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The cytomegalovirus gB/MF59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread
Vaccination against human cytomegalovirus (CMV) infection remains high priority. A recombinant form of a protein essential for CMV entry, glycoprotein B (gB), demonstrated partial protection in a clinical trial (NCT00299260) when delivered with the MF59 adjuvant. Although the antibody titre against...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950427/ https://www.ncbi.nlm.nih.gov/pubmed/36823200 http://dx.doi.org/10.1038/s41467-023-36683-x |
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author | Gomes, A. C. Baraniak, I. A. Lankina, A. Moulder, Z. Holenya, P. Atkinson, C. Tang, G. Mahungu, T. Kern, F. Griffiths, P. D. Reeves, M. B. |
author_facet | Gomes, A. C. Baraniak, I. A. Lankina, A. Moulder, Z. Holenya, P. Atkinson, C. Tang, G. Mahungu, T. Kern, F. Griffiths, P. D. Reeves, M. B. |
author_sort | Gomes, A. C. |
collection | PubMed |
description | Vaccination against human cytomegalovirus (CMV) infection remains high priority. A recombinant form of a protein essential for CMV entry, glycoprotein B (gB), demonstrated partial protection in a clinical trial (NCT00299260) when delivered with the MF59 adjuvant. Although the antibody titre against gB correlated with protection poor neutralising responses against the 5 known antigenic domains (AD) of gB were evident. Here, we show that vaccination of CMV seronegative patients induces an antibody response against a region of gB we term AD-6. Responses to the polypeptide AD-6 are detected in >70% of vaccine recipients yet in <5% of naturally infected people. An AD-6 antibody binds to gB and to infected cells but not the virion directly. Consistent with this, the AD-6 antibody is non-neutralising but, instead, prevents cell-cell spread of CMV in vitro. The discovery of AD-6 responses has the potential to explain part of the protection mediated by gB vaccines against CMV following transplantation. |
format | Online Article Text |
id | pubmed-9950427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99504272023-02-25 The cytomegalovirus gB/MF59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread Gomes, A. C. Baraniak, I. A. Lankina, A. Moulder, Z. Holenya, P. Atkinson, C. Tang, G. Mahungu, T. Kern, F. Griffiths, P. D. Reeves, M. B. Nat Commun Article Vaccination against human cytomegalovirus (CMV) infection remains high priority. A recombinant form of a protein essential for CMV entry, glycoprotein B (gB), demonstrated partial protection in a clinical trial (NCT00299260) when delivered with the MF59 adjuvant. Although the antibody titre against gB correlated with protection poor neutralising responses against the 5 known antigenic domains (AD) of gB were evident. Here, we show that vaccination of CMV seronegative patients induces an antibody response against a region of gB we term AD-6. Responses to the polypeptide AD-6 are detected in >70% of vaccine recipients yet in <5% of naturally infected people. An AD-6 antibody binds to gB and to infected cells but not the virion directly. Consistent with this, the AD-6 antibody is non-neutralising but, instead, prevents cell-cell spread of CMV in vitro. The discovery of AD-6 responses has the potential to explain part of the protection mediated by gB vaccines against CMV following transplantation. Nature Publishing Group UK 2023-02-23 /pmc/articles/PMC9950427/ /pubmed/36823200 http://dx.doi.org/10.1038/s41467-023-36683-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gomes, A. C. Baraniak, I. A. Lankina, A. Moulder, Z. Holenya, P. Atkinson, C. Tang, G. Mahungu, T. Kern, F. Griffiths, P. D. Reeves, M. B. The cytomegalovirus gB/MF59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread |
title | The cytomegalovirus gB/MF59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread |
title_full | The cytomegalovirus gB/MF59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread |
title_fullStr | The cytomegalovirus gB/MF59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread |
title_full_unstemmed | The cytomegalovirus gB/MF59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread |
title_short | The cytomegalovirus gB/MF59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread |
title_sort | cytomegalovirus gb/mf59 vaccine candidate induces antibodies against an antigenic domain controlling cell-to-cell spread |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950427/ https://www.ncbi.nlm.nih.gov/pubmed/36823200 http://dx.doi.org/10.1038/s41467-023-36683-x |
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