Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.

Two cardinal manifestations of viral immunity are efficient clearance of acute infection and the capacity to vaccinate against secondary viral exposure. For noroviruses, the contributions of T cells to viral clearance and vaccination have not been elucidated. We report here that both CD4 and CD8 T c...

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Main Authors: Karen A Chachu, Anna D LoBue, David W Strong, Ralph S Baric, Herbert W Virgin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-12-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC2587711?pdf=render
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spelling doaj-d0c260ff2dd74d88a704f168a628a3e52020-11-25T02:20:06ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742008-12-01412e100023610.1371/journal.ppat.1000236Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.Karen A ChachuAnna D LoBueDavid W StrongRalph S BaricHerbert W VirginTwo cardinal manifestations of viral immunity are efficient clearance of acute infection and the capacity to vaccinate against secondary viral exposure. For noroviruses, the contributions of T cells to viral clearance and vaccination have not been elucidated. We report here that both CD4 and CD8 T cells are required for efficient clearance of primary murine norovirus (MNV) infection from the intestine and intestinal lymph nodes. Further, long-lasting protective immunity was generated by oral live virus vaccination. Systemic vaccination with the MNV capsid protein also effectively protected against mucosal challenge, while vaccination with the capsid protein of the distantly related human Lordsdale virus provided partial protection. Fully effective vaccination required a broad immune response including CD4 T cells, CD8 T cells, and B cells, but the importance of specific immune cell types varied between the intestine and intestinal lymph nodes. Perforin, but not interferon gamma, was required for clearance of MNV infection by adoptively transferred T lymphocytes from vaccinated hosts. These studies prove the feasibility of both mucosal and systemic vaccination against mucosal norovirus infection, demonstrate tissue specificity of norovirus immune cells, and indicate that efficient vaccination strategies should induce potent CD4 and CD8 T cell responses.http://europepmc.org/articles/PMC2587711?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Karen A Chachu
Anna D LoBue
David W Strong
Ralph S Baric
Herbert W Virgin
spellingShingle Karen A Chachu
Anna D LoBue
David W Strong
Ralph S Baric
Herbert W Virgin
Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.
PLoS Pathogens
author_facet Karen A Chachu
Anna D LoBue
David W Strong
Ralph S Baric
Herbert W Virgin
author_sort Karen A Chachu
title Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.
title_short Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.
title_full Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.
title_fullStr Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.
title_full_unstemmed Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.
title_sort immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2008-12-01
description Two cardinal manifestations of viral immunity are efficient clearance of acute infection and the capacity to vaccinate against secondary viral exposure. For noroviruses, the contributions of T cells to viral clearance and vaccination have not been elucidated. We report here that both CD4 and CD8 T cells are required for efficient clearance of primary murine norovirus (MNV) infection from the intestine and intestinal lymph nodes. Further, long-lasting protective immunity was generated by oral live virus vaccination. Systemic vaccination with the MNV capsid protein also effectively protected against mucosal challenge, while vaccination with the capsid protein of the distantly related human Lordsdale virus provided partial protection. Fully effective vaccination required a broad immune response including CD4 T cells, CD8 T cells, and B cells, but the importance of specific immune cell types varied between the intestine and intestinal lymph nodes. Perforin, but not interferon gamma, was required for clearance of MNV infection by adoptively transferred T lymphocytes from vaccinated hosts. These studies prove the feasibility of both mucosal and systemic vaccination against mucosal norovirus infection, demonstrate tissue specificity of norovirus immune cells, and indicate that efficient vaccination strategies should induce potent CD4 and CD8 T cell responses.
url http://europepmc.org/articles/PMC2587711?pdf=render
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