Thesis icon

Thesis

Characterisation of AQP4-specific monoclonal antibodies in neuromyelitis optica spectrum disorders

Abstract:

Neuromyelitis optica spectrum disorders (NMOSD) is among a small but growing group of inflammatory conditions of the central nervous system (CNS) associated with autoantibodies of the IgG class against aquaporin-4 (AQP4), a principal water channel protein in astrocytes. Activation of the classical complement pathway by AQP4-IgG has been thought to initiate the formation of NMOSD lesions. However, clinical and histopathological data suggest the existence of AQP4-IgM and its potential contri...

Expand abstract

Actions

Access Document

Files:

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Research group:
Oxford Autoimmune Neurology Group
Oxford college:
Exeter College
Role:
Author
ORCID:
0000-0003-0179-1644

Contributors

Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Research group:
Oxford Autoimmune Neurology Group
Role:
Supervisor
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Research group:
Oxford Autoimmune Neurology Group
Role:
Supervisor
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Research group:
Experimental Neuropathology Group
Role:
Supervisor
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Examiner
ORCID:
0000-0002-4277-9855
Role:
Examiner


More from this funder
Programme:
Jardine Foundation Scholarship


DOI:
Type of award:
DPhil
Level of award:
Doctoral
Awarding institution:
University of Oxford

Terms of use


Views and Downloads

Views and downloads will return soon






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP