High-throughput specificity profiling of antibody libraries using ribosome display and microfluidics
Ellen K. Wagner,
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Kyle P. Carter,
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Yoong Wearn Lim
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et al.
Cell Reports Methods,
Journal Year:
2024,
Volume and Issue:
4(12), P. 100934 - 100934
Published: Dec. 1, 2024
In
this
work,
we
developed
PolyMap
(polyclonal
mapping),
a
high-throughput
method
for
mapping
protein-protein
interactions.
We
demonstrated
the
of
thousands
antigen-antibody
interactions
between
diverse
antibody
libraries
isolated
from
convalescent
and
vaccinated
COVID-19
donors
set
clinically
relevant
SARS-CoV-2
spike
variants.
identified
over
150
antibodies
with
variety
distinctive
binding
patterns
toward
antigen
variants
found
broader
profile,
including
targeting
Omicron
variant,
in
repertoires
more
recent
donors.
then
used
these
data
to
select
mixtures
small
number
clones
complementary
reactivity
that
together
provide
strong
potency
broad
neutralization.
is
generalizable
platform
can
be
one-pot
epitope
mapping,
immune
repertoire
profiling,
therapeutic
design
and,
future,
could
expanded
other
families
interacting
proteins.
Language: Английский
Improving antibody-mediated protection against HSV infection by eliminating interactions with the viral Fc receptor gE/gI
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 22, 2024
Herpes
simplex
virus
(HSV)
encodes
surface
glycoproteins
that
are
host
defense
evasion
molecules,
allowing
the
to
escape
immune
clearance.
In
addition
their
role
in
neuropathogenesis
and
cell-cell
spread,
E
I
(gE/gI)
form
a
viral
Fc
receptor
(vFcR)
for
most
subclasses
allotypes
of
human
IgG
promote
humoral
responses.
While
monoclonal
antibodies
(mAbs)
protect
mice
from
neonatal
HSV
(nHSV)
infections,
impact
vFcR
on
mAb-mediated
protection
by
binding
is
unknown.
Using
HSV-1
with
intact
ablated
gE-mediated
binding,
Fc-engineered
modified
ability
interact
gE/gI,
we
investigated
pathogenesis
nHSV.
The
gD-specific
mAb
HSV8
lack
gE
exhibited
enhanced
neutralization
Language: Английский
Pre-exposure prophylaxis of COVID-19 with tixagevimab/cilgavimab (Evusheld) in 63 rituximab-treated patients with ANCA-associated systemic vasculitis: two-year follow-up results
Т. V. Beketova,
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N. О. Levina,
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Yu. A. Uskova
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et al.
Rheumatology Science and Practice,
Journal Year:
2024,
Volume and Issue:
62(5), P. 465 - 473
Published: Oct. 31, 2024
Patients
with
ANCA-associated
systemic
vasculitis
(AAV)
are
at
risk
of
severe
COVID-19.
At
the
same
time,
in
immunocompromised
patients,
particular
those
receiving
anti-B
cell
therapy
rituximab
(RTX),
post-vaccination
effect
may
be
insufficient.
Since
2022
long-acting
virus-neutralizing
monoclonal
antibodies
(MAB)
tixagevimab
and
cilgavimab
(Evushheld,
AZD7442)
have
been
used
as
pre-exposure
prophylaxis
for
The
aim
study
is
to
evaluate
effectiveness
(TC)
COVID-19
its
safety
RTX
treated
patients
AAV.
Materials
methods
.
prospective
included
63
AAV
RTX.
Median
age
53
(19–
79)
years,
M:F
1:1.1.
From
March
June
2023,
TC
was
administered
a
total
dose
300
mg
and/or
600
mg.
Observation
continued
until
April
2024.
In
November
2023
2024
telephone
online
survey
conducted
simultaneously
identify
confirmed
cases
adverse
reactions.
also
Treatment
Satisfaction
Questionnaire
version
9
(TSQM-9).
Considering
duration
(6
months),
were
divided
into
two
groups
depending
on
interval
after
last
administration
TC:
up
6
months
inclusive
–
group
1;
more
than
2.
Results
During
two-year
follow-up
period,
detected
31.7%
median
between
development
5.5
[2–19]
months.
1,
which
12
COVID-19,
92%
had
mild
form
disease,
only
one
lung
damage,
there
no
fatal
outcomes.
2,
cessation
accompanied
by
damage
89%
cases,
required
hospitalization
78%,
patients.
Four
prolonged
course
persistence
SARS-CoV-2
(pCOVID,
persistent
COVID).
4
including
3
pCOVID,
treatment
carried
out
combined
antiviral
drug
nirmarelvir
+
ritonavir
(Skyvira)
combination
intravenous
human
immunoglobulin
(IVIG)
effect.
There
statistically
significant
differences
incidence
secondary
immunodeficiency
without
it
(p=0.868).
final
stage
study,
serum
level
IgG
examined
34
70.4
(0.33–1086.1)
binding
antibody
units
(BAU),
indicates
lack
neutralizing
most
patients;
statistical
their
(p=0.685).
No
reactions
directly
related
use
observed.
A
high
TSQM-9
global
satisfaction
domain
noted
71.4
(14.3–100);
72,4%
respondents
answered
“satisfied”–
“extremely
satisfied”
first
question
(effectiveness
domain).
Conclusions
Pre-exposure
using
RTM
safe
allowed
reduce
avoid
deaths
during
period
action.
After
TC,
an
increase
frequency
need
observed,
pCOVID
noted.
Skyvira
IVIG
effective
all
cases.
MAB
other
rheumatic
diseases
requires
further
in-depth
study.
Language: Английский