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Novel clinical features of recurrent human respiratory syncytial virus infections

Children and elderly individuals are often infected easily and repeatedly with human respiratory syncytial virus (HRSV); however, the features of recurrent infection in the same individual are defined poorly. To clarify the clinical significance of repeated HRSV infections in relation to subgroup ep...

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Autores principales: Yui, Ikuko, Fujino, Motoko, Sawada, Akihito, Nakayama, Tetsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282436/
https://www.ncbi.nlm.nih.gov/pubmed/24166209
http://dx.doi.org/10.1002/jmv.23809
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author Yui, Ikuko
Fujino, Motoko
Sawada, Akihito
Nakayama, Tetsuo
author_facet Yui, Ikuko
Fujino, Motoko
Sawada, Akihito
Nakayama, Tetsuo
author_sort Yui, Ikuko
collection PubMed
description Children and elderly individuals are often infected easily and repeatedly with human respiratory syncytial virus (HRSV); however, the features of recurrent infection in the same individual are defined poorly. To clarify the clinical significance of repeated HRSV infections in relation to subgroup epidemiology, this study performed prospective and longitudinal analyses in children with lower respiratory tract infections over 20 consecutive epidemics between 1985 and 2005 at a pediatric outpatient clinic in Kawasaki, Japan. HRSV infections were confirmed by 2 types of reverse-transcription PCR. Samples obtained from patients with repeated infections were subjected to sequence analysis and cloning analysis. A total of 1,312 lower respiratory tract infections observed in 1,010 patients were diagnosed as HRSV infections. Repeated HRSV infections occurred in 208 of the 1,010 patients. Analysis of the patients with repeated infections revealed that children were often infected multiple times even within a single short epidemic. Some patients were re-infected with strains having the same or virtually identical N gene sequences. In patients infected more than 4 times, cloning analysis revealed more frequent dual infections with both subgroups (23.8%). The HRSV-A subgroup caused subsequent homologous infections more frequently than did HRSV-B; furthermore, HRSV-A infections provided no protection from a second homologous infection. In contrast, HRSV-B infections offered significant protection against a second homologous infection. Statistical analysis revealed alleviation of symptoms with a reduced rate of dyspnoeic attacks only in the group re-infected with homologous HRSV-A strains. Thus, this study elucidates new clinical features of recurrent HRSV infection. J. Med. Virol 86: 1629–1638, 2014.
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spelling pubmed-42824362015-01-15 Novel clinical features of recurrent human respiratory syncytial virus infections Yui, Ikuko Fujino, Motoko Sawada, Akihito Nakayama, Tetsuo J Med Virol Research Articles Children and elderly individuals are often infected easily and repeatedly with human respiratory syncytial virus (HRSV); however, the features of recurrent infection in the same individual are defined poorly. To clarify the clinical significance of repeated HRSV infections in relation to subgroup epidemiology, this study performed prospective and longitudinal analyses in children with lower respiratory tract infections over 20 consecutive epidemics between 1985 and 2005 at a pediatric outpatient clinic in Kawasaki, Japan. HRSV infections were confirmed by 2 types of reverse-transcription PCR. Samples obtained from patients with repeated infections were subjected to sequence analysis and cloning analysis. A total of 1,312 lower respiratory tract infections observed in 1,010 patients were diagnosed as HRSV infections. Repeated HRSV infections occurred in 208 of the 1,010 patients. Analysis of the patients with repeated infections revealed that children were often infected multiple times even within a single short epidemic. Some patients were re-infected with strains having the same or virtually identical N gene sequences. In patients infected more than 4 times, cloning analysis revealed more frequent dual infections with both subgroups (23.8%). The HRSV-A subgroup caused subsequent homologous infections more frequently than did HRSV-B; furthermore, HRSV-A infections provided no protection from a second homologous infection. In contrast, HRSV-B infections offered significant protection against a second homologous infection. Statistical analysis revealed alleviation of symptoms with a reduced rate of dyspnoeic attacks only in the group re-infected with homologous HRSV-A strains. Thus, this study elucidates new clinical features of recurrent HRSV infection. J. Med. Virol 86: 1629–1638, 2014. BlackWell Publishing Ltd 2014-09 2013-10-25 /pmc/articles/PMC4282436/ /pubmed/24166209 http://dx.doi.org/10.1002/jmv.23809 Text en © 2014 Wiley Periodicals, Inc. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Yui, Ikuko
Fujino, Motoko
Sawada, Akihito
Nakayama, Tetsuo
Novel clinical features of recurrent human respiratory syncytial virus infections
title Novel clinical features of recurrent human respiratory syncytial virus infections
title_full Novel clinical features of recurrent human respiratory syncytial virus infections
title_fullStr Novel clinical features of recurrent human respiratory syncytial virus infections
title_full_unstemmed Novel clinical features of recurrent human respiratory syncytial virus infections
title_short Novel clinical features of recurrent human respiratory syncytial virus infections
title_sort novel clinical features of recurrent human respiratory syncytial virus infections
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282436/
https://www.ncbi.nlm.nih.gov/pubmed/24166209
http://dx.doi.org/10.1002/jmv.23809
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