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Anti-NMDA receptor encephalitis and nonencephalitic HSV-1 infection

OBJECTIVE: To determine whether there is an association between nonencephalitic herpes simplex virus 1 (HSV-1) infection and anti-NMDA receptor encephalitis (anti-NMDARE). METHODS: Antibody testing was performed using samples from 2 cohorts in a case-control observational study. The cohort “Philadel...

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Autores principales: Salovin, Amy, Glanzman, Jason, Roslin, Kylie, Armangue, Thais, Lynch, David R., Panzer, Jessica A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886833/
https://www.ncbi.nlm.nih.gov/pubmed/29629396
http://dx.doi.org/10.1212/NXI.0000000000000458
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author Salovin, Amy
Glanzman, Jason
Roslin, Kylie
Armangue, Thais
Lynch, David R.
Panzer, Jessica A.
author_facet Salovin, Amy
Glanzman, Jason
Roslin, Kylie
Armangue, Thais
Lynch, David R.
Panzer, Jessica A.
author_sort Salovin, Amy
collection PubMed
description OBJECTIVE: To determine whether there is an association between nonencephalitic herpes simplex virus 1 (HSV-1) infection and anti-NMDA receptor encephalitis (anti-NMDARE). METHODS: Antibody testing was performed using samples from 2 cohorts in a case-control observational study. The cohort “Philadelphia” included 16 serum samples of pediatric anti-NMDARE cases and 42 age-matched controls with other neuroinflammatory disorders studied at the Children's Hospital of Philadelphia and University of Pennsylvania. The cohort “Barcelona” contained 23 anti-NMDARE patient samples and 26 age-matched participants with other neuroinflammatory disorders studied at IDIBAPS-Hospital Clinic, University of Barcelona. The presence of HSV-1 IgG antibodies was examined by ELISA. As an additional control, IgG antibodies to cytomegalovirus (CMV) and Epstein-Barr virus viral capsid antigen (EBV-VCA) were determined. RESULTS: In each cohort, more participants with anti-NMDARE than controls had anti-HSV-1 IgG antibodies. In the Philadelphia cohort (58 participants), 44% of anti-NMDARE cases had antibodies to HSV-1 compared with 14% controls (OR 4.67, 95% CI 1.3–17.3, p = 0.031). In the Barcelona cohort (49 participants), 52% of participants with anti-NMDARE had antibodies to HSV-1 compared with 31% of controls (OR 2.45, 95% CI 0.7–7.9, p = 0.155). Overall, 49% of anti-NMDARE cases have antibodies to HSV-1 in these 2 combined cohorts compared with 21% of controls (Mantel-Haenszel OR 3.21, 95% CI 1.3–7.7, p = 0.007). CONCLUSION: Past HSV-1 infection was found in significantly more anti-NMDARE cases than controls. This suggests a meaningful association between nonencephalitic HSV-1 infection and development of anti-NMDARE.
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spelling pubmed-58868332018-04-06 Anti-NMDA receptor encephalitis and nonencephalitic HSV-1 infection Salovin, Amy Glanzman, Jason Roslin, Kylie Armangue, Thais Lynch, David R. Panzer, Jessica A. Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To determine whether there is an association between nonencephalitic herpes simplex virus 1 (HSV-1) infection and anti-NMDA receptor encephalitis (anti-NMDARE). METHODS: Antibody testing was performed using samples from 2 cohorts in a case-control observational study. The cohort “Philadelphia” included 16 serum samples of pediatric anti-NMDARE cases and 42 age-matched controls with other neuroinflammatory disorders studied at the Children's Hospital of Philadelphia and University of Pennsylvania. The cohort “Barcelona” contained 23 anti-NMDARE patient samples and 26 age-matched participants with other neuroinflammatory disorders studied at IDIBAPS-Hospital Clinic, University of Barcelona. The presence of HSV-1 IgG antibodies was examined by ELISA. As an additional control, IgG antibodies to cytomegalovirus (CMV) and Epstein-Barr virus viral capsid antigen (EBV-VCA) were determined. RESULTS: In each cohort, more participants with anti-NMDARE than controls had anti-HSV-1 IgG antibodies. In the Philadelphia cohort (58 participants), 44% of anti-NMDARE cases had antibodies to HSV-1 compared with 14% controls (OR 4.67, 95% CI 1.3–17.3, p = 0.031). In the Barcelona cohort (49 participants), 52% of participants with anti-NMDARE had antibodies to HSV-1 compared with 31% of controls (OR 2.45, 95% CI 0.7–7.9, p = 0.155). Overall, 49% of anti-NMDARE cases have antibodies to HSV-1 in these 2 combined cohorts compared with 21% of controls (Mantel-Haenszel OR 3.21, 95% CI 1.3–7.7, p = 0.007). CONCLUSION: Past HSV-1 infection was found in significantly more anti-NMDARE cases than controls. This suggests a meaningful association between nonencephalitic HSV-1 infection and development of anti-NMDARE. Lippincott Williams & Wilkins 2018-04-05 /pmc/articles/PMC5886833/ /pubmed/29629396 http://dx.doi.org/10.1212/NXI.0000000000000458 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Salovin, Amy
Glanzman, Jason
Roslin, Kylie
Armangue, Thais
Lynch, David R.
Panzer, Jessica A.
Anti-NMDA receptor encephalitis and nonencephalitic HSV-1 infection
title Anti-NMDA receptor encephalitis and nonencephalitic HSV-1 infection
title_full Anti-NMDA receptor encephalitis and nonencephalitic HSV-1 infection
title_fullStr Anti-NMDA receptor encephalitis and nonencephalitic HSV-1 infection
title_full_unstemmed Anti-NMDA receptor encephalitis and nonencephalitic HSV-1 infection
title_short Anti-NMDA receptor encephalitis and nonencephalitic HSV-1 infection
title_sort anti-nmda receptor encephalitis and nonencephalitic hsv-1 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886833/
https://www.ncbi.nlm.nih.gov/pubmed/29629396
http://dx.doi.org/10.1212/NXI.0000000000000458
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