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1. Full Text Mediators of innate immune recognition of bacteria concentrate in lipid rafts and facilitate lipopolysaccharide-induced cell activation
by Triantafilou, Martha and Miyake, Kensuke and Golenbock, Douglas T and Triantafilou, Kathy
Journal of Cell Science, ISSN 0021-9533, 06/2002, Volume 115, Issue 12, pp. 2603 - 2611
The plasma membrane of cells is composed of lateral heterogeneities, patches and microdomains. These membrane microdomains or lipid rafts are enriched in... 
Heat shock proteins | CXCR4 | Lipid rafts | GDF5 | TLR4 | LPS | lipid rafts | HLA CLASS-I | N-TERMINAL KINASE | RESONANCE ENERGY-TRANSFER | CLASS-II MOLECULES | FLUID MOSAIC MODEL | CELL BIOLOGY | SIGNAL-TRANSDUCTION | TOLL-LIKE RECEPTOR-4 | HUMAN LYMPHOBLASTOID-CELLS | heat shock proteins | GPI-ANCHORED PROTEINS | INFLUENZA-VIRUS HEMAGGLUTININ | Toll-Like Receptor 4 | Bone Morphogenetic Proteins - immunology | Humans | Lipopolysaccharides - immunology | Membrane Microdomains - immunology | Growth Differentiation Factor 5 | Signal Transduction - immunology | Toll-Like Receptors | Bacteria - immunology | Lymphocyte Activation - immunology | G(M1) Ganglioside - immunology | HSP90 Heat-Shock Proteins - immunology | Receptors, Cell Surface - drug effects | Bacterial Infections - immunology | HSP70 Heat-Shock Proteins - drug effects | Bone Morphogenetic Proteins - drug effects | Nystatin - pharmacology | Mitogen-Activated Protein Kinases - immunology | Membrane Glycoproteins - immunology | CHO Cells | Drosophila Proteins | Cricetinae | HSP70 Heat-Shock Proteins - immunology | HSP90 Heat-Shock Proteins - drug effects | Lipopolysaccharide Receptors - immunology | Receptors, Cell Surface - immunology | Receptors, CXCR4 - drug effects | Animals | Mitogen-Activated Protein Kinase 8 | Receptors, CXCR4 - immunology | Signal Transduction - drug effects | Lymphocyte Activation - drug effects | Membrane Microdomains - drug effects | Lipopolysaccharides - pharmacology | Membrane Glycoproteins - drug effects
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2. Full Text Antitumor activity and long-term fate of chimeric antigen receptor-positive T cells in patients with neuroblastoma
by Louis, Chrystal U and Savoldo, Barbara and Dotti, Gianpietro and Pule, Martin and Yvon, Eric and Myers, G. Doug and Rossig, Claudia and Russell, Heidi V and Diouf, Oumar and Liu, Enli and Liu, Hao and Wu, Meng-Fen and Gee, Adrian P and Mei, Zhuyong and Rooney, Cliona M and Heslop, Helen E and Brenner, Malcolm K
Blood, ISSN 0006-4971, 12/2011, Volume 118, Issue 23, pp. 6050 - 6056
We generated MHC-independent chimeric antigen receptors (CARs) directed to the GD2 antigen expressed by neuroblastoma tumor cells and treated patients with... 
TRIAL | ANTIBODY CH14.18 | COLONY-STIMULATING FACTOR | ADOPTIVE TRANSFER | IMMUNOTHERAPY | ANTI-GD2 ANTIBODY | CHILDRENS CANCER GROUP | HEMATOLOGY | PHASE-I | PRESENTING CELL | LYMPHOCYTES | Recombinant Fusion Proteins - immunology | Bone Neoplasms - therapy | Follow-Up Studies | Humans | Bone Marrow Neoplasms - immunology | Child, Preschool | Male | Antigens, Tumor-Associated, Carbohydrate - immunology | Neuroblastoma - therapy | Bone Marrow Neoplasms - genetics | Young Adult | Neuroblastoma - immunology | Female | Neoplasm, Residual - immunology | Receptors, Antigen, T-Cell - immunology | Bone Neoplasms - genetics | Child | Bone Marrow Neoplasms - therapy | Immunologic Memory - immunology | T-Lymphocytes, Cytotoxic - immunology | Neuroblastoma - genetics | Bone Neoplasms - immunology | Gangliosides - immunology | Neoplasm, Residual - genetics | Adoptive Transfer - methods | Adolescent | Cell Line, Tumor | Recombinant Fusion Proteins - genetics | Receptors, Antigen, T-Cell - genetics | Neoplasm, Residual - therapy | Genetic Therapy - methods | Gene Therapy | Immunobiology
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3. Full Text Cross-Linking of GM1 Ganglioside by Galectin-1 Mediates Regulatory T Cell Activity Involving TRPC5 Channel Activation: Possible Role in Suppressing Experimental Autoimmune Encephalomyelitis
by Wang, Jianfeng and Lu, Zi-Hua and Gabius, Hans-Joachim and Rohowsky-Kochan, Christine and Ledeen, Robert W and Wu, Gusheng
The Journal of Immunology, ISSN 0022-1767, 04/2009, Volume 182, Issue 7, pp. 4036 - 4045
Several animal autoimmune disorders are suppressed by treatment with the GM1 cross-linking units of certain toxins such as B subunit of cholera toxin (CtxB).... 
MYELIN OLIGODENDROCYTE GLYCOPROTEIN | HUMAN NEUROBLASTOMA-CELLS | BACTERIAL TOXINS | NOD MICE | MULTIPLE-SCLEROSIS | COMPLEX GANGLIOSIDES | ESCHERICHIA-COLI | GROWTH | IMMUNOLOGY | B-SUBUNIT | CHOLERA-TOXIN | T-Lymphocytes, Regulatory - metabolism | Galectin 1 - immunology | Immunoprecipitation | Spinal Cord - metabolism | Encephalomyelitis, Autoimmune, Experimental - metabolism | Encephalomyelitis, Autoimmune, Experimental - immunology | Galectin 1 - metabolism | T-Lymphocytes, Regulatory - immunology | CD4-Positive T-Lymphocytes - immunology | Lymphocyte Activation - immunology | Flow Cytometry | G(M1) Ganglioside - immunology | Spinal Cord - pathology | CD8-Positive T-Lymphocytes - metabolism | Cholera Toxin - immunology | Female | TRPC Cation Channels - immunology | Cross-Linking Reagents | Encephalomyelitis, Autoimmune, Experimental - pathology | Cholera Toxin - metabolism | CD4-Positive T-Lymphocytes - metabolism | Mice, Knockout | Spinal Cord - immunology | Animals | Mice | CD8-Positive T-Lymphocytes - immunology | G(M1) Ganglioside - metabolism | Index Medicus | Abridged Index Medicus
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4. Full Text The immunobiology of Campylobacter jejuni : Innate immunity and autoimmune diseases
by Phongsisay, Vongsavanh
Immunobiology, ISSN 0171-2985, 2015, Volume 221, Issue 4, pp. 535 - 543
Abstract The Gram-negative bacterium Campylobacter jejuni causes gastroenteritis and Guillain-Barré syndrome in humans. Recent advances in the immunobiology of... 
Allergy and Immunology | Advanced Basic Science | Innate immunity | Autoimmune diseases | Receptor | Campylobacter jejuni | ACTIVATION | DENDRITIC CELLS | GUILLAIN-BARRE-SYNDROME | PROTEOMICS ANALYSIS | IMMUNOLOGY | CEREBROSPINAL-FLUID | MYELOID CELLS | BINDING PROTEIN | PERTUSSIS TOXIN | TOLL-LIKE RECEPTORS | T-CELLS | Campylobacter jejuni - pathogenicity | NLR Family, Pyrin Domain-Containing 3 Protein | Humans | Adaptor Proteins, Vesicular Transport - genetics | Lectins, C-Type - immunology | Gastroenteritis - microbiology | Lectins, C-Type - genetics | Host-Pathogen Interactions - immunology | Sialic Acid Binding Immunoglobulin-like Lectins - immunology | Molecular Mimicry | Campylobacter jejuni - immunology | Glycoconjugates - immunology | Myeloid Differentiation Factor 88 - immunology | Membrane Glycoproteins - immunology | Receptors, Immunologic - immunology | Gastroenteritis - immunology | Carrier Proteins - immunology | Gene Expression Regulation | Myeloid Differentiation Factor 88 - genetics | Adaptor Proteins, Vesicular Transport - immunology | Campylobacter Infections - genetics | Guillain-Barre Syndrome - genetics | Campylobacter Infections - microbiology | Immunity, Innate | Guillain-Barre Syndrome - microbiology | Glycoconjugates - secretion | Membrane Glycoproteins - genetics | Sialic Acid Binding Immunoglobulin-like Lectins - genetics | Carrier Proteins - genetics | Animals | Campylobacter Infections - immunology | Guillain-Barre Syndrome - immunology | Inflammasomes - immunology | Gastroenteritis - genetics | Guillain-Barre Syndrome - pathology | Receptors, Immunologic - genetics | Campylobacter Infections - pathology | Gastroenteritis - pathology | Autoimmunity | Guillain-Barre syndrome | Lymphocytes | Analysis | Gastroenteritis | Interferon | Galactose | Macrophages | Gangliosides | Immunity
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5. Full Text Platelets Recognize Brain-Specific Glycolipid Structures, Respond to Neurovascular Damage and Promote Neuroinflammation
by Sotnikov, Ilya and Veremeyko, Tatyana and Starossom, Sarah C and Barteneva, Natalia and Weiner, Howard L and Ponomarev, Eugene D
PLoS ONE, ISSN 1932-6203, 03/2013, Volume 8, Issue 3, p. e58979
Platelets respond to vascular damage and contribute to inflammation, but their role in the neurodegenerative diseases is unknown. We found that the systemic... 
ALZHEIMER-DISEASE | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | MULTIPLE-SCLEROSIS | MULTIDISCIPLINARY SCIENCES | MICROVASCULAR ENDOTHELIAL-CELLS | SPINAL-CORD | GANGLIOSIDES | SIALIC-ACID | ISCHEMIC-STROKE | PERTUSSIS TOXIN | BLOOD | Blood Platelets - immunology | Central Nervous System - metabolism | Encephalomyelitis, Autoimmune, Experimental - metabolism | Membrane Microdomains - metabolism | Encephalomyelitis, Autoimmune, Experimental - immunology | Cerebrovascular Disorders - metabolism | Central Nervous System - immunology | Brain - metabolism | Membrane Microdomains - immunology | Inflammation - metabolism | Astrocytes - immunology | Biological Transport | Cerebrovascular Disorders - immunology | Anaphylaxis - immunology | Neurons - metabolism | Disease Models, Animal | Cell Degranulation | Neurons - immunology | Membrane Microdomains - chemistry | Receptors, Cell Surface - metabolism | Inflammation - immunology | Glycolipids - metabolism | Gangliosides - immunology | Blood-Brain Barrier - metabolism | Animals | Blood Platelets - metabolism | Glycolipids - immunology | Protein Binding | Mice | Anaphylaxis - metabolism | Brain - immunology | Astrocytes - metabolism | Nervous system diseases | Inflammation | B cells | Neurons | Gangliosides | Brain | Cardiac arrhythmia | Disease | Pathogenesis | Central nervous system | Rafts | Parenchyma | Lipids | Lipid rafts | Medical schools | Receptors | Dyspnea | Anaphylaxis | Blood platelets | Cascades | Immune system | Rigid structures | Phenotypes | Immune response | Neurodegenerative diseases | Neurological diseases | Hospitals | Glycosphingolipids | Womens health | Structural damage | Degranulation | Brain damage | Platelets | P-selectin
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6. Full Text Clustering T-cell GM1 lipid rafts increases cellular resistance to shear on fibronectin through changes in integrin affinity and cytoskeletal dynamics
by Mitchell, Jason S and Brown, Wells S and Woodside, Darren G and Vanderslice, Peter and McIntyre, Bradley W
Immunology and Cell Biology, ISSN 0818-9641, 05/2009, Volume 87, Issue 4, pp. 324 - 336
Lipid rafts are small laterally mobile microdomains that are highly enriched in lymphocyte signaling molecules. GM1 gangliosides are a common lipid raft... 
cell trafficking | T cells | adhesion molecules | inflammation | human | Human | Adhesion molecules | Inflammation | Cell trafficking | CYTOPLASMIC DOMAIN | PHOSPHATIDYLINOSITOL 3-KINASE | ACTIN POLYMERIZATION | TRANSIENT UP-REGULATION | SOLUBLE VCAM-1 BINDING | IMMUNOLOGY | CELL BIOLOGY | SIGNAL-TRANSDUCTION | MEDIATED ADHESION | ADHESION MOLECULE-1 | MEMBRANE RAFTS | ANTIGEN RECEPTOR | Vascular Cell Adhesion Molecule-1 - immunology | Fibronectins - immunology | Signal Transduction | Cytoskeleton - immunology | Jurkat Cells | Humans | Integrins - immunology | Cell Adhesion - immunology | Membrane Microdomains - immunology | G(M1) Ganglioside - immunology | Cell Line, Tumor | T-Lymphocytes - immunology | Chemotaxis - immunology | Cytoskeleton, immunology | G(M1) Ganglioside, immunology | Vascular Cell Adhesion Molecule-1, immunology | Cell Adhesion, immunology | Membrane Microdomains, immunology | T-Lymphocytes, immunology | Fibronectins, immunology | Chemotaxis, immunology | Integrins, immunology | Cell Trafficking | Adhesion Molecules
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7. Full Text Both ganglioside GM2 and cholesterol in the cell membrane are essential for Bombyx mori cypovirus cell entry
by Zhu, Min and Zhu, Liyuan and Hu, Xiaolong and Kumar, Dhiraj and Chen, Fei and Feng, Yongjie and Liang, Zi and Huang, Lixu and Yu, Lei and Xu, Jian and Xue, Renyu and Cao, Guangli and Gong, Chengliang
Developmental and Comparative Immunology, ISSN 0145-305X, 11/2018, Volume 88, pp. 161 - 168
cypovirus (BmCPV) enters permissive cells via clathrin-mediated endocytosis pathway. However, the distinct entry mechanism for BmCPV is still ambiguous. The... 
Ganglioside GM2 | Bombyx mori | Cytoplasmic polyhedrosis virus | Membrane cholesterol | Infectivity | ENDOCYTIC PATHWAY | RECEPTOR | IMMUNOLOGY | CYTOPLASMIC POLYHEDROSIS-VIRUS | GENOME | MAMMALIAN REOVIRUS | INTERNALIZATION | FISHERIES | ZOOLOGY | JUNCTIONAL ADHESION MOLECULE | VP4 | REVEALS | G(M2) Ganglioside - immunology | Cholesterol - immunology | Biosynthetic Pathways - immunology | beta-Cyclodextrins - pharmacology | Virus Internalization | Host-Pathogen Interactions - immunology | Biosynthetic Pathways - genetics | Hydroxymethylglutaryl CoA Reductases - metabolism | Capsid Proteins - immunology | Agriculture | Cell Membrane - drug effects | Endocytosis - immunology | Virion - immunology | Bombyx - immunology | Cell Line | Endocytosis - drug effects | Virus Replication - immunology | Arthropod Proteins - genetics | Arthropod Proteins - immunology | Animals | Reoviridae - pathogenicity | Bombyx - virology | Cell Membrane - immunology | Cholesterol - biosynthesis | Hydroxymethylglutaryl CoA Reductases - genetics | Physiological aspects | Cyclodextrins | Gangliosides | Health aspects | Cholesterol
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8. Full Text CD4 and CD8 T cells require different membrane gangliosides for activation
by Masakazu Nagafuku and Kaori Okuyama and Yuri Onimaru and Akemi Suzuki and Yuta Odagiri and Tadashi Yamashita and Katsunori Iwasaki and Michihiro Fujiwara and Motoaki Takayanagi and Isao Ohno and Jin-ichi Inokuchi
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 02/2012, Volume 109, Issue 6, pp. E336 - E342
Initial events of T-cell activation involve movement of the T-cell receptor into lipid rafts. Gangliosides are major components of lipid rafts. While... 
Glycosphingolipids | Repertoire selection | HUMAN-LYMPHOCYTES | NERVOUS-SYSTEM | LOCALIZATION | repertoire selection | MULTIDISCIPLINARY SCIENCES | GLYCOSYLATION | CYTOKINE PRODUCTION | glycosphingolipids | LIPID RAFTS | ASTHMA | FUNCTIONAL RAFTS | MICE | GLYCOSPHINGOLIPID LEVELS | T-Lymphocyte Subsets - immunology | CD8-Positive T-Lymphocytes - cytology | T-Lymphocyte Subsets - cytology | CD4-Positive T-Lymphocytes - cytology | Mice, Inbred C57BL | Sialyltransferases - deficiency | Pneumonia - pathology | Hypersensitivity - immunology | Hypersensitivity - complications | Sialyltransferases - metabolism | Gangliosides - immunology | Thymocytes - immunology | CD4-Positive T-Lymphocytes - immunology | Epitopes - immunology | Cell Differentiation - immunology | Lymphocyte Activation - immunology | Animals | Hypersensitivity - pathology | Pneumonia - complications | Pneumonia - immunology | Thymocytes - cytology | Cell Membrane - immunology | Mice | CD8-Positive T-Lymphocytes - immunology | Molecules | T cell receptors | Gene expression | Rodents | Immune system | Biological Sciences | PNAS Plus
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9. Full Text Efficient killing of high risk neuroblastoma using natural killer cells activated by plasmacytoid dendritic cells
by Cordeau, Martine and Belounis, Assila and Lelaidier, Martin and Cordeiro, Paulo and Sartelet, Hervé and Herblot, Sabine and Duval, Michel
PLoS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, p. e0164401
High-risk neuroblastoma ( NB) remains a major therapeutic challenge despite the recent advent of disialoganglioside (GD2)-antibody treatment combined with... 
INTERLEUKIN-2 | STEM-CELLS | TRAIL | MULTIDISCIPLINARY SCIENCES | BONE-MARROW | GENE-EXPRESSION | NK-CELLS | CHEMORESISTANCE | INDUCTION | CANCER | TUMOR-INITIATING CELLS | Antigens, CD - immunology | Antigens, Differentiation, T-Lymphocyte - immunology | Dendritic Cells - immunology | Humans | Lectins, C-Type - immunology | TNF-Related Apoptosis-Inducing Ligand - immunology | Interferon-alpha - immunology | Toll-Like Receptor 9 - immunology | Lymphocyte Activation - immunology | Interferon-gamma - immunology | Neuroblastoma - immunology | Cell Line, Tumor | Killer Cells, Natural - immunology | CD56 Antigen - immunology | Viral antibodies | Killer cells | Interleukins | Dendritic cells | Immunotherapy | Antibodies | Interferon | Neuroblastoma | Gangliosides | Pediatrics | Transplants & implants | Toxicity | Leukemia | Interleukin | Cytotoxicity | Risk | Stimulation | Activation | Metastasis | Cerebrospinal fluid | Proteins | CD69 antigen | Cell activation | Immunology | Toll-like receptors | Colony-stimulating factor | Natural killer cells | Immune system | Killing | Antigens | Cytokines | Risk groups | Granulocyte-macrophage colony-stimulating factor | T cell receptors | Gene expression | Patients | TLR9 protein | Monocytes | Stem cells | Ligands | TRAIL protein | Leukocytes (granulocytic) | Apoptosis | Tumors | Cancer
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10. Full Text Glycosylation Changes Triggered by the Differentiation of Monocytic THP-1 Cell Line into Macrophages
by Delannoy, Clément P and Rombouts, Yoann and Groux-Degroote, Sophie and Holst, Stephanie and Coddeville, Bernadette and Harduin-Lepers, Anne and Wuhrer, Manfred and Elass-Rochard, Elisabeth and Guérardel, Yann
Journal of Proteome Research, ISSN 1535-3893, 01/2017, Volume 16, Issue 1, pp. 156 - 169
The human acute monocytic leukemia cell line THP-1 is widely used as an in vitro phagocytic cell model because it exhibits several immune properties similar to... 
monocyte-to-macrophage differentiation | glycosyltransferases | glycosylation | mass spectrometry | glycosphingolipids | DENDRITIC CELLS | BIOCHEMICAL RESEARCH METHODS | HL-60 CELLS | N-GLYCOSYLATION | IN-VITRO | E-SELECTIN | LEUKEMIA-CELLS | SIALIDASE ACTIVITY | MYELOID FIBRONECTIN RECEPTORS | PROTEIN GLYCOSYLATION | EXPRESSION | Macrophages - chemistry | Mannose - immunology | Monocytes - cytology | Humans | N-Acetylglucosaminyltransferases - genetics | Neuraminidase - genetics | Sialyltransferases - immunology | G(M3) Ganglioside - chemistry | Monocytes - immunology | Glycosphingolipids - immunology | Sialic Acids - chemistry | Neuraminidase - immunology | Polysaccharides - chemistry | Glycosyltransferases - genetics | Fucosyltransferases - immunology | Sialic Acids - immunology | Macrophages - immunology | Mannose - chemistry | Carbohydrate Sequence | Cell Line | Fucosyltransferases - genetics | Glycosyltransferases - immunology | N-Acetylglucosaminyltransferases - immunology | Gene Expression Regulation | Sialyltransferases - genetics | Glycosylation | Polysaccharides - immunology | Macrophages - cytology | Monocytes - chemistry | Cell Differentiation - immunology | G(M3) Ganglioside - immunology | Carbohydrate Conformation | Glycosphingolipids - chemistry | Life Sciences | Populations and Evolution | Biotechnology | Quantitative Methods | Biochemistry, Molecular Biology | Genomics | Biomolecules | Molecular biology | Molecular Networks | Biodiversity | Systematics, Phylogenetics and taxonomy | Cancer
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11. Full Text Antecedent infections in Fisher syndrome: A common pathogenesis of molecular mimicry
by Koga, M and Gilbert, M and Li, J and Koike, S and Takahashi, M and Furukawa, K and Hirata, K and Yuki, N
Neurology, ISSN 0028-3878, 05/2005, Volume 64, Issue 9, pp. 1605 - 1611
Objective: To assess the production mechanism of anti-GQ1b autoantibody in Fisher syndrome (FS). Methods: The authors conducted a prospective case-control... 
CAMPYLOBACTER-JEJUNI | IGG ANTIBODY | BEARING LIPOPOLYSACCHARIDE | GUILLAIN-BARRE-SYNDROME | GANGLIOSIDE MIMICS | HAEMOPHILUS-INFLUENZAE | CORE OLIGOSACCHARIDE | CLINICAL-FEATURES | CLOSE ASSOCIATION | ANTI-GQ1B ANTIBODY | CLINICAL NEUROLOGY | Campylobacter Infections - complications | Prospective Studies | Autoantibodies - blood | Humans | Middle Aged | Male | Cytomegalovirus Infections - complications | Cytomegalovirus Infections - immunology | Haemophilus Infections - complications | Lipopolysaccharides - immunology | Case-Control Studies | Campylobacter jejuni - immunology | Adult | Female | Mycoplasma Infections - immunology | Epstein-Barr Virus Infections - immunology | Molecular Mimicry - immunology | Miller Fisher Syndrome - immunology | Miller Fisher Syndrome - virology | Gangliosides - immunology | Mice, Knockout | Mycoplasma Infections - complications | Autoantibodies - immunology | Animals | Campylobacter Infections - immunology | Miller Fisher Syndrome - blood | Haemophilus influenzae - immunology | Epstein-Barr Virus Infections - complications | Mice | Haemophilus Infections - immunology
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