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Localization of epitopes recognized by monoclonal antibodies that neutralized the H3N2 influenza viruses in man
Through extensive isolation of neutralizing mAbs against H3N2 influenza viruses representing the in vivo repertoire in a human donor, we examined the relationships between antigenic drift of influenza virus and protective antibodies generated in an infected individual. The majority of mAbs isolated...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Society for General Microbiology
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081080/ https://www.ncbi.nlm.nih.gov/pubmed/21068214 http://dx.doi.org/10.1099/vir.0.026419-0 |
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author | Okada, Jun Ohshima, Nobuko Kubota-Koketsu, Ritsuko Iba, Yoshitaka Ota, Sayuri Takase, Wakana Yoshikawa, Tetsushi Ishikawa, Toyokazu Asano, Yoshizo Okuno, Yoshinobu Kurosawa, Yoshikazu |
author_facet | Okada, Jun Ohshima, Nobuko Kubota-Koketsu, Ritsuko Iba, Yoshitaka Ota, Sayuri Takase, Wakana Yoshikawa, Tetsushi Ishikawa, Toyokazu Asano, Yoshizo Okuno, Yoshinobu Kurosawa, Yoshikazu |
author_sort | Okada, Jun |
collection | PubMed |
description | Through extensive isolation of neutralizing mAbs against H3N2 influenza viruses representing the in vivo repertoire in a human donor, we examined the relationships between antigenic drift of influenza virus and protective antibodies generated in an infected individual. The majority of mAbs isolated from a donor born in 1960 were divided into three major groups with distinct strain specificity: 1968–1973, 1977–1993 and 1997–2003. In the present study, we developed a new method that allowed us to comprehensively determine the location of epitopes recognized by many mAbs. Original haemagglutinins (HAs) of several strains and chimaeric variants, in which one of the seven sites (A, B1, B2, C1, C2, D or E) was replaced by some other strain-derived sequence, were artificially expressed on the cell surface. The binding activity of mAbs to the HAs was examined by flow cytometry. By using this method, we determined the location of epitopes recognized by 98 different mAbs. Clones that neutralize the 1968–1973 strains bind to site B2/D, A or A/B1. While sites C, E and B were recognized by clones that neutralized the 1977–1993 strains, the majority of these clones bind to site C. Clones that neutralize the 1997–2003 strains bind to site B, A/B1, A/B2 or E/C2. |
format | Text |
id | pubmed-3081080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Society for General Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-30810802011-07-22 Localization of epitopes recognized by monoclonal antibodies that neutralized the H3N2 influenza viruses in man Okada, Jun Ohshima, Nobuko Kubota-Koketsu, Ritsuko Iba, Yoshitaka Ota, Sayuri Takase, Wakana Yoshikawa, Tetsushi Ishikawa, Toyokazu Asano, Yoshizo Okuno, Yoshinobu Kurosawa, Yoshikazu J Gen Virol Animal Through extensive isolation of neutralizing mAbs against H3N2 influenza viruses representing the in vivo repertoire in a human donor, we examined the relationships between antigenic drift of influenza virus and protective antibodies generated in an infected individual. The majority of mAbs isolated from a donor born in 1960 were divided into three major groups with distinct strain specificity: 1968–1973, 1977–1993 and 1997–2003. In the present study, we developed a new method that allowed us to comprehensively determine the location of epitopes recognized by many mAbs. Original haemagglutinins (HAs) of several strains and chimaeric variants, in which one of the seven sites (A, B1, B2, C1, C2, D or E) was replaced by some other strain-derived sequence, were artificially expressed on the cell surface. The binding activity of mAbs to the HAs was examined by flow cytometry. By using this method, we determined the location of epitopes recognized by 98 different mAbs. Clones that neutralize the 1968–1973 strains bind to site B2/D, A or A/B1. While sites C, E and B were recognized by clones that neutralized the 1977–1993 strains, the majority of these clones bind to site C. Clones that neutralize the 1997–2003 strains bind to site B, A/B1, A/B2 or E/C2. Society for General Microbiology 2011-02 /pmc/articles/PMC3081080/ /pubmed/21068214 http://dx.doi.org/10.1099/vir.0.026419-0 Text en Copyright © 2011, SGM http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Animal Okada, Jun Ohshima, Nobuko Kubota-Koketsu, Ritsuko Iba, Yoshitaka Ota, Sayuri Takase, Wakana Yoshikawa, Tetsushi Ishikawa, Toyokazu Asano, Yoshizo Okuno, Yoshinobu Kurosawa, Yoshikazu Localization of epitopes recognized by monoclonal antibodies that neutralized the H3N2 influenza viruses in man |
title | Localization of epitopes recognized by monoclonal antibodies that neutralized the H3N2 influenza viruses in man |
title_full | Localization of epitopes recognized by monoclonal antibodies that neutralized the H3N2 influenza viruses in man |
title_fullStr | Localization of epitopes recognized by monoclonal antibodies that neutralized the H3N2 influenza viruses in man |
title_full_unstemmed | Localization of epitopes recognized by monoclonal antibodies that neutralized the H3N2 influenza viruses in man |
title_short | Localization of epitopes recognized by monoclonal antibodies that neutralized the H3N2 influenza viruses in man |
title_sort | localization of epitopes recognized by monoclonal antibodies that neutralized the h3n2 influenza viruses in man |
topic | Animal |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081080/ https://www.ncbi.nlm.nih.gov/pubmed/21068214 http://dx.doi.org/10.1099/vir.0.026419-0 |
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