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Prevalent levels of RSV serum neutralizing antibodies in healthy adults outside the RSV-season
One of the main challenges in early clinical research with respiratory syncytial virus (RSV) live-attenuated vaccines (LAVs) is to assess immunogenicity in healthy adults. Healthy adults will have preexisting levels of serum neutralizing antibodies that could prematurely neutralize the LAV and under...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482755/ https://www.ncbi.nlm.nih.gov/pubmed/31674870 http://dx.doi.org/10.1080/21645515.2019.1688040 |
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author | Van Der Plas, Johan L. Verdijk, Pauline Van Brummelen, Emilie M. J. Jeeninga, Rienk E. Roestenberg, Meta Burggraaf, Jacobus Kamerling, Ingrid M.C. |
author_facet | Van Der Plas, Johan L. Verdijk, Pauline Van Brummelen, Emilie M. J. Jeeninga, Rienk E. Roestenberg, Meta Burggraaf, Jacobus Kamerling, Ingrid M.C. |
author_sort | Van Der Plas, Johan L. |
collection | PubMed |
description | One of the main challenges in early clinical research with respiratory syncytial virus (RSV) live-attenuated vaccines (LAVs) is to assess immunogenicity in healthy adults. Healthy adults will have preexisting levels of serum neutralizing antibodies that could prematurely neutralize the LAV and underestimate the potential effect of the vaccine on the immune system. Data on prevalence and distribution of virus neutralizing titers (VNTs) in healthy adults is limited and there is no absolute threshold for protection against RSV-infection that can serve as an eligibility criterion in early phase trials. We assessed the RSV-specific serum VNT in healthy adults outside the Dutch RSV-Season in two clinical studies performed in 2017 (exploratory study, n = 100) and 2018 (first-in-human LAV-study, n = 190) using the same neutralizing assay. Our findings show that the prevalence and distribution of serum VNT was overall consistent in the two clinical studies. Log(2) VNTs were normally distributed, distributions of VNTs were similar and there was no statistical difference in mean log(2) VNT for both studies (p = .3). Serum VNTs were comparable during the 6 months of screening in the FIH LAV-study. Our findings will help to determine a cutoff serum VNT to be used as an eligibility criterion in future early phase clinical trials. |
format | Online Article Text |
id | pubmed-7482755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74827552020-09-16 Prevalent levels of RSV serum neutralizing antibodies in healthy adults outside the RSV-season Van Der Plas, Johan L. Verdijk, Pauline Van Brummelen, Emilie M. J. Jeeninga, Rienk E. Roestenberg, Meta Burggraaf, Jacobus Kamerling, Ingrid M.C. Hum Vaccin Immunother Short Report One of the main challenges in early clinical research with respiratory syncytial virus (RSV) live-attenuated vaccines (LAVs) is to assess immunogenicity in healthy adults. Healthy adults will have preexisting levels of serum neutralizing antibodies that could prematurely neutralize the LAV and underestimate the potential effect of the vaccine on the immune system. Data on prevalence and distribution of virus neutralizing titers (VNTs) in healthy adults is limited and there is no absolute threshold for protection against RSV-infection that can serve as an eligibility criterion in early phase trials. We assessed the RSV-specific serum VNT in healthy adults outside the Dutch RSV-Season in two clinical studies performed in 2017 (exploratory study, n = 100) and 2018 (first-in-human LAV-study, n = 190) using the same neutralizing assay. Our findings show that the prevalence and distribution of serum VNT was overall consistent in the two clinical studies. Log(2) VNTs were normally distributed, distributions of VNTs were similar and there was no statistical difference in mean log(2) VNT for both studies (p = .3). Serum VNTs were comparable during the 6 months of screening in the FIH LAV-study. Our findings will help to determine a cutoff serum VNT to be used as an eligibility criterion in future early phase clinical trials. Taylor & Francis 2019-12-20 /pmc/articles/PMC7482755/ /pubmed/31674870 http://dx.doi.org/10.1080/21645515.2019.1688040 Text en © 2019 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Short Report Van Der Plas, Johan L. Verdijk, Pauline Van Brummelen, Emilie M. J. Jeeninga, Rienk E. Roestenberg, Meta Burggraaf, Jacobus Kamerling, Ingrid M.C. Prevalent levels of RSV serum neutralizing antibodies in healthy adults outside the RSV-season |
title | Prevalent levels of RSV serum neutralizing antibodies in healthy adults outside the RSV-season |
title_full | Prevalent levels of RSV serum neutralizing antibodies in healthy adults outside the RSV-season |
title_fullStr | Prevalent levels of RSV serum neutralizing antibodies in healthy adults outside the RSV-season |
title_full_unstemmed | Prevalent levels of RSV serum neutralizing antibodies in healthy adults outside the RSV-season |
title_short | Prevalent levels of RSV serum neutralizing antibodies in healthy adults outside the RSV-season |
title_sort | prevalent levels of rsv serum neutralizing antibodies in healthy adults outside the rsv-season |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482755/ https://www.ncbi.nlm.nih.gov/pubmed/31674870 http://dx.doi.org/10.1080/21645515.2019.1688040 |
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