Research Square (Research Square),
Год журнала:
2023,
Номер
unknown
Опубликована: Окт. 19, 2023
Abstract
Background:
Following
SARS-CoV-2
outbreak,
another
crisis
has
been
established
by
progress
or
persistence
of
COVID-19
symptoms,
as
post
long
COVID,
which
is
critical
to
be
recognized
according
increasing
number
late
symptoms
reports.
In
this
study,
we
investigated
long-term
disorders
in
vaccinated
individuals
who
developed
adverse
events/side
effects
post-vaccination
and/or
episode
owing
the
challenging
differentiation
between
them.
Methods:
The
four
vaccine
regimens
including
inactivated
virus-based/prime-boost
group,
virus-based
prime/subunit
protein-based
boost,
adenovirus-based
prime/boost
and
boost
were
followed
from
first
dose
vaccination
up
6-month
booster
shot.
All
events
documented
through
in-depth
interview
using
a
researcher-made
questionnaire
well
history
demographics.
medical
all
cases
also
collected
Adverse
Events
Committee
Pasteur
Institute
Iran.
Results:
Totally
329
got
3
doses
6
months
after
shots
among
whom
41
(12.4%)
(including
31
females)
with
mean
age
40.9±10.48
years
had
type
disorder
following
vaccination.
captured
various
forms
gynecological
osteoarticular
involvements
most
common
ones.
After
evaluation
background,
age,
date
initiation,
39%
complains
have
found
linked
long-COVID-19
trigger.
Interestingly,
average
time
was
155±10.4
days
mostly
continued
end
study.
Conclusion:
era
vast
majority
global
population
against
it,
identification
side
effect
long-COVID
manifestation
difficult.
Therefore,
some
complications
though
ones,
might
possible
consequence
any
infection
This
study
takes
advantage
follow-up
presents
each
rate
late-disorders
present
highlights
importance
studies
worldwide.
PLoS Pathogens,
Год журнала:
2023,
Номер
19(11), С. e1011744 - e1011744
Опубликована: Ноя. 1, 2023
Background
This
study
aimed
at
evaluation
and
comparison
of
PastoCovac
Plus
protein-subunit
vaccine
in
parallel
with
ChAdOx1-S
(AstraZeneca)
BBIBP-CorV
(Sinopharm)
primarily
vaccinated
volunteers
two
doses
or
BBIBP-CorV.
Materials
methods
194
enrolled
the
who
were
previously
primed
2
vaccines.
They
divided
into
heterologous
regimens
receiving
a
third
dose
Plus,
homologous
groups
ChAdOx1-S.
Serum
samples
obtained
just
before
4
weeks
after
booster
dose.
Anti-spike
IgG
neutralizing
antibodies
quantified
conventional
live-virus
neutralization
titer,
(cVNT50)
assay
was
done
against
Omicron
BA.5
variant.
Moreover,
adverse
events
data
recorded
doses.
Results
ChAdOx1-S/PastoCovac
group
reached
73.0
units
increase
anti-Spike
rise
compared
to
ChAdOx1-S/
(
P
:
0.016).
No
significant
difference
observed
between
regarding
antibody
0.256),
indicating
equivalency
both
types.
Adjusting
for
baseline
titers,
BBIBP-CorV/PastoCovac
showed
135.2
<0.0001)
IgG,
3.1
0.008)
unit
mean
group.
Adjustment
COVID-19
history,
age,
underlying
diseases,
titers
increased
odds
fourfold
(OR:
1.9;
0.199)
BBIBP
CorV
37.3;
<
0.0001)
their
corresponding
arms.
The
rise,
adjustment
same
variables,
2.4
0.610)
5.4
0.286)
groups.
All
types
had
potency
neutralize
variant
no
difference.
highest
rate
event
incidence
Conclusions
application
individuals
successfully
specific
antibodies’
levels
without
any
serious
events.
could
be
administrated
regimen
effectively
boost
humoral
immune
responses.
Journal of Infection and Public Health,
Год журнала:
2025,
Номер
18(3), С. 102676 - 102676
Опубликована: Янв. 19, 2025
Given
the
limited
available
data
about
to
number
of
vaccine
doses
administered
over
an
extended
time
in
Iran,
immune
status
vaccinated
individuals
and
any
potential
disparities
this
regard
among
those
who
received
different
numbers
remain
unknown.
Therefore,
study
aimed
assess
humoral
immunity
COVID-19
vaccines
Iran.
This
was
conducted
from
February,
2022
December
2023
including
605
subjects.
The
durability
anti-spike,
anti-nucleocapsid
(NCP),
neutralizing
antibody,
interferon-γ
(IFN-γ)
evaluated
at
least
6
months
after
last
vaccination,
as
well
60
120
days
it,
two
or
three
vaccine.
Furthermore,
evaluation
cellular
response
performed
before
fourth
dose
(second
booster)
21
thereafter.
3-dose
group
showed
significantly
higher
levels
antibodies,
IFN-γ
compared
2-dose
group.
Both
groups
experienced
a
slight
decrease
dynamic
SARS-CoV-2
Abs,
though
associated
remained
within
positive
range.
After
receiving
PastoCovac,
most
participants
had
high
IFN-γ,
regardless
type
three-dose
regimen
they
previously
received.
average
antibody
titer
decreased
dose,
but
relatively
stable
during
follow-up
period.
found
that
level
anti-SARS-CoV-2
antibodies
their
durability,
were
still
range
long-term
follow-up.
PastoCovac
enhanced
responses
could
be
recommended
booster
for
with
European journal of medical research,
Год журнала:
2023,
Номер
28(1)
Опубликована: Ноя. 26, 2023
Abstract
There
have
been
massive
studies
to
develop
an
effective
vaccine
against
SARS-CoV-2
which
fortunately
led
manage
the
recent
pandemic,
COVID-19.
According
quite
rapidly
developed
vaccines
in
a
fast
window
time,
large
investigations
assess
probable
vaccine-related
adverse
events
are
crucially
required.
COVID-19
available
of
different
platforms
and
primary
clinical
trials
results
presented
acceptable
safety
profile
approved
vaccines.
Nevertheless,
long-term
assessment
or
rare
conditions
need
be
investigated.
The
present
systematic
review,
aimed
at
classification
unsolicited
Iranian
population
through
data
collection
published
case
report
studies.
related
reports
were
explored
via
PubMed,
Web
Science
Google
scholar
according
up
14
th
Dec,
2022
using
PRISMA
guideline.
Out
437
studies,
relevant
fully
investigated
totally
40
including
64
with
new
onset
problem
post-vaccination.
cases
then
classified
various
items,
such
as
type
event
reported
studied
included
BBIBP-CorV,
ChAdOx1-S,
Sputnik
V
COVAXIN.
showed
that
8
categories,
cutaneous
involvements
43.7%
(
n
=
28),
neurologic
problems
16),
blood/vessel
involvement
6),
cardiovascular
5),
ocular
disorders
4),
liver
disorder/failure
2),
graft
rejection
2)
one
metabolic
disorder.
Notably,
almost
60%
had
no
comorbidities.
Moreover,
obtained
revealed
nearly
half
incidences
occurred
after
first
dose
injection
median
duration
improvement
symptom
was
10
days
(range:
2–120).
In
addition,
73%
all
either
significantly
improved
recovered.
Liver
failure
following
ChAdOx1-S
vaccination
most
serious
death
two
individuals
medical
history.
Although
advantages
is
undoubtedly
significant,
history
disease,
comorbidities
immunodeficiency
should
vaccinated
utmost
caution.
This
study
provides
comprehensive
overview
implications
possible
considered
further
strategies.
there
might
bias
regarding
potential
under-reporting
missing
study.
not
proven
direct
outcomes
could
immune
response
over
stimulation,
people
medium/high
risk
monitored
getting
any
platforms.
achieved
by
carefull
attention
subjects
‘
also
consulting
healthcare
providers
before
vaccination.
Deleted Journal,
Год журнала:
2024,
Номер
28(1), С. 1 - 7
Опубликована: Янв. 1, 2024
The
present
study
aims
to
provide
an
insight
the
comprehensive
efforts
of
PII
regarding
COVID-19
management,
research,
achievements,
and
vaccine
production,
though
there
are
many
challenges.The
relevant
literature
review
was
investigated
through
national
international
database
also
reports
from
related
research
departments.Six
strategies
were
taken
by
manage
pandemic
COVID-19.While
this
has
been
hopefully
controlled,
SARS-CoV-2
could
still
be
a
potential
threat.Therefore,
data
management
updated
studies,
as
well
longterm
safety
efficacy
vaccines
on
agenda.
Heliyon,
Год журнала:
2024,
Номер
10(3), С. e24982 - e24982
Опубликована: Янв. 18, 2024
COVID-19
is
now
established
as
a
multi-organ
involvement
disease
with
broad
range
of
manifestations.
Identification
post-acute
incidence
critical
according
to
increasing
number
late
symptoms
reports.
Hereby,
we
report
case
past
history
who
presented
different
manifestations
including
osteoarticular
and
neurological
within
long-term
follow-up.
The
organs
initiated
lately
after
primary
vaccinations
(with
inactivated
vaccine)
lasted
few
months
without
any
pre-existing
medical
condition.
However,
upon
the
completion
vaccine
schedule
receiving
protein
subunit
vaccine,
PastoCovac
Plus,
booster,
improved
substantially
resolved,
though
in
reinfection
episode
partial,
reoccurrence
was
recorded.
This
presentation
can
be
challenging
issue
owing
fact
that
majority
global
population
are
vaccinated
also
experience
this
era
sometimes
differentiation
between
consequences
virus
post
or
vaccination
side
effects
difficult.
Journal of Medical Virology,
Год журнала:
2024,
Номер
96(2)
Опубликована: Фев. 1, 2024
Abstract
This
study
evaluated
the
possible
effects
of
blood
types
on
coronavirus
disease
(COVID‐19)
vaccine
immunogenicity
and
antibody
(Ab)
persistency.
Five
different
vaccinated
groups
against
COVID‐19
were
investigated
at
Pasteur
Institute
Iran
from
April
2021
to
December
2022.
Anti‐Spike
IgG
neutralizing
Ab
rise
tracked
Day
21
as
well
humoral
immune
persistency
assessment
180
after
booster
shots.
Late
adverse
events
up
6
months
dose
collected.
The
results
showed
that
type
A,
led
a
significantly
higher
anti‐Spike
in
AstraZeneca
primed
recipients
comparison
with
Sinopharm
ones
heterologous
regimens
(
p
:
0.019).
Furthermore,
O
was
great
co‐effector
homologous
regarding
(0.013).
In
addition,
better
group
whereas
A
had
best
effect
durability
same
group.
What
is
more,
Rh‐positive
individuals
+
PastoCovac
Plus
rate
=
0.001).
Neutralizing
also
induced
than
cases.
present
potential
impact
A/O
responses
It
proposed
could
increase
individuals.
Moreover,
might
be
recipients.
Scientific Reports,
Год журнала:
2024,
Номер
14(1)
Опубликована: Ноя. 5, 2024
During
COVID-19
pandemic,
international
pharmaceutical
companies
put
effort
to
build
global
manufacturing
networks
for
vaccines.
Soberana
Plus
vaccine,
a
recombinant
protein
based
vaccine
(RBD
dimer),
with
the
trade
name
of
PastoCovac
in
Iran,
is
on
subunit
platform
Cuba
and
completed
preclinical
toxicological
assessments.
This
study
aimed
at
presenting
steps
technology
transfer
from
Iran.
provides
first
practical
comparability
results
Iran
ensure
quality,
safety
efficacy
against
after
successful
Cuba.
was
transferred
formulation
stage.
The
assessment
active
ingredient
(API)
achieved
through
physicochemical
clinical
data
collection
tests
assure
if
there
any
adverse
impact
vaccination
results.
In
order
assess
quality
product
transfer,
we
sought
different
properties
including
regulatory
features,
potency
stability
as
well
its
immunogenicity
safety.
Following
evaluation
attributes
(CQAs)
standard
protocols,
showed
that
two
vaccines
are
highly
similar
comparable,
no
considerable
effect
or
profiles.
CQAs
were
all
acceptance
limits
terms
also
confirmed
significant
differences
between
regarding
reinfection
(P
=
0.199)
breakthrough
0.176).
Furthermore,
level
anti-spike
neutralizing
antibodies
both
groups
not
significantly
indicating
equality
performance
According
this
study,
an
acceptable
acceptant
pre
post
transfer.
Vaccines,
Год журнала:
2024,
Номер
12(3), С. 243 - 243
Опубликована: Фев. 26, 2024
PastoCovac
is
a
subunit
protein
vaccine
against
COVID-19
which
contains
the
tetanus
toxoid
as
carrier
conjugated
to
SARS-CoV-2
RBD.
The
primary
goal
of
application
was
elicit
stronger
specific
response
in
individuals.
However,
conjugate
vaccines
have
potency
generate
anticarrier
antibodies
addition
target
antigen.
Therefore,
present
study
aimed
evaluate
humoral
immune
induction
tetanus.
Six
groups
individuals,
including
those
who
received
one,
two,
or
three
doses
vaccine,
Td
and
also
controls
other
(except
PastoCovac),
were
investigated.
anti-tetanus
IgG
assessed
by
an
ELISA
assay
all
vaccinated
groups.
antibody
persistency
group
one
dose
on
day
60,
90,
180
after
last
injection.
titer
recipients
positive,
though
additional
led
significant
rise
(p
=
0.003).
Notably,
comparison
mean
between
one/two
showed
that
before
injection
not
significant.
Although
decreased
lower
level
than
21,
it
still
estimated
be
highly
positive
Eventually,
none
presented
side-effects
during
follow-up.
current
data
indicate
COVID-19,
PastoCovac,
could
induce
responses
tetanus,
can
persist
for
at
least
6
months.
Combination
formulae
containing
TT
DT
carriers
considered
instead
and/or
boosters
adults
if
they
are
indicated.
Obstetrics and Gynecology International,
Год журнала:
2024,
Номер
2024(1)
Опубликована: Янв. 1, 2024
Considering
menstruation
as
a
crucial
factor
in
females'
health
and
fertility,
any
that
could
change
its
cycle
is
important.
This
study
was
conducted
from
April
2021
to
October
2022
on
females
who
got
3
doses
of
vaccines
against
SARS-CoV-2
through
different
platforms.
The
participants
were
requested
provide
the
trained
experts
with
changes
regarding
menstrual
cycles
after
each
dose
vaccine
up
6
months
booster
shots.
disturbances
related
identified
by
adverse
events
committee
find
possible
associations
applied
vaccines.
Of
308
women
participated
until
end
study,
22
(7.1%)
complained
about
at
least
one
abnormality
their
patterns.
most
common
disturbance
metrorrhagia
10
(48%)
incidences
followed
menorrhagia
(24.2%).
Notably,
complaints
persistent
59%
patients.
In
addition,
14
studied
cases
developed
COVID-19
infection
disorders.
these
cases,
also
play
role
persistence
postvaccine
disturbances.
vaccination
affect
no
remarkable
previous
medical
history.
More
longitudinal
studies
are
required
this
issue.
Viral Immunology,
Год журнала:
2024,
Номер
37(10), С. 480 - 488
Опубликована: Дек. 1, 2024
Coronavirus
disease
2019
(COVID-19),
caused
by
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
and
first
identified
in
Wuhan,
China,
December
2019,
has
led
to
global
efforts
vaccination
mitigate
rising
morbidity
mortality,
with
vaccines
proving
crucial
controlling
the
pandemic.
This
study
evaluated
humoral
responses
inactivated
virus
vaccine
Sinopharm
or
Koxing
Kerlafor,
protein
subunit
ZF001,
adenoviral
vector
Convidecia
after
18
months
of
heterologous
homologous
booster
patients
previous
SARS-CoV-2
infection
healthy
individuals.
We
discovered
that
who
had
recovered
from
then
received
a
third
dose
(booster)
exhibited
durable
immunity.
Furthermore,
induced
higher
neutralizing
antibody
compared
booster.
These
findings
offer
valuable
insights
into
efficacy
different
COVID-19
strategies
following
immunization.