ABSTRACT
HLA‐G,
an
important
immune‐checkpoint
(IC)
molecule
that
exerts
inhibitory
signalling
on
immune
effector
cells,
has
been
suggested
to
represent
a
key
player
in
regulating
the
response
Severe
Acute
Respiratory
Syndrome
Coronavirus
Type
2
(SARS‐CoV‐2).
Since
specific
single‐nucleotide
polymorphisms
(SNP)
HLA‐G
3′untranslated
region
(UTR),
which
arrange
as
haplotypes,
are
crucial
for
regulation
of
expression,
we
analysed
contribution
these
genetic
variants
host
factors
SARS‐CoV‐2
infection
during
acute
and
post‐acute
phases.
gene
3′UTR
were
investigated
by
sequencing
unvaccinated
Disease
2019
(COVID‐19)
cohort
(
N
=
505)
phase
253).
The
haplotype
known
UTR‐3
p
0.002)
variant
rs17875408
(also
+3422)
T
0.004)
independent
prognostic
risk
fatal
COVID‐19.
+3422T
0.006)
predicted
also
early
loss
neutralising
antibodies.
In
addition,
UTR‐7
0.023)
emerged
factor
increased
susceptibility
Long‐COVID
symptoms
after
infection.
Our
study
highlights
due
variability
background,
potential
contribute
progression
infection,
extending
development
symptoms,
despite
likely
alterations
microenvironment
associated
HLA‐G‐specific
regulatory
elements
over
course
disease.
By
spotlighting
importance
background
IC
their
pivotal
role
modulating
responses
COVID‐19
emphasised.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(5), P. 697 - 697
Published: April 28, 2024
Since
the
SARS-CoV-2
Omicron
virus
has
gained
dominance
worldwide,
its
continual
evolution
with
unpredictable
mutations
and
patterns
revoked
all
authorized
immunotherapeutics.
Rapid
viral
also
necessitated
several
rounds
of
vaccine
updates
in
order
to
provide
adequate
immune
protection.
It
remains
imperative
understand
how
evolves
into
different
subvariants
causes
escape
as
this
could
help
reevaluate
current
intervention
strategies
mostly
implemented
clinics
emergency
measures
counter
pandemic
and,
importantly,
develop
new
solutions.
Here,
we
a
review
focusing
on
major
events
evolution,
including
features
spike
mutation
that
lead
evasion
against
monoclonal
antibody
(mAb)
therapy
vaccination,
suggest
alternative
durable
options
such
ACE2-based
experimental
therapies
superior
mAbs
address
unprecedented
virus.
In
addition,
type
unique
virus-trapping
molecules
can
zoonotic
SARS
coronaviruses,
either
from
unknown
animal
hosts
or
established
wild-life
reservoirs
SARS-CoV-2,
even
seasonal
alpha
coronavirus
NL63
depends
human
ACE2
for
infection.
Vaccines,
Journal Year:
2024,
Volume and Issue:
13(1), P. 17 - 17
Published: Dec. 28, 2024
The
COVID-19
pandemic,
driven
by
the
rapid
evolution
of
SARS-CoV-2
virus,
presents
ongoing
challenges
to
global
public
health.
is
characterized
rapidly
evolving
mutations,
especially
in
(but
not
limited
to)
spike
protein,
complicating
predictions
about
its
evolutionary
trajectory.
These
mutations
have
significantly
affected
transmissibility,
immune
evasion,
and
vaccine
efficacy,
leading
multiple
pandemic
waves
with
over
half
a
billion
cases
seven
million
deaths
globally.
Despite
several
strategies,
from
development
administration
design
availability
antivirals,
including
monoclonal
antibodies,
already
having
been
employed,
persistent
circulation
virus
emergence
new
variants
continue
result
high
case
numbers
fatalities.
In
past
four
years,
immense
research
efforts
contributed
much
our
understanding
viral
pathogenesis
mechanism,
syndrome,
host-microbe
interactions,
effective
vaccines,
diagnostic
tools,
treatments.
focus
this
review
provide
comprehensive
analysis
functional
impact
on
diagnosis,
treatments,
effectiveness.
We
further
discuss
safety
pregnancy
implications
hybrid
immunity
long-term
protection
against
infection,
as
well
latest
developments
pan-coronavirus
nasal
formulations,
emphasizing
need
for
continued
surveillance,
research,
adaptive
health
strategies
response
race.
Vaccines,
Journal Year:
2023,
Volume and Issue:
11(10), P. 1613 - 1613
Published: Oct. 19, 2023
Assessing
immune
responses
post-SARS-CoV-2
vaccination
is
crucial
for
optimizing
vaccine
strategies.
This
prospective
study
aims
to
evaluate
and
breakthrough
infection
in
235
infection-naïve
healthcare
workers
up
13-15
months
after
initial
two
groups
(108
BNT/BNT/BNT
127
ChAd/ChAd/BNT).
Immune
were
assessed
using
the
interferon-gamma
enzyme-linked
immunospot
(ELISPOT)
assay,
total
immunoglobulin,
neutralizing
activity
through
surrogate
virus
neutralization
test
at
nine
different
time
points.
Both
exhibited
peak
one
second
or
third
dose,
followed
by
gradual
declines
over
six
months.
Notably,
ChAd
group
a
increase
ELISPOT
results,
but
their
antibody
levels
declined
more
rapidly
reaching
response
compared
BNT
group.
Six
both
had
substantial
cellular
responses,
with
superior
humoral
(p
<
0.05).
As
many
as
55
participants
displayed
higher
activities
against
Omicron
variants,
similar
individuals,
suggesting
cross-immunity.
Distinct
classifications
(<30%,
>80%
inhibition)
correlated
results.
Our
reveals
diverse
patterns
based
on
strategies
infections,
emphasizing
importance
of
understanding
these
dynamics
optimized
decisions.
BMC Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: Oct. 7, 2024
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2),
which
causes
disease
2019
(COVID-19),
led
to
a
global
pandemic
from
2020.
In
Thailand,
five
waves
of
outbreaks
were
recorded,
with
the
fourth
and
fifth
driven
by
Delta
Omicron
variants,
resulting
in
over
20,000
new
confirmed
cases
daily
at
their
peaks.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(7), P. 785 - 785
Published: July 17, 2024
While
SARS-CoV-2
has
transitioned
to
an
endemic
phase,
infections
caused
by
newly
emerged
variants
continue
result
in
severe,
and
sometimes
fatal,
outcomes
or
lead
long-term
COVID-19
symptoms.
Vulnerable
populations,
such
as
PLWH,
face
elevated
risk
of
severe
illness.
Emerging
SARS-CoV-2,
including
numerous
Omicron
subvariants,
are
increasingly
associated
with
breakthrough
infections.
Adapting
mRNA
vaccines
these
new
may
offer
improved
protection
against
for
vulnerable
individuals.
In
this
study,
we
examined
humoral
cellular
immune
responses
before
after
administering
adapted
booster
vaccinations
alongside
a
control
group
healthy
Four
weeks
following
vaccination,
both
groups
exhibited
significant
increase
neutralizing
antibodies
responses.
Notably,
there
was
no
difference
response
between
PLWH
the
controls.
Immune
declined
rapidly
three
months
post
vaccination.
However,
still
showed
significantly
increased
antibody
titers
even
months.
These
findings
demonstrate
efficacy
vaccination
regimen.
The
results
suggest
that
regular
immunizations
be
necessary
sustain
protective
immunity.
Journal of Medical Virology,
Journal Year:
2024,
Volume and Issue:
96(2)
Published: Feb. 1, 2024
Abstract
The
continuous
evolution
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS‐CoV‐2)
has
been
accompanied
by
the
emergence
viral
mutations
that
pose
a
great
challenge
to
existing
vaccine
strategies.
It
is
not
fully
understood
with
regard
role
on
SARS‐CoV‐2
spike
protein
from
emerging
variants
in
T
cell
immunity.
In
current
study,
recombinant
eukaryotic
plasmids
were
constructed
as
DNA
vaccines
express
multiple
strains.
These
used
immunize
BALB/c
mice,
and
cross‐T
responses
these
strains
quantitated
using
interferon‐γ
(IFN‐γ)
Elispot.
Peptides
covering
full‐length
different
detect
epitope‐specific
IFN‐γ
+
CD4
CD8
fluorescence‐activated
sorting.
Delta
Omicron
BA.1
found
have
broad
cross‐reactivity,
followed
Beta
strain.
landscapes
epitopes
demonstrated
at
least
30
Alpha
BA.5
can
mediate
escape
its
sublineages
19
out
mutations,
most
which
are
new,
few
inherited
ancient
circulating
concerns.
immunity
between
prototype
strain
be
attributed
located
N‐terminal
domain
(181–246
aa
[amino
acids],
271–318
aa)
C‐terminal
(1171–1273
protein.
findings
provide
vivo
evidence
for
optimizing
manufacturing
immunization
strategies
or
future
variants.
The
pandemic
caused
by
SARS-CoV-2
is
still
a
major
health
problem.
Newly
emerging
variants
and
long-COVID-19
represent
challenge
for
the
global
system.
In
particular,
individuals
in
developing
countries
with
insufficient
care
need
easily
accessible,
affordable
effective
treatments
of
COVID-19.
Previous
studies
have
demonstrated
efficacy
functional
inhibitors
acid
sphingomyelinase
(FIASMA)
against
infections
various
viruses,
including
early
SARS-CoV-2.
This
work
investigated
whether
fluoxetine
sertraline,
usually
used
as
antidepressant
molecules
clinical
practice,
can
inhibit
replication
former
recently
emerged
vitro.
Fluoxetine
sertraline
potently
inhibited
infection
pseudotyped
virus
like
particles
D614G,
alpha,
delta,
omicron
BA.1
BA.5.
These
results
highlight
priority
candidates
large-scale
phase
3
trials
at
different
stages
infections,
either
alone
or
combination
other
medications.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(4), P. 545 - 545
Published: March 30, 2024
The
pandemic
caused
by
SARS-CoV-2
is
still
a
major
health
problem.
Newly
emerging
variants
and
long-COVID-19
represent
challenge
for
the
global
system.
In
particular,
individuals
in
developing
countries
with
insufficient
care
need
easily
accessible,
affordable
effective
treatments
of
COVID-19.
Previous
studies
have
demonstrated
efficacy
functional
inhibitors
acid
sphingomyelinase
against
infections
various
viruses,
including
early
SARS-CoV-2.
This
work
investigated
whether
fluoxetine
sertraline,
usually
used
as
antidepressant
molecules
clinical
practice,
can
inhibit
replication
former
recently
emerged
vitro.
Fluoxetine
sertraline
potently
inhibited
infection
pseudotyped
virus-like
particles
D614G,
alpha,
delta,
omicron
BA.1
BA.5.
These
results
highlight
priority
candidates
large-scale
phase
3
trials
at
different
stages
infections,
either
alone
or
combination
other
medications.
Vaccine X,
Journal Year:
2024,
Volume and Issue:
18, P. 100489 - 100489
Published: April 19, 2024
SARS-CoV-2
mRNA
vaccination,
recognized
for
high
immunogenicity,
frequently
induces
adverse
reactions,
especially
fever.
We
previously
reported
a
correlation
between
post-vaccination
fever
and
specific
antibody
responses
to
the
primary
series
first
booster.
herein
report
changes
in
reactions
across
successive
vaccinations,
from
monovalent
bivalent
vaccines.
Biomolecules,
Journal Year:
2024,
Volume and Issue:
14(10), P. 1217 - 1217
Published: Sept. 26, 2024
COVID-19
remains
a
significant
threat,
particularly
to
vulnerable
populations.
The
emergence
of
new
variants
necessitates
the
development
treatments
and
vaccines
that
induce
both
humoral
cellular
immunity.
This
study
aimed
identify
potentially
immunogenic
SARS-CoV-2
peptides
explore
intricate
host–pathogen
interactions
involving
peripheral
immune
responses,
memory
profiles,
various
demographic,
clinical,
lifestyle
factors.
Using
in
silico
experimental
methods,
we
identified
several
CD8-restricted
are
either
poorly
studied
or
have
previously
unreported
immunogenicity:
fifteen
from
Spike
three
each
non-structural
proteins
Nsp1-2-3-16.
A
peptide,
LA-9,
demonstrated
57%
response
rate
ELISpot
assays
using
PBMCs
14
HLA-A*02:01
positive,
vaccinated,
mild-COVID-19
recovered
subjects,
indicating
its
potential
for
diagnostics,
research,
multi-epitope
vaccine
platforms.
We
also
found
younger
individuals,
with
fewer
doses
longer
intervals
since
infection,
showed
lower
anti-Spike
(ELISA)
anti-Wuhan
neutralizing
antibodies
(pseudovirus
assay),
higher
naïve
T
cells,
central
memory,
effector
CD4hiCD8low
cells
(flow
cytometry)
compared
older
subjects.
In
our
cohort,
prevalence
Vδ2-γδ
DN
CD8
seemed
correlate
strong
anti-NP
antibody
responses
associate
Omicron
absence
confusional
state,
habitual
sporting
activity.