Seminars in Immunology,
Journal Year:
2023,
Volume and Issue:
69, P. 101794 - 101794
Published: June 20, 2023
During
the
three
years
since
SARS-CoV-2
infections
were
first
described
a
wealth
of
information
has
been
gathered
about
viral
variants
and
their
changing
properties,
disease
presentations
they
elicit
how
many
vaccines
developed
in
record
time
protect
from
COVID-19
severe
different
populations.
A
general
theme
throughout
pandemic
observation
that
children
young
people
fare
well,
with
mild
symptoms
during
acute
infection
full
recovery
thereafter.
It
also
become
clear
this
is
not
universally
true,
as
some
develop
hypoxic
pneumonia
even
succumb
to
infection,
while
another
group
rare
but
serious
multisystem
inflammatory
syndrome
(MIS-C)
other
experience
prolonged
illness
following
post-COVID.
Here
I
will
discuss
findings
made
explain
these
diverse
manifestations
infected
by
SARS-CoV-2.
at
speed
efficacy
protecting
disease.
Science,
Journal Year:
2022,
Volume and Issue:
377(6611), P. 1144 - 1149
Published: Sept. 8, 2022
There
has
been
substantial
research
on
adult
COVID-19
and
how
to
treat
it.
But
do
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
infections
afflict
children?
The
pandemic
yielded
many
surprises,
not
least
that
children
generally
develop
less
disease
than
older
adults,
which
is
unusual
for
a
disease.
However,
some
can
serious
complications
from
COVID-19,
such
as
multisystem
inflammatory
in
(MIS-C)
Long
Covid,
even
after
mild
or
asymptomatic
COVID-19.
Why
this
occurs
others
an
important
question.
Moreover,
when
contract
understanding
their
role
transmission,
especially
schools
at
home,
crucial
ensuring
effective
mitigation
measures.
Therefore,
addition
nonpharmaceutical
interventions,
improved
ventilation,
there
strong
case
vaccinate
so
reduce
possible
long-term
effects
infection
decrease
transmission.
questions
remain
about
whether
vaccination
might
skew
immune
responses
variants
the
long
term.
As
experts
discuss
below,
more
being
learned
these
issues,
but
much
needed
understand
of
children.
BMJ Medicine,
Journal Year:
2023,
Volume and Issue:
2(1), P. e000468 - e000468
Published: Nov. 1, 2023
The
T
cell
memory
response
is
a
crucial
component
of
adaptive
immunity
responsible
for
limiting
or
preventing
viral
reinfection.
after
infection
with
the
SARS-CoV-2
virus
vaccination
broad,
and
spans
multiple
proteins
epitopes,
about
20
in
each
individual.
So
far
long
lasting
provides
high
level
cross
reactivity
hence
resistance
to
escape
by
variants
virus,
such
as
omicron
variant.
All
current
vaccine
regimens
tested
produce
robust
responses,
heterologous
will
probably
enhance
protective
responses
through
increased
breadth.
could
have
major
role
protecting
against
severe
covid-19
disease
rapid
clearance
early
presentation
presence
reactive
cells
might
this
protection.
likely
provide
ongoing
protection
admission
hospital
death,
development
pan-coronovirus
future
proof
new
pandemic
strains.
Nature Immunology,
Journal Year:
2023,
Volume and Issue:
24(6), P. 966 - 978
Published: May 29, 2023
High-risk
groups,
including
Indigenous
people,
are
at
risk
of
severe
COVID-19.
Here
we
found
that
Australian
First
Nations
peoples
elicit
effective
immune
responses
to
COVID-19
BNT162b2
vaccination,
neutralizing
antibodies,
receptor-binding
domain
(RBD)
SARS-CoV-2
spike-specific
B
cells,
and
CD4+
CD8+
T
cells.
In
participants,
RBD
IgG
antibody
titers
were
correlated
with
body
mass
index
negatively
age.
Reduced
cells
follicular
helper
in
vaccinated
participants
chronic
conditions
(diabetes,
renal
disease)
strongly
associated
altered
glycosylation
increased
interleukin-18
levels
the
plasma.
These
perturbations
also
non-Indigenous
people
comorbidities,
indicating
they
related
comorbidities
rather
than
ethnicity.
However,
our
study
is
a
great
importance
who
have
disproportionate
rates
provides
evidence
robust
after
vaccination
people.
Child s Nervous System,
Journal Year:
2024,
Volume and Issue:
40(4), P. 1221 - 1237
Published: March 8, 2024
Abstract
Background
COVID-19
pandemic
is
thought
to
have
changed
the
epidemiology
of
some
pediatric
neurosurgical
disease:
among
them
are
intracranial
complications
sinusitis
and
otitis
(ICSO).
According
studies
on
a
limited
number
cases,
both
streptococci-related
ICSO
would
increased
immediately
after
pandemic,
although
reason
not
clear
yet
(seasonal
changes
versus
pandemic-related
effects).
The
goal
present
survey
European
Society
for
Pediatric
Neurosurgery
(ESPN)
was
collect
large
cases
from
different
countries
encompassing
pre-COVID
(2017–2019),
COVID
(2020–2021),
post-COVID
period
(2022–June
2023)
looking
possible
epidemiological
and/or
clinical
changes.
Material
methods
An
English
language
questionnaire
sent
ESPN
members
about
year
event,
patient’s
age
gender,
presence
immune-deficit
or
other
favoring
risk
factors,
infection,
signs
symptoms
at
onset,
site
primary
type
complication,
identified
germ,
surgical
operations,
duration
medical
treatment,
radiological
outcome,
follow-up.
Results
Two
hundred
fifty-four
were
collected
by
30
centers
coming
14
countries.
There
statistically
significant
difference
between
(129
children,
86
cases/year,
50.7%
whole
series)
(40
20
15.7%)
(85
28.3
33.5%).
Other
differences
concerned
predisposing
factors/concurrent
diseases
(higher
in
period)
previous
infection
period).
No
relevant
occurred
as
far
demographic,
microbiological,
clinical,
radiological,
morbidity,
mortality
data
concerned.
Paranasal
sinuses
middle
ear/mastoid
most
involved
(71%
27%,
respectively),
while
extradural
subdural
empyema
brain
abscess
common
(73%
17%,
respectively).
Surgery
required
95%
(neurosurgical
ENT
procedure
71%
62%
respectively)
antibiotics
99%
cases.
After
12.4-month
follow-up,
full
recovery
obtained
85%
84%
respectively.
rate
2.7%.
Conclusions
These
results
suggest
that
occurrence
significantly
pandemic.
Such
an
increase
seems
be
related
indirect
effects
(e.g.,
immunity
debt)
rather
than
direct
effect
seasonal
fluctuations.
remain
challenging
but
did
affect
management
strategies
nor
their
prognosis.
change
sinusitis/otitis
should
alert
appropriate
follow-up
children
with
sinusitis/otitis.
Nature Immunology,
Journal Year:
2023,
Volume and Issue:
24(11), P. 1890 - 1907
Published: Sept. 25, 2023
Abstract
CD8
+
T
cells
provide
robust
antiviral
immunity,
but
how
epitope-specific
evolve
across
the
human
lifespan
is
unclear.
Here
we
defined
cell
immunity
directed
at
prominent
influenza
epitope
HLA-A*02:01-M1
58–66
(A2/M1
58
)
four
age
groups
phenotypic,
transcriptomic,
clonal
and
functional
levels.
We
identify
a
linear
differentiation
trajectory
from
newborns
to
children
then
adults,
followed
by
divergence
reset
in
older
adults.
Gene
profiles
adults
closely
resemble
those
of
children,
despite
being
clonally
distinct.
Only
child-derived
adult-derived
A2/M1
had
potential
differentiate
into
highly
cytotoxic
cells,
which
was
linked
public
receptor
(TCR)αβ
signatures.
Suboptimal
TCRαβ
signatures
led
less
proliferation,
polyfunctionality,
avidity
recognition
peptide
mutants,
although
displayed
no
signs
exhaustion.
These
data
suggest
that
priming
different
stages
life
might
greatly
affect
responses
toward
viral
infections.
Cell Reports Medicine,
Journal Year:
2023,
Volume and Issue:
4(4), P. 101017 - 101017
Published: March 27, 2023
Immunocompromised
hematology
patients
are
vulnerable
to
severe
COVID-19
and
respond
poorly
vaccination.
Relative
deficits
in
immunity
are,
however,
unclear,
especially
after
3
vaccine
doses.
We
evaluated
immune
responses
across
three
vaccination
Seropositivity
was
low
a
first
dose
of
BNT162b2
ChAdOx1
(∼26%),
increased
59%-75%
second
dose,
85%
third
dose.
While
prototypical
antibody-secreting
cells
(ASCs)
T
follicular
helper
(Tfh)
cell
were
elicited
healthy
participants,
showed
prolonged
ASCs
skewed
Tfh2/17
responses.
Importantly,
vaccine-induced
expansions
spike-specific
peptide-HLA
tetramer-specific
CD4+/CD8+
cells,
together
with
their
receptor
(TCR)
repertoires,
robust
patients,
irrespective
B
numbers,
comparable
participants.
Vaccinated
breakthrough
infections
developed
higher
antibody
responses,
while
groups.
induces
varying
diseases
treatments
numbers
response.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 21, 2024
T
cell
activation
is
governed
through
receptors
(TCRs),
heterodimers
of
two
sequence-variable
chains
(often
an
alpha
[
α
]
and
beta
β
chain)
that
recognise
linear
antigen
fragments
presented
on
the
surfaces.
Early
sequencing
technologies
limited
study
immune
repertoire
TCRs
to
unpaired
transcripts,
leading
extensive
analysis
-chain
data
alone
as
its
greater
sequence
diversity
suggested
it
should
dominate
recognition.
Over
time,
structural
has
revealed
both
contribute
binding
most
antigens
highthroughput
single-cell
handling
have
been
increasingly
applied
obtain
samples
complete
TCR
variable
region
sequences
from
repertoires.
Despite
this,
there
currently
no
repository
dedicated
curation
publicly
available
paired
data.
We
addressed
this
gap
by
creating
Observed
receptor
Space
(OTS)
database,
a
source
consistently
processed
annotated,
full-length,
paired-chain
50
studies
at
least
75
individuals.
Currently,
OTS
contains
5.35M
redundant
(1.63M
nonredundant)
predominantly
human
and,
based
recent
availability
trends,
will
grow
rapidly.
perform
initial
OTS,
identification
pairing
biases,
public
TCRs,
distinct
chain
coherence
patterns
relative
antibodies.
also
harness
build
language
model,
providing
embedding
representations
method
for
residue
in-filling
conditional
partner
chain.
be
updated
maintained
central
community
resource
freely
downloadable
web
application
https://opig.stats.ox.ac.uk/webapps/ots
.
Patients
affected
by
different
types
of
autoimmune
diseases,
including
common
conditions
such
as
multiple
sclerosis
(MS)
and
rheumatoid
arthritis
(RA),
are
often
treated
with
immunosuppressants
to
suppress
disease
activity.
It
is
not
fully
understood
how
the
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)-specific
humoral
cellular
immunity
induced
infection
and/or
upon
vaccination
immunosuppressants.The
dynamics
immune
reactivation
SARS-CoV-2
experienced
MS
patients
humanized
anti-CD20
monoclonal
antibody
ocrelizumab
(OCR)
RA
methotrexate
(MTX)
monotherapy
were
analyzed
at
great
depth
via
high-dimensional
flow
cytometry
whole
blood
samples
mRNA-1273
(Moderna)
vaccine.
Longitudinal
B
T
cell
responses
compared
healthy
controls
(HCs)
before
7
days
after
first
second
vaccination.OCR-treated
exhibit
a
preserved
recall
response
CD8+
central
memory
cells
following
HCs
similar
CD4+
circulating
follicular
helper
1
dynamics,
whereas
strongly
impaired
resulting
in
absence
SARS-CoV-2-specific
immunity.
MTX
treatment
significantly
delayed
levels
vaccination,
sustained
inhibition
overall
marker
responding
cells.Together,
these
findings
indicate
that
MS-OCR
may
still
benefit
from
inducing
broad
which
has
been
associated
milder
outcome.
The
vaccine-induced
IgG
kinetics
RA-MTX
an
increased
risk
might
require
additional
shielding
or
alternative
strategies
interruptions
vulnerable
patients.This
research
project
was
supported
ZonMw
(The
Netherlands
Organization
for
Health
Research
Development,
#10430072010007),
European
Union's
Horizon
2020
innovation
program
under
Marie
Skłodowska-Curie
grant
agreement
(#792532
#860003),
Commission
(SUPPORT-E,
#101015756)
PPOC
(#20_21
L2506),
NHMRC
Leadership
Investigator
Grant
(#1173871).