Journal of Infection and Public Health,
Journal Year:
2024,
Volume and Issue:
18(1), P. 102618 - 102618
Published: Dec. 6, 2024
Research
has
demonstrated
the
association
between
susceptibility
to
coronavirus
disease
2019
(COVID-19)
and
single
nucleotide
polymorphisms
(SNPs).
On
other
hand,
cytotoxic
T
lymphocyte-associated
antigen-4
(CTLA-4)
serves
as
a
pivotal
inhibitory
receptor
with
substantial
impact
on
advancement
of
viral
infections.
Besides,
disintegrin
metalloproteinase33
(ADAM33)
gene
is
associated
both
asthma
heightened
airway
responsiveness.
Hence,
this
investigation
sought
elucidate
potential
CTLA-4
rs5742909
ADAM33
rs2280091
SNPs
fatality
rate
COVID-19
across
various
variants
severe
acute
respiratory
syndrome
2
(SARS-CoV-2).
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 14, 2024
Abstract
The
ongoing
COVID-19
pandemic,
intensified
by
emerging
SARS-CoV-2
mutations,
highlights
the
urgent
need
for
enhanced
vaccines.
Despite
considerable
efforts
in
vaccine
design,
improvements
are
still
required
formulating
vaccines
targeting
novel
coronavirus.
This
study,
utilized
immunoinformatics
and
reverse
vaccinology
to
design
multi-epitope
variations.
B
T
cell
epitopes
were
generated
analyzing
mutation
sites
of
prevalent
variant
strains,
two
designed
linking
with
different
adjuvants.
Interaction
model
four
Toll-like
receptors
(TLR)
revealed
a
relatively
high
affinity
between
immune
receptors.
Codon
optimization
computational
cloning
conducted
validate
robustness
immunogenic
simulations
performed
assess
antigenicity
antibody
generation
capability
vaccine.
L455S
JN.1
its
adjacent
F456L
on
effectiveness
against
XBB
that
15
structures
maintained
certain
level
binding
affinity.
study
offers
an
immunological
evaluation
from
mutation-centric
perspective
integrates
co-evolutionary
analysis
effective
various
strains.
methodologies
applied
this
research
can
also
be
extended
development
other
pathogens.
Signal Transduction and Targeted Therapy,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Nov. 6, 2024
Abstract
Variants
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
continue
to
emerge
and
evade
immunity,
resulting
in
breakthrough
infections
vaccinated
populations.
There
is
an
urgent
need
for
the
development
vaccines
with
broad
protective
effects.
In
this
study,
we
selected
hotspot
mutations
receptor-binding
domain
(RBD)
that
contribute
immune
escape
properties
integrated
them
into
original
RBD
protein
obtain
a
complex
(cRBD),
found
cRBDs
have
effects
against
SARS-CoV-2
variants.
Three
were
designed
our
study.
Compared
BA.1
protein,
induced
production
higher
levels
broader-spectrum
neutralizing
antibodies,
suggesting
stronger
broader
efficacy.
viral
challenge
experiments,
more
effective
than
attenuating
lung
pathologic
injury.
Among
three
constructs,
cRBD3
showed
optimal
broad-spectrum
promising
candidate
vaccine.
conclusion,
immunization
triggered
immunity
wide
range
variants,
including
those
emerged
after
had
completed
designing
cRBDs.
This
study
preliminarily
explores
validates
feasibility
incorporating
evasion
expand
activity
spectrum
antigen-induced
antibodies.
Clinical and Experimental Vaccine Research,
Journal Year:
2024,
Volume and Issue:
13(4), P. 329 - 329
Published: Jan. 1, 2024
This
study
evaluated
the
safety
and
immunogenicity
of
PIKA-adjuvanted
recombinant
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
spike
protein
subunit
vaccine
as
a
booster
dose
for
healthy
adults
who
had
previously
received
two
or
more
doses
an
inactivated
disease
2019
(COVID-19)
vaccine.
Journal of Infection and Public Health,
Journal Year:
2024,
Volume and Issue:
18(1), P. 102618 - 102618
Published: Dec. 6, 2024
Research
has
demonstrated
the
association
between
susceptibility
to
coronavirus
disease
2019
(COVID-19)
and
single
nucleotide
polymorphisms
(SNPs).
On
other
hand,
cytotoxic
T
lymphocyte-associated
antigen-4
(CTLA-4)
serves
as
a
pivotal
inhibitory
receptor
with
substantial
impact
on
advancement
of
viral
infections.
Besides,
disintegrin
metalloproteinase33
(ADAM33)
gene
is
associated
both
asthma
heightened
airway
responsiveness.
Hence,
this
investigation
sought
elucidate
potential
CTLA-4
rs5742909
ADAM33
rs2280091
SNPs
fatality
rate
COVID-19
across
various
variants
severe
acute
respiratory
syndrome
2
(SARS-CoV-2).