medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Feb. 13, 2024
Abstract
During
the
COVID-19
pandemic
it
was
widely
described
that
certain
individuals
infected
by
SARS-CoV-2
experience
persistent
disease
signs
and
symptoms,
Long
COVID,
which
in
some
cases
is
very
severe
with
life
changing
consequences.
To
maximize
our
chances
of
identifying
underpinnings
this
illness,
we
have
focused
on
121
most
from
>1000
patients
screened
specialized
clinics
Sweden
Belgium.
We
restricted
study
to
subjects
objective
measures
organ
damage
or
dysfunction,
>3
months
following
a
verified,
but
mild-to-moderate
infection.
By
performing
systems-level
immunological
testing
comparisons
controls
fully
convalescent
similar
mild/moderate
episode,
identify
elevated
serological
responses
COVID
suggestive
chronic
antigen
stimulation.
Persistent
viral
reservoirs
been
proposed
using
multiple
orthogonal
methods
for
detection
RNA
protein
plasma
subset
detectable
antigens,
minimal
overlap
across
assays,
no
correlation
symptoms
immune
measurements.
Elevated
serologic
other
hand
were
inversely
correlated
clonally
expanded
memory
CD8
+
T
cells,
indicating
restrained
clonal
expansion
enables
persistence,
exposure
IgG
responses,
even
if
antigen-detection
blood
not
universally
possible.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: May 10, 2023
Abstract
The
ongoing
global
pandemic
of
coronavirus
disease
2019
(COVID-19),
caused
by
severe
acute
respiratory
syndrome
2
(SARS‐CoV‐2),
has
devastating
impacts
on
the
public
health
and
economy.
Rapid
viral
antigenic
evolution
led
to
continual
generation
new
variants.
Of
special
note
is
recently
expanding
Omicron
subvariants
that
are
capable
immune
evasion
from
most
existing
neutralizing
antibodies
(nAbs).
This
posed
challenges
for
prevention
treatment
COVID-19.
Therefore,
exploring
broad-spectrum
antiviral
agents
combat
emerging
variants
imperative.
In
sharp
contrast
massive
accumulation
mutations
within
SARS-CoV-2
receptor-binding
domain
(RBD),
S2
fusion
subunit
remained
highly
conserved
among
Hence,
S2-based
therapeutics
may
provide
effective
cross-protection
against
Here,
we
summarize
developed
inhibitors
(e.g.,
nAbs,
peptides,
proteins,
small-molecule
compounds)
candidate
vaccines
targeting
elements
in
subunit.
main
focus
includes
all
targetable
elements,
namely,
peptide,
stem
helix,
heptad
repeats
1
(HR1-HR2)
bundle.
Moreover,
a
detailed
summary
characteristics
action-mechanisms
each
class
cross-reactive
inhibitors,
which
should
guide
promote
future
design
coronaviruses.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: May 27, 2024
Abstract
Considering
the
significant
burden
of
post-acute
COVID-19
conditions
among
patients
infected
with
SARS-CoV-2,
we
aimed
to
identify
risk
acute
respiratory
complications
or
sequelae.
A
binational
population-based
cohort
study
was
conducted
analyze
sequelae
after
SARS-CoV-2
infection.
We
used
a
Korean
nationwide
claim-based
(K-COV-N;
n
=
2,312,748;
main
cohort)
and
Japanese
(JMDC;
3,115,606;
replication
multi-to-one
propensity
score
matching.
Among
2,312,748
participants
(mean
age,
47.2
years
[SD,
15.6];
1,109,708
[48.0%]
female),
17.1%
(394,598/2,312,748)
were
SARS-CoV-2.
The
is
significantly
increased
in
people
infection
compared
general
population
(acute
complications:
HR,
8.06
[95%
CI,
6.92-9.38];
sequelae:
1.68
[1.62-1.75]),
increasing
severity.
identified
vaccination
as
an
attenuating
factor,
showing
protective
association
against
conditions.
Furthermore,
while
excess
diminished
time
following
infection,
it
persisted
beyond
6
months
post-infection.
showed
similar
pattern
association.
Our
comprehensively
evaluates
post-COVID-19
conditions,
considering
factors
such
status,
post-infection
duration,
severity,
specific
PubMed,
Journal Year:
2025,
Volume and Issue:
50(2), P. 61 - 68
Published: Feb. 1, 2025
T-cell-mediated
immunity
is
essential
for
controlling
severe
acute
respiratory
syndrome
coronavirus
2
(SARSCoV2)
infection,
preventing
disease,
and
potentially
reducing
the
risk
of
long-term
disease
(COVID).
This
study
investigated
impact
natural
vaccination,
hybrid
on
T-cell
responses,
with
a
particular
emphasis
role
memory
T-cells
in
COVID-19.
The
present
reviewed
current
literature
including
development,
individuals
SARS-CoV-2
those
vaccinated
messenger
RNA
(mRNA)
vaccines,
immunity.
It
examined
studies
that
compared
activity,
immune
regulation,
prevalence
COVID-19
across
these
groups.
Natural
infection
induces
variable
cases
showing
stronger
but
sometimes
dysregulated
immunological
which
may
contribute
to
prolonged
Vaccination,
particularly
mRNA
elicits
targeted
consistent
T-cells,
severity,
incidence
Hybrid
combines
provides
most
robust
protection,
enhanceds
reduces
through
balanced
regulation.
Memory
play
critical
mitigating
Vaccination
significantly
enhances
immunity,
minimizing
chronic
symptoms
alone.
effective
defense,
emphasizing
importance
even
after
prevent
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Oct. 26, 2023
Abstract
Respiratory
mucosal
immunity
induced
by
vaccination
is
vital
for
protection
from
coronavirus
infection
in
animal
models.
In
humans,
the
capacity
of
peripheral
to
generate
sustained
lung
mucosa,
and
how
this
influenced
prior
SARS-CoV-2
infection,
unknown.
Here
we
show
using
bronchoalveolar
lavage
samples
that
donors
with
history
both
have
more
airway
antibodies
memory
B
cells
than
those
only
vaccinated.
Infection
also
induces
populations
spike-specific
CD4+
CD8+
T
are
not
expanded
alone.
Airway
a
distinct
hierarchy
antigen
specificity
compared
periphery.
Spike-specific
persist
mucosa
7
months
after
last
immunising
event.
Thus,
alone
does
appear
induce
durable
against
SARS-CoV-2,
supporting
an
argument
need
vaccines
targeting
airways.
JCI Insight,
Journal Year:
2024,
Volume and Issue:
9(5)
Published: March 8, 2024
Understanding
the
immune
responses
to
SARS-CoV-2
vaccination
is
critical
optimizing
strategies
for
individuals
with
autoimmune
diseases,
such
as
systemic
lupus
erythematosus
(SLE).
Here,
we
comprehensively
analyzed
innate
and
adaptive
in
19
patients
SLE
receiving
a
complete
2-dose
Pfizer-BioNTech
mRNA
vaccine
(BNT162b2)
regimen
compared
control
cohort
of
56
healthy
(HC)
volunteers.
Patients
exhibited
impaired
neutralizing
antibody
production
antigen-specific
CD4+
CD8+
T
cell
relative
HC.
Interestingly,
were
only
altered
treated
immunosuppressive
therapies,
whereas
impairment
numbers
was
independent
medication.
also
displayed
reduced
levels
circulating
CXC
motif
chemokine
ligands,
CXCL9,
CXCL10,
CXCL11,
IFN-γ
after
secondary
well
downregulation
gene
expression
pathways
indicative
compromised
responses.
Single-cell
RNA-Seq
analysis
reveals
that
showed
vaccine-inducible
monocyte
population
characterized
by
overexpression
IFN-response
transcription
factors.
Thus,
although
2
doses
BNT162b2
induced
relatively
robust
SLE,
our
data
demonstrate
both
HC,
highlighting
need
population-specific
studies.