Development of Acquired Immunity following Repeated Respiratory Syncytial Virus Infections in Cotton Rats.

Respiratory syncytial virus (RSV) infections occur every year worldwide. Most infants are infected with RSV by one year of age and are reinfected because immune responses after the first infection are too weak to protect against subsequent infections. In the present study, immune responses against R...

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Main Authors: Yoshiaki Yamaji, Yosuke Yasui, Tetsuo Nakayama
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4880180?pdf=render
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spelling doaj-1704ccabbcf8405680dbcca4ae7a099e2020-11-25T02:47:06ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01115e015577710.1371/journal.pone.0155777Development of Acquired Immunity following Repeated Respiratory Syncytial Virus Infections in Cotton Rats.Yoshiaki YamajiYosuke YasuiTetsuo NakayamaRespiratory syncytial virus (RSV) infections occur every year worldwide. Most infants are infected with RSV by one year of age and are reinfected because immune responses after the first infection are too weak to protect against subsequent infections. In the present study, immune responses against RSV were investigated in order to obtain a better understanding of repetitive RSV infections in cotton rats. No detectable neutralizing antibody (NT) was developed after the first infection, and the second infection was not prevented. The results of histological examinations revealed severe inflammation, viral antigens were detected around bronchial epithelial cells, and infectious viruses were recovered from lung homogenates. Following the second infection neutralizing antibodies were significantly elevated, and CD8+ cells were activated in response to RSV-F253-265. No viral antigens was detected thereafter in lung tissues and infectious viruses were not recovered. Similar results were obtained in the present study using the subgroups A and B. These results support the induction of humoral and cellular immune responses following repetitive infections with RSV; however, these responses were insufficient to eliminate viruses in the first and second infections.http://europepmc.org/articles/PMC4880180?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yoshiaki Yamaji
Yosuke Yasui
Tetsuo Nakayama
spellingShingle Yoshiaki Yamaji
Yosuke Yasui
Tetsuo Nakayama
Development of Acquired Immunity following Repeated Respiratory Syncytial Virus Infections in Cotton Rats.
PLoS ONE
author_facet Yoshiaki Yamaji
Yosuke Yasui
Tetsuo Nakayama
author_sort Yoshiaki Yamaji
title Development of Acquired Immunity following Repeated Respiratory Syncytial Virus Infections in Cotton Rats.
title_short Development of Acquired Immunity following Repeated Respiratory Syncytial Virus Infections in Cotton Rats.
title_full Development of Acquired Immunity following Repeated Respiratory Syncytial Virus Infections in Cotton Rats.
title_fullStr Development of Acquired Immunity following Repeated Respiratory Syncytial Virus Infections in Cotton Rats.
title_full_unstemmed Development of Acquired Immunity following Repeated Respiratory Syncytial Virus Infections in Cotton Rats.
title_sort development of acquired immunity following repeated respiratory syncytial virus infections in cotton rats.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Respiratory syncytial virus (RSV) infections occur every year worldwide. Most infants are infected with RSV by one year of age and are reinfected because immune responses after the first infection are too weak to protect against subsequent infections. In the present study, immune responses against RSV were investigated in order to obtain a better understanding of repetitive RSV infections in cotton rats. No detectable neutralizing antibody (NT) was developed after the first infection, and the second infection was not prevented. The results of histological examinations revealed severe inflammation, viral antigens were detected around bronchial epithelial cells, and infectious viruses were recovered from lung homogenates. Following the second infection neutralizing antibodies were significantly elevated, and CD8+ cells were activated in response to RSV-F253-265. No viral antigens was detected thereafter in lung tissues and infectious viruses were not recovered. Similar results were obtained in the present study using the subgroups A and B. These results support the induction of humoral and cellular immune responses following repetitive infections with RSV; however, these responses were insufficient to eliminate viruses in the first and second infections.
url http://europepmc.org/articles/PMC4880180?pdf=render
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