Temporal profiling of human lymphoid tissues reveals coordinated defense against viral challenge
Nature Immunology,
Год журнала:
2025,
Номер
26(2), С. 215 - 229
Опубликована: Янв. 31, 2025
Язык: Английский
SARS-CoV-2 Vaccines: The Advantage of Mucosal Vaccine Delivery and Local Immunity
Vaccines,
Год журнала:
2024,
Номер
12(7), С. 795 - 795
Опубликована: Июль 18, 2024
Immunity
against
respiratory
pathogens
is
often
short-term,
and,
consequently,
there
an
unmet
need
for
the
effective
prevention
of
such
infections.
One
infectious
disease
coronavirus
19
(COVID-19),
which
caused
by
novel
Beta
SARS-CoV-2
that
emerged
around
end
2019.
The
World
Health
Organization
declared
illness
a
pandemic
on
11
March
2020,
and
since
then
it
has
killed
or
sickened
millions
people
globally.
development
COVID-19
systemic
vaccines,
impressively
led
to
significant
reduction
in
severity,
hospitalization,
mortality,
contained
pandemic’s
expansion.
However,
these
vaccines
have
not
been
able
stop
virus
from
spreading
because
restricted
mucosal
immunity.
As
result,
breakthrough
infections
frequently
occurred,
new
strains
emerging.
Furthermore,
will
likely
continue
circulate
like
influenza
virus,
co-exist
with
humans.
upper
tract
nasal
cavity
are
primary
sites
infection
thus,
mucosal/nasal
vaccination
induce
response
virus’
transmission
warranted.
In
this
review,
we
present
status
both
approved
those
under
evaluation
clinical
trials.
our
approach
B-cell
peptide-based
applied
prime-boost
schedule
elicit
Язык: Английский
Natural and induced immune responses in oral cavity and saliva
BMC Immunology,
Год журнала:
2025,
Номер
26(1)
Опубликована: Апрель 18, 2025
Язык: Английский
Why Should Vaccines against Respiratory Diseases Go Mucosal? B Cell Epitope-Based Vaccines against SARS-CoV-2
Опубликована: Июнь 13, 2024
Immunity
against
respiratory
pathogens
is
often
short-term,
and
consequently
there
an
unmet
need
for
effective
prevention
of
such
infections.
One
infectious
disease
COVID-19,
which
caused
by
the
novel
Beta
coronavirus
SARS-CoV-2
that
emerged
around
end
2019.
The
World
Health
Organization
declared
illness
a
pandemic
on
March
11,
2020,
since
then
it
has
killed
or
sickened
millions
people
globally.
development
COVID-19
systemic
vaccines,
impressively
led
to
significant
reduction
in
severity,
hospitalization,
mortality,
con-tained
pandemic's
expansion.
However,
these
vaccines
have
not
been
able
stop
virus
from
spreading
because
restricted
mucosal
immunity.
As
result,
breakthrough
infections
frequently
occurred
new
strains
emerging.
Furthermore,
will
likely
continue
circulate
and,
like
influenza
virus,
co-exist
with
humans.
upper
tract
nasal
cavity
are
primary
sites
infection
thus,
mucosal/nasal
vaccination
induce
response
transmission
warrant-ed.
In
this
review,
we
present
status
approved
those
under
evaluation
clinical
trials.
our
approach
B-cell
pep-tide-based
applied
prime-boost
schedule
eliciting
both
Язык: Английский
mRNA vaccine-induced IgG mediates nasal SARS-CoV-2 clearance in mice
Molecular Therapy — Nucleic Acids,
Год журнала:
2024,
Номер
35(4), С. 102360 - 102360
Опубликована: Окт. 16, 2024
Coronavirus
disease
2019
(COVID-19)
mRNA
vaccines
that
have
contributed
to
controlling
the
SARS-CoV-2
pandemic
induce
specific
serum
antibodies,
which
correlate
with
protection.
However,
neutralizing
capacity
of
antibodies
for
emerging
variants
is
altered.
Suboptimal
antibody
responses
are
observed
in
patients
humoral
immunodeficiency
diseases,
ongoing
B
cell
depletion
therapy,
and
aging.
Common
experimental
mouse
models
altered
compartments,
such
as
or
deficiency,
do
not
fully
recapitulate
scenarios
declining
suboptimal
levels
humans.
We
report
on
immunity
a
transgenic
model
restricted
virus-specific
antibodies.
Vaccination
C57BL/6-Tg(IghelMD4)4Ccg/J
mice
unmodified
N1mΨ-modified
encoding
ancestral
spike
(S)
protein
subsequent
challenge
mouse-adapted
provided
insights
into
antibody-independent
impact
titers
mucosal
immunity.
Protection
against
fatal
was
independent
seroconversion
following
vaccination,
suggesting
T
cells
can
compensate
levels.
In
contrast,
mRNA-induced
IgG
nasal
conchae
limited
local
viral
load
progression.
Our
results
indicate
parenteral
immunization
elicit
effectively
suppress
replication,
highlighting
potential
transmission
epidemiology.
Язык: Английский
Role of IgA1 protease-producing bacteria in SARS-CoV-2 infection and transmission: a hypothesis
mBio,
Год журнала:
2024,
Номер
15(10)
Опубликована: Авг. 29, 2024
Secretory
(S)
IgA
antibodies
against
severe
acute
respiratory
syndrome
(SARS)-CoV-2
are
induced
in
saliva
and
upper
tract
(URT)
secretions
by
natural
infection
may
be
critical
determining
the
outcome
of
initial
infection.
IgA1
(SIgA1)
is
predominant
isotype
these
secretions.
Neutralization
SARS-CoV-2
most
effectively
accomplished
polymeric
such
as
SIgA.
We
hypothesize
that
cleavage
SIgA1
unique
bacterial
proteases
to
univalent
Fabα
antibody
fragments
with
diminished
virus
neutralizing
activity
would
facilitate
descent
into
lungs
cause
serious
disease
also
enhance
its
airborne
transmission
others.
Recent
studies
nasopharyngeal
microbiota
patients
have
revealed
significant
increases
proportions
protease-producing
bacteria
comparison
healthy
subjects.
Similar
considerations
might
apply
other
viral
infections
including
influenza,
possibly
explaining
original
attribution
influenza
Язык: Английский
Next-Generation SARS-CoV-2 Vaccine Formulations and Alternative Routes of Administration
The Journal of Infectious Diseases,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 16, 2024
Abstract
The
development
of
SARS-CoV-2
next-generation
vaccines
with
the
potential
for
increased
effectiveness,
durability,
breadth,
and
ability
to
decrease
transmission
are
public
health
importance.
We
highlight
alternative
routes
administration
such
as
mucosal
intradermal
administration.
Язык: Английский
mRNA Vaccines Against COVID-19 as Trailblazers for Other Human Infectious Diseases
Vaccines,
Год журнала:
2024,
Номер
12(12), С. 1418 - 1418
Опубликована: Дек. 16, 2024
mRNA
vaccines
represent
a
milestone
in
the
history
of
vaccinology,
because
they
are
safe,
very
effective,
quick
and
cost-effective
to
produce,
easy
adapt
should
antigen
vary,
able
induce
humoral
cellular
immunity.
Methods:
To
date,
only
two
COVID-19
one
RSV
have
been
approved.
However,
several
currently
under
development
for
prevention
human
viral
(influenza,
immunodeficiency
virus
[HIV],
Epstein–Barr
virus,
cytomegalovirus,
Zika,
respiratory
syncytial
metapneumovirus/parainfluenza
3,
Chikungunya,
Nipah,
rabies,
varicella
zoster
herpes
simplex
1
2),
bacterial
(tuberculosis),
parasitic
(malaria)
diseases.
Results:
RNA
viruses,
such
as
severe
acute
syndrome
coronavirus
(SARS-CoV)-2,
HIV,
influenza,
characterized
by
high
variability,
thus
creating
need
rapidly
circulating
strain,
task
that
can
easily
accomplish;
however,
speed
variability
may
be
higher
than
time
needed
vaccine
adapted.
vaccines,
using
lipid
nanoparticles
delivery
system,
act
adjuvants,
powerfully
stimulating
innate
well
adaptive
immunity,
both
humoral,
which
is
waning,
cell-mediated,
highly
persistent.
Safety
profiles
were
satisfactory,
considering
slight
increase
prognostically
favorable
anaphylactic
reactions
young
females
myopericarditis
males
has
observed.
Conclusions:
The
pandemic
determined
shift
use
RNA:
after
having
used
medicine
micro-RNAs
tumor
new
era
anti-infectious
begun,
great
development,
either
improve
already
available,
but
unsatisfactory,
or
develop
protective
against
infectious
agents
no
preventative
tools
realized
yet.
Язык: Английский