Autoantibodies to N-methyl D-aspartate receptors in autoimmune encephalitis

N-methyl-D-aspartate receptor (NMDAR) antibody encephalitis is a recently described autoimmune encephalopathy defined by the presence of serum antibodies that bind NMDARs (NMDAR-Abs). NMDAR-Ab encephalitis is a severe, but treatmentresponsive encephalitis with subacute onset. It can be associated wi...

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Autor principal: Bera, K
Outros Autores: Vincent, A
Formato: Tese
Idioma:English
Publicado em: 2011
Assuntos:
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author Bera, K
author2 Vincent, A
author_facet Vincent, A
Bera, K
author_sort Bera, K
collection OXFORD
description N-methyl-D-aspartate receptor (NMDAR) antibody encephalitis is a recently described autoimmune encephalopathy defined by the presence of serum antibodies that bind NMDARs (NMDAR-Abs). NMDAR-Ab encephalitis is a severe, but treatmentresponsive encephalitis with subacute onset. It can be associated with tumours and affects mainly young adults. Patients present with cognitive dysfunction, seizures, psychiatric and sleep disorders and most develop dyskinesias, autonomic instability and reduced consciousness. To explore further the NMDAR-Abs and their potential pathogenicity, a series of <em>in vitro</em> investigations were performed and preliminary attempts at passive transfer of disease. Human embryonic kidney (HEK) cells transfected with the NR1 and NR2B subunits, and live cultured neurons, were used first to detect NMDAR-Ab binding. Immunocytochemistry and ow cytometry demonstrated that binding to transfected HEK cells could be improved when NMDAR were presented in clusters by cotransfection with the postsynaptic density protein PSD-95. The NR1 subunit was identified as the target of NMDAR-Abs, and a novel quantitative assay based on immunoprecipitation of NR1 tagged by fusion with green uorescent protein was developed. Measurement of NMDAR-Ab levels showed that antibody levels corresponded to the clinical disease score within individual patients. Although the purification of full length NR1 was not successful, a secreted N-terminal construct was created and expressed in HEK cells. The binding of NMDAR-Abs was confirmed and this construct will be used for active immunisation in future. To explore pathogenic mechanisms <em>in vitro</em>, the main antibody subclasses were shown to be IgG1 and IgG3. Moreover the patients' autoantibodies, but not healthy control antibodies, were able to activate the complement cascade <em>in vitro</em> in cell lines and primary cultures. Finally, the NMDAR-Abs were shown to bind to primary microglial cultures and to cause morphological changes corresponding to early activation processes after prolonged exposure. The research has developed new assays that could be used for diagnosis and serial studies and revealed new potential mechanisms in NMDAR-Ab encephalitis.
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spelling oxford-uuid:6bbda982-ab5c-4982-b23a-0478c689869c2022-03-26T19:06:09ZAutoantibodies to N-methyl D-aspartate receptors in autoimmune encephalitisThesishttp://purl.org/coar/resource_type/c_db06uuid:6bbda982-ab5c-4982-b23a-0478c689869cNeuroscienceImmunologyNeurologyEnglishOxford University Research Archive - Valet2011Bera, KVincent, AN-methyl-D-aspartate receptor (NMDAR) antibody encephalitis is a recently described autoimmune encephalopathy defined by the presence of serum antibodies that bind NMDARs (NMDAR-Abs). NMDAR-Ab encephalitis is a severe, but treatmentresponsive encephalitis with subacute onset. It can be associated with tumours and affects mainly young adults. Patients present with cognitive dysfunction, seizures, psychiatric and sleep disorders and most develop dyskinesias, autonomic instability and reduced consciousness. To explore further the NMDAR-Abs and their potential pathogenicity, a series of <em>in vitro</em> investigations were performed and preliminary attempts at passive transfer of disease. Human embryonic kidney (HEK) cells transfected with the NR1 and NR2B subunits, and live cultured neurons, were used first to detect NMDAR-Ab binding. Immunocytochemistry and ow cytometry demonstrated that binding to transfected HEK cells could be improved when NMDAR were presented in clusters by cotransfection with the postsynaptic density protein PSD-95. The NR1 subunit was identified as the target of NMDAR-Abs, and a novel quantitative assay based on immunoprecipitation of NR1 tagged by fusion with green uorescent protein was developed. Measurement of NMDAR-Ab levels showed that antibody levels corresponded to the clinical disease score within individual patients. Although the purification of full length NR1 was not successful, a secreted N-terminal construct was created and expressed in HEK cells. The binding of NMDAR-Abs was confirmed and this construct will be used for active immunisation in future. To explore pathogenic mechanisms <em>in vitro</em>, the main antibody subclasses were shown to be IgG1 and IgG3. Moreover the patients' autoantibodies, but not healthy control antibodies, were able to activate the complement cascade <em>in vitro</em> in cell lines and primary cultures. Finally, the NMDAR-Abs were shown to bind to primary microglial cultures and to cause morphological changes corresponding to early activation processes after prolonged exposure. The research has developed new assays that could be used for diagnosis and serial studies and revealed new potential mechanisms in NMDAR-Ab encephalitis.
spellingShingle Neuroscience
Immunology
Neurology
Bera, K
Autoantibodies to N-methyl D-aspartate receptors in autoimmune encephalitis
title Autoantibodies to N-methyl D-aspartate receptors in autoimmune encephalitis
title_full Autoantibodies to N-methyl D-aspartate receptors in autoimmune encephalitis
title_fullStr Autoantibodies to N-methyl D-aspartate receptors in autoimmune encephalitis
title_full_unstemmed Autoantibodies to N-methyl D-aspartate receptors in autoimmune encephalitis
title_short Autoantibodies to N-methyl D-aspartate receptors in autoimmune encephalitis
title_sort autoantibodies to n methyl d aspartate receptors in autoimmune encephalitis
topic Neuroscience
Immunology
Neurology
work_keys_str_mv AT berak autoantibodiestonmethyldaspartatereceptorsinautoimmuneencephalitis