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Age-Specific Profiles of Antibody Responses against Respiratory Syncytial Virus Infection
Respiratory syncytial virus (RSV) is one of the most prevalent causative agents of lower respiratory tract infections worldwide, especially in infants around 3 to 4 months old. Infants at such a young age have maternally-transferred passive antibodies against RSV but do not have active immune system...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474434/ https://www.ncbi.nlm.nih.gov/pubmed/28111238 http://dx.doi.org/10.1016/j.ebiom.2017.01.014 |
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author | Jounai, Nao Yoshioka, Megumi Tozuka, Miyuki Inoue, Kazue Oka, Tatsuya Miyaji, Kazuki Ishida, Katsuyasu Kawai, Naoki Ikematsu, Hideyuki Kawakami, Chiaki Shimizu, Hiroyuki Mori, Masaaki Ishii, Ken J. Takeshita, Fumihiko |
author_facet | Jounai, Nao Yoshioka, Megumi Tozuka, Miyuki Inoue, Kazue Oka, Tatsuya Miyaji, Kazuki Ishida, Katsuyasu Kawai, Naoki Ikematsu, Hideyuki Kawakami, Chiaki Shimizu, Hiroyuki Mori, Masaaki Ishii, Ken J. Takeshita, Fumihiko |
author_sort | Jounai, Nao |
collection | PubMed |
description | Respiratory syncytial virus (RSV) is one of the most prevalent causative agents of lower respiratory tract infections worldwide, especially in infants around 3 to 4 months old. Infants at such a young age have maternally-transferred passive antibodies against RSV but do not have active immune systems efficient enough for the control of RSV infection. In order to elucidate age-specific profiles of immune responses against RSV protection, antibody responses were examined by using blood samples in both acute and convalescent phases obtained from child patients and adult patients. In addition to the serum neutralization activity, antibody responses to the RSV fusion protein (F protein) were dissected by analyzing levels of total IgG, IgG subclasses, the binding stability, and the levels of antibody for the neutralization epitopes. It was suggested that children's antibody responses against RSV are matured over months and years in at least 5 stages based on 1) levels of the neutralization titer and IgG3 for F protein in the convalescent phase, 2) geometric mean ratios of the neutralization titers and levels of IgG1 and IgG2 for F protein in the convalescent phase compared to those levels in the acute phase, 3) the affinity maturation of IgG for F protein and the cross reactivity of IgG for RSV glycoproteins of groups A and B, 4) levels of neutralization epitope-specific IgG, and 5) augmentation of overall antibody responses due to repetitive RSV infection. |
format | Online Article Text |
id | pubmed-5474434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-54744342017-06-26 Age-Specific Profiles of Antibody Responses against Respiratory Syncytial Virus Infection Jounai, Nao Yoshioka, Megumi Tozuka, Miyuki Inoue, Kazue Oka, Tatsuya Miyaji, Kazuki Ishida, Katsuyasu Kawai, Naoki Ikematsu, Hideyuki Kawakami, Chiaki Shimizu, Hiroyuki Mori, Masaaki Ishii, Ken J. Takeshita, Fumihiko EBioMedicine Research Paper Respiratory syncytial virus (RSV) is one of the most prevalent causative agents of lower respiratory tract infections worldwide, especially in infants around 3 to 4 months old. Infants at such a young age have maternally-transferred passive antibodies against RSV but do not have active immune systems efficient enough for the control of RSV infection. In order to elucidate age-specific profiles of immune responses against RSV protection, antibody responses were examined by using blood samples in both acute and convalescent phases obtained from child patients and adult patients. In addition to the serum neutralization activity, antibody responses to the RSV fusion protein (F protein) were dissected by analyzing levels of total IgG, IgG subclasses, the binding stability, and the levels of antibody for the neutralization epitopes. It was suggested that children's antibody responses against RSV are matured over months and years in at least 5 stages based on 1) levels of the neutralization titer and IgG3 for F protein in the convalescent phase, 2) geometric mean ratios of the neutralization titers and levels of IgG1 and IgG2 for F protein in the convalescent phase compared to those levels in the acute phase, 3) the affinity maturation of IgG for F protein and the cross reactivity of IgG for RSV glycoproteins of groups A and B, 4) levels of neutralization epitope-specific IgG, and 5) augmentation of overall antibody responses due to repetitive RSV infection. Elsevier 2017-01-16 /pmc/articles/PMC5474434/ /pubmed/28111238 http://dx.doi.org/10.1016/j.ebiom.2017.01.014 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Jounai, Nao Yoshioka, Megumi Tozuka, Miyuki Inoue, Kazue Oka, Tatsuya Miyaji, Kazuki Ishida, Katsuyasu Kawai, Naoki Ikematsu, Hideyuki Kawakami, Chiaki Shimizu, Hiroyuki Mori, Masaaki Ishii, Ken J. Takeshita, Fumihiko Age-Specific Profiles of Antibody Responses against Respiratory Syncytial Virus Infection |
title | Age-Specific Profiles of Antibody Responses against Respiratory Syncytial Virus Infection |
title_full | Age-Specific Profiles of Antibody Responses against Respiratory Syncytial Virus Infection |
title_fullStr | Age-Specific Profiles of Antibody Responses against Respiratory Syncytial Virus Infection |
title_full_unstemmed | Age-Specific Profiles of Antibody Responses against Respiratory Syncytial Virus Infection |
title_short | Age-Specific Profiles of Antibody Responses against Respiratory Syncytial Virus Infection |
title_sort | age-specific profiles of antibody responses against respiratory syncytial virus infection |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474434/ https://www.ncbi.nlm.nih.gov/pubmed/28111238 http://dx.doi.org/10.1016/j.ebiom.2017.01.014 |
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