Journal of Clinical Investigation,
Journal Year:
2023,
Volume and Issue:
133(1)
Published: Jan. 2, 2023
Infections
with
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
and
vaccinations
targeting
the
spike
protein
(S)
offer
protective
immunity
against
disease
2019
(COVID-19).
This
may
further
be
shaped
by
cross-reactivity
common
cold
coronaviruses.
Mutations
arising
in
S
that
are
associated
altered
intrinsic
virus
properties
immune
escape
result
continued
circulation
of
SARS-CoV-2
variants.
Potentially,
vaccine
updates
will
required
to
protect
future
variants
concern,
as
for
influenza.
To
potent
protection
variants,
these
second-generation
vaccines
need
redirect
epitopes
not
merely
boost
toward
conserved
domains
preimmune
individuals.
For
influenza,
efficacy
repeated
vaccination
is
hampered
original
antigenic
sin,
an
attribute
memory
leads
greater
induction
antibodies
specific
first-encountered
variant
immunogen
compared
subsequent
In
this
Review,
recent
findings
on
sin
discussed
context
evolution.
Unanswered
questions
directions
highlighted,
emphasis
impact
outcome
design.
Nature,
Journal Year:
2022,
Volume and Issue:
603(7902), P. 679 - 686
Published: Jan. 7, 2022
Abstract
The
SARS-CoV-2
epidemic
in
southern
Africa
has
been
characterized
by
three
distinct
waves.
first
was
associated
with
a
mix
of
lineages,
while
the
second
and
third
waves
were
driven
Beta
(B.1.351)
Delta
(B.1.617.2)
variants,
respectively
1–3
.
In
November
2021,
genomic
surveillance
teams
South
Botswana
detected
new
variant
rapid
resurgence
infections
Gauteng
province,
Africa.
Within
days
genome
being
uploaded,
it
designated
concern
(Omicron,
B.1.1.529)
World
Health
Organization
and,
within
weeks,
had
identified
87
countries.
Omicron
is
exceptional
for
carrying
over
30
mutations
spike
glycoprotein,
which
are
predicted
to
influence
antibody
neutralization
function
4
Here
we
describe
profile
early
transmission
dynamics
Omicron,
highlighting
spread
regions
high
levels
population
immunity.
Signal Transduction and Targeted Therapy,
Journal Year:
2022,
Volume and Issue:
7(1)
Published: April 28, 2022
Abstract
Since
the
outbreak
of
coronavirus
disease
2019
(COVID-19)
pandemic,
there
have
been
a
few
variants
severe
acute
respiratory
syndrome
2
(SARS-CoV-2),
one
which
is
Omicron
variant
(B.1.1.529).
The
most
mutated
SARS-CoV-2
variant,
and
its
high
transmissibility
immune
evasion
ability
raised
global
concerns.
Owing
to
enhanced
transmissibility,
has
rapidly
replaced
Delta
as
dominant
in
several
regions.
However,
recent
studies
shown
that
exhibits
reduced
pathogenicity
due
altered
cell
tropism.
In
addition,
significant
resistance
neutralizing
activity
vaccines,
convalescent
serum,
antibody
therapies.
present
review,
advances
molecular
clinical
characteristics
infectivity,
pathogenicity,
was
summarized,
potential
therapeutic
applications
response
infection
were
discussed.
Furthermore,
we
highlighted
future
waves
strategies
end
pandemic.
New England Journal of Medicine,
Journal Year:
2022,
Volume and Issue:
387(11), P. 1011 - 1020
Published: Aug. 31, 2022
T
he
coronavirus
disease
2019
(Covid-19)
pandemic
has
claimed
an
estimated
15
million
lives,
including
more
than
1
lives
in
the
United
States
alone.The
rapid
development
of
multiple
Covid-19
vaccines
been
a
triumph
biomedical
research,
and
billions
vaccine
doses
have
administered
worldwide.Challenges
facing
field
include
inequitable
distribution,
hesitancy,
waning
immunity,
emergence
highly
transmissible
viral
variants
that
partially
escape
antibodies.This
review
summarizes
current
state
knowledge
about
immune
responses
to
importance
both
humoral
cellular
immunity
for
durable
protection
against
severe
disease.
A
nti
v
ir
l
Immunit
yThe
system
is
broadly
divided
into
innate
adaptive
systems.Innate
are
first
line
defense
viruses
rapidly
triggered
when
pattern-recognition
receptors,
such
as
toll-like
recognize
pathogen-associated
molecular
patterns.Innate
antiviral
includes
secretion
type
I
interferons,
cytokines,
certain
responses,
neutrophils,
monocytes
macrophages,
dendritic
cells,
natural
killer
cells.
Adaptive
second
viruses,
involve
antigen-specific
recognition
epitopes.Adaptive
two
complementary
branches
system:
immunity.Humoral
acute
respiratory
syndrome
2
(SARS-CoV-2)
antibodies
bind
SARS-CoV-2
spike
protein
either
neutralize
virus
or
eliminate
it
through
other
effector
mechanisms.
2,3ellular
virus-specific
B
cells
which
provide
long-term
immunologic
memory
expand
on
reexposure
antigen.B
produce
antibodies,
CD8+
directly
virally
infected
CD4+
help
support
responses.5][6][7]
For
variant
largely
escapes
neutralizing
may
be
particularly
important
longterm
Science,
Journal Year:
2022,
Volume and Issue:
377(6603)
Published: June 14, 2022
The
Omicron,
or
Pango
lineage
B.1.1.529,
variant
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
carries
multiple
spike
mutations
with
high
transmissibility
and
partial
neutralizing
antibody
(nAb)
escape.
Vaccinated
individuals
show
protection
against
disease,
often
attributed
to
primed
cellular
immunity.
We
investigated
T
B
cell
immunity
B.1.1.529
in
triple
BioNTech
BNT162b2
messenger
RNA-vaccinated
health
care
workers
(HCWs)
different
SARS-CoV-2
infection
histories.
previous
variants
concern
was
enhanced
triple-vaccinated
individuals,
but
the
magnitude
responses
protein
reduced.
Immune
imprinting
by
earlier
B.1.1.7
(Alpha)
resulted
less
durable
binding
B.1.1.529.
Previously
infection-naïve
HCWs
who
became
infected
during
wave
showed
reduced
nAb
potency
itself.
Previous
Wuhan
Hu-1
abrogated
recognition
any
cross-reactive
on
Immunological Reviews,
Journal Year:
2022,
Volume and Issue:
310(1), P. 6 - 26
Published: June 5, 2022
Antibodies
against
epitopes
in
S1
give
the
most
accurate
CoP
infection
by
SARS-CoV-2
coronavirus.
Measurement
of
those
antibodies
neutralization
or
binding
assays
both
have
predictive
value,
with
antibody
titers
giving
highest
statistical
correlation.
However,
protective
functions
are
multiple.
multiple
other
than
influence
efficacy.
The
role
cellular
responses
can
be
discerned
respect
to
CD4
Immunological Reviews,
Journal Year:
2022,
Volume and Issue:
310(1), P. 27 - 46
Published: June 22, 2022
Immunological
memory
is
the
basis
of
protective
immunity
provided
by
vaccines
and
previous
infections.
can
develop
from
multiple
branches
adaptive
immune
system,
including
CD4
T
cells,
CD8
B
long-lasting
antibody
responses.
Extraordinary
progress
has
been
made
in
understanding
to
SARS-CoV-2
infection
COVID-19
vaccines,
addressing
development;
quantitative
qualitative
features
different
cellular
anatomical
compartments;
durability
each
component
antibodies.
Given
sophistication
measurements;
size
human
studies;
use
longitudinal
samples
cross-sectional
head-to-head
comparisons
between
or
for
1
year
already
supersedes
that
any
other
acute
infectious
disease.
This
knowledge
may
help
inform
public
policies
regarding
as
well
scientific
development
future
against
diseases.
Cold Spring Harbor Perspectives in Medicine,
Journal Year:
2022,
Volume and Issue:
12(5), P. a041390 - a041390
Published: April 20, 2022
Our
understanding
of
the
still
unfolding
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
pandemic
would
have
been
extremely
limited
without
study
genetics
and
evolution
this
new
human
coronavirus.
Large-scale
genome-sequencing
efforts
provided
close
to
real-time
tracking
global
spread
diversification
SARS-CoV-2
since
its
entry
into
population
in
late
2019.
These
data
underpinned
analysis
origins,
epidemiology,
adaptations
population:
principally
immune
evasion
increasing
transmissibility.
SARS-CoV-2,
despite
being
a
pathogen,
was
highly
capable
human-to-human
transmission.
During
rapid
humans,
has
evolved
independent
forms,
so-called
"variants
concern,"
that
are
better
optimized
for
The
most
important
adaptation
bat
progenitor
both
SARS-CoV-1
infection
(and
other
mammals)
is
use
angiotensin-converting
enzyme
(ACE2)
receptor.
Relaxed
structural
constraints
provide
plasticity
SARS-related
spike
protein
permitting
it
accommodate
significant
amino
acid
replacements
antigenic
consequence
compromising
ability
bind
ACE2.
Although
bulk
research
justifiably
concentrated
on
viral
as
main
determinant
changes
transmissibility,
there
accumulating
evidence
contribution
regions
proteome
virus-host
interaction.
Whereas
levels
community
transmission
recombinants
genetically
distinct
variants
at
present
low,
when
divergent
cocirculate,
recombination
between
clades
detected,
risk
viruses
with
properties
emerge.
Applying
computational
machine
learning
methods
genome
sequence
sets
generate
experimentally
verifiable
predictions
will
serve
an
early
warning
system
novel
variant
surveillance
be
future
vaccine
planning.
Omicron,
latest
concern,
focused
attention
step
change
events,
"shift,"
opposed
incremental
"drift"
antigenicity.
Both
increase
transmissibility
shift
Omicron
led
readily
causing
infections
fully
vaccinated
and/or
previously
infected.
Omicron's
virulence,
while
reduced
relative
concern
replaced,
Delta,
very
much
premised
past
exposure
individuals
clear
signal
boosted
vaccination
protects
from
disease.
Currently,
proven
itself
dangerous
pathogen
unpredictable
evolutionary
capacity,
leading
too
great
not
ensure
all
world
screened
by
sequencing,
protected
through
available
affordable
vaccines,
non-punitive
strategies
place
detecting
responding
concern.