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Fractional Dosing of Yellow Fever Vaccine to Extend Supply: A Modeling Study

BACKGROUND: The ongoing yellow fever (YF) epidemic in Angola strains the global vaccine supply, prompting WHO to adopt dose sparing for its vaccination campaign in Kinshasa in July–August 2016. Although a 5-fold fractional-dose vaccine is similar to standard-dose vaccine in safety and immunogenicity...

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Autores principales: Wu, Joseph T., Peak, Corey M., Leung, Gabriel M., Lipsitch, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5161610/
https://www.ncbi.nlm.nih.gov/pubmed/27837923
http://dx.doi.org/10.1016/S0140-6736(16)31838-4
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author Wu, Joseph T.
Peak, Corey M.
Leung, Gabriel M.
Lipsitch, Marc
author_facet Wu, Joseph T.
Peak, Corey M.
Leung, Gabriel M.
Lipsitch, Marc
author_sort Wu, Joseph T.
collection PubMed
description BACKGROUND: The ongoing yellow fever (YF) epidemic in Angola strains the global vaccine supply, prompting WHO to adopt dose sparing for its vaccination campaign in Kinshasa in July–August 2016. Although a 5-fold fractional-dose vaccine is similar to standard-dose vaccine in safety and immunogenicity, efficacy is untested. There is an urgent need to ensure the robustness of fractional-dose vaccination by elucidating the conditions under which dose fractionation would reduce transmission. METHODS: We estimate the effective reproductive number for YF in Angola using disease natural history and case report data. With simple mathematical models of YF transmission, we calculate the infection attack rate (IAR, the proportion of population infected over the course of an epidemic) under varying levels of transmissibility and five-fold fractional-dose vaccine efficacy for two vaccination scenarios: (i) random vaccination in a hypothetical population that is completely susceptible; (ii) the Kinshasa vaccination campaign in July–August 2016 with different age cutoff for fractional-dose vaccines. FINDINGS: We estimate the effective reproductive number early in the Angola outbreak was between 5·2 and 7·1. If vaccine action is all-or-nothing (i.e. a proportion VE of vaccinees receives complete and the remainder receive no protection), n-fold fractionation can dramatically reduce IAR as long as efficacy VE exceeds 1/n. This benefit threshold becomes more stringent if vaccine action is leaky (i.e. the susceptibility of each vaccinee is reduced by a factor that is equal to the vaccine efficacy VE). The age cutoff for fractional-dose vaccines chosen by the WHO for the Kinshasa vaccination campaign (namely, 2 years) provides the largest reduction in IAR if the efficacy of five-fold fractional-dose vaccines exceeds 20%. INTERPRETATION: Dose fractionation is a very effective strategy for reducing infection attack rate that would be robust with a large margin for error in case fractional-dose VE is lower than expected.
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spelling pubmed-51616102017-12-10 Fractional Dosing of Yellow Fever Vaccine to Extend Supply: A Modeling Study Wu, Joseph T. Peak, Corey M. Leung, Gabriel M. Lipsitch, Marc Lancet Article BACKGROUND: The ongoing yellow fever (YF) epidemic in Angola strains the global vaccine supply, prompting WHO to adopt dose sparing for its vaccination campaign in Kinshasa in July–August 2016. Although a 5-fold fractional-dose vaccine is similar to standard-dose vaccine in safety and immunogenicity, efficacy is untested. There is an urgent need to ensure the robustness of fractional-dose vaccination by elucidating the conditions under which dose fractionation would reduce transmission. METHODS: We estimate the effective reproductive number for YF in Angola using disease natural history and case report data. With simple mathematical models of YF transmission, we calculate the infection attack rate (IAR, the proportion of population infected over the course of an epidemic) under varying levels of transmissibility and five-fold fractional-dose vaccine efficacy for two vaccination scenarios: (i) random vaccination in a hypothetical population that is completely susceptible; (ii) the Kinshasa vaccination campaign in July–August 2016 with different age cutoff for fractional-dose vaccines. FINDINGS: We estimate the effective reproductive number early in the Angola outbreak was between 5·2 and 7·1. If vaccine action is all-or-nothing (i.e. a proportion VE of vaccinees receives complete and the remainder receive no protection), n-fold fractionation can dramatically reduce IAR as long as efficacy VE exceeds 1/n. This benefit threshold becomes more stringent if vaccine action is leaky (i.e. the susceptibility of each vaccinee is reduced by a factor that is equal to the vaccine efficacy VE). The age cutoff for fractional-dose vaccines chosen by the WHO for the Kinshasa vaccination campaign (namely, 2 years) provides the largest reduction in IAR if the efficacy of five-fold fractional-dose vaccines exceeds 20%. INTERPRETATION: Dose fractionation is a very effective strategy for reducing infection attack rate that would be robust with a large margin for error in case fractional-dose VE is lower than expected. 2016-11-10 2016-12-10 /pmc/articles/PMC5161610/ /pubmed/27837923 http://dx.doi.org/10.1016/S0140-6736(16)31838-4 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This manuscript version is made available under the CC BY-NC-ND 4.0 license.
spellingShingle Article
Wu, Joseph T.
Peak, Corey M.
Leung, Gabriel M.
Lipsitch, Marc
Fractional Dosing of Yellow Fever Vaccine to Extend Supply: A Modeling Study
title Fractional Dosing of Yellow Fever Vaccine to Extend Supply: A Modeling Study
title_full Fractional Dosing of Yellow Fever Vaccine to Extend Supply: A Modeling Study
title_fullStr Fractional Dosing of Yellow Fever Vaccine to Extend Supply: A Modeling Study
title_full_unstemmed Fractional Dosing of Yellow Fever Vaccine to Extend Supply: A Modeling Study
title_short Fractional Dosing of Yellow Fever Vaccine to Extend Supply: A Modeling Study
title_sort fractional dosing of yellow fever vaccine to extend supply: a modeling study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5161610/
https://www.ncbi.nlm.nih.gov/pubmed/27837923
http://dx.doi.org/10.1016/S0140-6736(16)31838-4
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