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NMDAR encephalitis: passive transfer from man to mouse by a recombinant antibody

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dc.contributor.author Malviya, Manish
dc.contributor.author Mannara, Francesco
dc.contributor.author Martín García, Elena, 1975-
dc.contributor.author Maldonado, Rafael, 1961-
dc.contributor.author Goebels, Norbert
dc.date.accessioned 2018-02-14T11:52:53Z
dc.date.available 2018-02-14T11:52:53Z
dc.date.issued 2017
dc.identifier.citation Malviya M, Barman S, Golombeck KS, Planagumà J, Mannara F, Strutz-Seebohm N et al. NMDAR encephalitis: passive transfer from man to mouse by a recombinant antibody. Ann Clin Transl Neurol. 2017 Oct 3;4(11):768-83. DOI: 10.1002/acn3.444
dc.identifier.issn 2328-9503
dc.identifier.uri http://hdl.handle.net/10230/33851
dc.description.abstract Objective: Autoimmune encephalitis is most frequently associated with anti-NMDAR autoantibodies. Their pathogenic relevance has been suggested by passive transfer of patients' cerebrospinal fluid (CSF) in mice in vivo. We aimed to analyze the intrathecal plasma cell repertoire, identify autoantibody-producing clones, and characterize their antibody signatures in recombinant form. Methods: Patients with recent onset typical anti-NMDAR encephalitis were subjected to flow cytometry analysis of the peripheral and intrathecal immune response before, during, and after immunotherapy. Recombinant human monoclonal antibodies (rhuMab) were cloned and expressed from matching immunoglobulin heavy- (IgH) and light-chain (IgL) amplicons of clonally expanded intrathecal plasma cells (cePc) and tested for their pathogenic relevance. Results: Intrathecal accumulation of B and plasma cells corresponded to the clinical course. The presence of cePc with hypermutated antigen receptors indicated an antigen-driven intrathecal immune response. Consistently, a single recombinant human GluN1-specific monoclonal antibody, rebuilt from intrathecal cePc, was sufficient to reproduce NMDAR epitope specificity in vitro. After intraventricular infusion in mice, it accumulated in the hippocampus, decreased synaptic NMDAR density, and caused severe reversible memory impairment, a key pathogenic feature of the human disease, in vivo. Interpretation: A CNS-specific humoral immune response is present in anti-NMDAR encephalitis specifically targeting the GluN1 subunit of the NMDAR. Using reverse genetics, we recovered the typical intrathecal antibody signature in recombinant form, and proved its pathogenic relevance by passive transfer of disease symptoms from man to mouse, providing the critical link between intrathecal immune response and the pathogenesis of anti-NMDAR encephalitis as a humorally mediated autoimmune disease.
dc.format.mimetype application/pdf
dc.language.iso eng
dc.publisher Wiley
dc.relation.ispartof Annals of Clinical and Translational Neurology. 2017 Oct 3;4(11):768-83
dc.rights © 2017 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association.This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.title NMDAR encephalitis: passive transfer from man to mouse by a recombinant antibody
dc.type info:eu-repo/semantics/article
dc.identifier.doi http://dx.doi.org/10.1002/acn3.444
dc.subject.keyword Autoimmune encephalitis
dc.subject.keyword NMDAR encephalitis
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.type.version info:eu-repo/semantics/publishedVersion


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