGS | MULTIDISCIPLINARY SCIENCES | EFFECTOR FUNCTION | TRANSCRIPTION | plasmacytoid dendritic cell | POLYMERASE | CD8(+) T-CELLS | acquired immunodeficiency syndrome | PLASMACYTOID DENDRITIC CELLS | persistent viral infections | viral tropism | viral polymerase | HEPATITIS-C VIRUS | IN-VIVO | MICE | Lymphocytic choriomeningitis virus - immunology | Genome, Viral | Viremia | Mice, Inbred C57BL | Viral Proteins - genetics | Viral Proteins - metabolism | Point Mutation | Animals | Virus Replication | Lymphocytic choriomeningitis virus - genetics | Lymphocytic choriomeningitis virus - physiology | Mice | CD8-Positive T-Lymphocytes - immunology | Viral meningitis | Physiological aspects | Research | Properties | Immunotherapy | Biological Sciences
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, p. e0161507
Immunomodulatory Foxp3(+) regulatory T cells (Tregs) form a heterogeneous population consisting of subsets with different activation states, migratory...
RESPONSES | VISCERAL ADIPOSE-TISSUE | LYMPHOID ORGANS | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | REG CELLS | IN-VIVO | MEDIATED SUPPRESSION | MICE | CYTOKINE | TRANSCRIPTION FACTOR GATA-3 | GATA3 Transcription Factor - genetics | Cell Proliferation | GATA3 Transcription Factor - immunology | Interleukin-13 - immunology | Interleukin-5 - genetics | Interleukin-1 Receptor-Like 1 Protein - deficiency | Interleukin-33 - immunology | T-Lymphocytes, Regulatory - immunology | Interleukin-13 - genetics | T-Lymphocytes, Regulatory - cytology | Interleukin-1 Receptor-Like 1 Protein - genetics | Transforming Growth Factor beta - immunology | Signal Transduction | Lymphocyte Activation | Interleukin-1 Receptor-Like 1 Protein - immunology | Mice, Inbred C57BL | Gene Expression Regulation | Immunophenotyping | Mice, Knockout | Interleukin-5 - immunology | Interleukin-33 - genetics | Animals | Transforming Growth Factor beta - genetics | Interleukin-10 - genetics | Mice | Interleukin-10 - immunology | Cell Lineage - immunology | Cell proliferation | Homing behavior | Transcription factors | Laboratories | Activation | Lymphocytes T | Arthritis | Homing | Genotype & phenotype | Receptors | Cell growth | Immunology | Interleukin 5 | Lymphocytes | Animal tissues | Rheumatism | Foxp3 protein | Growth factors | Antigens | Cytokines | Immunoregulation | Immunomodulation | Rheumatology | Inflammation | Interleukin 13 | Lymphoid tissue | Gene expression | Chemokine receptors | CD4 antigen | Medicine | Interleukin 10 | GATA-3 protein | Clinical medicine
RESPONSES | VISCERAL ADIPOSE-TISSUE | LYMPHOID ORGANS | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | REG CELLS | IN-VIVO | MEDIATED SUPPRESSION | MICE | CYTOKINE | TRANSCRIPTION FACTOR GATA-3 | GATA3 Transcription Factor - genetics | Cell Proliferation | GATA3 Transcription Factor - immunology | Interleukin-13 - immunology | Interleukin-5 - genetics | Interleukin-1 Receptor-Like 1 Protein - deficiency | Interleukin-33 - immunology | T-Lymphocytes, Regulatory - immunology | Interleukin-13 - genetics | T-Lymphocytes, Regulatory - cytology | Interleukin-1 Receptor-Like 1 Protein - genetics | Transforming Growth Factor beta - immunology | Signal Transduction | Lymphocyte Activation | Interleukin-1 Receptor-Like 1 Protein - immunology | Mice, Inbred C57BL | Gene Expression Regulation | Immunophenotyping | Mice, Knockout | Interleukin-5 - immunology | Interleukin-33 - genetics | Animals | Transforming Growth Factor beta - genetics | Interleukin-10 - genetics | Mice | Interleukin-10 - immunology | Cell Lineage - immunology | Cell proliferation | Homing behavior | Transcription factors | Laboratories | Activation | Lymphocytes T | Arthritis | Homing | Genotype & phenotype | Receptors | Cell growth | Immunology | Interleukin 5 | Lymphocytes | Animal tissues | Rheumatism | Foxp3 protein | Growth factors | Antigens | Cytokines | Immunoregulation | Immunomodulation | Rheumatology | Inflammation | Interleukin 13 | Lymphoid tissue | Gene expression | Chemokine receptors | CD4 antigen | Medicine | Interleukin 10 | GATA-3 protein | Clinical medicine
Journal Article
11.
Full Text
Superoxide Dismutase 1 Protects Hepatocytes from Type I Interferon-Driven Oxidative Damage
Immunity, ISSN 1074-7613, 11/2015, Volume 43, Issue 5, pp. 974 - 986
Tissue damage caused by viral hepatitis is a major cause of morbidity and mortality worldwide. Using a mouse model of viral hepatitis, we...
PATHOGENESIS | VIRUS-INFECTION | MACROPHAGES | LIVER FIBROSIS | DISEASE | FUNCTIONAL-ROLE | ALPHA | IMMUNOLOGY | STRESS | T-CELLS | VIRAL-INFECTION | Hepatitis, Viral, Animal - immunology | Oxidation-Reduction | Antioxidants - metabolism | Mice, Inbred C57BL | Oxidative Stress - immunology | Inflammation - immunology | Hepatocytes - immunology | Interferon Type I - immunology | Immunity, Innate - immunology | Signal Transduction - immunology | Superoxide Dismutase - immunology | Liver - immunology | Animals | Killer Cells, Natural - immunology | Transcription, Genetic - immunology |
PATHOGENESIS | VIRUS-INFECTION | MACROPHAGES | LIVER FIBROSIS | DISEASE | FUNCTIONAL-ROLE | ALPHA | IMMUNOLOGY | STRESS | T-CELLS | VIRAL-INFECTION | Hepatitis, Viral, Animal - immunology | Oxidation-Reduction | Antioxidants - metabolism | Mice, Inbred C57BL | Oxidative Stress - immunology | Inflammation - immunology | Hepatocytes - immunology | Interferon Type I - immunology | Immunity, Innate - immunology | Signal Transduction - immunology | Superoxide Dismutase - immunology | Liver - immunology | Animals | Killer Cells, Natural - immunology | Transcription, Genetic - immunology |