Clinical indices and laboratory markers for evaluating the immune-mediated inflammation in rheumatoid arthritis: the impact of COVID-19
Patient-Oriented Medicine and Pharmacy,
Journal Year:
2025,
Volume and Issue:
3(1), P. 49 - 58
Published: March 25, 2025
Rheumatoid
arthritis
(RA)
is
an
immune-mediated
inflammatory
disease
of
unknown
etiology
that
represents
a
considerable
burden
for
both
the
patient
and
healthcare
system.
The
degree
to
which
inflammation
being
controlled
determines
prognosis;
therefore,
achieving
remission
or
low
activity
paramount
importance
medical
practitioners.
effectiveness
currently
employed
treatment
regimen
specific
determined
by
indices
change
in
their
values
during
treatment.
commonly
used
RA
are
result
painstaking
search
optimal
set
clinical,
laboratory
instrumental
parameters
reflecting
underlying
pathogenesis
spanning
half
century.
Routine
tests
not
included
these
can
nevertheless
provide
additional
valuable
information
regarding
disease.
new
coronavirus
infection,
COVID-19,
has
similar
pathogenetic
mechanisms
with
immunoinflammatory
rheumatic
diseases,
its
clinical
consequences
form
postcovid-19
syndrome,
make
it
difficult
assess
using
existing
indices,
raise
question
need
take
them
into
account
when
assessing
choosing
tactics
RA.
Language: Английский
Dynamics of specific immune response and autoantibodies against the background of vaccination with the Gam-COVID-Vac in healthy young individuals
А. А. Баранов,
No information about this author
O. P. Rechkina,
No information about this author
Марина Бородина
No information about this author
et al.
Patient-Oriented Medicine and Pharmacy,
Journal Year:
2025,
Volume and Issue:
3(1), P. 64 - 76
Published: March 26, 2025
Relevance
.
The
Coronavirus
2019
(COVID-19)
pandemic
has
affected
all
countries
of
the
world
and
renewed
attention
to
timely
prevention
viral
infections
through
specific
immunization
general
population.
However,
some
issues
related
safety
vaccine
administration
production
autoantibodies
after
remain
unclear.
Objective.
To
evaluate
dynamics
formation
a
immune
response
SARS-CoV-2
virus,
autoantibody
interrelationships
between
them
during
vaccination
with
Gam-COVID-Vac
(Sputnik
V)
in
healthy
young
adults.
Material
methods
retrospective
study
included
45
practically
students
who
were
fully
vaccinated
two
components
at
university
medical
center
made
3
follow-up
visits
center.
There
32
females
(71.0%)
13
males
(29.0%)
aged
19
28
years,
median
age
23.00
[22.00;24.00]
years.
All
trainees
analyzed
for
IgG
IgM
antibodies
serum
by
enzyme-linked
immunosorbent
assay
(ELISA)
using
SARS-CoV-2-IgG-IgG-IFA-BEST
SARS-CoV-2-IgM-IFA-BEST
test
systems,
as
well
double-helix
deoxyribonucleic
acid
(anti-dsDNA)
kits
(Vecto-dsDNA-IgG)
Vector-Best
JSC
(Russia).
concentration
cardiolipin
(IgM
aCL,
aCL)
ELISA
method
(kits
ORGenTec
Diagnostika,
Germany)
was
investigated
three
times
29
patients.
Statistical
processing
results
performed
generally
accepted
parametric
nonparametric
analysis.
Results.
In
examined
individuals
before
Gam-COVID-Vac,
levels
low
within
reference
values.
After
first
component
vaccine,
level
increased
significantly
compared
period
(KP:
0.28
[0.17;1.25]
u.u.
0.07
[0.04;0.09]
u.u.,
respectively,
p
<0.001).
It
remained
high,
baseline,
stage
2
0.13
[0.07;0.37]
<0.001),
but
underwent
significant
decrease
second
component,
data
1
(p
<0.01).
vaccination,
KP
exceeded
values
1.1
cfu
14
(31.11%)
individuals,
decreased
11.11%
stage.
baseline
period,
there
dramatic
increase
both
(KP:10.24
[6.78;12.44]
0.06
[0.05;0.11]
<0.001)
occurrence
their
high
detection
rate
greater
than
u.u.)
91.11%,
it
reached
100.0%.
higher
found
men
women
(KP
12.44
[10.24;15.78]
9.75
[4.50;11.95]
women,
aCL
(1.41
[1.02;1.62]
GPL
U/mL
1.00
[0.87;1.32]
U/mL,
<0.05)
trend
toward
anti-dsDNA
concentrations
>0.05)
those
opposite
sex.
not
different
>0.05).
step,
almost
differences
initial
one
(p=0.05).
increased,
reaching
second-stage
(1.37
[1.02;1.51]
[0.81;1.40]
<0.05).
Only
detected
titer
or
drug.
any
case.
Conclusions.
age,
antiviral
is
effectively
formed
when
Gam-COVID
Vac.
more
pronounced
especially
associated
certain
types
characteristic
immunoinflammatory
rheumatic
diseases.
cases
induction
synthesis,
transient.
Language: Английский
Pharmacotherapy of autoimmune rheumatic diseases – from monoclonal antibodies to CAR T cells: 20 years later
Rheumatology Science and Practice,
Journal Year:
2024,
Volume and Issue:
62(3), P. 262 - 279
Published: June 26, 2024
Autoimmunity
is
a
pathological
process
associated
with
violation
of
immunological
tolerance
to
normal
structural
components
the
body
(autoantigens),
predominance
active
(adaptive)
immunity
and
manifested
by
hyperproduction
autoantibodies.
Systemic
autoimmune
rheumatic
diseases
(SARDs)
are
among
most
common
severe
nosological
forms
this
pathology
autoimmunity.
Problems
pharmacotherapy
SARDs
subject
intensive
research.
At
beginning
21st
century,
more
than
20
biologic
agents
were
developed
for
treatment
rheumatoid
arthritis
–
monoclonal
antibodies
(mAbs)
recombinant
proteins
that
control
inflammation
overproduction
“pro-inflammatory”
cytokines,
use
which
has
dramatically
improved
results
pharmacotherapy.
However,
much
less
research
been
devoted
studying
possibilities
aimed
at
selective
suppression
“autoimmune”
component
pathogenesis
SADRs
uncontrolled
activation
B
cells
restoration
autoantigens.
In
spectrum
drugs
whose
mechanism
action
cells,
leading
place
occupied
rituximab
(RTM).
It
noteworthy
years
ago
(2004),
group
researchers
led
prof.
J.C.
Edwards
first
demonstrated
effectiveness
RTM
in
patients
RA,
was
soon
successfully
repositioned
treat
wide
range
SARDs.
A
major
achievement
CAR
(сhimeric
antigen
receptor)
T
cell
therapy,
refractory
hematological
tumors.
The
main
CART-cells
genetically
engineered
T-cell
receptor
recognizes
target
without
participation
histocompatibility
complex.
Although
limited,
extremely
impressive
data
regarding
high
remission
rates
have
obtained
adapting
CD19
CART-cell
therapy
systemic
lupus
erythematosus
(SLE)
other
standard
immunosuppressive
medications.
article
discusses
SLE
prospects
further
Language: Английский
Results of a 24-week open-label, non-interventional study on the efficacy and safety of olokizumab therapy in patients with rheumatoid arthritis after switching from anti-B-cell therapy during the SARS-CoV-2 pandemic
A. V. Fedorova,
No information about this author
N. E. Banshchikova,
No information about this author
А. Э. Сизиков
No information about this author
et al.
Modern Rheumatology Journal,
Journal Year:
2024,
Volume and Issue:
18(3), P. 25 - 31
Published: June 14, 2024
In
the
context
of
new
coronavirus
infection
(NCI)
COVID-19
pandemic,
rheumatological
community
is
facing
challenges
in
treatment
immune-inflammatory
rheumatic
diseases
(IIRDs).
It
has
been
shown
that
patients
have
an
increased
risk
infections
and
a
severe
course
NCI
IIRD
therapy
also
influences
disease
outcomes.
particular,
use
anti-B-cell
medication
rituximab
(RTM)
associated
with
higher
mortality.
The
pandemic
highlighted
need
to
find
alternative
safe
options
for
these
patients.
This
work
continuation
12-week
study
on
efficacy
safety
olok-izumab
(OKZ)
rheumatoid
arthritis
(RA)
after
switching
from
during
SARS-CoV-2
pandemic.
Objective:
evaluate
OKZ
(Artlegia®;
solution
subcutaneous
administration,
160
mg/ml
–
0.4
ml)
RA
real-life
clinical
practice
RTM
Material
methods.
included
19
confirmed
diagnosis
who
had
received
at
dose
500–1000
mg
twice
every
14
days
least
6
months
ago.
As
activity
increased,
was
replaced
while
synthetic
disease-modifying
anti-rheumatic
drugs
(DMARDs)
continued.
At
weeks
0,
4,
8,
12
24
biologic
DMARD,
number
tender
(TJN)
swollen
(SJN)
joints
out
28,
pain
intensity
visual
analogue
scale,
ESR,
CRP
level,
indices
CDAI,
DAS28-ESR,
DAS28-CRP,
HAQ
index
profile
were
assessed
each
visit.
Results
discussion.
After
there
statistically
significant
decrease
mean
TJN
(from
10
6.0,
3.0,
5.0
4.0,
respectively;
p
<
0.05)
SJN
7.0
3.0
by
week
4
2.0
24;
0.05).
same
time,
ESR
values
observed:
median
decreased
18
0.6
mg/l
0.5
(p
0.05),
30
5
mm/h
period
levels
normalized
regardless
baseline
values.
All
showed
positive
dynamic
compared
onwards
assessment
period.
24,
DAS28-ESR
5.50
3.57;
3.30;
3.08
3.01
0.05);
DAS28-CRP
5.30
3.46;
3.23;
3.26
3.12
CDAI
27.0
17.0;
12.0;
15.0
12.0
respectively.
th
observation.
A
improvement
functional
status
observed
maintained
until
24.
1.62
1.50
8
1.12
Conclusion.
non-medical
switch
effective
safe.
Language: Английский
Chronic neuroborreliosis and post-COVID syndrome: a clinical case
N. S. Baranova,
No information about this author
Ya. S. Ostapenko,
No information about this author
J. A. Malysheva
No information about this author
et al.
Patient-Oriented Medicine and Pharmacy,
Journal Year:
2024,
Volume and Issue:
2(3), P. 37 - 49
Published: Nov. 1, 2024
Lyme
borreliosis
is
a
natural
focal,
vector-borne
disease
caused
by
Borrelia
burgdorferi
sensu
lato.
The
transmission
of
ixodes
ticks
characterized
staged
course
with
damage
to
various
organs
and
systems.
This
an
urgent
problem
in
medicine
because
the
peculiarities
its
clinical
course,
including
late
period.
Not
infrequently,
due
lack
vigilance
physicians
polymorphism
presentation
disease,
runs
under
masks
other
diagnoses.
In
Covid-19,
new
coronavirus
SARS-CoV-2,
both
acute
period
later
develop
systemic
manifestations
central
peripheral
nervous
systems
musculoskeletal
system.
These
features
are
particularly
characteristic
post-Covid-19
syndrome.
A
case
chronic
neuroborreliosis
post-COVID-19
syndrome
lesions
muscular
presented.
Language: Английский
Efficacy, Immunogenicity, and Safety of the Combined Vector Vaccine Gam-COVID-Vac in Patients with Rheumatic Diseases
Antibiot Khimioter = Antibiotics and Chemotherapy,
Journal Year:
2024,
Volume and Issue:
69(7-8), P. 44 - 52
Published: Nov. 21, 2024
The
aim
of
the
study
is
to
assess
efficacy,
immunogenicity,
and
safety
combined
vector
vaccine
Gam-COVID-Vac
determine
risk
factors
for
development
adverse
events
(AEs)
in
patients
with
rheumatic
diseases
(RD).
Patients
methods
.
present
consisted
a
retrospective
prospective
parts,
which
included
295
42
RD,
as
well
113
57
healthy
controls,
respectively.
Information
about
efficacy
was
obtained
from
291
RD
146
assessed
by
incidence
PCR-confirmed
COVID-19
cases
31
365
days
after
vaccination.
concentration
antibodies
SARS-CoV-2
enzyme
immunoassay
cohort
at
1,
3,
6,
12
months
administration
second
component
vaccine.
Safety
studied
all
participants
based
on
AEs
exacerbation
underlying
RD.
Results.
After
vaccination,
29
(9.97%)
were
recorded
27
them
mild,
2
required
hospitalization,
ended
recovery.
Treatment
rituximab
before
vaccination
increased
developing
2.3
times.
A
sig-nificant
increase
antibody
titers
observed
full
immunization
(P<0.006
points).
absent
40.72%
24.71%
P<0.001.
Exacerbations
registered
(0.6%)
cases.
local
systemic
(depending
administered
component)
women,
under
age
60
year,
duration
less
than
10
years,
methotrexate
therapy
(P<0.016
cases).
Conclusions
According
data
obtained,
use
characterized
good
sufficient
safety.
Language: Английский
Colchicine: Repositioning an “ancient” medicine in the 21st century
Rheumatology Science and Practice,
Journal Year:
2024,
Volume and Issue:
62(5), P. 445 - 464
Published: Oct. 31, 2024
The
main
indications
for
colchicine
treatment
until
recently
were
gout,
pericarditis,
familial
Mediterranean
fever
and
some
other
auto-inflammatory
diseases.
expansion
of
(repositioning)
the
use
in
direction
prevention
cardiovascular
complications
should
be
considered
as
one
major
events
medicine
XXI
century.
Deciphering
role
inflammation
most
important
mechanism
development
atherosclerosis
has
created
prerequisites
concept
anti-inflammatory
therapy
atherosclerosis,
which
low-dose
can
take
an
place,
complementing
effects
aspirin,
statins
antihypertensive
therapy.
analysis
materials
from
randomized
placebo-controlled
studies
indicates
a
decrease
frequency
patients
with
coronary
heart
disease
(by
31%)
who
have
suffered
myocardial
infarction
23%),
well
33%),
stroke,
need
revascularization
mortality.
low
dose
(0.5
mg/day)
is
approved
by
U.S.
Food
Drug
Administration
disease.
It
assumed
that
future
will
place
pathology
associated
atherosclerotic
vascular
Language: Английский