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Duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study
In 2009, Bio-Manguinhos conducted a dose-response study with the yellow fever vaccine, administering the vaccine in the usual mean dose of 27,476 IU (full dose, reference) and in tapered doses (10,447 IU, 3013 IU, 587 IU, 158 IU, and 31 IU) by the usual subcutaneous route and usual volume (0.5 mL)....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026294/ https://www.ncbi.nlm.nih.gov/pubmed/29784469 http://dx.doi.org/10.1016/j.vaccine.2018.05.041 |
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author | de Menezes Martins, Reinaldo Maia, Maria de Lourdes S. de Lima, Sheila Maria Barbosa de Noronha, Tatiana Guimarães Xavier, Janaina Reis Camacho, Luiz Antonio Bastos de Albuquerque, Elizabeth Maciel Farias, Roberto Henrique Guedes da Matta de Castro, Thalita Homma, Akira |
author_facet | de Menezes Martins, Reinaldo Maia, Maria de Lourdes S. de Lima, Sheila Maria Barbosa de Noronha, Tatiana Guimarães Xavier, Janaina Reis Camacho, Luiz Antonio Bastos de Albuquerque, Elizabeth Maciel Farias, Roberto Henrique Guedes da Matta de Castro, Thalita Homma, Akira |
author_sort | de Menezes Martins, Reinaldo |
collection | PubMed |
description | In 2009, Bio-Manguinhos conducted a dose-response study with the yellow fever vaccine, administering the vaccine in the usual mean dose of 27,476 IU (full dose, reference) and in tapered doses (10,447 IU, 3013 IU, 587 IU, 158 IU, and 31 IU) by the usual subcutaneous route and usual volume (0.5 mL). Tapered doses were obtained by dilution in the manufacturer’s laboratory, and the test batches presented industrial quality. Doses down to 587 IU showed similar immunogenicity to the full dose (27,476, reference), while the 158 IU and 31 IU doses displayed lower immunogenicity. Seropositivity was maintained at 10 months, except in the group that received the 31 IU dose. The current study aims to determine whether yellow fever seropositivity was maintained eight years after YF vaccination in non-revaccinated individuals. According to the current study’s results, seropositivity was maintained in 85% of 318 participants and was similar across groups. The findings support the use of the yellow fever vaccine in fractional doses during outbreaks, but each fractional dose should have at least 587 IU. This study also supports the minimum dose required by WHO, 1000 IU. Clinical trials registration: Clinicaltrials.gov NCT 03338231. |
format | Online Article Text |
id | pubmed-6026294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60262942018-07-06 Duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study de Menezes Martins, Reinaldo Maia, Maria de Lourdes S. de Lima, Sheila Maria Barbosa de Noronha, Tatiana Guimarães Xavier, Janaina Reis Camacho, Luiz Antonio Bastos de Albuquerque, Elizabeth Maciel Farias, Roberto Henrique Guedes da Matta de Castro, Thalita Homma, Akira Vaccine Article In 2009, Bio-Manguinhos conducted a dose-response study with the yellow fever vaccine, administering the vaccine in the usual mean dose of 27,476 IU (full dose, reference) and in tapered doses (10,447 IU, 3013 IU, 587 IU, 158 IU, and 31 IU) by the usual subcutaneous route and usual volume (0.5 mL). Tapered doses were obtained by dilution in the manufacturer’s laboratory, and the test batches presented industrial quality. Doses down to 587 IU showed similar immunogenicity to the full dose (27,476, reference), while the 158 IU and 31 IU doses displayed lower immunogenicity. Seropositivity was maintained at 10 months, except in the group that received the 31 IU dose. The current study aims to determine whether yellow fever seropositivity was maintained eight years after YF vaccination in non-revaccinated individuals. According to the current study’s results, seropositivity was maintained in 85% of 318 participants and was similar across groups. The findings support the use of the yellow fever vaccine in fractional doses during outbreaks, but each fractional dose should have at least 587 IU. This study also supports the minimum dose required by WHO, 1000 IU. Clinical trials registration: Clinicaltrials.gov NCT 03338231. Elsevier Science 2018-06-27 /pmc/articles/PMC6026294/ /pubmed/29784469 http://dx.doi.org/10.1016/j.vaccine.2018.05.041 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article de Menezes Martins, Reinaldo Maia, Maria de Lourdes S. de Lima, Sheila Maria Barbosa de Noronha, Tatiana Guimarães Xavier, Janaina Reis Camacho, Luiz Antonio Bastos de Albuquerque, Elizabeth Maciel Farias, Roberto Henrique Guedes da Matta de Castro, Thalita Homma, Akira Duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study |
title | Duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study |
title_full | Duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study |
title_fullStr | Duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study |
title_full_unstemmed | Duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study |
title_short | Duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study |
title_sort | duration of post-vaccination immunity to yellow fever in volunteers eight years after a dose-response study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026294/ https://www.ncbi.nlm.nih.gov/pubmed/29784469 http://dx.doi.org/10.1016/j.vaccine.2018.05.041 |
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