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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3463485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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