npj Vaccines,
Journal Year:
2022,
Volume and Issue:
7(1)
Published: Feb. 9, 2022
Two
doses
of
the
MVA-CoV2-S
vaccine
candidate
expressing
SARS-CoV-2
spike
(S)
protein
protected
K18-hACE2
transgenic
mice
from
a
lethal
dose
SARS-CoV-2.
This
vaccination
regimen
prevented
virus
replication
in
lungs,
reduced
lung
pathology,
and
diminished
levels
pro-inflammatory
cytokines.
High
titers
IgG
antibodies
against
S
receptor-binding
domain
(RBD)
proteins
neutralizing
were
induced
parental
variants
concern,
markers
that
correlated
with
protection.
Similar
SARS-CoV-2-specific
antibody
responses
observed
at
prechallenge
postchallenge
two-dose
regimen,
while
single-dose
treatment
does
not
avoid
breakthrough
infection.
All
vaccinated
animals
survived
infection
also
to
reinfection.
Furthermore,
two
long-term
memory
S-specific
humoral
cellular
immune
C57BL/6
mice,
6
months
after
immunization.
The
efficacy
immunological
benefits
COVID-19
supports
its
consideration
for
human
clinical
trials.
The Lancet Microbe,
Journal Year:
2022,
Volume and Issue:
3(5), P. e348 - e356
Published: March 24, 2022
The
memory
immune
response
is
crucial
for
preventing
reinfection
or
reducing
disease
severity.
However,
the
robustness
and
functionality
of
humoral
T-cell
to
SARS-CoV-2
remains
unknown
12
months
after
initial
infection.
aim
this
study
investigate
durability
original
strain
variants
in
recovered
patients
infection.In
longitudinal
cohort
study,
we
recruited
participants
who
had
from
COVID-19
were
discharged
Wuhan
Research
Center
Communicable
Disease
Diagnosis
Treatment
at
Chinese
Academy
Medical
Sciences,
Wuhan,
China,
between
Jan
7
May
29,
2020.
Patients
received
a
follow-up
visit
Dec
16,
2020,
27,
2021.
We
evaluated
presence
IgM,
IgA,
IgG
antibodies
against
nucleoprotein,
Spike
protein,
receptor-binding
domain
infection,
using
ELISA.
Neutralising
strain,
D614G,
beta
(B.1.351),
delta
(B.1.617.2)
analysed
microneutralisation
assay
subset
plasma
samples.
magnitude
breadth
SARS-CoV-2-specific
responses
interferon
γ
(IFNγ)
enzyme-linked
absorbent
spot
(ELISpot)
intracellular
cytokine
staining
(ICS)
assay.
antibody
(ie,
IFN-γ,
interleukin-2
[IL-2],
tumour
necrosis
factor
α
[TNFα])
by
age
Antibody
titres
also
according
sequelae
symptoms.We
enrolled
1096
patients,
including
289
(26·4%)
with
moderate
disease,
734
(67·0%)
severe
73
(6·7%)
critical
disease.
Paired
samples
collected
141
during
visits
PBMCs
92
individuals
12-month
visit,
which
80
ELISpot
ICS
detect
responses.
N-IgG
(899
[82·0%]),
S-IgG
(1043
[95·2%]),
RBD-IgG
(1032
[94·2%]),
neutralising
(115
[81·6%]
141)
detectable
infection
most
individuals.
remained
stable
6
younger
than
60
years.
Multifunctional
detected
all
viral
proteins
tested.
There
was
no
difference
profiles
different
symptom
Moreover,
both
beta,
strains.
degree
reduced
in-vitro
D614G
variants,
but
not
variant,
associated
found
poor
variant;
83
(72·2%)
115
showed
all.
titre
reduction
patient
variant
similar
that
lower
variant.
By
contrast,
cross-reactive
Importantly,
could
be
lost
infection.SARS-CoV-2-specific
retained
strains
compared
those
diminished
general.
Memory
disrupted
new
variants.
This
suggests
particularly
important
protection
caused
concern
whereas
seem
reduce
over
time.Chinese
National
Natural
Science
Foundation,
UK
Council.
The
COVID-19
global
pandemic
caused
by
the
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
infection
has
infected
hundreds
of
millions
individuals.
Following
infection,
a
subset
can
develop
wide
range
chronic
symptoms
affecting
diverse
organ
systems
referred
to
as
post-acute
sequelae
SARS-CoV-2
(PASC),
also
known
long
COVID.
A
National
Institutes
Health-sponsored
initiative,
RECOVER:
Researching
COVID
Enhance
Recovery,
sought
understand
basis
in
large
cohort.
Given
that
occur
COVID,
mechanisms
may
underlie
these
be
diverse.
In
this
review,
we
focus
on
emerging
literature
supporting
role(s)
viral
persistence
or
reactivation
viruses
play
PASC.
Persistence
RNA
antigens
is
reported
some
organs,
yet
mechanism
which
they
do
so
and
how
associated
with
pathogenic
immune
responses
unclear.
Understanding
RNA,
antigen
other
reactivated
relate
specific
inflammatory
drive
PASC
provide
rationale
for
treatment.
Annual Review of Immunology,
Journal Year:
2023,
Volume and Issue:
41(1), P. 343 - 373
Published: Feb. 8, 2023
A
large
body
of
evidence
generated
in
the
last
two
and
a
half
years
addresses
roles
T
cells
SARS-CoV-2
infection
following
vaccination.
Infection
or
vaccination
induces
multi-epitope
CD4
CD8
cell
responses
with
polyfunctionality.
Early
have
been
associated
mild
COVID-19
outcomes.
In
concert
animal
model
data,
these
results
suggest
that
while
antibody
are
key
to
prevent
infection,
may
also
play
valuable
reducing
disease
severity
controlling
infection.
memory
after
is
sustained
for
at
least
six
months.
While
neutralizing
impacted
by
variants,
most
preserved.
This
review
highlights
extensive
progress
made,
data
knowledge
gaps
remain,
our
understanding
vaccines.
Science,
Journal Year:
2023,
Volume and Issue:
380(6641), P. 203 - 210
Published: April 13, 2023
Certain
bacterial
colonists
induce
a
highly
specific
T
cell
response.
A
hallmark
of
this
encounter
is
that
adaptive
immunity
develops
preemptively,
in
the
absence
an
infection.
However,
functional
properties
colonist-induced
cells
are
not
well
defined,
limiting
our
ability
to
understand
anticommensal
and
harness
it
therapeutically.
We
addressed
both
challenges
by
engineering
skin
bacterium
Staphylococcus
epidermidis
express
tumor
antigens
anchored
secreted
or
cell-surface
proteins.
Upon
colonization,
engineered
S.
elicits
tumor-specific
circulate,
infiltrate
local
metastatic
lesions,
exert
cytotoxic
activity.
Thus,
immune
response
colonist
can
promote
cellular
at
distal
site
be
redirected
against
target
therapeutic
interest
expressing
target-derived
antigen
commensal.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: May 4, 2022
Since
the
onset
of
COVID-19
pandemic,
medical
field
has
been
forced
to
apply
basic
knowledge
immunology
with
most
up-to-date
SARS-CoV-2
findings
and
translate
it
population
whole
world
in
record
time.
Following
infection
viral
antigen,
adaptive
immune
responses
are
activated
mainly
by
particle
encounters
antigen-presenting
cells
or
B
cell
receptors,
which
induce
further
biological
interactions
defend
host
against
virus.
After
warded
off,
immunological
memory
is
developed.
The
SARS-CoV
cellular
immunity
shown
persist
even
17
years
after
infection,
despite
undetectable
humoral
component.
Similar
demonstrated
for
T
a
shorter
period
assessing
interferon-gamma
levels
when
heparinized
blood
stimulated
virus-specific
peptides.
also
play
an
irreplaceable
part
reaction
as
backbone
response.
They
both
provide
signals
activation
maturation,
competence,
production
IgA
was
be
significant
influence
mediating
mucosal
first
defense
mechanism
development
nasal
vaccines.
Here,
we
interpret
recent
available
research,
encompasses
significance
current
understanding
activity,
compare
among
naive,
exposed,
vaccinated
donors.
Our
data
showed
that
those
who
recovered
from
EMA-approved
vaccines
had
long-lasting
immunity.
Additionally,
analyze
immunocompromised
patients
mediated
impact
clonality
pandemic
regarding
breakthrough
infections
variants
concern,
B.1.617.2
(Delta)
B.1.1.529
(Omicron)
variants.
Nature reviews. Immunology,
Journal Year:
2021,
Volume and Issue:
21(12), P. 762 - 768
Published: Oct. 19, 2021
An
important
challenge
during
the
COVID-19
pandemic
has
been
to
understand
asymptomatic
disease
and
extent
which
this
may
be
a
source
of
transmission.
As
is
by
definition
hard
screen
for,
there
lack
clarity
about
aspect
spectrum.
Studies
have
considered
whether
prevalence
determined
differences
in
age,
demographics,
viral
load,
duration
shedding,
magnitude
or
durability
immunity.
It
clear
that
adaptive
immunity
strongly
activated
infection,
but
some
features
T
cell
antibody
response
differ
from
those
symptomatic
disease.
Areas
need
greater
include
leads
persistent
symptoms
(long
COVID),
quality,
quantity
immune
priming
required
confer
subsequent
protection.
Individuals
with
can
transmit
virus
at
risk
long-term
In
Progress
article,
Boyton
Altman
present
current
insights
into
responses
SARS-CoV-2
infection
discuss
relevance
for
public
health
strategies.
Expert Review of Vaccines,
Journal Year:
2021,
Volume and Issue:
20(8), P. 1013 - 1025
Published: June 26, 2021
Several
vaccine
candidates
have
been
developed
using
different
platforms,
including
nucleic
acids
(DNA
and
RNA),
viral
vectors
(replicating
non-replicating),
virus-like
particles,
peptide-based,
recombinant
proteins,
live
attenuated,
inactivated
virus
modalities.
Although
many
of
these
vaccines
are
undergoing
pre-clinical
trials,
several
large
clinical
trials
investigating
the
efficacy
safety
coronavirus
disease
2019
(COVID-19)
produced
promising
findings.In
this
review,
we
provide
a
status
update
on
COVID-19
currently
discuss
issues
concern
beyond
safety,
dosing
regimens,
mixed
strategy,
prior
severe
acute
respiratory
syndrome
coronavirus-2
infection,
antibody
levels,
cellular
immunity
protection,
variants
concern,
distribution,
vaccination
willingness,
herd
immunity,
passports,
indications.Four
obtained
emergency
use
authorization,
87
at
development
stage,
186
in
development.
While
knowledge
is
rapidly
expanding,
benefits
must
outweigh
potential
risks
adverse
events.
To
combat
pandemic,
clinicians
should
consistently
COVID-19-associated
information,
healthcare
authorities
manufacturers
work
together
to
adequate
appropriate
vaccinations
for
prevention
COVID-19.What
context?Severe
(SARS-CoV-2)
caused
global
pandemic:
outbreak.
The
implementation
could
be
an
important
measure
control
pandemic.What
new?Several
phase
3
demonstrated
effectiveness
SARS-CoV-2
infections.
authorization
implemented
countries.
concerns
regarding
unusual
blood
clots
low
platelet
counts
raised,
events.What
impact?Except
children,
recommended
all
people,
those
pregnant
or
immunocompromised.
Healthcare
advise
people
receiving
that
they
seek
medical
attention
if
associated
thromboembolism
thrombocytopenia
symptoms.
More
studies
necessary
determine
dose
regimen
as
well
against
concerns.
A
effort
made
achieve
widespread
immunity.