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A multivalent T-antigen-based vaccine for Group A Streptococcus
Pili of Group A Streptococcus (GAS) are surface-exposed structures involved in adhesion and colonisation of the host during infection. The major protein component of the GAS pilus is the T-antigen, which multimerises to form the pilus shaft. There are currently no licenced vaccines against GAS infec...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902606/ https://www.ncbi.nlm.nih.gov/pubmed/33623073 http://dx.doi.org/10.1038/s41598-021-83673-4 |
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author | Loh, Jacelyn M. S. Rivera-Hernandez, Tania McGregor, Reuben Khemlani, Adrina Hema J. Tay, Mei Lin Cork, Amanda J. M. Raynes, Jeremy Moreland, Nicole J. Walker, Mark J. Proft, Thomas |
author_facet | Loh, Jacelyn M. S. Rivera-Hernandez, Tania McGregor, Reuben Khemlani, Adrina Hema J. Tay, Mei Lin Cork, Amanda J. M. Raynes, Jeremy Moreland, Nicole J. Walker, Mark J. Proft, Thomas |
author_sort | Loh, Jacelyn M. S. |
collection | PubMed |
description | Pili of Group A Streptococcus (GAS) are surface-exposed structures involved in adhesion and colonisation of the host during infection. The major protein component of the GAS pilus is the T-antigen, which multimerises to form the pilus shaft. There are currently no licenced vaccines against GAS infections and the T-antigen represents an attractive target for vaccination. We have generated a multivalent vaccine called TeeVax1, a recombinant protein that consists of a fusion of six T-antigen domains. Vaccination with TeeVax1 produces opsonophagocytic antibodies in rabbits and confers protective efficacy in mice against invasive disease. Two further recombinant proteins, TeeVax2 and TeeVax3 were constructed to cover 12 additional T-antigens. Combining TeeVax1–3 produced a robust antibody response in rabbits that was cross-reactive to a full panel of 21 T-antigens, expected to provide over 95% vaccine coverage. These results demonstrate the potential for a T-antigen-based vaccine to prevent GAS infections. |
format | Online Article Text |
id | pubmed-7902606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79026062021-02-24 A multivalent T-antigen-based vaccine for Group A Streptococcus Loh, Jacelyn M. S. Rivera-Hernandez, Tania McGregor, Reuben Khemlani, Adrina Hema J. Tay, Mei Lin Cork, Amanda J. M. Raynes, Jeremy Moreland, Nicole J. Walker, Mark J. Proft, Thomas Sci Rep Article Pili of Group A Streptococcus (GAS) are surface-exposed structures involved in adhesion and colonisation of the host during infection. The major protein component of the GAS pilus is the T-antigen, which multimerises to form the pilus shaft. There are currently no licenced vaccines against GAS infections and the T-antigen represents an attractive target for vaccination. We have generated a multivalent vaccine called TeeVax1, a recombinant protein that consists of a fusion of six T-antigen domains. Vaccination with TeeVax1 produces opsonophagocytic antibodies in rabbits and confers protective efficacy in mice against invasive disease. Two further recombinant proteins, TeeVax2 and TeeVax3 were constructed to cover 12 additional T-antigens. Combining TeeVax1–3 produced a robust antibody response in rabbits that was cross-reactive to a full panel of 21 T-antigens, expected to provide over 95% vaccine coverage. These results demonstrate the potential for a T-antigen-based vaccine to prevent GAS infections. Nature Publishing Group UK 2021-02-23 /pmc/articles/PMC7902606/ /pubmed/33623073 http://dx.doi.org/10.1038/s41598-021-83673-4 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Loh, Jacelyn M. S. Rivera-Hernandez, Tania McGregor, Reuben Khemlani, Adrina Hema J. Tay, Mei Lin Cork, Amanda J. M. Raynes, Jeremy Moreland, Nicole J. Walker, Mark J. Proft, Thomas A multivalent T-antigen-based vaccine for Group A Streptococcus |
title | A multivalent T-antigen-based vaccine for Group A Streptococcus |
title_full | A multivalent T-antigen-based vaccine for Group A Streptococcus |
title_fullStr | A multivalent T-antigen-based vaccine for Group A Streptococcus |
title_full_unstemmed | A multivalent T-antigen-based vaccine for Group A Streptococcus |
title_short | A multivalent T-antigen-based vaccine for Group A Streptococcus |
title_sort | multivalent t-antigen-based vaccine for group a streptococcus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902606/ https://www.ncbi.nlm.nih.gov/pubmed/33623073 http://dx.doi.org/10.1038/s41598-021-83673-4 |
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