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Herd Immunity to Ebolaviruses Is Not a Realistic Target for Current Vaccination Strategies

The recent West African Ebola virus pandemic, which affected >28,000 individuals increased interest in anti-Ebolavirus vaccination programs. Here, we systematically analyzed the requirements for a prophylactic vaccination program based on the basic reproductive number (R(0), i.e., the number of s...

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Autores principales: Masterson, Stuart G., Lobel, Leslie, Carroll, Miles W., Wass, Mark N., Michaelis, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954026/
https://www.ncbi.nlm.nih.gov/pubmed/29867992
http://dx.doi.org/10.3389/fimmu.2018.01025
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author Masterson, Stuart G.
Lobel, Leslie
Carroll, Miles W.
Wass, Mark N.
Michaelis, Martin
author_facet Masterson, Stuart G.
Lobel, Leslie
Carroll, Miles W.
Wass, Mark N.
Michaelis, Martin
author_sort Masterson, Stuart G.
collection PubMed
description The recent West African Ebola virus pandemic, which affected >28,000 individuals increased interest in anti-Ebolavirus vaccination programs. Here, we systematically analyzed the requirements for a prophylactic vaccination program based on the basic reproductive number (R(0), i.e., the number of secondary cases that result from an individual infection). Published R(0) values were determined by systematic literature research and ranged from 0.37 to 20. R(0)s ≥ 4 realistically reflected the critical early outbreak phases and superspreading events. Based on the R(0), the herd immunity threshold (I(c)) was calculated using the equation I(c) = 1 − (1/R(0)). The critical vaccination coverage (V(c)) needed to provide herd immunity was determined by including the vaccine effectiveness (E) using the equation V(c) = I(c)/E. At an R(0) of 4, the I(c) is 75% and at an E of 90%, more than 80% of a population need to be vaccinated to establish herd immunity. Such vaccination rates are currently unrealistic because of resistance against vaccinations, financial/logistical challenges, and a lack of vaccines that provide long-term protection against all human-pathogenic Ebolaviruses. Hence, outbreak management will for the foreseeable future depend on surveillance and case isolation. Clinical vaccine candidates are only available for Ebola viruses. Their use will need to be focused on health-care workers, potentially in combination with ring vaccination approaches.
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spelling pubmed-59540262018-06-04 Herd Immunity to Ebolaviruses Is Not a Realistic Target for Current Vaccination Strategies Masterson, Stuart G. Lobel, Leslie Carroll, Miles W. Wass, Mark N. Michaelis, Martin Front Immunol Immunology The recent West African Ebola virus pandemic, which affected >28,000 individuals increased interest in anti-Ebolavirus vaccination programs. Here, we systematically analyzed the requirements for a prophylactic vaccination program based on the basic reproductive number (R(0), i.e., the number of secondary cases that result from an individual infection). Published R(0) values were determined by systematic literature research and ranged from 0.37 to 20. R(0)s ≥ 4 realistically reflected the critical early outbreak phases and superspreading events. Based on the R(0), the herd immunity threshold (I(c)) was calculated using the equation I(c) = 1 − (1/R(0)). The critical vaccination coverage (V(c)) needed to provide herd immunity was determined by including the vaccine effectiveness (E) using the equation V(c) = I(c)/E. At an R(0) of 4, the I(c) is 75% and at an E of 90%, more than 80% of a population need to be vaccinated to establish herd immunity. Such vaccination rates are currently unrealistic because of resistance against vaccinations, financial/logistical challenges, and a lack of vaccines that provide long-term protection against all human-pathogenic Ebolaviruses. Hence, outbreak management will for the foreseeable future depend on surveillance and case isolation. Clinical vaccine candidates are only available for Ebola viruses. Their use will need to be focused on health-care workers, potentially in combination with ring vaccination approaches. Frontiers Media S.A. 2018-05-09 /pmc/articles/PMC5954026/ /pubmed/29867992 http://dx.doi.org/10.3389/fimmu.2018.01025 Text en Copyright © 2018 Masterson, Lobel, Carroll, Wass and Michaelis. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Masterson, Stuart G.
Lobel, Leslie
Carroll, Miles W.
Wass, Mark N.
Michaelis, Martin
Herd Immunity to Ebolaviruses Is Not a Realistic Target for Current Vaccination Strategies
title Herd Immunity to Ebolaviruses Is Not a Realistic Target for Current Vaccination Strategies
title_full Herd Immunity to Ebolaviruses Is Not a Realistic Target for Current Vaccination Strategies
title_fullStr Herd Immunity to Ebolaviruses Is Not a Realistic Target for Current Vaccination Strategies
title_full_unstemmed Herd Immunity to Ebolaviruses Is Not a Realistic Target for Current Vaccination Strategies
title_short Herd Immunity to Ebolaviruses Is Not a Realistic Target for Current Vaccination Strategies
title_sort herd immunity to ebolaviruses is not a realistic target for current vaccination strategies
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954026/
https://www.ncbi.nlm.nih.gov/pubmed/29867992
http://dx.doi.org/10.3389/fimmu.2018.01025
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