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CMV-associated encephalitis and antineuronal autoantibodies - a case report
BACKGROUND: Human cytomegalovirus (CMV) is an ubiquitous pathogen capable of modulating the host immune system. Immune dysfunction is common during CMV infection and includes autoimmune phenomena. Here we focus on a case of primary CMV infection associated with encephalopathy in a patient with a rud...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502587/ https://www.ncbi.nlm.nih.gov/pubmed/22947340 http://dx.doi.org/10.1186/1471-2377-12-87 |
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author | Xu, Xinling Bergman, Peter Willows, Thomas Tammik, Charlotte Sund, Marie Hökfelt, Tomas Söderberg-Naucler, Cecilia Varani, Stefania |
author_facet | Xu, Xinling Bergman, Peter Willows, Thomas Tammik, Charlotte Sund, Marie Hökfelt, Tomas Söderberg-Naucler, Cecilia Varani, Stefania |
author_sort | Xu, Xinling |
collection | PubMed |
description | BACKGROUND: Human cytomegalovirus (CMV) is an ubiquitous pathogen capable of modulating the host immune system. Immune dysfunction is common during CMV infection and includes autoimmune phenomena. Here we focus on a case of primary CMV infection associated with encephalopathy in a patient with a rudimentary spleen. We discuss diagnostic challenges and immunological aspects as well as the hypothesis that CMV may break tolerance and induce potentially encephalitogenic autoantibodies. CASE PRESENTATION: A 33-year-old woman was admitted with features of encephalitis, rapidly progressing into a catatonic state. The patient tested negative for presence of herpes simplex virus DNA in cerebrospinal fluid (CSF), and had elevated liver enzymes and hepatomegaly at computed tomography scan (CT) examination. CT scan and magnetic resonance imaging (MRI) showed only a rudimentary spleen. Initially, serum was negative for anti-CMV IgM, but borderline for anti-CMV IgG by enzyme-linked immunosorbent assay. However, a more sensitive assay resulted in a positive specific IgM Western blot profile and low IgG avidity, suggesting primary CMV infection. Further, CMV DNA was retrospectively detected in a CSF sample collected at admission. We also detected antineuronal autoantibodies, which stained GAD-positive neurons in the hippocampus. The patient was treated by a combination of prednisone, intravenous immunoglobulins (IVIg) and antivirals, which resulted in a dramatic amelioration of the patient’s neurological status. One year after admission the patient exhibited a nearly complete recovery with mild deficits in attention and memory. CONCLUSIONS: A possible reason for the critical course of CMV infection could be the lack of a functional spleen in this patient, a condition previously associated with severe CMV infection. Prompt treatment with antiviral drugs, steroids and IVIg was most likely important for the positive outcome in this case and should be considered for similar cases of severe primary CMV infection associated with immunopathological phenomena. |
format | Online Article Text |
id | pubmed-3502587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35025872012-11-22 CMV-associated encephalitis and antineuronal autoantibodies - a case report Xu, Xinling Bergman, Peter Willows, Thomas Tammik, Charlotte Sund, Marie Hökfelt, Tomas Söderberg-Naucler, Cecilia Varani, Stefania BMC Neurol Case Report BACKGROUND: Human cytomegalovirus (CMV) is an ubiquitous pathogen capable of modulating the host immune system. Immune dysfunction is common during CMV infection and includes autoimmune phenomena. Here we focus on a case of primary CMV infection associated with encephalopathy in a patient with a rudimentary spleen. We discuss diagnostic challenges and immunological aspects as well as the hypothesis that CMV may break tolerance and induce potentially encephalitogenic autoantibodies. CASE PRESENTATION: A 33-year-old woman was admitted with features of encephalitis, rapidly progressing into a catatonic state. The patient tested negative for presence of herpes simplex virus DNA in cerebrospinal fluid (CSF), and had elevated liver enzymes and hepatomegaly at computed tomography scan (CT) examination. CT scan and magnetic resonance imaging (MRI) showed only a rudimentary spleen. Initially, serum was negative for anti-CMV IgM, but borderline for anti-CMV IgG by enzyme-linked immunosorbent assay. However, a more sensitive assay resulted in a positive specific IgM Western blot profile and low IgG avidity, suggesting primary CMV infection. Further, CMV DNA was retrospectively detected in a CSF sample collected at admission. We also detected antineuronal autoantibodies, which stained GAD-positive neurons in the hippocampus. The patient was treated by a combination of prednisone, intravenous immunoglobulins (IVIg) and antivirals, which resulted in a dramatic amelioration of the patient’s neurological status. One year after admission the patient exhibited a nearly complete recovery with mild deficits in attention and memory. CONCLUSIONS: A possible reason for the critical course of CMV infection could be the lack of a functional spleen in this patient, a condition previously associated with severe CMV infection. Prompt treatment with antiviral drugs, steroids and IVIg was most likely important for the positive outcome in this case and should be considered for similar cases of severe primary CMV infection associated with immunopathological phenomena. BioMed Central 2012-09-04 /pmc/articles/PMC3502587/ /pubmed/22947340 http://dx.doi.org/10.1186/1471-2377-12-87 Text en Copyright ©2012 Xu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Xu, Xinling Bergman, Peter Willows, Thomas Tammik, Charlotte Sund, Marie Hökfelt, Tomas Söderberg-Naucler, Cecilia Varani, Stefania CMV-associated encephalitis and antineuronal autoantibodies - a case report |
title | CMV-associated encephalitis and antineuronal autoantibodies - a case report |
title_full | CMV-associated encephalitis and antineuronal autoantibodies - a case report |
title_fullStr | CMV-associated encephalitis and antineuronal autoantibodies - a case report |
title_full_unstemmed | CMV-associated encephalitis and antineuronal autoantibodies - a case report |
title_short | CMV-associated encephalitis and antineuronal autoantibodies - a case report |
title_sort | cmv-associated encephalitis and antineuronal autoantibodies - a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502587/ https://www.ncbi.nlm.nih.gov/pubmed/22947340 http://dx.doi.org/10.1186/1471-2377-12-87 |
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