Modeling the public health impact of different meningococcal vaccination strategies with 4CMenB and MenACWY versus the current toddler MenACWY national immunization program in Chile
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Graña, María Gabriela
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Modeling the public health impact of different meningococcal vaccination strategies with 4CMenB and MenACWY versus the current toddler MenACWY national immunization program in Chile
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Abstract
Invasive meningococcal disease (IMD) is an uncommon yet unpredictable, severe, and life-threatening
disease with the highest burden in young children. In Chile, most IMD is caused by meningococcal
serogroup B (MenB) and W (MenW) infection. In response to a MenW outbreak in 2012, a toddler
vaccination program was implemented using quadrivalent meningococcal conjugate vaccine against
serogroups A, C, W and Y (MenACWY). The vaccine program, however, does not protect infants or other
unvaccinated age groups and does not protect against MenB IMD. Since 2017, MenB IMD cases are
becoming increasingly prevalent. Using a dynamic transmission model adapted for Chile, this analysis
assessed the public health impact (reduction in IMD cases, long-term sequelae, deaths, and qualityadjusted
life-years) of six alternative vaccination strategies using MenACWY and/or the four-component
MenB (4CMenB) vaccine in infants, toddlers, and/or adolescents compared to the National Immunization
Program (NIP) implemented in 2014. Strategies that added infant 4CMenB to MenACWY in toddlers or
adolescents would prevent more IMD than the current NIP, observed within the first 5 years of the
program. Replacing the NIP by an adolescent MenACWY strategy would prevent more IMD in the longer
term, once herd immunity is established to protect unvaccinated infants or older age groups. The strategy
that maximized reduction of IMD cases and associated sequelae in all age groups with immediate plus
long-term benefits included infant 4CMenB and MenACWY in both toddlers and adolescents. This analysis
can help policymakers determine the best strategy to control IMD in Chile and improve public health. A set
of audio slides linked to this manuscript can be found at https://doi.org/10.6084/m9.figshare.16837543.
PLAIN LANGUAGE SUMMARY (PLS)
What is the context?
Invasive meningococcal disease (IMD) is a severe, sometimes fatal, unpredictable disease with highest
rates in infants, young children, and adolescents. It is caused by different serogroups of Neisseria
meningitidis bacteria. Most cases in Chile are due to meningococcal serogroups B (MenB) and W
(MenW). Following a MenW IMD outbreak in 2012, vaccination was introduced, leading to the current
National Immunization Program (NIP) in toddlers with quadrivalent meningococcal conjugate vaccine
(MenACWY) (protecting against IMD caused by MenA, C, W, and Y).
What is new?
A disease model to predict the impact of vaccination strategies in the Chilean population compared six
alternative strategies, using the multi-component MenB (4CMenB) vaccine for infants (protecting against
MenB, with potential cross-protection against MenW and Y IMD) and/or the MenACWY vaccine for
toddlers and/or adolescents.
What is the impact?
Results, compared to the NIP, show that: Strategy 1 (a program targeting only infants with 4CMenB) would
reduce more MenB cases but fewer MenA, C, W and Y cases resulting in a lower reduction of total IMD
cases in the long term; Strategy 3 (a program targeting only adolescents with MenACWY) would have
a similar effect to the NIP in the short term but a far greater IMD reduction in the long term (as vaccinating
this age group eventually reduces transmission to other age groups, reducing their risk of disease); all the
other strategies targeted more than one age group, further reducing numbers of IMD cases compared
with the NIP. The greatest benefits were seen with infant 4CMenB vaccination combined with toddler and
adolescent MenACWY vaccination. Results can help policymakers determine the best IMD strategy to
maximize the benefits of available meningococcal vaccines.
Patrocinador
GlaxoSmithKline Biologicals SA
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Artículo de publícación WoS Artículo de publicación SCOPUS
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Human Vaccines & Immunotherapeutics 2021, Vol. 17, No. 12, 5603–5613
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