Humanised effector-null FcγRIIA antibody inhibits immune complex-mediated proinflammatory responses.


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
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

228-237

Commentaires 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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Auteurs

Bo Chen (B)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA Chenb@medimmune.com SimsG@MedImmune.com.

Katherine A Vousden (KA)

Department of Antibody Discovery and Protein Engineering, MedImmune Ltd, Granta Park, Great Abington, UK.

Brian Naiman (B)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.

Sean Turman (S)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.

Hong Sun (H)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.

Shu Wang (S)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.
Viela Bio, Gaithersburg, Maryland, USA.

Lisa M K Vinall (LMK)

Department of Antibody Discovery and Protein Engineering, MedImmune Ltd, Granta Park, Great Abington, UK.

Benjamin P Kemp (BP)

Department of Antibody Discovery and Protein Engineering, MedImmune Ltd, Granta Park, Great Abington, UK.

Srinath Kasturiangan (S)

Department of Antibody Discovery and Protein Engineering, MedImmune LLC, Gaithersburg, Maryland, USA.

D Gareth Rees (DG)

Department of Antibody Discovery and Protein Engineering, MedImmune Ltd, Granta Park, Great Abington, UK.

Ethan Grant (E)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Mary Jane Hinrichs (MJ)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Steven Eck (S)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Antonio DiGiandomenico (A)

Microbial Sciences, MedImmune, LLC, Gaithersburg, Maryland, USA.

M Jack Borrok (M)

Department of Antibody Discovery and Protein Engineering, MedImmune LLC, Gaithersburg, Maryland, USA.

Neang Ly (N)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Ximing Xiong (X)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.

Carlos Gonzalez (C)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Christopher Morehouse (C)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Yue Wang (Y)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.

Yebin Zhou (Y)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.

Jennifer Cann (J)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Weiguang Zhao (W)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Holly Koelkebeck (H)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Koshu Okubo (K)

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.

Tanya N Mayadas (TN)

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.

David Howe (D)

Department of Clinical Development, MedImmune Ltd, Granta Park, Great Abington, UK.

Janet Griffiths (J)

Department of Translational Medicine, MedImmune LLC, Gaithersburg, Maryland, USA.

Roland Kolbeck (R)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.

Ronald Herbst (R)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA.

Gary P Sims (GP)

Department of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, Maryland, USA Chenb@medimmune.com SimsG@MedImmune.com.

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