medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: April 17, 2022
ABSTRACT
Background
Beginning
in
March
2021,
Mexico
vaccinated
childcare
workers
with
a
single-dose
CanSino
Biologics
(Adv5-nCoV)
COVID-19
vaccine.
Although
is
currently
approved
for
use
10
Latin
American,
Asian,
and
European
countries,
little
information
available
about
its
vaccine
effectiveness
(VE).
Methods
We
evaluated
VE
within
worker
cohort
that
included
1,408
facilities.
Participants
were
followed
during
March–December
2021
tested
through
SARS-CoV-2
RT-PCR
or
rapid
antigen
test
if
they
developed
any
symptom
compatible
COVID-19.
Vaccination
status
was
obtained
registries.
calculated
as
100%
×
(1−hazard
ratio
infection
fully
vs.
unvaccinated
participants),
using
an
Andersen-Gill
model
adjusted
age,
sex,
state,
local
viral
circulation.
Results
The
43,925
persons
who
mostly
(96%)
female
median
age
of
32
years;
37,646
(86%)
CanSino.
During
2,250
(5%)
participants
had
laboratory-confirmed
COVID-19,
whom
25
hospitalized
6
died.
Adjusted
20%
(95%
CI
=
10–29%)
against
illness,
76%
(42–90%)
hospitalization,
94%
(66–99%)
death.
illness
declined
from
48%
33–61)
after
14–60
days
following
full
vaccination
to
9–31)
61–120
days.
Conclusions
effective
at
preventing
highly
hospitalization
It
will
be
useful
further
evaluate
duration
protection
assess
the
value
booster
doses
prevent
severe
outcomes.
Summary
across
Mexico.
decreased
risk
by
20%,
76%,
death
94%.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: Jan. 3, 2022
Abstract
Vaccines
based
on
the
spike
protein
of
SARS-CoV-2
are
a
cornerstone
public
health
response
to
COVID-19.
The
emergence
hypermutated,
increasingly
transmissible
variants
concern
(VOCs)
threaten
this
strategy.
Omicron,
fifth
VOC
be
described,
harbours
30
amino
acid
mutations
in
including
15
receptor-binding
domain.
Here,
we
demonstrate
substantial
evasion
neutralisation
by
Omicron
vitro
using
sera
from
vaccinated
individuals.
Importantly,
these
data
mirrored
reduction
real-world
vaccine
effectiveness
that
is
partially
restored
booster
vaccination.
We
also
does
not
induce
cell
syncytia
and
favours
TMPRSS2-independent
endosomal
entry
pathway.
Such
marked
changes
antigenicity
replicative
biology
may
underlie
rapid
global
spread
altered
pathogenicity
variant.
PLoS Medicine,
Journal Year:
2022,
Volume and Issue:
19(9), P. e1003992 - e1003992
Published: Sept. 1, 2022
The
continued
occurrence
of
more
contagious
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
(SARS-CoV-2)
variants
and
waning
immunity
over
time
require
ongoing
reevaluation
the
vaccine
effectiveness
(VE).
This
study
aimed
to
estimate
in
age
groups
(12
59
60
years
or
above)
3
doses
(BNT162b2
mRNA
mRNA-1273)
by
since
vaccination
against
SARS-CoV-2
infection
Disease
2019
(COVID-19)
hospitalization
an
Alpha-,
Delta-,
Omicron-dominated
period.A
Danish
nationwide
cohort
design
was
used
VE
COVID-19
with
Alpha,
Delta,
Omicron
variant.
Information
obtained
from
registries
linked
using
a
unique
personal
identification
number.
included
all
previously
uninfected
residents
Denmark
aged
12
above
(18
for
analysis
doses)
Alpha
(February
20
June
15,
2021),
Delta
(July
4
November
20,
(December
21,
2021
January
31,
2022)
dominated
periods.
estimates
including
95%
confidence
intervals
(CIs)
were
calculated
(1-hazard
ratio∙100)
Cox
proportional
hazard
regression
models
underlying
calendar
adjustments
age,
sex,
comorbidity,
geographical
region.
Vaccination
status
as
time-varying
exposure.
In
oldest
group,
after
90.7%
(95%
CI:
88.2;
92.7)
variant,
82.3%
75.5;
87.2)
39.9%
26.3;
50.9)
variant
14
30
days
vaccination.
waned
73.2%
(Alpha,
57.1;
83.3),
50.0%
(Delta,
46.7;
53.0),
4.4%
(Omicron,
-0.1;
8.7)
>120
Higher
observed
third
dose
86.1%
83.3;
88.4)
57.7%
55.9;
59.5)
Among
both
groups,
98.1%
variants.
95.5%
main
limitation
this
is
nonrandomized
potential
differences
between
unvaccinated
(reference
group)
vaccinated
individuals.Two
provided
high
protection
protection,
notably
infection,
time.
Two
only
limited
short-lived
Omicron.
However,
following
higher.
substantially
increased
level
duration
sustained
among
+60-year-olds.
Vaccines,
Journal Year:
2022,
Volume and Issue:
10(3), P. 350 - 350
Published: Feb. 23, 2022
The
coronavirus
disease
2019
(COVID-19)
pandemic
has
threatened
global
health
and
prompted
the
need
for
mass
vaccination.
We
aimed
to
assess
efficacy
effectiveness
of
COVID-19
vaccines
prevent
mortality
reduce
risk
developing
severe
after
1st
2nd
doses.
From
conception
28
June
2021,
we
searched
PubMed,
Cochrane,
EBSCO,
Scopus,
ProQuest,
Web
Science,
WHO-ICTRP,
Google
Scholar.
included
both
observational
randomized
controlled
trials.
pooled
vaccine
following
vaccination,
as
well
their
95
percent
confidence
intervals
(CI),
were
estimated
using
random-effects
model.
In
total,
22
21,567
screened
articles
eligible
quantitative
analysis.
Mortality
7
14
days
full
vaccination
decreased
significantly
among
vaccinated
group
compared
unvaccinated
(OR
=
0.10,
([95%
CI,
0.04-0.27],
I2
54%)
0.46,
[95%
0.35-0.61],
0%),
respectively.
probability
having
one
or
two
weeks
dose
0.29
0.19-0.46],
25%)
0.08
0.03-0.25],
74%),
incidence
infection
any
time
doses
diminished
0.14
0.07-0.4],
100%)
0.179
0.15-0.19],
98%),
Also,
week
significantly,
0.04,
CI
(0.01-0.2],
100%).
After
meta-regression,
type
country
main
predictors
outcome
[non-mRNA
type,
ß
2.99,
p
0.0001;
UK,
-0.75,
0.038;
USA,
0.8,
0.02].
This
study
showed
that
most
have
comparable
effectiveness,
it
is
purported
may
help
end
this
pandemic.
JAMA Network Open,
Journal Year:
2022,
Volume and Issue:
5(10), P. e2238871 - e2238871
Published: Oct. 27, 2022
Importance
Data
on
the
association
of
COVID-19
vaccination
with
intensive
care
unit
(ICU)
admission
and
outcomes
patients
SARS-CoV-2–related
pneumonia
are
scarce.
Objective
To
evaluate
whether
is
associated
preventing
ICU
for
to
compare
baseline
characteristics
vaccinated
unvaccinated
admitted
an
ICU.
Design,
Setting,
Participants
This
retrospective
cohort
study
regional
data
sets
reports:
(1)
daily
number
administered
vaccines
(2)
all
consecutive
in
Lombardy,
Italy,
from
August
1
December
15,
2021
(Delta
variant
predominant).
Vaccinated
received
either
mRNA
(BNT162b2
or
mRNA-1273)
adenoviral
vector
(ChAdOx1-S
Ad26.COV2).
Incident
rate
ratios
(IRRs)
were
computed
1,
2021,
January
31,
2022;
analyzed
2021.
Exposures
status
(no
vaccination,
vaccine,
vaccine).
Main
Outcomes
Measures
The
incidence
IRR
was
evaluated,
comparing
people
unvaccinated,
adjusted
age
sex.
at
investigated.
between
mortality
hospital
discharge
also
studied,
adjusting
possible
confounders.
Results
Among
10
107
674
inhabitants
time
this
study,
median
[IQR]
48
[28-64]
years
5
154
914
(51.0%)
female.
Of
7
863
417
individuals
who
(median
age:
53
[33-68]
years;
4
010
343
[51.4%]
female),
6
251
(79.5%)
550
439
(7.0%)
061
561
(13.5%)
a
mix
497
875
(57.2%)
boosted.
Compared
people,
vaccine
within
120
days
last
dose
0.03
(95%
CI,
0.03-0.04;
P
<
.001),
whereas
after
0.21
0.19-0.24;
.001).
There
553
during
period:
139
(25.1%)
414
(74.9%)
unvaccinated.
patients,
older
[IQR]:
72
[66-76]
vs
60
[51-69]
primarily
male
(110
[79.1%]
252
[60.9%];
more
comorbidities
2
[1-3]
0
[0-1]
comorbidities;
.001)
had
higher
ratio
arterial
partial
pressure
oxygen
(Pa
o
)
fraction
inspiratory
(FiO
138
[100-180]
[90-158]
mm
Hg;
=
.007).
Factors
age,
premorbid
heart
disease,
lower
Pa
/FiO
admission,
female
sex
(this
factor
only
mortality).
similar
patients.
Conclusions
Relevance
In
significantly
risk
pneumonia.
not
status.
These
findings
suggest
substantial
reduction
developing
COVID-19–related
severe
acute
respiratory
failure
requiring
among
people.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2021,
Volume and Issue:
unknown
Published: Sept. 25, 2021
ABSTRACT
Billions
of
doses
COVID-19
vaccines
have
been
administered
globally,
dramatically
reducing
SARS-CoV-2
incidence
and
severity
in
some
settings.
Many
studies
suggest
provide
a
high
degree
protection
against
infection
disease,
but
precise
estimates
vary
differ
design,
outcomes
measured,
dosing
regime,
location,
circulating
virus
strains.
Here
we
conduct
systematic
review
through
February
2022.
We
included
efficacy
data
from
Phase
3
clinical
trials
for
15
undergoing
WHO
Emergency
Use
Listing
evaluation
real-world
effectiveness
8
with
observational
meeting
inclusion
criteria.
Vaccine
metrics
collected
include
asymptomatic
infection,
any
symptomatic
COVID-19,
severe
including
hospitalization
death,
partial
or
complete
vaccination,
variants
concern
Alpha,
Beta,
Gamma,
Delta,
Omicron.
additionally
the
epidemiological
principles
behind
design
interpretation
vaccine
studies,
important
sources
heterogeneity.
Transplant Infectious Disease,
Journal Year:
2022,
Volume and Issue:
24(6)
Published: Aug. 4, 2022
We
aimed
to
analyze
the
humoral
and
cellular
response
standard
booster
(additional
doses)
COVID-19
vaccination
in
solid
organ
transplantation
(SOT)
risk
factors
involved
for
an
impaired
response.We
did
a
systematic
review
meta-analysis
of
studies
published
up
until
January
11,
2022,
that
reported
immunogenicity
vaccine
among
SOT.
The
study
is
registered
with
PROSPERO,
number
CRD42022300547.Of
1527
studies,
112
which
15391
SOT
2844
healthy
controls,
were
included.
showed
low
(effect
size
[ES]:
0.44
[0.40-0.48])
overall
control
(log-Odds-ratio
[OR]:
-4.46
[-8.10
-2.35]).
was
highest
liver
(ES:
0.67
[0.61-0.74])
followed
by
heart
0.45
[0.32-0.59]),
kidney
0.40
[0.36-0.45]),
kidney-pancreas
0.33
[0.13-0.53]),
lung
(0.27
[0.17-0.37]).
dose
0.43
[0.39-0.47]
vs.
0.51
[0.43-0.54])
marginal
increase
18%
efficacy.
prior
infection
had
higher
0.94
[0.92-0.96]
ES:
[0.39-0.41];
p-value
<
.01).
seroresponse
mRNA-12723
mRNA
0.52
(0.40-0.64).
Mycophenolic
acid
(OR:
1.42
[1.21-1.63])
Belatacept
1.89
[1.3-2.49])
nonresponse.
parallelly
decreased
0.42
[0.32-0.52])
-3.12
[-0.4.12
-2.13]).Overall,
develops
suboptimal
compared
general
population.
Immunosuppression
including
mycophenolic
acid,
belatacept,
tacrolimus
associated
response.
Booster
doses
immune
response,
but
further
upgradation
strategy
required.
Proceedings of the National Academy of Sciences,
Journal Year:
2022,
Volume and Issue:
119(8)
Published: Feb. 7, 2022
Due
to
the
enormous
economic,
health,
and
social
costs
of
COVID-19
pandemic,
there
are
high
expected
returns
investing
in
parallel
multiple
approaches
accelerating
vaccination.
We
argue
investigating
scope
for
lowering
dosage
some
vaccines.
While
existing
evidence
is
not
dispositive,
available
clinical
data
on
immunogenicity
lower
doses
combined
with
a
correlation
between
neutralizing
antibody
response
vaccine
efficacy
suggests
that
half
or
even
quarter
vaccines
could
generate
levels
protection,
particularly
against
severe
disease
death,
while
potentially
expanding
supply
by
450
million
1.55
billion
per
month,
based
projections
2021.
An
epidemiological
model
that,
if
fractional
less
effective
than
standard
doses,
vaccinating
more
people
faster
substantially
reduce
total
infections
deaths.
The
further
testing
alternative
much
public
health
economic
benefits.
However,
commercial
incentives
dosing
weak,
suggesting
may
occur
without
investment.
Governments
support
either
experimental
observational
evaluations
dosing,
primary
booster
shots.
Discussions
researchers
government
officials
countries
where
scarce
strong
interest
these
approaches.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: April 20, 2022
Abstract
Background
The
continued
occurrence
of
more
contagious
SARS-CoV-2
variants
and
waning
immunity
over
time
require
ongoing
re-evaluation
the
vaccine
effectiveness
(VE).
This
study
aimed
to
estimate
in
two
age
groups
(12-59
60
years
or
above)
three
doses
(BNT162b2
mRNA
mRNA-1273
vaccine)
by
since
vaccination
against
infection
COVID-19-related
hospitalization
an
Alpha,
Delta
Omicron
dominated
period.
Methods
A
Danish
nationwide
cohort
design
was
used
VE
with
variants.
Information
obtained
from
registries
linked
using
a
unique
personal
identification
number.
included
all
residents
Denmark
aged
12
above
(18
for
analysis
doses)
Alpha
(February
20
June
15,
2021),
(July
4
November
20,
2021)
(December
21,
2021
January
31,
2022)
periods.
estimates
including
95%
confidence
intervals
(CIs)
were
calculated
Cox
proportional
hazard
regression
models
adjustments
age,
sex
geographical
region.
Vaccination
status
as
time-varying
exposure.
Findings
In
oldest
group,
after
91.0%
(95%
CI:
88.5;
92.9)
variant,
82.2%
75.3;
87.1)
variant
39.9%
26.4;
50.9)
14-30
days
vaccination.
waned
71.5%
54.7;
82.8),
49.8%
46.5;
52.8)
4.7%
0.2;
8.9)
>120
variants,
respectively.
Higher
observed
third
dose
86.0%
(Delta,
83.3;
88.3)
57.6%
(Omicron,
55.8;
59.4)
Among
both
groups,
94.8%
whereas
among
youngest
62.4%
46.3;
73.6)
89.8%
87.9;
91.3),
Conclusions
Two
provided
high
protection
time.
only
limited
variant.
substantially
increased
Omicron.