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Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera
Chikungunya virus (CHIKV) is a reemerging mosquito-borne alphavirus responsible for numerous outbreaks. Chikungunya can cause debilitating acute and chronic disease. Thus, the development of a safe and effective CHIKV vaccine is an urgent global health priority. This study evaluated the effectivenes...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Clinical Investigation
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9431671/ https://www.ncbi.nlm.nih.gov/pubmed/35700051 http://dx.doi.org/10.1172/jci.insight.160173 |
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author | Roques, Pierre Fritzer, Andrea Dereuddre-Bosquet, Nathalie Wressnigg, Nina Hochreiter, Romana Bossevot, Laetitia Pascal, Quentin Guehenneux, Fabienne Bitzer, Annegret Corbic Ramljak, Irena Le Grand, Roger Lundberg, Urban Meinke, Andreas |
author_facet | Roques, Pierre Fritzer, Andrea Dereuddre-Bosquet, Nathalie Wressnigg, Nina Hochreiter, Romana Bossevot, Laetitia Pascal, Quentin Guehenneux, Fabienne Bitzer, Annegret Corbic Ramljak, Irena Le Grand, Roger Lundberg, Urban Meinke, Andreas |
author_sort | Roques, Pierre |
collection | PubMed |
description | Chikungunya virus (CHIKV) is a reemerging mosquito-borne alphavirus responsible for numerous outbreaks. Chikungunya can cause debilitating acute and chronic disease. Thus, the development of a safe and effective CHIKV vaccine is an urgent global health priority. This study evaluated the effectiveness of the live-attenuated CHIKV vaccine VLA1553 against WT CHIKV infection by using passive transfer of sera from vaccinated volunteers to nonhuman primates (NHP) subsequently exposed to WT CHIKV and established a serological surrogate of protection. We demonstrated that human VLA1553 sera transferred to NHPs conferred complete protection from CHIKV viremia and fever after challenge with homologous WT CHIKV. In addition, serum transfer protected animals from other CHIKV-associated clinical symptoms and from CHIKV persistence in tissue. Based on this passive transfer study, a 50% micro–plaque reduction neutralization test titer of ≥ 150 was determined as a surrogate of protection, which was supported by analysis of samples from a seroepidemiological study. In conclusion, considering the unfeasibility of an efficacy trial due to the unpredictability and explosive, rapidly moving nature of chikungunya outbreaks, the definition of a surrogate of protection for VLA1553 is an important step toward vaccine licensure to reduce the medical burden caused by chikungunya. |
format | Online Article Text |
id | pubmed-9431671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-94316712022-09-02 Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera Roques, Pierre Fritzer, Andrea Dereuddre-Bosquet, Nathalie Wressnigg, Nina Hochreiter, Romana Bossevot, Laetitia Pascal, Quentin Guehenneux, Fabienne Bitzer, Annegret Corbic Ramljak, Irena Le Grand, Roger Lundberg, Urban Meinke, Andreas JCI Insight Research Article Chikungunya virus (CHIKV) is a reemerging mosquito-borne alphavirus responsible for numerous outbreaks. Chikungunya can cause debilitating acute and chronic disease. Thus, the development of a safe and effective CHIKV vaccine is an urgent global health priority. This study evaluated the effectiveness of the live-attenuated CHIKV vaccine VLA1553 against WT CHIKV infection by using passive transfer of sera from vaccinated volunteers to nonhuman primates (NHP) subsequently exposed to WT CHIKV and established a serological surrogate of protection. We demonstrated that human VLA1553 sera transferred to NHPs conferred complete protection from CHIKV viremia and fever after challenge with homologous WT CHIKV. In addition, serum transfer protected animals from other CHIKV-associated clinical symptoms and from CHIKV persistence in tissue. Based on this passive transfer study, a 50% micro–plaque reduction neutralization test titer of ≥ 150 was determined as a surrogate of protection, which was supported by analysis of samples from a seroepidemiological study. In conclusion, considering the unfeasibility of an efficacy trial due to the unpredictability and explosive, rapidly moving nature of chikungunya outbreaks, the definition of a surrogate of protection for VLA1553 is an important step toward vaccine licensure to reduce the medical burden caused by chikungunya. American Society for Clinical Investigation 2022-07-22 /pmc/articles/PMC9431671/ /pubmed/35700051 http://dx.doi.org/10.1172/jci.insight.160173 Text en © 2022 Roques et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Roques, Pierre Fritzer, Andrea Dereuddre-Bosquet, Nathalie Wressnigg, Nina Hochreiter, Romana Bossevot, Laetitia Pascal, Quentin Guehenneux, Fabienne Bitzer, Annegret Corbic Ramljak, Irena Le Grand, Roger Lundberg, Urban Meinke, Andreas Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera |
title | Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera |
title_full | Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera |
title_fullStr | Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera |
title_full_unstemmed | Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera |
title_short | Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera |
title_sort | effectiveness of chikv vaccine vla1553 demonstrated by passive transfer of human sera |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9431671/ https://www.ncbi.nlm.nih.gov/pubmed/35700051 http://dx.doi.org/10.1172/jci.insight.160173 |
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