Controlled tetra-Fc sialylation of IVIg results in a drug candidate with consistent enhanced anti-inflammatory activity.
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Induction of Regulatory T Cells by Intravenous Immunoglobulin: A Bridge between Adaptive and Innate ImmunityImmune recruitment or suppression by glycan engineering of endogenous and therapeutic antibodiesDesensitization: Overcoming the Immunologic Barriers to TransplantationMechanisms of Autoantibody-Induced Pathology.Protection in antibody- and T cell-mediated autoimmune diseases by antiinflammatory IgG Fcs requires type II FcRs.Comparison of Fc N-Glycosylation of Pharmaceutical Products of Intravenous Immunoglobulin GAnti-HA Glycoforms Drive B Cell Affinity Selection and Determine Influenza Vaccine Efficacy.Time-Dependent Structural Alteration of Rituximab Analyzed by LC/TOF-MS after a Systemic Administration to Rats.Sialylation of IgG Fc domain impairs complement-dependent cytotoxicity.Protection from experimental autoimmune encephalomyelitis by polyclonal IgG requires adjuvant-induced inflammation.Sialylation converts arthritogenic IgG into inhibitors of collagen-induced arthritis.Differences in Anti-Inflammatory Actions of Intravenous Immunoglobulin between Mice and Men: More than Meets the Eye.Using glyco-engineering to produce therapeutic proteins.bIgG time for large eaters: monocytes and macrophages as effector and target cells of antibody-mediated immune activation and repression.Epidermolysis Bullosa Acquisita: From Pathophysiology to Novel Therapeutic Options.IVIG-mediated effector functions in autoimmune and inflammatory diseases.State-of-the-art technologies for rapid and high-throughput sample preparation and analysis of N-glycans from antibodies.The Emerging Importance of IgG Fab Glycosylation in Immunity.Sweet but dangerous - the role of immunoglobulin G glycosylation in autoimmunity and inflammation.Intravenous immunoglobulin: pharmacological properties and use in polyneuropathies.Engineering the fragment crystallizable (Fc) region of human IgG1 multimers and monomers to fine-tune interactions with sialic acid-dependent receptors.Regulation of antibody effector functions through IgG Fc N-glycosylation.Modulators of IgG penetration through the blood-brain barrier: Implications for Alzheimer's disease immunotherapy.Improving Antibody-Based Cancer Therapeutics Through Glycan Engineering.Decoding the Human Immunoglobulin G-Glycan Repertoire Reveals a Spectrum of Fc-Receptor- and Complement-Mediated-Effector Activities.Combining measurements to estimate properties and characterization extent of complex biochemical mixtures; applications to Heparan Sulfate.Translating Inhibitory Fc Receptor Biology into Novel Therapeutic Approaches.High-resolution physicochemical characterization of different intravenous immunoglobulin products.Unlocking the bone: Fcγ-receptors and antibody glycosylation are keys to connecting bone homeostasis to humoral immunity.Glycosynthase Mutants of Endoglycosidase S2 Show Potent Transglycosylation Activity and Remarkably Relaxed Substrate Specificity for Antibody Glycosylation Remodeling.Antibody production using a ciliate generates unusual antibody glycoforms displaying enhanced cell-killing activity.Evaluation of a glycoengineered monoclonal antibody via LC-MS analysis in combination with multiple enzymatic digestion.Sialylated intravenous immunoglobulin suppress anti-ganglioside antibody mediated nerve injuryMassive immune response against IVIg interferes with response against other antigens in mice: A new mode of action?Piperidine-based glycodendrons as protein N-glycan prosthetics.Pro-inflammatory State in Monoclonal Gammopathy of Undetermined Significance and in Multiple Myeloma Is Characterized by Low Sialylation of Pathogen-Specific and Other Monoclonal Immunoglobulins.Engineered Sialylation of Pathogenic Antibodies In Vivo Attenuates Autoimmune Disease.Solid-Phase Enzymatic Remodeling Produces High Yields of Single Glycoform Antibodies.Desensitisation strategies in high-risk children before kidney transplantation.Differential antibody glycosylation in autoimmunity: sweet biomarker or modulator of disease activity?
P2860
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P2860
Controlled tetra-Fc sialylation of IVIg results in a drug candidate with consistent enhanced anti-inflammatory activity.
description
2015 nî lūn-bûn
@nan
2015 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի մարտին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Controlled tetra-Fc sialylatio ...... ed anti-inflammatory activity.
@ast
Controlled tetra-Fc sialylatio ...... ed anti-inflammatory activity.
@en
type
label
Controlled tetra-Fc sialylatio ...... ed anti-inflammatory activity.
@ast
Controlled tetra-Fc sialylatio ...... ed anti-inflammatory activity.
@en
prefLabel
Controlled tetra-Fc sialylatio ...... ed anti-inflammatory activity.
@ast
Controlled tetra-Fc sialylatio ...... ed anti-inflammatory activity.
@en
P2093
P2860
P50
P356
P1476
Controlled tetra-Fc sialylatio ...... ed anti-inflammatory activity.
@en
P2093
Amy Medeiros
Anthony M Manning
Birgit C Schultes
Carlos J Bosques
Daniel Ortiz
Divya Mekala
Edward Cochran
Ganesh V Kaundinya
Hetal Sarvaiya
Inessa Schwab
P2860
P304
P356
10.1073/PNAS.1422481112
P407
P577
2015-03-02T00:00:00Z