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Expression of human cytomegalovirus components in the brain tissues of patients with Rasmussen’s encephalitis
Rasmussen’s encephalitis (RE) is a rare and severe progressive epileptic syndrome with unknown etiology. Infection by viruses, including human cytomegalovirus (HCMV), has been speculated to be a potential trigger for RE. However, no viral antigens have been detected in the brains of patients with RE...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702243/ https://www.ncbi.nlm.nih.gov/pubmed/28303446 http://dx.doi.org/10.1007/s12250-016-3917-z |
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author | Zhang, Yao Wang, Yisong Chen, Sichang Chen, Shuai Guan, Yuguang Liu, Changqing Li, Tianfu Luan, Guoming An, Jing |
author_facet | Zhang, Yao Wang, Yisong Chen, Sichang Chen, Shuai Guan, Yuguang Liu, Changqing Li, Tianfu Luan, Guoming An, Jing |
author_sort | Zhang, Yao |
collection | PubMed |
description | Rasmussen’s encephalitis (RE) is a rare and severe progressive epileptic syndrome with unknown etiology. Infection by viruses, including human cytomegalovirus (HCMV), has been speculated to be a potential trigger for RE. However, no viral antigens have been detected in the brains of patients with RE; thus, a possible clinical linkage between viral infections and RE has not been firmly established. In this study, we evaluated the expression of HCMV pp65 antigen in brain sections from 26 patients with RE and 20 non-RE patients by immunohistochemistry and in situ hybridization, and assessed the associations between HCMV infection and clinical parameters. Elevated expression of HCMV pp65 protein and DNA was observed in 88.5% (23/26) and 69.2% (18/26) of RE cases, respectively. In the non-RE group, HCMV pp65 antigen was detected only in two cases (10%), both of which were negative for DNA staining. Additionally, the intensity of HCMV pp65 staining was correlated with a shorter duration of the prodromal stage, younger age of seizure onset, and more severe unilateral cortical atrophy. Elevated expression of HCMV pp65 was observed in RE brain tissue and was correlated with the clinical features of RE disease. In summary, our results suggested that HCMV infection may be involved in the occurrence and progression of RE disease. Thus, further studies are needed to determine whether early treatment with anti-HCMV antibodies could modulate the course of RE. [Image: see text] |
format | Online Article Text |
id | pubmed-6702243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-67022432019-08-21 Expression of human cytomegalovirus components in the brain tissues of patients with Rasmussen’s encephalitis Zhang, Yao Wang, Yisong Chen, Sichang Chen, Shuai Guan, Yuguang Liu, Changqing Li, Tianfu Luan, Guoming An, Jing Virol Sin Research Article Rasmussen’s encephalitis (RE) is a rare and severe progressive epileptic syndrome with unknown etiology. Infection by viruses, including human cytomegalovirus (HCMV), has been speculated to be a potential trigger for RE. However, no viral antigens have been detected in the brains of patients with RE; thus, a possible clinical linkage between viral infections and RE has not been firmly established. In this study, we evaluated the expression of HCMV pp65 antigen in brain sections from 26 patients with RE and 20 non-RE patients by immunohistochemistry and in situ hybridization, and assessed the associations between HCMV infection and clinical parameters. Elevated expression of HCMV pp65 protein and DNA was observed in 88.5% (23/26) and 69.2% (18/26) of RE cases, respectively. In the non-RE group, HCMV pp65 antigen was detected only in two cases (10%), both of which were negative for DNA staining. Additionally, the intensity of HCMV pp65 staining was correlated with a shorter duration of the prodromal stage, younger age of seizure onset, and more severe unilateral cortical atrophy. Elevated expression of HCMV pp65 was observed in RE brain tissue and was correlated with the clinical features of RE disease. In summary, our results suggested that HCMV infection may be involved in the occurrence and progression of RE disease. Thus, further studies are needed to determine whether early treatment with anti-HCMV antibodies could modulate the course of RE. [Image: see text] Springer Singapore 2017-03-02 /pmc/articles/PMC6702243/ /pubmed/28303446 http://dx.doi.org/10.1007/s12250-016-3917-z Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Article Zhang, Yao Wang, Yisong Chen, Sichang Chen, Shuai Guan, Yuguang Liu, Changqing Li, Tianfu Luan, Guoming An, Jing Expression of human cytomegalovirus components in the brain tissues of patients with Rasmussen’s encephalitis |
title | Expression of human cytomegalovirus components in the brain
tissues of patients with Rasmussen’s encephalitis |
title_full | Expression of human cytomegalovirus components in the brain
tissues of patients with Rasmussen’s encephalitis |
title_fullStr | Expression of human cytomegalovirus components in the brain
tissues of patients with Rasmussen’s encephalitis |
title_full_unstemmed | Expression of human cytomegalovirus components in the brain
tissues of patients with Rasmussen’s encephalitis |
title_short | Expression of human cytomegalovirus components in the brain
tissues of patients with Rasmussen’s encephalitis |
title_sort | expression of human cytomegalovirus components in the brain
tissues of patients with rasmussen’s encephalitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702243/ https://www.ncbi.nlm.nih.gov/pubmed/28303446 http://dx.doi.org/10.1007/s12250-016-3917-z |
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