Yonsei Medical Journal,
Journal Year:
2021,
Volume and Issue:
62(11), P. 961 - 961
Published: Jan. 1, 2021
Since
the
COVID-19
pandemic
first
began
in
December
2019,
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
virus
has
continuously
evolved
with
many
variants
emerging
across
world.
These
are
categorized
as
variant
of
interest
(VOI),
concern
(VOC),
and
under
monitoring
(VUM).
As
September
15,
2021,
there
four
SARS-CoV-2
lineages
designated
VOC
(alpha,
beta,
gamma,
delta
variants).
VOCs
have
increased
transmissibility
compared
to
original
virus,
potential
for
increasing
disease
severity.
In
addition,
exhibit
decreased
susceptibility
vaccine-induced
infection-induced
immune
responses,
thus
possess
ability
reinfect
previously
infected
recovered
individuals.
Given
their
evade
less
susceptible
monoclonal
antibody
treatments.
can
also
impact
effectiveness
mRNA
adenovirus
vector
vaccines,
although
currently
authorized
vaccines
still
effective
preventing
infection
disease.
Current
measures
reduce
transmission
well
efforts
monitor
understand
should
be
continued.
Here,
we
review
molecular
features,
epidemiology,
on
transmissibility,
severity,
vaccine
VOCs.
Science,
Journal Year:
2022,
Volume and Issue:
376(6593)
Published: March 15, 2022
We
provide
two
methods
for
monitoring
reinfection
trends
in
routine
surveillance
data
to
identify
signatures
of
changes
risk
and
apply
these
approaches
from
South
Africa's
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
epidemic
date.
Although
we
found
no
evidence
increased
associated
with
circulation
the
Beta
(B.1.351)
or
Delta
(B.1.617.2)
variants,
did
find
clear,
population-level
suggest
immune
evasion
by
Omicron
(B.1.1.529)
variant
previously
infected
individuals
Africa.
Reinfections
occurring
between
1
November
2021
31
January
2022
were
detected
all
three
previous
waves,
there
has
been
an
increase
having
a
third
infection
since
mid-November
2021.
Nature,
Journal Year:
2022,
Volume and Issue:
608(7923), P. 603 - 608
Published: July 5, 2022
Abstract
SARS-CoV-2
Omicron
subvariants
BA.2.12.1
and
BA.4/5
have
surged
notably
to
become
dominant
in
the
United
States
South
Africa,
respectively
1,2
.
These
new
carrying
further
mutations
their
spike
proteins
raise
concerns
that
they
may
evade
neutralizing
antibodies,
thereby
compromising
efficacy
of
COVID-19
vaccines
therapeutic
monoclonals.
We
now
report
findings
from
a
systematic
antigenic
analysis
these
surging
subvariants.
is
only
modestly
(1.8-fold)
more
resistant
sera
vaccinated
boosted
individuals
than
BA.2.
However,
substantially
(4.2-fold)
thus
likely
lead
vaccine
breakthrough
infections.
Mutation
at
residue
L452
found
both
facilitates
escape
some
antibodies
directed
so-called
class
2
3
regions
receptor-binding
domain
The
F486V
mutation
certain
1
but
compromises
affinity
for
viral
receptor.
R493Q
reversion
mutation,
however,
restores
receptor
consequently
fitness
BA.4/5.
Among
authorized
clinical
use,
bebtelovimab
retains
full
potency
against
lineage
continues
evolve,
successively
yielding
are
not
transmissible
also
evasive
antibodies.
Nature,
Journal Year:
2021,
Volume and Issue:
602(7896), P. 300 - 306
Published: Nov. 25, 2021
Abstract
During
the
current
coronavirus
disease
2019
(COVID-19)
pandemic,
a
variety
of
mutations
have
accumulated
in
viral
genome
severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
and,
at
time
writing,
four
variants
concern
are
considered
to
be
potentially
hazardous
human
society
1
.
The
recently
emerged
B.1.617.2/Delta
variant
is
closely
associated
with
COVID-19
surge
that
occurred
India
spring
2021
(ref.
).
However,
virological
properties
remain
unclear.
Here
we
show
highly
fusogenic
and
notably
more
pathogenic
than
prototypic
SARS-CoV-2
infected
hamsters.
P681R
mutation
spike
protein,
which
conserved
this
lineage,
facilitates
cleavage
protein
enhances
fusogenicity.
Moreover,
demonstrate
P681R-bearing
virus
exhibits
higher
pathogenicity
compared
its
parental
virus.
Our
data
suggest
hallmark
phenotype
enhanced
pathogenicity.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Jan. 24, 2022
Abstract
The
SARS-CoV-2
Delta
variant
has
spread
rapidly
worldwide.
To
provide
data
on
its
virological
profile,
we
here
report
the
first
local
transmission
of
in
mainland
China.
All
167
infections
could
be
traced
back
to
index
case.
Daily
sequential
PCR
testing
quarantined
individuals
indicated
that
viral
loads
infections,
when
they
become
PCR-positive,
were
average
~1000
times
greater
compared
lineage
A/B
during
epidemic
wave
China
early
2020,
suggesting
potentially
faster
replication
and
infectiousness
infection.
estimated
bottleneck
size
was
generally
narrow,
with
1-3
virions
29
donor-recipient
pairs.
However,
minor
iSNVs
resulted
at
least
3
34
substitutions
identified
outbreak,
highlighting
contribution
intra-host
variants
population-level
diversity
rapid
spread.
Cell,
Journal Year:
2022,
Volume and Issue:
185(10), P. 1728 - 1744.e16
Published: April 1, 2022
As
the
emerging
variants
of
SARS-CoV-2
continue
to
drive
worldwide
pandemic,
there
is
a
constant
demand
for
vaccines
that
offer
more
effective
and
broad-spectrum
protection.
Here,
we
report
circular
RNA
(circRNA)
vaccine
elicited
potent
neutralizing
antibodies
T
cell
responses
by
expressing
trimeric
RBD
spike
protein,
providing
robust
protection
against
in
both
mice
rhesus
macaques.
Notably,
circRNA
enabled
higher
durable
antigen
production
than
1mΨ-modified
mRNA
proportion
distinct
Th1-skewed
immune
responses.
Importantly,
found
circRNARBD-Omicron
induced
Omicron
but
not
Delta
variant.
In
contrast,
circRNARBD-Delta
protected
or
functioned
as
booster
after
two
doses
either
native-
Delta-specific
vaccination,
making
it
favorable
choice
current
concern
(VOCs)
SARS-CoV-2.
Nature Medicine,
Journal Year:
2022,
Volume and Issue:
28(3), P. 477 - 480
Published: Jan. 19, 2022
The
Omicron
variant
of
SARS-CoV-2
is
causing
a
rapid
increase
in
infections
across
the
globe.
This
new
concern
carries
an
unusually
high
number
mutations
key
epitopes
neutralizing
antibodies
on
viral
spike
glycoprotein,
suggesting
potential
immune
evasion.
Here
we
assessed
serum
capacity
longitudinal
cohorts
vaccinated
and
convalescent
individuals,
as
well
monoclonal
antibody
activity
against
using
pseudovirus
neutralization
assays.
We
report
near-complete
lack
polyclonal
sera
from
individuals
with
two
doses
BNT162b2
COVID-19
vaccine
resistance
to
different
clinical
use.
However,
mRNA
booster
immunizations
resulted
significant
Omicron.
study
demonstrates
that
can
critically
improve
humoral
response
variant.