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Capsomer Vaccines Protect Mice from Vaginal Challenge with Human Papillomavirus
Capsomers were produced in bacteria as glutathione-S-transferase (GST) fusion proteins with human papillomavirus type 16 L1 lacking the first nine and final 29 residues (GST-HPV16L1Δ) alone or linked with residues 13–47 of HPV18, HPV31 and HPV45 L2 in tandem (GST-HPV16L1Δ-L2x3). Subcutaneous immuniz...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206079/ https://www.ncbi.nlm.nih.gov/pubmed/22069498 http://dx.doi.org/10.1371/journal.pone.0027141 |
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author | Wu, Wai-Hong Gersch, Elizabeth Kwak, Kihyuck Jagu, Subhashini Karanam, Balasubramanyam Huh, Warner K. Garcea, Robert L. Roden, Richard B. S. |
author_facet | Wu, Wai-Hong Gersch, Elizabeth Kwak, Kihyuck Jagu, Subhashini Karanam, Balasubramanyam Huh, Warner K. Garcea, Robert L. Roden, Richard B. S. |
author_sort | Wu, Wai-Hong |
collection | PubMed |
description | Capsomers were produced in bacteria as glutathione-S-transferase (GST) fusion proteins with human papillomavirus type 16 L1 lacking the first nine and final 29 residues (GST-HPV16L1Δ) alone or linked with residues 13–47 of HPV18, HPV31 and HPV45 L2 in tandem (GST-HPV16L1Δ-L2x3). Subcutaneous immunization of mice with GST-HPV16L1Δ or GST-HPV16L1Δ-L2x3 in alum and monophosphoryl lipid A induced similarly high titers of HPV16 neutralizing antibodies. GST-HPV16L1Δ-L2x3 also elicited moderate L2-specific antibody titers. Intravaginal challenge studies showed that immunization of mice with GST-HPV16 L1Δ or GST-HPV16L1Δ-L2x3 capsomers, like Cervarix®, provided complete protection against HPV16. Conversely, vaccination with GST-HPV16 L1Δ capsomers failed to protect against HPV18 challenge, whereas mice immunized with either GST-HPV16L1Δ-L2x3 capsomers or Cervarix® were each completely protected. Thus, while the L2-specific response was moderate, it did not interfere with immunity to L1 in the context of GST-HPV16L1Δ-L2x3 and is sufficient to mediate L2-dependent protection against an experimental vaginal challenge with HPV18. |
format | Online Article Text |
id | pubmed-3206079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32060792011-11-08 Capsomer Vaccines Protect Mice from Vaginal Challenge with Human Papillomavirus Wu, Wai-Hong Gersch, Elizabeth Kwak, Kihyuck Jagu, Subhashini Karanam, Balasubramanyam Huh, Warner K. Garcea, Robert L. Roden, Richard B. S. PLoS One Research Article Capsomers were produced in bacteria as glutathione-S-transferase (GST) fusion proteins with human papillomavirus type 16 L1 lacking the first nine and final 29 residues (GST-HPV16L1Δ) alone or linked with residues 13–47 of HPV18, HPV31 and HPV45 L2 in tandem (GST-HPV16L1Δ-L2x3). Subcutaneous immunization of mice with GST-HPV16L1Δ or GST-HPV16L1Δ-L2x3 in alum and monophosphoryl lipid A induced similarly high titers of HPV16 neutralizing antibodies. GST-HPV16L1Δ-L2x3 also elicited moderate L2-specific antibody titers. Intravaginal challenge studies showed that immunization of mice with GST-HPV16 L1Δ or GST-HPV16L1Δ-L2x3 capsomers, like Cervarix®, provided complete protection against HPV16. Conversely, vaccination with GST-HPV16 L1Δ capsomers failed to protect against HPV18 challenge, whereas mice immunized with either GST-HPV16L1Δ-L2x3 capsomers or Cervarix® were each completely protected. Thus, while the L2-specific response was moderate, it did not interfere with immunity to L1 in the context of GST-HPV16L1Δ-L2x3 and is sufficient to mediate L2-dependent protection against an experimental vaginal challenge with HPV18. Public Library of Science 2011-11-01 /pmc/articles/PMC3206079/ /pubmed/22069498 http://dx.doi.org/10.1371/journal.pone.0027141 Text en Wu et al. http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited. |
spellingShingle | Research Article Wu, Wai-Hong Gersch, Elizabeth Kwak, Kihyuck Jagu, Subhashini Karanam, Balasubramanyam Huh, Warner K. Garcea, Robert L. Roden, Richard B. S. Capsomer Vaccines Protect Mice from Vaginal Challenge with Human Papillomavirus |
title | Capsomer Vaccines Protect Mice from Vaginal Challenge with Human Papillomavirus |
title_full | Capsomer Vaccines Protect Mice from Vaginal Challenge with Human Papillomavirus |
title_fullStr | Capsomer Vaccines Protect Mice from Vaginal Challenge with Human Papillomavirus |
title_full_unstemmed | Capsomer Vaccines Protect Mice from Vaginal Challenge with Human Papillomavirus |
title_short | Capsomer Vaccines Protect Mice from Vaginal Challenge with Human Papillomavirus |
title_sort | capsomer vaccines protect mice from vaginal challenge with human papillomavirus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206079/ https://www.ncbi.nlm.nih.gov/pubmed/22069498 http://dx.doi.org/10.1371/journal.pone.0027141 |
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