Frontiers in Medicine,
Journal Year:
2022,
Volume and Issue:
9
Published: May 6, 2022
The
emergence
of
several
novel
SARS-CoV-2
variants
regarded
as
concern
(VOCs)
has
exacerbated
pathogenic
and
immunologic
prominences,
well
reduced
diagnostic
sensitivity
due
to
phenotype
modification-capable
mutations.
Furthermore,
latent
more
virulent
strains
that
have
arisen
a
result
unique
mutations
with
increased
evolutionary
potential
represent
threat
vaccine
effectiveness
in
terms
incoming
existing
variants.
As
result,
resisting
natural
immunity,
which
leads
higher
reinfection
rates,
avoiding
vaccination-induced
immunization,
lack
effectiveness,
become
crucial
problem
for
public
health
around
the
world.
This
study
attempts
review
genomic
variation
pandemic
impact
emerging
variations
based
on
clinical
characteristics
management
immunization
effectiveness.
goal
this
is
gain
better
understanding
link
between
genome
level
polymorphism,
symptom
manifestation,
current
vaccination
instance
VOCs.
Vaccines,
Journal Year:
2022,
Volume and Issue:
10(3), P. 456 - 456
Published: March 16, 2022
The
development
of
antiviral
resistance
has
exacerbated
a
growing
threat
to
public
health.
As
result,
there
is
increasing
demand
for
unconventional
antivirals
that
can
effectively
replace
the
presently
in-use
drugs.
Lactic
acid-producing
bacteria
(LAB)
are
among
most
common
used
in
food
industry.
These
play
an
essential
role
fermentation
many
foods
and
feed.
Additionally,
these
considered
more
economical,
efficient,
safe
“nutraceuticals”
health
care
arsenal.
Therefore,
we
carried
out
screening
molecular
characterization
raw
camel
milk
LAB
isolates
tested
their
inhibitory
activity
against
influenza
virus
H1N1.
strain
exhibited
highest
H1N1
virus,
confirmed
by
hemagglutination
assay,
was
identified
as
Lactiplantibacillus
plantarum
KAU007.
study
also
non-cytotoxic
behavior
CFCS
isolated
from
KAU007
MDCK
cells,
approving
its
safety
concern
mammalian
cells.
Besides,
at
5
10
mg/mL
significantly
decreased
level
IFN-γ
(p
<
0.001
p
0.001)
IL-6
0.005)
dose-dependent
manner,
respectively.
This
preliminary
report
about
anti-influenza
milk.
reinforces
contains
beneficial
with
antagonistic
properties
virus.
Diagnostic Microbiology and Infectious Disease,
Journal Year:
2024,
Volume and Issue:
109(2), P. 116253 - 116253
Published: March 16, 2024
Our
study
aimed
to
evaluate
the
safety
of
CoronaVac,
an
inactivated
vaccine
made
by
Sinovac,
in
children
aged
7-14.
We
conducted
a
parent-administered
online
survey
monitor
adverse
reactions
after
vaccinating
Taizhou,
China,
from
February
15,
2021,
January
19,
2022.
767
parents
completed
receiving
questionnaire
via
WeChat.
Overall,
15.3
%
(117/767)
experienced
effects
first
dose,
and
12.2
(88/724)
second.
Muscle
pain
was
most
common
reaction
post-first
dose
(10.0
%),
while
localized
or
itching
at
injection
site
second
(7.6
%).
In
conclusion,
has
low
incidence
side
effects.
The
mild
moderate,
transient,
nature
these
further
boosts
parents'
confidence
their
children.
The Lancet Global Health,
Journal Year:
2022,
Volume and Issue:
10(6), P. e774 - e775
Published: April 23, 2022
As
we
enter
the
third
year
of
COVID-19
pandemic,
policy
makers
need
pragmatic
data
about
performance
different
vaccination
regimens
for
informed
decisions
and
prioritisation,
because
placebo-controlled
studies
are
no
longer
feasible
ethical
reasons.
Furthermore,
there
is
a
evidence
protective
effectiveness
vaccines
against
symptomatic
or
severe
in
real-world
settings,
which
unselected
individuals
from
every
age
risk
groups
vaccinated.In
The
Lancet
Global
Health,
Alejandro
Jara
colleagues1Jara
A
Undurraga
EA
Zubizarreta
JR
et
al.Effectiveness
homologous
heterologous
booster
doses
an
inactivated
SARS-CoV-2
vaccine:
large-scale
prospective
cohort
study.Lancet
Glob
Health.
2022;
(published
online
April
23.)https://doi.org/10.1016/S2214-109X(22)00112-7Summary
Full
Text
PDF
PubMed
Scopus
(25)
Google
Scholar
report
CoronaVac
(Sinovac
Biotech),
AZD1222
(Oxford-AstraZeneca),
BNT162b2
(Pfizer-BioNTech)
boosters
after
completion
primary
schedule
with
two
CoronaVac.
results
based
on
analyses
dataset
gathered
single
centralised
immunisation
registry
nearly
11·2
million
aged
16
years
older,
representing
80%
Chilean
population.
Participants
study
were
followed
up
until
Nov
10,
2021;
therefore,
follow-up
potentially
excludes
three
omicron
subvariants
(BA.1,
BA.1.1,
BA.2).Compared
vaccination,
adjusted
vaccine
was
calculated
as
78·8%
(95%
CI
76·8–80·6)
CoronaVac,
96·5%
(96·2–96·7)
booster,
93·2%
(92·9–93·6)
booster.
rates
86·3%
hospitalisation
86·7%
COVID-19-associated
deaths
following
three-dose
schedule.
Corresponding
higher
schedules,
at
96·1%
97·7%
96·8%
98·1%
deaths.
Additional
indicated
that
provided
improved
high
level
protection
outcomes
death
than
two-dose
Although
strategy
showed
effectiveness,
it
note
median
women
men
who
received
69·1
years,
compared
43·5
45·2
67·0
66·3
difference
when
evaluating
relatively
lower
regimen
has
been
shown
both
antibody
T-cell
responses
compromised
people
55
older.2Medeiros
GX
Sasahara
GL
Magawa
JY
al.Reduced
t
cell
to
coronavirus
among
above
old.Front
Immunol.
13812126
Crossref
(4)
ScholarAlthough
by
supports
so-called
mix-and-match
approach,
optimum
strategies
dosing
intervals
provide
maximum
benefit
context
variants
circulation
be
defined.
Zeng
colleagues3Zeng
G
Wu
Q
Pan
H
al.Immunogenicity
safety
dose
immune
persistence
schedule,
healthy
adults:
interim
single-centre,
double-blind,
randomised,
phase
2
clinical
trials.Lancet
Infect
Dis.
22:
483-495Summary
(78)
reported
neutralising
titres
induced
declined
near
below
limit
seropositivity
6
months;
however,
given
8
months
second
led
strong
boost
response.
Aikawa
colleagues4Aikawa
NE
Kupa
LVK
Medeiros-Ribeiro
AC
al.Increment
immunogenicity
large
population
patients
autoimmune
rheumatic
diseases.Ann
Rheum
March
11.)https://doi.org/10.1136/annrheumdis-2021-222096Crossref
(7)
initial
series
resulted
robust
response
even
diseases,
greater
those
still
seronegative
first
vaccinations.
Khong
colleagues5Khong
KW
Liu
D
Leung
KY
al.Antibody
combination
platforms
covid-19
variant.Vaccines.
10:
160Crossref
(19)
combinations
(BNT162b2-CoronaVac-BNT162b2
CoronaVac-CoronaVac-BNT162b2)
delta
(B.1.617.2)
variant,
but
much
titre
BA.1
subvariant.
Two-dose
mRNA
rapid
pronounced
loss
infection
variant6Andrews
N
Stowe
J
Kirsebom
F
al.Covid-19
(B.1.1.529)
Variant.N
Engl
Med.
2.)https://doi.org/10.1056/NEJMoa2119451Crossref
(364)
disease
before
surge
variant.7Nordström
P
Ballin
M
Nordström
Risk
infection,
hospitalisation,
9
retrospective,
total
Sweden.Lancet.
399:
814-823Summary
(48)
Because
do
not
cover
surge,
cannot
estimate
schedules
settings.
McMenamin
colleagues8McMenamin
ME
Nealon
Lin
Y
al.Vaccine
1
Hong
Kong.medRxiv.
24.)
(preprint).https://doi.org/10.1101/2022.03.22.22272769Google
analysed
Dec
31,
2021,
8,
2022,
covering
fifth
wave
BA.2
lineage
Kong.
Three
highly
mortality
all
groups,
yet
effects
have
investigated.The
insights
how
manage
vaccination.
It
now
clear
that,
world
where
equity
utopia,
scientists
can
only
strive
best
use
available
reach
attainable
benefit.
mix
match
strategy,
including
priming
thereafter,
seems
realistic
policy.
vaccinated.
In
BA.2).
Compared
investigated.
We
declare
competing
interests.
Effectiveness
studyOur
suggest
complete
provides
COVID-19,
death.
Heterologous
outcomes,
providing
additional
support
approach.
Full-Text
Open
Access
Vaccines,
Journal Year:
2023,
Volume and Issue:
11(8), P. 1329 - 1329
Published: Aug. 5, 2023
(1)
Background:
This
study
aimed
to
compare
the
immunogenicity
of
mix-and-match
CoronaVac/BNT162b2
vaccination
homologous
CoronaVac/CoronaVac
regimen.
(2)
Methods:
We
conducted
a
simple-blinded
randomized
superiority
trial
measure
SARS-CoV-2
neutralization
antibodies
and
anti-spike
receptor
binding
domain
(RBD)
IgG
concentrations
in
blood
samples
participants
who
had
received
first
dose
CoronaVac
vaccine
followed
by
BNT162b2
or
vaccine.
The
primary
endpoint
for
was
serum-neutralizing
antibody
level
with
percentage
inhibition
at
90%
21–35
days
after
boost.
A
difference
25%
between
groups
considered
clinically
relevant.
(3)
Results:
Among
240
eligible
participants,
data
were
available
100
randomly
allocated
group
versus
99
group.
regimen
elicited
significantly
higher
levels
neutralizing
(median
96%,
interquartile
range
(IQR)
(95–97)
median
94%,
IQR
(81–96)
13,460,
(2557–29,930)
1190,
(347–4964)
compared
Accordingly,
subjects
>
(90.0%)
(60.6%).
Interestingly,
no
severe
events
reported
within
30
second
both
groups.
(4)
Conclusions:
Our
showed
terms
immunogenicity,
thus
constituting
proof-of-concept
supporting
use
inactivated
vaccines
strategy
while
ensuring
good
safety.
Frontiers in Medicine,
Journal Year:
2022,
Volume and Issue:
9
Published: May 6, 2022
The
emergence
of
several
novel
SARS-CoV-2
variants
regarded
as
concern
(VOCs)
has
exacerbated
pathogenic
and
immunologic
prominences,
well
reduced
diagnostic
sensitivity
due
to
phenotype
modification-capable
mutations.
Furthermore,
latent
more
virulent
strains
that
have
arisen
a
result
unique
mutations
with
increased
evolutionary
potential
represent
threat
vaccine
effectiveness
in
terms
incoming
existing
variants.
As
result,
resisting
natural
immunity,
which
leads
higher
reinfection
rates,
avoiding
vaccination-induced
immunization,
lack
effectiveness,
become
crucial
problem
for
public
health
around
the
world.
This
study
attempts
review
genomic
variation
pandemic
impact
emerging
variations
based
on
clinical
characteristics
management
immunization
effectiveness.
goal
this
is
gain
better
understanding
link
between
genome
level
polymorphism,
symptom
manifestation,
current
vaccination
instance
VOCs.