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1. Full Text Ranking the impact of human health disorders on gut metabolism: Systemic lupus erythematosus and obesity as study cases
by Rojo, David and Hevia, Arancha and Bargiela, Rafael and López, Patricia and Cuervo, Adriana and González, Sonia and Suárez, Ana and Sánchez, Borja and Martínez-Martínez, Mónica and Milani, Christian and Ventura, Marco and Barbas, Coral and Moya, Andrés and Suárez, Antonio and Margolles, Abelardo and Ferrer, Manuel
Scientific Reports, ISSN 2045-2322, 02/2015, Volume 5, Issue 1, p. 8310
Multiple factors have been shown to alter intestinal microbial diversity. It remains to be seen, however, how multiple collective pressures impact the activity... 
RHEUMATOID-ARTHRITIS | STRAINS | DIET | INTESTINAL MICROBIOTA | PSEUDOMONAS-AERUGINOSA | MULTIDISCIPLINARY SCIENCES | DISEASE | QUORUM-QUENCHING ENZYMES | HOST | MICE | Body Mass Index | Metabolomics | Humans | Middle Aged | Gastrointestinal Tract - microbiology | Homeostasis | Lupus Erythematosus, Systemic - metabolism | Metabolome | N-Acetylneuraminic Acid - metabolism | Case-Control Studies | Gastrointestinal Tract - metabolism | Obesity - metabolism | Microbiota | Metabolic Networks and Pathways | Adult | Female | Lupus | Systemic lupus erythematosus | Immunology | Metabolism | Autoimmune diseases
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2. Full Text CD19(+)CD24(hi)CD38(hi) B Cells Exhibit Regulatory Capacity in Healthy Individuals but Are Functionally Impaired in Systemic Lupus Erythematosus Patients
by Blair, PA and Norena, LY and Flores-Borja, F and Rawlings, DJ and Isenberg, DA and Ehrenstein, MR and Mauri, C
IMMUNITY, ISSN 1074-7613, 01/2010, Volume 32, Issue 1, pp. 129 - 140
The immunosuppressive function of regulatory B cells has been shown in several murine models of chronic inflammation, including collagen-induced arthritis,... 
MULTIPLE-SCLEROSIS | AUTOIMMUNITY | IMMUNE-RESPONSES | INFLAMMATION | SUPPRESSIVE FUNCTION | DISEASE | CPG-OLIGODEOXYNUCLEOTIDES | MICE | IMMUNOLOGY | T-CELLS | LYMPHOCYTES | CD24 Antigen - metabolism | Humans | Middle Aged | Lupus Erythematosus, Systemic - metabolism | Male | Th1 Cells - immunology | Th1 Cells - metabolism | Young Adult | Signal Transduction - immunology | Flow Cytometry | ADP-ribosyl Cyclase 1 - immunology | Lupus Erythematosus, Systemic - immunology | Adult | B-Lymphocyte Subsets - immunology | Female | B-Lymphocytes - metabolism | Antigens, CD19 - immunology | Cytokines - immunology | Cell Separation | Cell Differentiation - immunology | B-Lymphocytes - immunology | B-Lymphocyte Subsets - metabolism | ADP-ribosyl Cyclase 1 - metabolism | Aged | Antigens, CD19 - metabolism | CD24 Antigen - immunology | Cytokines - biosynthesis
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3. Full Text Neutrophil extracellular traps induce endothelial dysfunction in systemic lupus erythematosus through the activation of matrix metalloproteinase-2
by Carmona-Rivera, Carmelo and Zhao, Wenpu and Yalavarthi, Srilakshmi and Kaplan, Mariana J
Annals of the Rheumatic Diseases, ISSN 0003-4967, 07/2015, Volume 74, Issue 7, pp. 1417 - 1424
RationaleThe structural and functional integrity of the endothelium is crucial in maintaining vascular homeostasis and preventing atherosclerosis. Patients... 
NETTING NEUTROPHILS | PEPTIDYLARGININE DEIMINASE INHIBITION | MEMBRANE-VESICLES | CORONARY | PATHWAY | TISSUE INHIBITORS | MATRIX-METALLOPROTEINASE-9 | RELEASE | RHEUMATOLOGY | EXPRESSION | DAMAGE | Up-Regulation | Autoantibodies - metabolism | Extracellular Traps - metabolism | Humans | Matrix Metalloproteinase 9 - immunology | Lupus Erythematosus, Systemic - metabolism | Matrix Metalloproteinase 9 - metabolism | Female | Granulocytes - pathology | Models, Animal | Umbilical Veins - pathology | Granulocytes - metabolism | Matrix Metalloproteinase 2 - metabolism | Mice, Inbred C57BL | Cells, Cultured | Endothelium, Vascular - physiopathology | Arthritis, Rheumatoid | Aorta - pathology | Autoantibodies - immunology | Animals | Endothelium, Vascular - metabolism | Endothelium, Vascular - pathology | Mice | Lupus Erythematosus, Systemic - physiopathology | Lupus Erythematosus, Systemic - pathology | Complications and side effects | Systemic lupus erythematosus | Research | Cardiovascular diseases | Risk factors | Endothelium | Lupus | Proteins | Rodents | Atherosclerosis | Neutrophils | Cytotoxicity | neutrophil extracellular traps | endothelial dysfunction | lupus | metalloproteinase
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4. Full Text Diversity, cellular origin and autoreactivity of antibody-secreting cell population expansions in acute systemic lupus erythematosus
by Tipton, Christopher M and Fucile, Christopher F and Darce, Jaime and Chida, Asiya and Ichikawa, Travis and Gregoretti, Ivan and Schieferl, Sandra and Hom, Jennifer and Jenks, Scott and Feldman, Ron J and Mehr, Ramit and Wei, Chungwen and Lee, F. Eun-Hyung and Cheung, Wan Cheung and Rosenberg, Alexander F and Sanz, Iñaki
Nature Immunology, ISSN 1529-2908, 07/2015, Volume 16, Issue 7, pp. 755 - 765
Acute systemic lupus erythematosus (SLE) courses with surges of antibody-secreting cells (ASCs) whose origin, diversity and contribution to serum... 
RESPONSES | ACTIVATION | MEMORY B-CELLS | AFFINITY MATURATION | AUTOIMMUNITY | PERIPHERAL-BLOOD | GERMINAL CENTER | IMMUNOLOGY | MONOCLONAL-ANTIBODIES | SLE | ANTIGEN | Autoantibodies - metabolism | Cell Proliferation | Immunoglobulin G - blood | Humans | Immunoglobulin Variable Region - metabolism | Lupus Erythematosus, Systemic - metabolism | Molecular Sequence Data | Immunoglobulin Variable Region - immunology | Tandem Mass Spectrometry | Antibody Diversity - genetics | Flow Cytometry | Antibody Diversity - immunology | Immunoglobulin G - immunology | Single-Cell Analysis - methods | Base Sequence | Proteome - immunology | Clone Cells - immunology | Lupus Erythematosus, Systemic - immunology | Proteomics - methods | Immunoglobulin Heavy Chains - immunology | B-Lymphocytes - metabolism | Amino Acid Sequence | Antibody-Producing Cells - metabolism | Acute Disease | Proteome - analysis | Clone Cells - metabolism | Sequence Homology, Amino Acid | Autoantibodies - immunology | Antibody-Producing Cells - immunology | B-Lymphocytes - immunology | Immunoglobulin G - genetics | Influenza Vaccines - immunology | Lupus Erythematosus, Systemic - genetics | Immunoglobulin Heavy Chains - metabolism | Immunoglobulin Variable Region - genetics | Autoantibodies - genetics | Tetanus Toxoid - immunology | Immunoglobulin Heavy Chains - genetics | Systemic lupus erythematosus | Immune response | Autoantibodies | Development and progression | Genetic aspects | Nucleotide sequencing | Identification and classification | Methods | DNA sequencing
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5. Full Text Immunometabolism in systemic lupus erythematosus
by Morel, Laurence
Nature Reviews Rheumatology, ISSN 1759-4790, 05/2017, Volume 13, Issue 5, pp. 280 - 290
Systemic lupus erythematosus (SLE) is an autoimmune disease mediated by pathogenic autoantibodies directed against nucleoprotein complexes. Beyond the... 
LIVER X RECEPTORS | INDUCIBLE FACTOR 1-ALPHA | RENAL GLYCOSPHINGOLIPID METABOLISM | DENDRITIC CELL | T-CELL-ACTIVATION | REDUCES DISEASE-ACTIVITY | MURINE LUPUS | TUBEROUS SCLEROSIS | REGULATORY T | RHEUMATOLOGY | MECHANISTIC TARGET | CD4-Positive T-Lymphocytes - immunology | Autoantibodies - immunology | Animals | B-Lymphocytes - immunology | Humans | CD4-Positive T-Lymphocytes - metabolism | Lupus Erythematosus, Systemic - immunology | Lupus Erythematosus, Systemic - metabolism | Mice | B-Lymphocytes - metabolism | Disease Models, Animal | Care and treatment | Systemic lupus erythematosus | Autoantibodies | Research | B cells | Dendritic cells
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6. Full Text Modular Transcriptional Repertoire Analyses of Adults With Systemic Lupus Erythematosus Reveal Distinct Type I and Type II Interferon Signatures
by Chiche, Laurent and Jourde‐Chiche, Noémie and Whalen, Elizabeth and Presnell, Scott and Gersuk, Vivian and Dang, Kristen and Anguiano, Esperanza and Quinn, Charlie and Burtey, Stéphane and Berland, Yvon and Kaplanski, Gilles and Harle, Jean‐Robert and Pascual, Virginia and Chaussabel, Damien
Arthritis & Rheumatology, ISSN 2326-5191, 06/2014, Volume 66, Issue 6, pp. 1583 - 1595
Objective. The role of interferon-alpha (IFN alpha) in the pathogenesis of systemic lupus erythematosus (SLE) is strongly supported by gene expression studies.... 
ALPHA MONOCLONAL-ANTIBODY | ANTIINTERFERON ALPHA | REVISED CRITERIA | INDUCIBLE GENE-EXPRESSION | AUTOIMMUNE-DISEASES | IFN-GAMMA | RHEUMATIC-DISEASES | RHEUMATOLOGY | PHASE-I | BLOOD MONONUCLEAR-CELLS | DISEASE-ACTIVITY | Biomarkers - metabolism | Interferon-alpha - metabolism | Prospective Studies | Follow-Up Studies | Humans | Middle Aged | Lupus Erythematosus, Systemic - metabolism | Gene Expression Profiling - methods | Male | Interferon-gamma - metabolism | Young Adult | Interferon-alpha - genetics | Interferon-beta - metabolism | Lupus Erythematosus, Systemic - genetics | Adolescent | Interferon Type I - genetics | Interferon Type I - metabolism | Interferon-beta - genetics | Adult | Female | Aged | Interferon-gamma - genetics | Lupus | Autoimmune diseases | Gene expression | Systemic Lupus Erythematosus | Interferon | Modular analyses | Transcriptional signature
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7. Full Text Normalization of CD4 + T cell metabolism reverses lupus
by Yin, Yiming and Choi, Seung-Chul and Xu, Zhiwei and Perry, Daniel J and Seay, Howard and Croker, Byron P and Sobel, Eric S and Brusko, Todd M and Morel, Laurence
Science Translational Medicine, ISSN 1946-6234, 02/2015, Volume 7, Issue 274, pp. 274ra18 - 274ra18
Systemic lupus erythematosus (SLE) is an autoimmune disease in which autoreactive CD4(+) T cells play an essential role. CD4(+) T cells rely on glycolysis for... 
MAMMALIAN TARGET | RAPAMYCIN | MEDICINE, RESEARCH & EXPERIMENTAL | ACTIVATION | RECEPTOR-GAMMA | MOUSE MODEL | REDUCES DISEASE-ACTIVITY | FATTY-ACID-METABOLISM | DIFFERENTIATION | SYSTEMIC AUTOIMMUNITY | ERYTHEMATOSUS | CELL BIOLOGY | Deoxyglucose - therapeutic use | Phenotype | Animals | Metformin - therapeutic use | CD4-Positive T-Lymphocytes - metabolism | Lupus Erythematosus, Systemic - drug therapy | Lupus Erythematosus, Systemic - metabolism | Mice | Disease Models, Animal
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8. Full Text Expanded Double Negative T Cells in Patients with Systemic Lupus Erythematosus Produce IL-17 and Infiltrate the Kidneys
by Crispin, Jose C and Oukka, Mohamed and Bayliss, George and Cohen, Robert A and Van Beek, Christine A and Stillman, Isaac E and Kyttaris, Vasileios C and Juang, Yuang-Taung and Tsokos, George C
The Journal of Immunology, ISSN 0022-1767, 12/2008, Volume 181, Issue 12, pp. 8761 - 8766
Double negative (DN) T cells are expanded in patients with systemic lupus erythematosus (SLE) and stimulate autoantibody production as efficiently as CD4(+) T... 
DENDRITIC CELLS | INTERLEUKIN-17 | INFLAMMATION | HELPER-CELLS | NEPHRITIS | PHENOTYPE | DIFFERENTIATION | IMMUNOLOGY | LESIONS | T-Lymphocyte Subsets - immunology | CD8-Positive T-Lymphocytes - pathology | Cell Proliferation | Kidney - pathology | Humans | Middle Aged | Kidney - immunology | Lupus Erythematosus, Systemic - metabolism | CD4-Positive T-Lymphocytes - pathology | CD4-Positive T-Lymphocytes - immunology | Cell Movement - immunology | Inflammation Mediators - metabolism | Lupus Erythematosus, Systemic - immunology | CD8-Positive T-Lymphocytes - metabolism | Adult | Inflammation Mediators - physiology | CD4-Positive T-Lymphocytes - metabolism | Cells, Cultured | Immunophenotyping | Interleukin-17 - biosynthesis | T-Lymphocyte Subsets - pathology | Up-Regulation - immunology | T-Lymphocyte Subsets - metabolism | CD8-Positive T-Lymphocytes - immunology | Lupus Erythematosus, Systemic - pathology
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9. Full Text The proteasome inhibitior bortezomib depletes plasma cells and ameliorates clinical manifestations of refractory systemic lupus erythematosus
by Alexander, Tobias and Sarfert, Ramona and Klotsche, Jens and Kühl, Anja A and Rubbert-Roth, Andrea and Lorenz, Hannes-Martin and Rech, Jürgen and Hoyer, Bimba F and Cheng, Qingyu and Waka, Aderajew and Taddeo, Adriano and Wiesener, Michael and Schett, Georg and Burmester, Gerd-Rüdiger and Radbruch, Andreas and Hiepe, Falk and Voll, Reinhard E
Annals of the Rheumatic Diseases, ISSN 0003-4967, 07/2015, Volume 74, Issue 7, pp. 1474 - 1478
ObjectivesTo investigate whether bortezomib, a proteasome inhibitor approved for treatment of multiple myeloma, induces clinically relevant plasma cell (PC)... 
CARFILZOMIB | THERAPY | DOSE DEXAMETHASONE | MEMORY | REJECTION | DISEASE | NEPHRITIS | RELAPSED MULTIPLE-MYELOMA | MICE | RHEUMATOLOGY | Humans | Pyrazines - administration & dosage | Lupus Erythematosus, Systemic - metabolism | Male | Pyrazines - therapeutic use | Boronic Acids - therapeutic use | Plasma Cells - pathology | Plasma Cells - drug effects | Lupus Erythematosus, Systemic - drug therapy | Lupus Erythematosus, Systemic - immunology | Interferon Type I - metabolism | Adult | Female | Boronic Acids - administration & dosage | Drug Therapy, Combination | Severity of Illness Index | Bortezomib | Dexamethasone - administration & dosage | DNA - immunology | Proteasome Inhibitors - pharmacology | Proteasome Inhibitors - administration & dosage | Treatment Outcome | Proteasome Inhibitors - therapeutic use | Administration, Intravenous | Dexamethasone - therapeutic use | Antibodies - blood | Pyrazines - pharmacology | Germany | Boronic Acids - pharmacology | Complications and side effects | Treatment outcome | Systemic lupus erythematosus | Analysis | Multiple myeloma | Dosage and administration | Drug therapy | Risk factors | Lupus | Studies | Immunoglobulins | Protease inhibitors | Disease | Bone marrow | Vaccines | Systemic Lupus Erythematosus | Autoimmunity | Treatment | Autoimmune Diseases | Basic and Translational Research | B cells | 1506
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10. Full Text Metabolic disturbances associated with systemic lupus erythematosus
by Wu, Tianfu and Xie, Chun and Han, Jie and Ye, Yujin and Weiel, Jim and Li, Quan and Blanco, Irene and Ahn, Chul and Olsen, Nancy and Putterman, Chaim and Saxena, Ramesh and Mohan, Chandra
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, p. e37210
The metabolic disturbances that underlie systemic lupus erythematosus are currently unknown. A metabolomic study was executed, comparing the sera of 20 SLE... 
PROFILES | ANTIOXIDANTS | BIOLOGY | ATHEROSCLEROSIS | FATTY-ACIDS | SLE | DISEASE-ACTIVITY | Humans | Carbohydrate Metabolism | Lupus Erythematosus, Systemic - metabolism | Metabolome | Lipid Metabolism | Male | Lupus Erythematosus, Systemic - blood | Metabolomics - methods | Young Adult | Amino Acids - metabolism | Sensitivity and Specificity | Adolescent | Adult | Female | Cluster Analysis | Lupus | Glucose metabolism | Medical research | Rheumatoid factor | Cysteine | Systemic lupus erythematosus | Metabolites | Physiological aspects | Medicine, Experimental | Biosynthesis | Fatty acids | Tricarboxylic acid cycle | Oxidative stress | Energy metabolism | Multiple sclerosis | Peptides | Lipid peroxidation | Amino acids | Chains | Lipids | Arthritis | Discriminators | Krebs cycle | Energy | Population | Oxidation | Glutathione | Peroxidation | Carbohydrates | Enzymes | Cytokines | Methionine | Metabolism | Gene expression | Cultural differences | Patients | Vitamins | Chronic conditions | Leukotriene B4 | Rheumatoid arthritis | Choline | Disturbances | Glycolysis | Insulin resistance | Acute coronary syndromes | Autoimmune diseases | Prostate cancer
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11. Full Text Deficient CD4+CD25high T Regulatory Cell Function in Patients with Active Systemic Lupus Erythematosus
by Valencia, Xavier and Yarboro, Cheryl and Illei, Gabor and Lipsky, Peter E
The Journal of Immunology, ISSN 0022-1767, 02/2007, Volume 178, Issue 4, pp. 2579 - 2588
CD4(+)CD25(+) T regulatory cells (Tregs) play an essential role in maintaining immunologic homeostasis and preventing autoimmunity. Systemic lupus... 
Forkhead Transcription Factors - immunology | Forkhead Transcription Factors - biosynthesis | T-Lymphocytes, Regulatory - metabolism | Cell Proliferation | Gene Expression Regulation - immunology | Humans | Middle Aged | Self Tolerance | Lupus Erythematosus, Systemic - metabolism | Male | T-Lymphocytes, Regulatory - pathology | T-Lymphocytes, Regulatory - immunology | Lymphocyte Activation - immunology | Lupus Erythematosus, Systemic - immunology | Adult | Female | Aged | Lupus Erythematosus, Systemic - pathology | Cytokines - biosynthesis | Cytokines - immunology
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12. Full Text Immunogenetics of systemic lupus erythematosus: A comprehensive review
by Ghodke-Puranik, Yogita and Niewold, Timothy B
Journal of Autoimmunity, ISSN 0896-8411, 2015, Volume 64, pp. 125 - 136
Abstract Our understanding of the genetic basis of systemic lupus erythematosus has progressed rapidly in recent years. While many genetic polymorphisms have... 
Allergy and Immunology | Genetics | Interferon | Systemic lupus erythematosus | Autoimmune diseases | GENETIC POLYMORPHISMS | DENDRITIC CELLS | AICARDI-GOUTIERES SYNDROME | SUSCEPTIBILITY LOCI | IMMUNOLOGY | OF-FUNCTION VARIANT | DISEASE RISK VARIANT | NF-KAPPA-B | INTERFERON-ALPHA ACTIVITY | GENOME-WIDE ASSOCIATION | IFN-ALPHA | Genetic Predisposition to Disease | Major Histocompatibility Complex - genetics | Signal Transduction | Epigenesis, Genetic | Humans | Open Reading Frames | Regulatory Sequences, Nucleic Acid | Autoimmune Diseases - immunology | Lupus Erythematosus, Systemic - metabolism | Genetic Loci | Multifactorial Inheritance | Polymorphism, Genetic | Autoimmune Diseases - genetics | Immunogenetics | Animals | Lupus Erythematosus, Systemic - genetics | Lupus Erythematosus, Systemic - immunology | Interferon Type I - genetics | Interferon Type I - metabolism | Major Histocompatibility Complex - immunology | Autoimmune Diseases - metabolism | Lupus | Epigenetic inheritance | Genetic polymorphisms | autoimmune diseases | systemic lupus erythematosus | genetics | interferon
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