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Autoimmune Encephalitis and CSF Anti-GluR3 Antibodies in an MS Patient after Alemtuzumab Treatment

A 45-year-old Italian woman, affected by relapsing–remitting multiple sclerosis (RR-MS) starting from 2011, started treatment with alemtuzumab in July 2016. Nine months after the second infusion, she had an immune thrombocytopenic purpura (ITP) with complete recovery after steroid treatment. Three m...

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Autores principales: Buscarinu, Maria Chiara, Fornasiero, Arianna, Pellicciari, Giulia, Reniè, Roberta, Landi, Anna Chiara, Bozzao, Alessandro, Cappelletti, Cristina, Bernasconi, Pia, Ristori, Giovanni, Salvetti, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895826/
https://www.ncbi.nlm.nih.gov/pubmed/31671619
http://dx.doi.org/10.3390/brainsci9110299
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author Buscarinu, Maria Chiara
Fornasiero, Arianna
Pellicciari, Giulia
Reniè, Roberta
Landi, Anna Chiara
Bozzao, Alessandro
Cappelletti, Cristina
Bernasconi, Pia
Ristori, Giovanni
Salvetti, Marco
author_facet Buscarinu, Maria Chiara
Fornasiero, Arianna
Pellicciari, Giulia
Reniè, Roberta
Landi, Anna Chiara
Bozzao, Alessandro
Cappelletti, Cristina
Bernasconi, Pia
Ristori, Giovanni
Salvetti, Marco
author_sort Buscarinu, Maria Chiara
collection PubMed
description A 45-year-old Italian woman, affected by relapsing–remitting multiple sclerosis (RR-MS) starting from 2011, started treatment with alemtuzumab in July 2016. Nine months after the second infusion, she had an immune thrombocytopenic purpura (ITP) with complete recovery after steroid treatment. Three months after the ITP, the patient presented with transient aphasia, cognitive deficits, and focal epilepsy. Serial brain magnetic resonance imaging showed a pattern compatible with encephalitis. Autoantibodies to glutamate receptor 3 peptide A and B were detected in cerebrospinal fluid and serum, in the absence of any other diagnostic cues. After three courses of intravenous immunoglobulin (0.4 mg/kg/day for 5 days, 1 month apart), followed by boosters (0.4 mg/kg/day) every 4–6 weeks, her neurological status improved and is currently comparable with that preceding the encephalitis. Autoimmune complications of the central nervous system during alemtuzumab therapy are relatively rare: only one previous case of autoimmune encephalitis following alemtuzumab treatment has been reported to date.
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spelling pubmed-68958262019-12-24 Autoimmune Encephalitis and CSF Anti-GluR3 Antibodies in an MS Patient after Alemtuzumab Treatment Buscarinu, Maria Chiara Fornasiero, Arianna Pellicciari, Giulia Reniè, Roberta Landi, Anna Chiara Bozzao, Alessandro Cappelletti, Cristina Bernasconi, Pia Ristori, Giovanni Salvetti, Marco Brain Sci Case Report A 45-year-old Italian woman, affected by relapsing–remitting multiple sclerosis (RR-MS) starting from 2011, started treatment with alemtuzumab in July 2016. Nine months after the second infusion, she had an immune thrombocytopenic purpura (ITP) with complete recovery after steroid treatment. Three months after the ITP, the patient presented with transient aphasia, cognitive deficits, and focal epilepsy. Serial brain magnetic resonance imaging showed a pattern compatible with encephalitis. Autoantibodies to glutamate receptor 3 peptide A and B were detected in cerebrospinal fluid and serum, in the absence of any other diagnostic cues. After three courses of intravenous immunoglobulin (0.4 mg/kg/day for 5 days, 1 month apart), followed by boosters (0.4 mg/kg/day) every 4–6 weeks, her neurological status improved and is currently comparable with that preceding the encephalitis. Autoimmune complications of the central nervous system during alemtuzumab therapy are relatively rare: only one previous case of autoimmune encephalitis following alemtuzumab treatment has been reported to date. MDPI 2019-10-30 /pmc/articles/PMC6895826/ /pubmed/31671619 http://dx.doi.org/10.3390/brainsci9110299 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Buscarinu, Maria Chiara
Fornasiero, Arianna
Pellicciari, Giulia
Reniè, Roberta
Landi, Anna Chiara
Bozzao, Alessandro
Cappelletti, Cristina
Bernasconi, Pia
Ristori, Giovanni
Salvetti, Marco
Autoimmune Encephalitis and CSF Anti-GluR3 Antibodies in an MS Patient after Alemtuzumab Treatment
title Autoimmune Encephalitis and CSF Anti-GluR3 Antibodies in an MS Patient after Alemtuzumab Treatment
title_full Autoimmune Encephalitis and CSF Anti-GluR3 Antibodies in an MS Patient after Alemtuzumab Treatment
title_fullStr Autoimmune Encephalitis and CSF Anti-GluR3 Antibodies in an MS Patient after Alemtuzumab Treatment
title_full_unstemmed Autoimmune Encephalitis and CSF Anti-GluR3 Antibodies in an MS Patient after Alemtuzumab Treatment
title_short Autoimmune Encephalitis and CSF Anti-GluR3 Antibodies in an MS Patient after Alemtuzumab Treatment
title_sort autoimmune encephalitis and csf anti-glur3 antibodies in an ms patient after alemtuzumab treatment
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895826/
https://www.ncbi.nlm.nih.gov/pubmed/31671619
http://dx.doi.org/10.3390/brainsci9110299
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