Frontiers in Pediatrics,
Год журнала:
2023,
Номер
11
Опубликована: Март 16, 2023
SARS-CoV-2
is
known
to
manifest
a
robust
innate
immune
response.
However,
little
about
inflammatory
influences
from
maternal
infection
or
mRNA
vaccination
upon
the
fetus.
In
addition,
it
unknown
if
Vitamin
D
deficiency
fetal
homeostasis
an
anti-inflammatory
mechanism
development
of
possible
cytokines
acute
phase
reactants
by
maternal/fetal
dyad,
in
form
cortisol
elevations,
occur.
effects
on
Complete
Blood
Count
(CBC)
are
not
known.To
evaluate
neonatal
and
responses
after
disease
vaccination.Samples
medical
records
reviews
mother/baby
dyads
(n
=
97)
were
collected
consecutively,
categorized
into
4
groups;
no
exposure
(Control),
Vaccinated
mothers,
positive/IgG
titer
positive
blood,
negative
blood.
IgG/IgM/IgA
titers,
CBC,
CRP,
ferritin,
cortisol,
obtained
examine
response
Student's
t-test,
Wilcoxon
rank-sum,
Chi-squared
with
Bonferroni
corrections
used
compare
groups.
Multiple
imputations
performed
for
missing
data.Cortisol
was
higher
babies
both
mothers
who
vaccinated
(p
0.001)
0.009)
as
compared
control
group
suggesting
attempt
maintain
these
Measurements
vitamin
did
reach
statistical
significance.
CBC
showed
variation,
except
mean
platelet
volume
(MPV),
which
elevated
whose
0.003)
0.007)
group.Acute
reactant
elevations
noted
our
neonates.
levels
unchanged
homeostatic
levels.
Cord
blood
at
birth,
Cortisol
MPV
IgG
Control
group,
indicating
that
generated.
The
implication
events
subsequent
and/or
elevation
fetus
merits
further
investigation.
Journal of Clinical Medicine,
Год журнала:
2023,
Номер
12(10), С. 3539 - 3539
Опубликована: Май 18, 2023
Severe
COVID-19
can
result
in
a
significant
and
irreversible
impact
on
long-term
recovery
subsequent
immune
protection.
Understanding
the
complex
reactions
may
be
useful
for
establishing
clinically
relevant
monitoring.Hospitalized
adults
with
SARS-CoV-2
between
March/October
2020
(n
=
64)
were
selected.
Cryopreserved
peripheral
blood
mononuclear
cells
(PBMCs)
plasma
samples
obtained
at
hospitalization
(baseline)
6
months
after
recovery.
Immunological
components'
phenotyping
SARS-CoV-2-specific
T-cell
response
studied
PBMCs
by
flow
cytometry.
Up
to
25
pro/anti-inflammatory
cytokines/chemokines
assessed
LEGENDplex
immunoassays.
The
group
was
compared
matched
healthy
donors.Biochemical
altered
parameters
during
infection
normalized
follow-up
time
point
group.
Most
of
cytokine/chemokine
levels
increased
baseline
This
showed
Natural
Killer
(NK)
activation
decreased
CD16high
NK
subset,
which
six
later.
They
also
presented
higher
intermediate
patrolling
monocyte
proportion
baseline.
T
an
terminally
differentiated
(TemRA)
effector
memory
(EM)
subsets
distribution
continued
increase
Interestingly,
(CD38)
this
point,
contrary
exhaustion
markers
(TIM3/PD1).
In
addition,
we
observed
highest
magnitude
TemRA
CD4
EM
CD8
six-months
point.The
immunological
is
reversed
point.
However,
marked
pattern
remains
over
time.
dysregulation
could
constitute
risk
factor
reinfection
development
other
pathologies.
Additionally,
high
T-cells
appear
associated
severity.
Maternal
SARS-CoV-2
infection
triggers
placental
inflammation
and
alters
cord
blood
immune
cell
composition.
However,
most
studies
focus
on
outcomes
of
severe
maternal
infection.
Therefore,
we
analyzed
chorionic
villi
from
newborns
unvaccinated
mothers
who
experienced
mild/asymptomatic
during
pregnancy.
We
investigated
rewiring
using
flow
cytometry,
single-cell
RNA
sequencing,
functional
readouts
ex
vivo
stimulation
with
TLR
agonists
pathogens.
was
associated
increased
frequency
memory
T
B
cells
nonclassical
monocytes
in
blood.
Ex
responses
to
were
attenuated,
suggesting
a
tolerogenic
state.
Maladaptive
also
observed
monocytes,
where
antiviral
dampened
but
bacterial
TLRs
increased.
expansion
activation
Hofbauer
cells,
secreting
elevated
levels
myeloid
cell–recruiting
chemokines.
Moreover,
reported
maternally
derived
monocytes/macrophages
the
fetal
placenta
that
transcriptionally
primed
for
responses.
Our
data
indicate
even
absence
vertical
transmission
or
symptoms
neonate,
COVID-19
altered
transcriptional
state
circulation
placenta.
Biomedicines,
Год журнала:
2022,
Номер
10(10), С. 2554 - 2554
Опубликована: Окт. 13, 2022
Pregnant
women
are
included
in
the
COVID-19
risk
groups
even
if
they
do
not
have
any
pathology.
This
requires
an
analysis
of
research
focused
on
pregnant
to
understand
impact
SARS-CoV-2
their
condition.
There
is
also
a
need
know
whether
there
vertical
mother-to-child
transmission,
as
well
other
consequences
case
woman
infected
and
positive.
A
systematic
review
was
carried
out
analyze
existing
information
complications
with
coronavirus
possibility
transmission
from
mother
child,
registered
PROSPERO
website
searched
PubMed,
Scopus,
CINAHL,
Cochrane
Library
databases.
Finally,
22
articles
were
review.
The
suggests
that
child
could
be
exceptionally
possible
at
time
delivery
or
breastfeeding,
but
through
placenta.
It
interesting
point
good
acceptance
vaccination
by
women,
which
may
reason
for
low
infectivity.
Further
should
provide
evidence
role
breast
milk
relation
SARS-CoV-2.
Abstract
This
study
is
a
crucial
step
in
understanding
the
dynamics
of
maternal
immune
response
directed
at
paternal
human
leukocyte
antigen
(HLA)
molecules.
HLA
molecules
are
proteins
on
cell
surfaces
that
play
critical
role
system
regulation.
Our
findings
focus
pivotal
antibodies
targeting
fetal
inhibiting
antigen-induced
activation
uterine
cells,
which
essential
for
successful
pregnancies.
Antibodies
produced
by
recognize
and
neutralize
foreign
substances.
The
primary
to
unravel
anti-fetal
rejection
drawing
parallels
transplant
emphasizing
allorecognition—the
process
an
individual’s
recognizes
responds
antigens
from
another
individual
same
species—in
both
cellular
(involving
cells)
humoral
antibodies)
refusal.
Although
exploring
anti-HLA
preventing
loss
patients
with
recurrent
spontaneous
abortion
captivating,
there
still
significant
knowledge
gaps
need
be
addressed.
Further
studies
imperative
reveal
precise
mechanism
these
generate
prevent
responses,
determinants
pregnancy
outcomes.
It
vital
investigate
specificity
whether
they
exclusively
target
specific
trophoblasts
(cells
forming
outer
layer
blastocyst,
providing
nutrients
embryo).
review
paper
not
only
offers
insights
into
development
protective
but
also
lays
foundation
future
research
therapeutic
implications,
particularly
cases
abortion.
Acta Paediatrica,
Год журнала:
2023,
Номер
112(4), С. 805 - 812
Опубликована: Фев. 11, 2023
The
immune
status
of
children
recovering
from
SARS-CoV-2
infection
is
not
completely
understood.
We
describe
IgG
antispike
persistence
in
infected
during
the
first
two
pandemic
waves.
In
addition,
we
compared
with
healthy
controls
their
leukocyte
populations
and
CD64
expression.Cross-sectional
study.
Carried
out
October
2021
to
February
2022
nonreinfected
nonvaccinated
2020.
presence
was
studied
using
chemiluminescent
immunoassay.
Leukocyte
were
analysed
flow
cytometry
marked
for
CD45,
CD4,
CD8
CD64.
Statistical
minor
than
0.05
considered
significant.One
hundred
eighty-three
control
77
patients
included.
determinations
performed
after
a
median
501
days
(262-464);
52
positive.
Cases
showed
significantly
higher
percentages
monocytes,
lymphocytes,
CD8+
CD4+
.
expression
monocytes
neutrophils.
accompanied
by
percentage
CD64+
neutrophils.In
our
series,
protein
usually
positive
beyond
1
year
infection.
Furthermore,
cases
differ
controls,
on
neutrophils
monocytes.
Prospective
clinical
observations
are
required
confirm
implications
these
findings.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Май 11, 2023
Few
studies
have
addressed
the
impact
of
maternal
mild/asymptomatic
SARS-CoV-2
infection
on
developing
neonatal
immune
system.
In
this
study,
we
analyzed
umbilical
cord
blood
and
placental
chorionic
villi
from
newborns
unvaccinated
mothers
with
SARSCoV-2
during
pregnancy
using
flow
cytometry,
single-cell
transcriptomics,
functional
assays.
Despite
lack
vertical
transmission,
levels
inflammatory
mediators
were
altered
in
blood.
Maternal
was
also
associated
increased
memory
T,
B
cells,
non-classical
monocytes
as
well
activation.
However,
ex
vivo
responses
to
stimulation
attenuated.
Finally,
within
villi,
report
an
expansion
fetal
Hofbauer
cells
infiltrating
macrophages
rewiring
towards
a
heightened
state.
contrast
monocytes,
myeloid
primed
for
antiviral
responses.
Taken
together,
study
highlights
dysregulated
cell
response
mild
pregnancy.
Iranian Journal of Microbiology,
Год журнала:
2024,
Номер
unknown
Опубликована: Фев. 10, 2024
Background
and
Objectives:
Newborns
as
a
vulnerable
population
are
exposed
to
congenital
acquired
infections
during
after
birth.
There
several
reports
of
the
isolation
reporting
infectious
agents
(IAs)
in
early
life
newborns
with
respiratory
manifestations,
present
comprehensive
study
provides
snapshot
current
global
situation
prevalence
IAs
symptoms.
Materials
Methods:
A
systematic
search
was
conducted
main
databases,
including
PubMed,
Scopus,
Web
science,
Google
scholar.
The
pooled
estimated
using
me-
ta-analysis
software
based
on
random
effects
model.
Results:
Out
44
inclusive
studies
(50
datasets)
for
newborns,
be
12.2%
(95%
CI:
6.40-22.0%)
highest
lowest
related
Brazil
(78.2%,
95%
31.0-96.6%),
UK
(0.01%,
CI
0.01-0.01%)
respectively.
Conclusion:
high
emphasizes
considers
necessary
measures
prevent
infections.
Heliyon,
Год журнала:
2024,
Номер
10(23), С. e40386 - e40386
Опубликована: Ноя. 13, 2024
Coronavirus
disease
2019
(COVID-19)
is
a
highly
contagious
viral
disease,
caused
by
the
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2).
It
can
manifest
as
mild
to
flu-like
and
non-flu-like
symptoms
signs,
which
are
associated
with
immune
dysfunction
increased
mortality.
The
findings
from
COVID-19
patients
imply
link
between
system
abnormalities
such
impaired
T-cell
responses
or
cytokine
imbalances
risk
for
worse
clinical
outcomes,
has
not
been
fully
understood.
Owing
regulatory
role
of
inhibitory
checkpoints
during
infection,
this
review
summarizes
available
studies
concerning
TIM3
relatively
less
characterized
checkpoint
in
patients.
Medical Microbiology and Immunology,
Год журнала:
2024,
Номер
214(1)
Опубликована: Дек. 26, 2024
While
the
general
immune
response
to
Severe
Acute
Respiratory
Syndrome-Coronavirus-2
(SARS-CoV-2)
is
well-understood,
long-term
effects
of
Human
Immunodeficiency
Virus-1/Severe
(HIV-1/SARS-CoV-2)
co-infection
on
system
remain
unclear.
This
study
investigates
in
people
with
HIV-1
(PWH)
co-infected
SARS-CoV-2
understand
its
health
consequences.
A
retrospective
longitudinal
PWH
suppressed
viral
load
and
infection
was
conducted.
Cryopreserved
peripheral
blood
mononuclear
cells
plasma
samples
were
collected
at
three
time-points:
HIV-1/pre-SARS-CoV-2
(n
=
18),
HIV-1/SARS-CoV-2
46),
HIV-1/post-SARS-CoV-2
36).
Plasma
levels
25
soluble
cytokines
chemokines,
anti-S/anti-N-IgG-SARS-CoV-2
antibodies
measured.
Immunophenotyping
innate
adaptive
components
SARS-CoV-2-specific
T/B-cell
responses
assessed
by
flow
cytometry.
associated
long-lasting
dysfunction,
characterized
elevated
pro-inflammatory
a
decrease
MIG-IP10-ITAC
chemokine
axis
HIV/SARS-CoV-2
time-point,
which
persisted
one
year
later.
Additionally,
alterations
distribution
subsets
increased
activation
(NKG2D/NKG2C)
maturation
(TIM3)
markers
NK
dendritic
observed
persisting
throughout
study.
Effector
memory
CD4
T-cell
decreased,
while
exhaustion/senescence
(PD1/TIM3/CD57)
all
time-points.
remained
stable
study,
HIV-1-specific
decreased
time-point
so.
Persistent
dysfunction
increases
risk
future
complications,
even
mild
symptoms.
Exacerbated
inflammation
may
contribute
reduce
vaccine
efficacy
potential
reinfections.