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CMV Infection Attenuates the Disease Course in a Murine Model of Multiple Sclerosis

Recent evidence in multiple sclerosis (MS) suggests that active CMV infection may result in more benign clinical disease. The goal of this pilot study was to determine whether underlying murine CMV (MCMV) infection affects the course of the Theiler's murine encephalitis virus (TMEV) induced mur...

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Autores principales: Pirko, Istvan, Cardin, Rhonda, Chen, Yi, Lohrey, Anne K., Lindquist, Diana M., Dunn, R. Scott, Zivadinov, Robert, Johnson, Aaron J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3290597/
https://www.ncbi.nlm.nih.gov/pubmed/22393447
http://dx.doi.org/10.1371/journal.pone.0032767
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author Pirko, Istvan
Cardin, Rhonda
Chen, Yi
Lohrey, Anne K.
Lindquist, Diana M.
Dunn, R. Scott
Zivadinov, Robert
Johnson, Aaron J.
author_facet Pirko, Istvan
Cardin, Rhonda
Chen, Yi
Lohrey, Anne K.
Lindquist, Diana M.
Dunn, R. Scott
Zivadinov, Robert
Johnson, Aaron J.
author_sort Pirko, Istvan
collection PubMed
description Recent evidence in multiple sclerosis (MS) suggests that active CMV infection may result in more benign clinical disease. The goal of this pilot study was to determine whether underlying murine CMV (MCMV) infection affects the course of the Theiler's murine encephalitis virus (TMEV) induced murine model of MS. A group of eight TMEV-infected mice were co-infected with MCMV at 2 weeks prior to TMEV infection while a second group of TMEV-infected mice received MCMV two weeks post TMEV. We also used 2 control groups, where at the above time points MCMV was replaced with PBS. Outcome measures included (1) monthly monitoring of disability via rotarod for 8 months; (2) in vivo MRI for brain atrophy studies and (3) FACS analysis of brain infiltrating lymphocytes at 8 months post TMEV infection. Co-infection with MCMV influenced the disease course in mice infected prior to TMEV infection. In this group, rotarod detectable motor performance was significantly improved starting 3 months post-infection and beyond (p≤0.024). In addition, their brain atrophy was close to 30% reduced at 8 months, but this was only present as a trend due to low power (p = 0.19). A significant reduction in the proportion of brain infiltrating CD3+ cells was detected in this group (p = 0.026), while the proportion of CD45+ Mac1+ cells significantly increased (p = 0.003). There was also a strong trend for a reduced proportion of CD4+ cells (p = 0.17) while CD8 and B220+ cell proportion did not change. These findings support an immunomodulatory effect of MCMV infection in this MS model. Future studies in this co-infection model will provide insight into mechanisms which modulate the development of demyelination and may be utilized for the development of novel therapeutic strategies.
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spelling pubmed-32905972012-03-05 CMV Infection Attenuates the Disease Course in a Murine Model of Multiple Sclerosis Pirko, Istvan Cardin, Rhonda Chen, Yi Lohrey, Anne K. Lindquist, Diana M. Dunn, R. Scott Zivadinov, Robert Johnson, Aaron J. PLoS One Research Article Recent evidence in multiple sclerosis (MS) suggests that active CMV infection may result in more benign clinical disease. The goal of this pilot study was to determine whether underlying murine CMV (MCMV) infection affects the course of the Theiler's murine encephalitis virus (TMEV) induced murine model of MS. A group of eight TMEV-infected mice were co-infected with MCMV at 2 weeks prior to TMEV infection while a second group of TMEV-infected mice received MCMV two weeks post TMEV. We also used 2 control groups, where at the above time points MCMV was replaced with PBS. Outcome measures included (1) monthly monitoring of disability via rotarod for 8 months; (2) in vivo MRI for brain atrophy studies and (3) FACS analysis of brain infiltrating lymphocytes at 8 months post TMEV infection. Co-infection with MCMV influenced the disease course in mice infected prior to TMEV infection. In this group, rotarod detectable motor performance was significantly improved starting 3 months post-infection and beyond (p≤0.024). In addition, their brain atrophy was close to 30% reduced at 8 months, but this was only present as a trend due to low power (p = 0.19). A significant reduction in the proportion of brain infiltrating CD3+ cells was detected in this group (p = 0.026), while the proportion of CD45+ Mac1+ cells significantly increased (p = 0.003). There was also a strong trend for a reduced proportion of CD4+ cells (p = 0.17) while CD8 and B220+ cell proportion did not change. These findings support an immunomodulatory effect of MCMV infection in this MS model. Future studies in this co-infection model will provide insight into mechanisms which modulate the development of demyelination and may be utilized for the development of novel therapeutic strategies. Public Library of Science 2012-02-29 /pmc/articles/PMC3290597/ /pubmed/22393447 http://dx.doi.org/10.1371/journal.pone.0032767 Text en Pirko et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pirko, Istvan
Cardin, Rhonda
Chen, Yi
Lohrey, Anne K.
Lindquist, Diana M.
Dunn, R. Scott
Zivadinov, Robert
Johnson, Aaron J.
CMV Infection Attenuates the Disease Course in a Murine Model of Multiple Sclerosis
title CMV Infection Attenuates the Disease Course in a Murine Model of Multiple Sclerosis
title_full CMV Infection Attenuates the Disease Course in a Murine Model of Multiple Sclerosis
title_fullStr CMV Infection Attenuates the Disease Course in a Murine Model of Multiple Sclerosis
title_full_unstemmed CMV Infection Attenuates the Disease Course in a Murine Model of Multiple Sclerosis
title_short CMV Infection Attenuates the Disease Course in a Murine Model of Multiple Sclerosis
title_sort cmv infection attenuates the disease course in a murine model of multiple sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3290597/
https://www.ncbi.nlm.nih.gov/pubmed/22393447
http://dx.doi.org/10.1371/journal.pone.0032767
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