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Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice
In contrast to C57BL/6 mice, BALB/c mice are relatively resistant to the induction of experimental autoimmune encephalomyelitis (EAE) after challenge with MOG(35–55) peptide. Here, we provide the first evidence that infection with murine cytomegalovirus (MCMV) in adulthood abrogates this resistance....
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326788/ https://www.ncbi.nlm.nih.gov/pubmed/28289417 http://dx.doi.org/10.3389/fimmu.2017.00192 |
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author | Milovanovic, Jelena Popovic, Branka Milovanovic, Marija Kvestak, Daria Arsenijevic, Aleksandar Stojanovic, Bojana Tanaskovic, Irena Krmpotic, Astrid Arsenijevic, Nebojsa Jonjic, Stipan Lukic, Miodrag L. |
author_facet | Milovanovic, Jelena Popovic, Branka Milovanovic, Marija Kvestak, Daria Arsenijevic, Aleksandar Stojanovic, Bojana Tanaskovic, Irena Krmpotic, Astrid Arsenijevic, Nebojsa Jonjic, Stipan Lukic, Miodrag L. |
author_sort | Milovanovic, Jelena |
collection | PubMed |
description | In contrast to C57BL/6 mice, BALB/c mice are relatively resistant to the induction of experimental autoimmune encephalomyelitis (EAE) after challenge with MOG(35–55) peptide. Here, we provide the first evidence that infection with murine cytomegalovirus (MCMV) in adulthood abrogates this resistance. Infected BALB/c mice developed clinical and histological signs similar to those seen in susceptible C57BL/6 mice. In addition to CD4(+) cells, large proportion of cells in the infiltrate of diseased BALB/c mice was CD8(+), similar with findings in multiple sclerosis. CD8(+) cells that responded to ex vivo restimulation with MOG(35–55) were not specific for viral epitopes pp89 and m164. MCMV infection favors proinflammatory type of dendritic cells (CD86(+)CD40(+)CD11c(+)) in the peripheral lymph organs, M1 type of microglia in central nervous system, and increases development of Th1/Th17 encephalitogenic cells. This study indicates that MCMV may enhance autoimmune neuropathology and abrogate inherent resistance to EAE in mouse strain by enhancing proinflammatory phenotype of antigen-presenting cells, Th1/Th17, and CD8 response to MOG(35–55). |
format | Online Article Text |
id | pubmed-5326788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53267882017-03-13 Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice Milovanovic, Jelena Popovic, Branka Milovanovic, Marija Kvestak, Daria Arsenijevic, Aleksandar Stojanovic, Bojana Tanaskovic, Irena Krmpotic, Astrid Arsenijevic, Nebojsa Jonjic, Stipan Lukic, Miodrag L. Front Immunol Immunology In contrast to C57BL/6 mice, BALB/c mice are relatively resistant to the induction of experimental autoimmune encephalomyelitis (EAE) after challenge with MOG(35–55) peptide. Here, we provide the first evidence that infection with murine cytomegalovirus (MCMV) in adulthood abrogates this resistance. Infected BALB/c mice developed clinical and histological signs similar to those seen in susceptible C57BL/6 mice. In addition to CD4(+) cells, large proportion of cells in the infiltrate of diseased BALB/c mice was CD8(+), similar with findings in multiple sclerosis. CD8(+) cells that responded to ex vivo restimulation with MOG(35–55) were not specific for viral epitopes pp89 and m164. MCMV infection favors proinflammatory type of dendritic cells (CD86(+)CD40(+)CD11c(+)) in the peripheral lymph organs, M1 type of microglia in central nervous system, and increases development of Th1/Th17 encephalitogenic cells. This study indicates that MCMV may enhance autoimmune neuropathology and abrogate inherent resistance to EAE in mouse strain by enhancing proinflammatory phenotype of antigen-presenting cells, Th1/Th17, and CD8 response to MOG(35–55). Frontiers Media S.A. 2017-02-27 /pmc/articles/PMC5326788/ /pubmed/28289417 http://dx.doi.org/10.3389/fimmu.2017.00192 Text en Copyright © 2017 Milovanovic, Popovic, Milovanovic, Kvestak, Arsenijevic, Stojanovic, Tanaskovic, Krmpotic, Arsenijevic, Jonjic and Lukic. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Milovanovic, Jelena Popovic, Branka Milovanovic, Marija Kvestak, Daria Arsenijevic, Aleksandar Stojanovic, Bojana Tanaskovic, Irena Krmpotic, Astrid Arsenijevic, Nebojsa Jonjic, Stipan Lukic, Miodrag L. Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice |
title | Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice |
title_full | Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice |
title_fullStr | Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice |
title_full_unstemmed | Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice |
title_short | Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice |
title_sort | murine cytomegalovirus infection induces susceptibility to eae in resistant balb/c mice |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326788/ https://www.ncbi.nlm.nih.gov/pubmed/28289417 http://dx.doi.org/10.3389/fimmu.2017.00192 |
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