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Identification of B cell epitopes reactive to human papillomavirus type-16L1- derived peptides

BACKGROUND: Persistent infection of human papillomavirus (HPV) types 16 and 18 causes cervical cancer. To better understand immune responses to the prophylactic vaccine, HPV 16/18 L1 virus-like particles (HPV-VLPs), we investigated B cell epitopes of HPV16 L1-derived peptides. METHODS: Sera from mic...

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Autores principales: Fukui, Akimasa, Matsueda, Satoko, Kawano, Kouichiro, Tsuda, Naotake, Komatsu, Nobukazu, Shichijo, Shigeki, Sasada, Tetsuro, Hattori, Satoshi, Ushijima, Kimio, Itoh, Kyogo, Kamura, Toshiharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463485/
https://www.ncbi.nlm.nih.gov/pubmed/22979950
http://dx.doi.org/10.1186/1743-422X-9-199
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author Fukui, Akimasa
Matsueda, Satoko
Kawano, Kouichiro
Tsuda, Naotake
Komatsu, Nobukazu
Shichijo, Shigeki
Sasada, Tetsuro
Hattori, Satoshi
Ushijima, Kimio
Itoh, Kyogo
Kamura, Toshiharu
author_facet Fukui, Akimasa
Matsueda, Satoko
Kawano, Kouichiro
Tsuda, Naotake
Komatsu, Nobukazu
Shichijo, Shigeki
Sasada, Tetsuro
Hattori, Satoshi
Ushijima, Kimio
Itoh, Kyogo
Kamura, Toshiharu
author_sort Fukui, Akimasa
collection PubMed
description BACKGROUND: Persistent infection of human papillomavirus (HPV) types 16 and 18 causes cervical cancer. To better understand immune responses to the prophylactic vaccine, HPV 16/18 L1 virus-like particles (HPV-VLPs), we investigated B cell epitopes of HPV16 L1-derived peptides. METHODS: Sera from mice immunized with HPV-16/18 L1 VLPs were analyzed for their IgG titers against 10 different HPV16 L1-derived peptides (20-mer) that contain human leukocyte antigen (HLA)-class I A-2, A-24 and class II DR. RESULTS: One 20-mer peptide at positions 300 to 319 was identified as a common B cell epitope in both Balb/c (H-2(d)) and C57BL/6 (H-2(b)) mice. Mapping analysis showed that the 10-amino-acid sequence at positions 304to 313 was an immunogenic portion. It is of note that the binding capability of this 10-mer peptide to the HLA-A2 and HLA-A24 molecules was confirmed by the HLA class I stabilization assay. In addition, one unique 20-mer was determined as a B cell epitope in each strain. CONCLUSIONS: These results might provide new information for better understanding of immune responses to HPV 16 L1.
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spelling pubmed-34634852012-10-04 Identification of B cell epitopes reactive to human papillomavirus type-16L1- derived peptides Fukui, Akimasa Matsueda, Satoko Kawano, Kouichiro Tsuda, Naotake Komatsu, Nobukazu Shichijo, Shigeki Sasada, Tetsuro Hattori, Satoshi Ushijima, Kimio Itoh, Kyogo Kamura, Toshiharu Virol J Research BACKGROUND: Persistent infection of human papillomavirus (HPV) types 16 and 18 causes cervical cancer. To better understand immune responses to the prophylactic vaccine, HPV 16/18 L1 virus-like particles (HPV-VLPs), we investigated B cell epitopes of HPV16 L1-derived peptides. METHODS: Sera from mice immunized with HPV-16/18 L1 VLPs were analyzed for their IgG titers against 10 different HPV16 L1-derived peptides (20-mer) that contain human leukocyte antigen (HLA)-class I A-2, A-24 and class II DR. RESULTS: One 20-mer peptide at positions 300 to 319 was identified as a common B cell epitope in both Balb/c (H-2(d)) and C57BL/6 (H-2(b)) mice. Mapping analysis showed that the 10-amino-acid sequence at positions 304to 313 was an immunogenic portion. It is of note that the binding capability of this 10-mer peptide to the HLA-A2 and HLA-A24 molecules was confirmed by the HLA class I stabilization assay. In addition, one unique 20-mer was determined as a B cell epitope in each strain. CONCLUSIONS: These results might provide new information for better understanding of immune responses to HPV 16 L1. BioMed Central 2012-09-14 /pmc/articles/PMC3463485/ /pubmed/22979950 http://dx.doi.org/10.1186/1743-422X-9-199 Text en Copyright ©2012 Fukui et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Fukui, Akimasa
Matsueda, Satoko
Kawano, Kouichiro
Tsuda, Naotake
Komatsu, Nobukazu
Shichijo, Shigeki
Sasada, Tetsuro
Hattori, Satoshi
Ushijima, Kimio
Itoh, Kyogo
Kamura, Toshiharu
Identification of B cell epitopes reactive to human papillomavirus type-16L1- derived peptides
title Identification of B cell epitopes reactive to human papillomavirus type-16L1- derived peptides
title_full Identification of B cell epitopes reactive to human papillomavirus type-16L1- derived peptides
title_fullStr Identification of B cell epitopes reactive to human papillomavirus type-16L1- derived peptides
title_full_unstemmed Identification of B cell epitopes reactive to human papillomavirus type-16L1- derived peptides
title_short Identification of B cell epitopes reactive to human papillomavirus type-16L1- derived peptides
title_sort identification of b cell epitopes reactive to human papillomavirus type-16l1- derived peptides
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463485/
https://www.ncbi.nlm.nih.gov/pubmed/22979950
http://dx.doi.org/10.1186/1743-422X-9-199
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