The
severe
acute
respiratory
syndrome
Coronavirus
2
(SARS-CoV-2)
Omicron
variant
of
concern
has
been
the
dominant
cause
worldwide
COVID-19
cases
since
2022.
All
sublineage
viruses
have
demonstrated
high
transmissibility
and
an
ability
to
escape
vaccine-induced
immunity.
While
first-generation
vaccines,
including
monovalent
continue
provide
protection
against
disease,
hospitalization
mortality,
their
efficacy
sub
variants
remains
sparse.
These
vaccines
also
associated
with
rapidly
waning
primary
reinfections
conferred
by
evolving
sublineages..
This
led
development
deployment
updated
introduction
bivalent
booster.
Through
this
review,
we
highlight
brief
journey
leading
dominance
effectiveness
key
these
variants,
(bivalent)
boosters.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: May 23, 2023
The
highly
transmissible
Omicron
(B.1.1.529)
variant
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
was
first
detected
in
late
2021.
Initial
waves
were
primarily
made
up
sub-lineages
BA.1
and/or
BA.2,
BA.4,
and
BA.5
subsequently
became
dominant
mid-2022,
several
descendants
these
have
since
emerged.
infections
generally
caused
less
disease
on
average
than
those
by
earlier
variants
concern
healthy
adult
populations,
at
least,
part,
due
to
increased
population
immunity.
Nevertheless,
healthcare
systems
many
countries,
particularly
with
low
immunity,
been
overwhelmed
unprecedented
surges
prevalence
during
waves.
Pediatric
admissions
also
higher
compared
previous
concern.
All
exhibit
partial
escape
from
wild-type
(Wuhan-Hu
1)
spike-based
vaccine-elicited
neutralizing
antibodies,
more
enhanced
immuno-evasive
properties
emerging
over
time.
Evaluating
vaccine
effectiveness
(VE)
against
has
become
challenging
a
complex
background
varying
coverage,
platforms,
prior
infection
rates,
hybrid
Original
messenger
RNA
booster
doses
substantially
improved
VE
or
BA.2
symptomatic
disease.
However,
protection
waned,
reductions
months
after
administration.
While
original
CD8
+
CD4
T-cell
responses
cross-recognize
sub-lineages,
thereby
retaining
outcomes,
variant-adapted
vaccines
are
required
expand
the
breadth
B-cell
improve
durability
protection.
Variant-adapted
rolled
out
2022
increase
overall
antigenically
aligned
immune
mechanisms.
Biomedicines,
Journal Year:
2023,
Volume and Issue:
11(2), P. 370 - 370
Published: Jan. 27, 2023
COVID-19
has
taken
a
severe
toll
on
the
global
population
through
infections,
hospitalizations,
and
deaths.
Elucidating
SARS-CoV-2
infection-derived
immunity
led
to
development
of
multiple
effective
vaccines
their
implementation
into
mass-vaccination
programs
worldwide.
After
~3
years,
substantial
proportion
human
possesses
from
infection
and/or
vaccination.
With
waning
immune
protection
over
time
against
emerging
variants,
it
is
essential
understand
duration
protection,
breadth
coverage,
effects
reinfection.
This
targeted
review
summarizes
available
research
literature
infection-derived,
vaccination-elicited,
hybrid
immunity.
Infection-derived
shown
93-100%
outcomes
for
up
8
months,
but
reinfection
observed
with
some
virus
variants.
Vaccination
elicits
high
levels
neutralizing
antibodies
CD4+
CD8+
T-cell
responses.
Hybrid
enables
strong,
broad
responses,
high-quality
memory
B
cells
generated
at
5-
10-fold
higher
levels,
versus
or
vaccination
alone
symptomatic
disease
lasting
6-8
months.
evolution
more
transmissible
immunologically
divergent
variants
necessitated
updating
vaccines.
To
ensure
continued
regulators
vaccine
technical
committees
recommend
variant-specific
bivalent
Science Advances,
Journal Year:
2023,
Volume and Issue:
9(29)
Published: July 21, 2023
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
breakthrough
infection
of
vaccinated
individuals
is
increasingly
common
with
the
circulation
highly
immune
evasive
and
transmissible
Omicron
variants.
Here,
we
report
dynamics
durability
recalled
spike-specific
humoral
immunity
following
BA.1
or
BA.2
infection,
longitudinal
sampling
up
to
8
months
after
infection.
Both
infections
robustly
boosted
neutralization
activity
against
infecting
strain
while
expanding
breadth
BA.4,
although
was
substantially
reduced
for
more
recent
XBB
BQ.1.1
strains.
Cross-reactive
memory
B
cells
both
ancestral
spike
were
predominantly
expanded
by
limited
recruitment
de
novo
Omicron-specific
antibodies.
Modeling
titers
predicts
that
protection
from
symptomatic
reinfection
antigenically
similar
strains
will
be
durable
but
undermined
new
emerging
further
escape.
Cell Reports,
Journal Year:
2023,
Volume and Issue:
42(8), P. 112888 - 112888
Published: July 31, 2023
Evolution
of
the
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
Omicron
variant
has
led
to
emergence
sublineages
with
different
patterns
neutralizing
antibody
evasion.
We
report
that
BA.4/BA.5
breakthrough
infection
individuals
immunized
SARS-CoV-2
wild-type-strain-based
mRNA
vaccines
results
in
a
boost
BA.4.6,
BF.7,
BQ.1.1,
and
BA.2.75
neutralization
but
does
not
efficiently
BA.2.75.2,
XBB,
or
XBB.1.5
neutralization.
In
silico
analyses
showed
spike
glycoprotein
lost
most
B
cell
epitopes,
especially
XBB.1.5.
contrast,
T
epitopes
are
conserved
across
variants
including
responses
mRNA-vaccinated,
SARS-CoV-2-naive
against
wild-type
strain,
BA.1,
were
comparable,
suggesting
immunity
recent
may
remain
largely
unaffected.
While
some
effectively
evade
immunity,
spike-protein-specific
due
nature
polymorphic
cell-mediated
immune
responses,
continue
contribute
prevention/limitation
COVID-19
manifestation.
Science Translational Medicine,
Journal Year:
2024,
Volume and Issue:
16(757)
Published: July 24, 2024
Messenger
RNA
(mRNA)
vaccines
were
pivotal
in
reducing
severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
infection
burden,
yet
they
have
not
demonstrated
robust
durability,
especially
older
adults.
Here,
we
describe
a
molecular
adjuvant
comprising
lipid
nanoparticle
(LNP)–encapsulated
mRNA
encoding
interleukin-12p70
(IL-12p70).
The
bioactive
was
engineered
with
multiorgan
protection
(MOP)
sequence
to
restrict
transcript
expression
the
intramuscular
injection
site.
Admixing
IL-12–MOP
(CTX-1796)
BNT162b2
SARS-CoV-2
vaccine
increased
spike
protein–specific
immune
responses
mice.
Specifically,
benefits
of
adjuvantation
included
amplified
humoral
and
cellular
immunity
durability
for
1
year
after
vaccination
An
additional
benefit
restoration
aged
mice
amounts
comparable
those
achieved
young
adult
animals,
alongside
amplification
single
immunization.
Associated
enhanced
dendritic
cell
germinal
center
observed.
Together,
these
data
demonstrate
that
an
LNP-encapsulated
mRNA-encoded
can
amplify
immunogenicity
independent
age,
demonstrating
translational
potential
vulnerable
populations.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(15), P. 8155 - 8155
Published: July 26, 2024
At
present,
COVID-19
remains
a
public
health
concern
due
to
the
ongoing
evolution
of
SARS-CoV-2
and
its
prevalence
in
particular
countries.
This
paper
provides
an
updated
overview
epidemiology
pathogenesis
COVID-19,
with
focus
on
emergence
variants
phenomenon
known
as
‘long
COVID’.
Meanwhile,
diagnostic
detection
advances
will
be
mentioned.
Though
many
inventions
have
been
made
combat
pandemic,
some
outstanding
ones
include
multiplex
RT-PCR,
which
can
used
for
accurate
diagnosis
infection.
ELISA-based
antigen
tests
also
appear
potential
tools
available
future.
discusses
current
treatments,
vaccination
strategies,
well
emerging
cell-based
therapies
The
underscores
necessity
us
continuously
update
scientific
understanding
treatments
it.
Expert Review of Vaccines,
Journal Year:
2023,
Volume and Issue:
22(1), P. 650 - 661
Published: July 7, 2023
Introduction
The
Omicron
BA.1
variant
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
and
subsequent
sub-lineages
exhibit
partial
escape
from
neutralizing
antibodies
elicited
by
vaccines
containing
or
encoding
wild-type
spike
protein.
In
response
to
the
emergence
sub-lineages,
variant-adapted
that
contain
encode
for
protein
components
have
been
developed.Areas
covered
This
review
presents
currently
available
clinical
immunogenicity
safety
data
on
versions
BNT162b2
messenger
RNA
(mRNA)
vaccine
summarizes
expected
mechanism
action,
rationale
development,
these
vaccines.
addition,
challenges
encountered
during
development
regulatory
approval
are
discussed.Expert
opinion
Omicron-adapted
provide
a
wider
breadth
potentially
more
durable
protection
against
antigenically
aligned
variants
when
compared
with
original
vaccine.
As
SARS-CoV-2
continues
evolve,
further
updates
may
be
required.
To
facilitate
this,
globally
harmonized
process
transition
updated
is
needed.
Next-generation
approaches
broader
future
variants.
JCI Insight,
Journal Year:
2023,
Volume and Issue:
8(7)
Published: April 9, 2023
Currently
authorized
COVID-19
vaccines
induce
humoral
and
cellular
responses
to
epitopes
in
the
SARS-CoV-2
spike
protein,
though
relative
roles
of
antibodies
T
cells
protection
are
not
well
understood.
To
understand
role
vaccine-elicited
cell
protection,
we
established
a
cell-only
vaccine
using
DC-targeted
lentiviral
vector
expressing
single
CD8+
viral
nucleocapsid,
spike,
ORF1.
Immunization
angiotensin-converting
enzyme
2-transgenic
mice
with
ex
vivo
vector-transduced
DCs
or
by
direct
injection
induced
proliferation
functional
antigen-specific
cells,
resulting
3-log
decrease
virus
load
upon
live
challenge
that
was
effective
against
ancestral
Omicron
variants.
The
Pfizer/BNT162b2
also
protective
mice,
but
elicited
did
cross-react
on
variants,
suggesting
mediated
cells.
studies
suggest
response
plays
an
important
protection.
findings
incorporation
additional
into
current
would
increase
their
effectiveness
broaden