Humanised effector-null FcγRIIA antibody inhibits immune complex-mediated proinflammatory responses.
Animals
Antibodies, Anti-Idiotypic
/ pharmacology
Antibodies, Antineutrophil Cytoplasmic
/ immunology
Antigen-Antibody Complex
/ drug effects
Autoimmune Diseases
/ drug therapy
Dendritic Cells
/ immunology
Humans
Immunoglobulin G
/ immunology
Immunologic Factors
/ pharmacology
Interleukin-6
/ immunology
Macaca fascicularis
Mice
Mice, Transgenic
Neutrophils
/ immunology
Reactive Oxygen Species
/ immunology
Receptors, IgG
/ immunology
Tumor Necrosis Factor-alpha
/ immunology
FcγRIIA
antibody
immune complex
inflammation
Journal
Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
04
04
2018
revised:
25
10
2018
accepted:
30
10
2018
pubmed:
22
11
2018
medline:
29
10
2019
entrez:
22
11
2018
Statut:
ppublish
Résumé
Immune complexes (ICs) play a critical role in the pathology of autoimmune diseases. The aim of this study was to generate and characterise a first-in-class anti-FcγRIIA antibody (Ab) VIB9600 (previously known as MEDI9600) that blocks IgG immune complex-mediated cellular activation for clinical development. VIB9600 was humanised and optimised from the IV.3 Ab. Binding affinity and specificity were determined by Biacore and ELISA. Confocal microscopy, Flow Cytometry-based assays and binding competition assays were used to assess the mode of action of the antibody. In vitro cell-based assays were used to demonstrate suppression of IC-mediated inflammatory responses. In vivo target suppression and efficacy was demonstrated in FcγRIIA-transgenic mice. Single-dose pharmacokinetic (PK)/pharmacodynamic study multiple dose Good Laboratory Practice (GLP) toxicity studies were conducted in non-human primates. We generated a humanised effector-deficient anti-FcγRIIA antibody (VIB9600) that potently blocks autoantibody and IC-mediated proinflammatory responses. VIB9600 suppresses FcγRIIA activation by blocking ligand engagement and by internalising FcγRIIA from the cell surface. VIB9600 inhibits IC-induced type I interferons from plasmacytoid dendritic cells (involved in SLE), antineutrophil cytoplasmic antibody (ANCA)-induced production of reactive oxygen species by neutrophils (involved in ANCA-associated vasculitis) and IC-induced tumour necrosis factor α and interleukin-6 production (involved in rheumatoid arthritis). In FcγRIIA transgenic mice, VIB9600 suppressed antiplatelet antibody-induced thrombocytopaenia, acute anti-GBM Ab-induced nephritis and anticollagen Ab-induced arthritis. VIB9600 also exhibited favourable PK and safety profiles in cynomolgus monkey studies. VIB9600 is a specific humanised antibody antagonist of FcγRIIA with null effector function that warrants further clinical development for the treatment of IC-mediated diseases.
Identifiants
pubmed: 30459279
pii: annrheumdis-2018-213523
doi: 10.1136/annrheumdis-2018-213523
pmc: PMC6352406
doi:
Substances chimiques
Antibodies, Anti-Idiotypic
0
Antibodies, Antineutrophil Cytoplasmic
0
Antigen-Antibody Complex
0
Fc gamma receptor IIA
0
Immunoglobulin G
0
Immunologic Factors
0
Interleukin-6
0
Reactive Oxygen Species
0
Receptors, IgG
0
Tumor Necrosis Factor-alpha
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
228-237Commentaires et corrections
Type : CommentIn
Informations de copyright
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: MedImmune employees hold stock in AstraZeneca. Shu Wang is the emploee of the Viela Bio. Viela Bio is the sole owner of VIB9600. Bing Yao (YaoB@vielabio.com) is the CEO of Viela Bio and VIB9600 is in clinical development.
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