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...
Main Authors: | , , |
---|---|
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 |
id |
doaj-1704ccabbcf8405680dbcca4ae7a099e |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT yoshiakiyamaji developmentofacquiredimmunityfollowingrepeatedrespiratorysyncytialvirusinfectionsincottonrats AT yosukeyasui developmentofacquiredimmunityfollowingrepeatedrespiratorysyncytialvirusinfectionsincottonrats AT tetsuonakayama developmentofacquiredimmunityfollowingrepeatedrespiratorysyncytialvirusinfectionsincottonrats |
_version_ |
1724754597832032256 |