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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6895826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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