Literature DB >> 15917112

Yellow fever vaccination: how much is enough?

Eduardo Massad1, Francisco Antonio Bezerra Coutinho, Marcelo Nascimento Burattini, Luis Fernandez Lopez, Cláudio José Struchiner.   

Abstract

In recent years, a growing number of serious adverse events (including deaths) associated with the yellow fever (YF) vaccine has been reported. If YF vaccination were incorporated in routine programs, administered to children, the risk of deaths from this vaccine would be minimized provided that mortality of children vaccinated below 1 year were negligible. However, in affected areas the vaccine is administered to all age groups. This poses a dilemma to public health authorities - what proportion of a population subject to low risk of YF outbreaks should be vaccinated in order to minimize the total number of serious adverse events (including deaths) due both to natural infection and vaccination? In other words, how much vaccination is safe? Our results suggest that, depending on the age-specific rates of developing vaccine-induced serious adverse events and the risk of yellow fever outbreaks, the optimum proportion to vaccinate may be lower than the proportion that would prevent an epidemics or even be zero. We also show that the vaccine should not be applied to individuals older than 60 years of age because the risk of serious adverse events (including deaths) is higher for that age class. Our work is instrumental to the discussion on the optimum strategy to vaccinate affected populations against yellow fever. Therefore, the aim of this work is to estimate the optimum proportion to vaccinate against YF taking into account the risks of serious adverse events associated with both the vaccine and natural infection.

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Year:  2005        PMID: 15917112     DOI: 10.1016/j.vaccine.2005.03.002

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  18 in total

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3.  Vaccinating in disease-free regions: a vaccine model with application to yellow fever.

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4.  A small animal peripheral challenge model of yellow fever using interferon-receptor deficient mice and the 17D-204 vaccine strain.

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Journal:  Vaccine       Date:  2012-03-13       Impact factor: 3.641

5.  A humanized IgG but not IgM antibody is effective in prophylaxis and therapy of yellow fever infection in an AG129/17D-204 peripheral challenge mouse model.

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6.  Incubation periods of Yellow fever virus.

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7.  Decision making with regard to antiviral intervention during an influenza pandemic.

Authors:  Eunha Shim; Gretchen B Chapman; Alison P Galvani
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Review 8.  Modeling transmission dynamics and control of vector-borne neglected tropical diseases.

Authors:  Paula M Luz; Claudio J Struchiner; Alison P Galvani
Journal:  PLoS Negl Trop Dis       Date:  2010-10-26

9.  Elderly subjects have a delayed antibody response and prolonged viraemia following yellow fever vaccination: a prospective controlled cohort study.

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Journal:  PLoS One       Date:  2011-12-07       Impact factor: 3.240

10.  Modeling the risk of malaria for travelers to areas with stable malaria transmission.

Authors:  Eduardo Massad; Ronald H Behrens; Marcelo N Burattini; Francisco A B Coutinho
Journal:  Malar J       Date:  2009-12-16       Impact factor: 2.979

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