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Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies

BACKGROUND: Current vaccines against HPVs are constituted of L1 protein self-assembled into virus-like particles (VLPs) and they have been shown to protect against natural HPV16 and HPV18 infections and associated lesions. In addition, limited cross-protection has been observed against closely relat...

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Autores principales: Combelas, Nicolas, Saussereau, Emilie, Fleury, Maxime JJ, Ribeiro, Tatiana, Gaitan, Julien, Duarte-Forero, Diego F, Coursaget, Pierre, Touzé, Antoine
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2852459/
https://www.ncbi.nlm.nih.gov/pubmed/20334659
http://dx.doi.org/10.1186/1479-5876-8-28
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author Combelas, Nicolas
Saussereau, Emilie
Fleury, Maxime JJ
Ribeiro, Tatiana
Gaitan, Julien
Duarte-Forero, Diego F
Coursaget, Pierre
Touzé, Antoine
author_facet Combelas, Nicolas
Saussereau, Emilie
Fleury, Maxime JJ
Ribeiro, Tatiana
Gaitan, Julien
Duarte-Forero, Diego F
Coursaget, Pierre
Touzé, Antoine
author_sort Combelas, Nicolas
collection PubMed
description BACKGROUND: Current vaccines against HPVs are constituted of L1 protein self-assembled into virus-like particles (VLPs) and they have been shown to protect against natural HPV16 and HPV18 infections and associated lesions. In addition, limited cross-protection has been observed against closely related types. Immunization with L2 protein in animal models has been shown to provide cross-protection against distant papillomavirus types, suggesting that the L2 protein contains cross-neutralizing epitopes. However, vaccination with L2 protein or L2 peptides does not induce high titers of anti-L2 antibodies. In order to develop a vaccine with the potential to protect against other high-risk HPV types, we have produced HPV58 pseudovirions encoding the HPV31 L2 protein and compared their capacity to induce cross-neutralizing antibodies with that of HPV L1 and HPV L1/L2 VLPs. METHODS: The titers of neutralizing antibodies against HPV16, HPV18, HPV31 and HPV58 induced in Balb/c mice were compared after immunization with L2-containing vaccines. RESULTS: Low titers of cross-neutralizing antibodies were detected in mice when immunized with L1/L2 VLPs, and the highest levels of cross-neutralizing antibodies were observed in mice immunized with HPV 58 L1/L2 pseudovirions encoding the HPV 31 L2 protein. CONCLUSIONS: The results obtained indicate that high levels of cross-neutralizing antibodies are only observed after immunization with pseudovirions encoding the L2 protein. HPV pseudovirions thus represent a possible new strategy for the generation of a broad-spectrum vaccine to protect against high-risk HPVs and associated neoplasia.
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spelling pubmed-28524592010-04-10 Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies Combelas, Nicolas Saussereau, Emilie Fleury, Maxime JJ Ribeiro, Tatiana Gaitan, Julien Duarte-Forero, Diego F Coursaget, Pierre Touzé, Antoine J Transl Med Research BACKGROUND: Current vaccines against HPVs are constituted of L1 protein self-assembled into virus-like particles (VLPs) and they have been shown to protect against natural HPV16 and HPV18 infections and associated lesions. In addition, limited cross-protection has been observed against closely related types. Immunization with L2 protein in animal models has been shown to provide cross-protection against distant papillomavirus types, suggesting that the L2 protein contains cross-neutralizing epitopes. However, vaccination with L2 protein or L2 peptides does not induce high titers of anti-L2 antibodies. In order to develop a vaccine with the potential to protect against other high-risk HPV types, we have produced HPV58 pseudovirions encoding the HPV31 L2 protein and compared their capacity to induce cross-neutralizing antibodies with that of HPV L1 and HPV L1/L2 VLPs. METHODS: The titers of neutralizing antibodies against HPV16, HPV18, HPV31 and HPV58 induced in Balb/c mice were compared after immunization with L2-containing vaccines. RESULTS: Low titers of cross-neutralizing antibodies were detected in mice when immunized with L1/L2 VLPs, and the highest levels of cross-neutralizing antibodies were observed in mice immunized with HPV 58 L1/L2 pseudovirions encoding the HPV 31 L2 protein. CONCLUSIONS: The results obtained indicate that high levels of cross-neutralizing antibodies are only observed after immunization with pseudovirions encoding the L2 protein. HPV pseudovirions thus represent a possible new strategy for the generation of a broad-spectrum vaccine to protect against high-risk HPVs and associated neoplasia. BioMed Central 2010-03-24 /pmc/articles/PMC2852459/ /pubmed/20334659 http://dx.doi.org/10.1186/1479-5876-8-28 Text en Copyright ©2010 Combelas 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
Combelas, Nicolas
Saussereau, Emilie
Fleury, Maxime JJ
Ribeiro, Tatiana
Gaitan, Julien
Duarte-Forero, Diego F
Coursaget, Pierre
Touzé, Antoine
Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies
title Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies
title_full Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies
title_fullStr Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies
title_full_unstemmed Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies
title_short Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies
title_sort papillomavirus pseudovirions packaged with the l2 gene induce cross-neutralizing antibodies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2852459/
https://www.ncbi.nlm.nih.gov/pubmed/20334659
http://dx.doi.org/10.1186/1479-5876-8-28
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