Persistence of virus-specific immune responses in the central nervous system of mice after West Nile virus infection
<p>Abstract</p> <p>Background</p> <p>West Nile virus (WNV) persists in humans and several animal models. We previously demonstrated that WNV persists in the central nervous system (CNS) of mice for up to 6 months post-inoculation. We hypothesized that the CNS immune res...
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doaj-7840eb363ebc448b9abee2c0d8eded392020-11-25T03:43:35ZengBMCBMC Immunology1471-21722011-01-01121610.1186/1471-2172-12-6Persistence of virus-specific immune responses in the central nervous system of mice after West Nile virus infectionWong Susan JDemarest Valerie LStewart Barbara SGreen SharoneBernard Kristen A<p>Abstract</p> <p>Background</p> <p>West Nile virus (WNV) persists in humans and several animal models. We previously demonstrated that WNV persists in the central nervous system (CNS) of mice for up to 6 months post-inoculation. We hypothesized that the CNS immune response is ineffective in clearing the virus.</p> <p>Results</p> <p>Immunocompetent, adult mice were inoculated subcutaneously with WNV, and the CNS immune response was examined at 1, 2, 4, 8, 12 and 16 weeks post-inoculation (wpi). Characterization of lymphocyte phenotypes in the CNS revealed elevation of CD19<sup>+ </sup>B cells for 4 wpi, CD138 plasma cells at 12 wpi, and CD4<sup>+ </sup>and CD8<sup>+ </sup>T cells for at least 12 wpi. T cells recruited to the brain were activated, and regulatory T cells (Tregs) were present for at least 12 wpi. WNV-specific antibody secreting cells were detected in the brain from 2 to 16 wpi, and virus-specific CD8<sup>+ </sup>T cells directed against an immunodominant WNV epitope were detected in the brain from 1 to 16 wpi. Furthermore, these WNV-specific immune responses occurred in mice with and without acute clinical disease.</p> <p>Conclusions</p> <p>Virus-specific immune cells persist in the CNS of mice after WNV infection for up to 16 wpi.</p> http://www.biomedcentral.com/1471-2172/12/6 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wong Susan J Demarest Valerie L Stewart Barbara S Green Sharone Bernard Kristen A |
spellingShingle |
Wong Susan J Demarest Valerie L Stewart Barbara S Green Sharone Bernard Kristen A Persistence of virus-specific immune responses in the central nervous system of mice after West Nile virus infection BMC Immunology |
author_facet |
Wong Susan J Demarest Valerie L Stewart Barbara S Green Sharone Bernard Kristen A |
author_sort |
Wong Susan J |
title |
Persistence of virus-specific immune responses in the central nervous system of mice after West Nile virus infection |
title_short |
Persistence of virus-specific immune responses in the central nervous system of mice after West Nile virus infection |
title_full |
Persistence of virus-specific immune responses in the central nervous system of mice after West Nile virus infection |
title_fullStr |
Persistence of virus-specific immune responses in the central nervous system of mice after West Nile virus infection |
title_full_unstemmed |
Persistence of virus-specific immune responses in the central nervous system of mice after West Nile virus infection |
title_sort |
persistence of virus-specific immune responses in the central nervous system of mice after west nile virus infection |
publisher |
BMC |
series |
BMC Immunology |
issn |
1471-2172 |
publishDate |
2011-01-01 |
description |
<p>Abstract</p> <p>Background</p> <p>West Nile virus (WNV) persists in humans and several animal models. We previously demonstrated that WNV persists in the central nervous system (CNS) of mice for up to 6 months post-inoculation. We hypothesized that the CNS immune response is ineffective in clearing the virus.</p> <p>Results</p> <p>Immunocompetent, adult mice were inoculated subcutaneously with WNV, and the CNS immune response was examined at 1, 2, 4, 8, 12 and 16 weeks post-inoculation (wpi). Characterization of lymphocyte phenotypes in the CNS revealed elevation of CD19<sup>+ </sup>B cells for 4 wpi, CD138 plasma cells at 12 wpi, and CD4<sup>+ </sup>and CD8<sup>+ </sup>T cells for at least 12 wpi. T cells recruited to the brain were activated, and regulatory T cells (Tregs) were present for at least 12 wpi. WNV-specific antibody secreting cells were detected in the brain from 2 to 16 wpi, and virus-specific CD8<sup>+ </sup>T cells directed against an immunodominant WNV epitope were detected in the brain from 1 to 16 wpi. Furthermore, these WNV-specific immune responses occurred in mice with and without acute clinical disease.</p> <p>Conclusions</p> <p>Virus-specific immune cells persist in the CNS of mice after WNV infection for up to 16 wpi.</p> |
url |
http://www.biomedcentral.com/1471-2172/12/6 |
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