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Recent years have seen unprecedented outbreaks of avian influenza A
viruses. In particular, highly pathogenic H5N1 viruses have not
only resulted in widespread outbreaks in domestic poultry, but have
been transmitted to humans, resulting in numerous fatalities. The
rapid expansion in their geographic distribution and the
possibility that these viruses could acquire the ability to spread
from person to person raises the risk that such a virus could cause
a global pandemic with high morbidity and mortality. An effective
influenza vaccine represents the best approach to prevent and
control such an emerging pandemic. However, current influenza
vaccines are directed at existing seasonal influenza viruses, which
have little or no antigenic relationship to the highly pathogenic
H5N1 strains. Concerns about pandemic preparedness have greatly
stimulated research activities to develop eff- tive vaccines for
pandemic influenza viruses, and to overcome the limitations inh-
ent in current approaches to vaccine production and distribution.
These limitations include the use of embryonated chicken eggs as
the substrate for vaccine prod- tion, which is time-consuming and
could involve potential biohazards in growth of new virus strains.
Other limitations include the requirement that the current inac-
vated influenza vaccines be administered using needles and
syringes, requiring trained personnel, which could be a bottleneck
when attempting to vaccinate large populations in mass campaigns.
In addition, the current inactivated vaccines that are delivered by
injection elicit limited protective immunity in the upper
respiratory tract where the infection process is initiated.
Recent years have seen unprecedented outbreaks of avian influenza A
viruses. In particular, highly pathogenic H5N1 viruses have not
only resulted in widespread outbreaks in domestic poultry, but have
been transmitted to humans, resulting in numerous fatalities. The
rapid expansion in their geographic distribution and the
possibility that these viruses could acquire the ability to spread
from person to person raises the risk that such a virus could cause
a global pandemic with high morbidity and mortality. An effective
influenza vaccine represents the best approach to prevent and
control such an emerging pandemic. However, current influenza
vaccines are directed at existing seasonal influenza viruses, which
have little or no antigenic relationship to the highly pathogenic
H5N1 strains. Concerns about pandemic preparedness have greatly
stimulated research activities to develop eff- tive vaccines for
pandemic influenza viruses, and to overcome the limitations inh-
ent in current approaches to vaccine production and distribution.
These limitations include the use of embryonated chicken eggs as
the substrate for vaccine prod- tion, which is time-consuming and
could involve potential biohazards in growth of new virus strains.
Other limitations include the requirement that the current inac-
vated influenza vaccines be administered using needles and
syringes, requiring trained personnel, which could be a bottleneck
when attempting to vaccinate large populations in mass campaigns.
In addition, the current inactivated vaccines that are delivered by
injection elicit limited protective immunity in the upper
respiratory tract where the infection process is initiated.
What you should know about the Covid-19 vaccines from top experts
in the field. As the SARS-Cov2 virus emerged and spread globally in
early 2020, unprecedented international efforts began to develop
and test vaccines to control the devastating pandemic. This book
focuses on the remarkable progress in developing vaccines, the
amazing effectiveness of the early vaccines, and the challenges of
delivering them to the population. To put this extraordinary
progress into perspective, the history of other vaccines is
presented and their roles in individual protection and protection
of the community, "vaccines that protect the unvaccinated," are
outlined. The rigorous processes whereby vaccines are evaluated in
distinct phases and the steps that must be met prior to obtaining
regulatory approval for both vaccine safety and effectiveness are
highlighted. Multiple vaccine approaches are reviewed, including
new approaches such as "messenger or mRNA vaccine" that may
revolutionize future vaccine development. The comprehensive models
used to provide recommendations and priorities for vaccination of
groups of people at risk are summarized. The book also focuses on
the questions that remain unanswered after the vaccines are
approved. These include duration of immunity, risk factors for
vaccine failure, impact of viral evolution and variant strains, and
assessment of both immediate and long-term safety. The authors also
address concerns about vaccine acceptance including roll-out,
access, and detailed and trusted sources of information.
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