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Case Report: Anti-GABA(A) Receptor Encephalitis in a Dog

Autoantibodies against neurotransmitter receptors detected in cerebrospinal fluid (CSF) and serum are increasingly recognized in people with human autoimmune encephalitis causing severe neurological deficits, such as seizures and behavioral abnormalities. This case report describes the first encepha...

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Autores principales: Huenerfauth, Enrice I., Bien, Christian G., Bien, Corinna, Volk, Holger A., Meyerhoff, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262380/
https://www.ncbi.nlm.nih.gov/pubmed/35812851
http://dx.doi.org/10.3389/fvets.2022.886711
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author Huenerfauth, Enrice I.
Bien, Christian G.
Bien, Corinna
Volk, Holger A.
Meyerhoff, Nina
author_facet Huenerfauth, Enrice I.
Bien, Christian G.
Bien, Corinna
Volk, Holger A.
Meyerhoff, Nina
author_sort Huenerfauth, Enrice I.
collection PubMed
description Autoantibodies against neurotransmitter receptors detected in cerebrospinal fluid (CSF) and serum are increasingly recognized in people with human autoimmune encephalitis causing severe neurological deficits, such as seizures and behavioral abnormalities. This case report describes the first encephalitis associated with antibodies against the γ-aminobutyric acid-A receptor (GABA(A)R) in a dog. A young male intact Cavalier King Charles Spaniel was presented with recent onset of initial multiple generalized tonic-clonic seizures progressing into a status epilepticus. Interictally, he showed alternating stupor and hyperexcitability, ataxia, pleurothotonus and circling behavior to the left side. Magnetic resonance imaging (MRI) of the brain showed breed-specific anatomical abnormalities. Standard CSF analysis was unremarkable. Despite treatment with multiple antiseizure medications (ASMs) seizures and behavior abnormalities sustained. Immunotherapy with dexamethasone was started on the fifth day after disease manifestation. This led to rapid improvement of clinical signs. An extensive antibody search in CSF and serum demonstrated a neuropil staining pattern on a tissue-based assay compatible with GABA(A)R antibodies. The diagnosis was confirmed by binding of serum and CSF antibodies to GABA(A)R transfected Human Embryonic Kidney cells. The serum titer was 1:320, the CSF titer 1:2. At the control visit 4.5 weeks after start of immunotherapy, the dog was clinically normal. The GABA(A)R antibody titer in serum had strongly decreased. The antibodies were no longer detectable in CSF. Based on clinical presentation and testing for GABA(A)R binding antibodies, this describes the first veterinary patient with an anti-GABA(A)R encephalitis with a good outcome following ASM and corticosteroid treatment.
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spelling pubmed-92623802022-07-08 Case Report: Anti-GABA(A) Receptor Encephalitis in a Dog Huenerfauth, Enrice I. Bien, Christian G. Bien, Corinna Volk, Holger A. Meyerhoff, Nina Front Vet Sci Veterinary Science Autoantibodies against neurotransmitter receptors detected in cerebrospinal fluid (CSF) and serum are increasingly recognized in people with human autoimmune encephalitis causing severe neurological deficits, such as seizures and behavioral abnormalities. This case report describes the first encephalitis associated with antibodies against the γ-aminobutyric acid-A receptor (GABA(A)R) in a dog. A young male intact Cavalier King Charles Spaniel was presented with recent onset of initial multiple generalized tonic-clonic seizures progressing into a status epilepticus. Interictally, he showed alternating stupor and hyperexcitability, ataxia, pleurothotonus and circling behavior to the left side. Magnetic resonance imaging (MRI) of the brain showed breed-specific anatomical abnormalities. Standard CSF analysis was unremarkable. Despite treatment with multiple antiseizure medications (ASMs) seizures and behavior abnormalities sustained. Immunotherapy with dexamethasone was started on the fifth day after disease manifestation. This led to rapid improvement of clinical signs. An extensive antibody search in CSF and serum demonstrated a neuropil staining pattern on a tissue-based assay compatible with GABA(A)R antibodies. The diagnosis was confirmed by binding of serum and CSF antibodies to GABA(A)R transfected Human Embryonic Kidney cells. The serum titer was 1:320, the CSF titer 1:2. At the control visit 4.5 weeks after start of immunotherapy, the dog was clinically normal. The GABA(A)R antibody titer in serum had strongly decreased. The antibodies were no longer detectable in CSF. Based on clinical presentation and testing for GABA(A)R binding antibodies, this describes the first veterinary patient with an anti-GABA(A)R encephalitis with a good outcome following ASM and corticosteroid treatment. Frontiers Media S.A. 2022-06-23 /pmc/articles/PMC9262380/ /pubmed/35812851 http://dx.doi.org/10.3389/fvets.2022.886711 Text en Copyright © 2022 Huenerfauth, Bien, Bien, Volk and Meyerhoff. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Huenerfauth, Enrice I.
Bien, Christian G.
Bien, Corinna
Volk, Holger A.
Meyerhoff, Nina
Case Report: Anti-GABA(A) Receptor Encephalitis in a Dog
title Case Report: Anti-GABA(A) Receptor Encephalitis in a Dog
title_full Case Report: Anti-GABA(A) Receptor Encephalitis in a Dog
title_fullStr Case Report: Anti-GABA(A) Receptor Encephalitis in a Dog
title_full_unstemmed Case Report: Anti-GABA(A) Receptor Encephalitis in a Dog
title_short Case Report: Anti-GABA(A) Receptor Encephalitis in a Dog
title_sort case report: anti-gaba(a) receptor encephalitis in a dog
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262380/
https://www.ncbi.nlm.nih.gov/pubmed/35812851
http://dx.doi.org/10.3389/fvets.2022.886711
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