Terapevticheskii arkhiv,
Journal Year:
2023,
Volume and Issue:
95(12), P. 1056 - 1063
Published: Dec. 28, 2023
Autoimmunity
and
autoinflammation,
co-potentiating
pathological
processes,
are
considered
within
the
"immune-inflammatory"
continuum
(continuity
with
a
variety
of
elements),
reflecting
close
relationship
between
innate
acquired
immune
responses.
is
leading
pathogenetic
mechanism
for
specific
type
human
chronic
inflammatory
disorders
–
autoimmune
diseases,
affecting
more
than
10%
people
in
general
population.
Advances
molecular
biology,
pharmacogenetics,
bioinformatics
provided
background
individualizing
therapy
systemic
rheumatic
diseases
personalized
medicine.
Studying
immunopathogenesis
mechanisms,
improving
diagnostics,
interpreting
taxonomy,
developing
approaches
to
prevention
priority
issues
modern
Rheumatology Science and Practice,
Journal Year:
2024,
Volume and Issue:
62(1), P. 32 - 54
Published: Feb. 29, 2024
The
pandemic
of
coronavirus
disease
2019
(COVID-19),
etiologically
related
to
the
SARS-CoV-2
virus
(severe
acute
respiratory
syndrome
coronavirus-2),
has
drawn
attention
new
clinical
and
fundamental
problems
in
immunopathology
human
diseases
associated
with
virus-induced
autoimmunity
autoinflammation.
provision
that
“the
experience
gained
rheumatology
process
studying
pathogenetic
mechanisms
pharmacotherapy
immunoinflammatory
rheumatic
as
most
common
severe
forms
autoimmune
autoinflammatory
pathology
humans
will
be
demand
for
deciphering
nature
pathological
processes
underlying
COVID-19
developing
approaches
effective
pharmacotherapy”
was
confirmed
numerous
studies
conducted
over
next
3
years
midst
pandemic.
main
focus
on
a
critical
analysis
data
regarding
role
inflammation,
which
basis
pathogenesis
immune-mediated
context
COVID-19.
У
пациентки
50
лет
с
достоверным
диагнозом
псориатического
артрита
на
фоне
лечения
нестероидными
противовоспалительными
препаратами
(НПВП)
развилось
осложнение
в
виде
экзокринной
недостаточности
поджелудочной
железы
синдромом
диспепсии,
не
позволившее
продолжить
противовоспалительную
терапию
согласно
клиническим
рекомендациям.
Представленный
клинический
случай
призван
продемонстрировать
врачам-специалистам
возможности
применения
биорегуляционных
препаратов
лечении
пациентов
аутовоспалительными
заболеваниями.
Особенностью
описанного
клинического
случая
является
«мягкое»
течение
артрита,
преимущественно
проявляющееся
у
энтезопатиями
различной
локализации,
а
также
болями
и
скованностью
нижней
части
спины
без
ярко
выраженных
артритов.
Окончательный
диагноз
был
верифицирован
2018
году
после
развертывания
полной
клинической
картины
заболевания,
позволившей
диагностировать
псориатический
артрит
критериям
CASPAR.
Инициированная
базисная
противовоспалительная
терапия
метотрексатом
дозе
12,5
мг
неделю
комбинации
нимесулидом
200
день
была
отменена
2021
виду
достижения
ремиссии
заболевания.
В
связи
рецидивом
симптомов
летом
2024
года
нарастания
болей
области
энтезисов
скованности
суставах,
пациентка
возобновила
прием
НПВП
увеличила
дозу
нимесулида
до
400
день,
что
спровоцировало
развитие
серьезного
нежелательного
явления
–
железы,
потребовавшей
госпитализации
пациентки.
последствии
амбулаторном
этапе
лечения,
находясь
под
наблюдением
врача-гастроэнтеролога,
обратилась
к
врачу-ревматологу
выраженными
(70
мм
из
100
по
визуально-аналоговой
шкале)
воспалительного
характера
левом
коленном
суставе,
локализующимися
верхнего
края
надколенника,
больших
вертелов
бедренных
костей
местах
прикрепления
ахилловых
сухожилий
пяточной
кости.
По
результатам
УЗИ
левого
коленного
сустава
установлена
причина
-
энтезит
латеральной
головки
четырехглавой
мышцы
бедра
признаков
артрита.
Принимая
во
внимание
невозможность
использования
НПВП,
пациентке
было
выполнено
трехкратное
введение
Траумель®
C
(Traumeel®
S)
2,2
мл
область
навигацией
периодичностью
1
раз
неделю,
дополнена
назначением
таблетированной
формы
C.
Через
месяц
терапии
биорегуляционным
препаратом
при
УЗИ-контроле
колена
отмечена
положительная
динамика
«стихания»
проявлений
энтезита,
снижение
уровня
боли
суставах
70
10
шкале.
Пациентка
повторном
визите
через
отметила
значительное
улучшение
своего
состояния,
практическое
полное
прекращение
спины.
практике
демонстрирует
успешное
применение
многокомпонентным
энтезопатий
псориатическим
артритом
условиях
невозможности
нестероидных
противовоспалительных
препаратов.
Terapevticheskii arkhiv,
Journal Year:
2024,
Volume and Issue:
96(1), P. 68 - 74
Published: Jan. 25, 2024
A
meeting
of
the
Expert
Council
on
September
9,
2023
considered
last
challenges
in
treatment
osteoarthritis
(OA)
including
OA
comorbid
patients.
Leading
experts
rheumatology,
traumatology
and
other
relevant
disciplines
participated
meeting.
The
key
goal
was
discussion
potential
application
a
combination
undenatured
(native)
type
II
collagen,
methylsulfonylmethane,
boswellic
acids,
vitamins
C
D
(Artneo
complex)
as
part
complex
therapy.
concluded
that
Artneo
for
stage
I–III
knee
patients
is
not
just
non-inferior
comparison
with
chondroitin
sulfate
glucosamine
hydrochloride
but
excels
it
decrease
magnetic
resonance
imaging
synovitis
markers
dynamics
Lequesne
index
severity.
proven
efficacy
favorable
safety
profile
6-months
course
deserve
attention
medical
community
active
implementation
into
ambulatory
practice,
first
all,
mild
or
moderate
and/or
burdened
comorbidities.
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
Rheumatology Science and Practice,
Journal Year:
2023,
Volume and Issue:
61(5), P. 513 - 530
Published: Oct. 27, 2023
Uncontrolled
activation
of
neutrophils
is
considered
an
important
mechanism
thromboinflammation
and
fibrosis
in
immunemediated
rheumatic
diseases
(IMRD),
malignant
neoplasms,
atherosclerosis,
COVID-19
many
other
acute
chronic
inflammatory
humans.
Particular
attention
has
been
drawn
to
the
ability
form
“network”
(web-like)
structures,
called
“neutrophil
extracellular
traps”
NETs.
The
process
associated
with
formation
NETs
weakening
their
degradation
“NETosis”.
publication
summarizes
data
on
role
NETosis
pathogenesis
IMRD
discusses
prospects
for
pharmacotherapy
aimed
at
preventing
destruction
Rheumatology Science and Practice,
Journal Year:
2024,
Volume and Issue:
62(2), P. 186 - 191
Published: April 28, 2024
The
aim
of
the
study
was
to
investigate
relationship
between
cytokine
levels
and
values
antibodies
cyclic
citrullinated
peptide
(anti-CCP)
carbamylated
proteins
(anti-CarP)
in
patients
with
rheumatoid
arthritis
(RA).
Materials
methods.
106
a
reliable
diagnosis
were
included
study.
Determination
anti-CarP
anti-CCP
performed
by
enzyme
immunoassay.
Patients
divided
into
subgroups
depending
on
anti-CarP.
concentration
27
cytokines
serum
determined
using
multiplex
xMAR
technology.
Results
discussion.
When
comparing
immunological
subgroups,
anti-CCP(+)
had
higher
concentrations
interleukin
(IL)
1β,
IL-1Ra,
IL-2,
IL-6,
IL-8,
IL-10,
IL-12,
IL-13,
IL-15,
IL-17,
fibroblast
growth
factor,
granulocyte
colony-stimulating
factor
(CSF),
granulocyte-macrophage
CSF,
interferon
(IFN)
γ,
IFN0γ-induced
protein
10,
monocyte
chemoattractant
1,
macrophage
inflammatory
1α
(MIP-1α),
transforming
bb,
tumor
necrosis
α
vascular
endothelial
factor.
IL-5,
IL-9,
eotaxin,
MIP-1β
RANTES
(regulated
activation,
normal
T
cell
expressed
secreted)
anti-CCP(–)
patients.
In
subgroup
patients,
an
inverse
correlation
found
IL-5
total
Sharpe
score,
IL-9
DAS28-CRP
(Disease
Activity
Score
C-reactive
calculation).
anti-Carp(–)
(n=73)
IL-17
recorded.
Conclusion.
Our
data
support
concept
RA
heterogeneity,
characterised
existence
different
clinical
subtypes,
which
may
have
implications
for
improving
personalised
therapy.
Clinical Medicine (Russian Journal),
Journal Year:
2024,
Volume and Issue:
102(3), P. 197 - 204
Published: June 1, 2024
Rheumatology
is
one
of
the
most
rapidly
developing
medical
specialties,
which
effectively
adapts
achievements
and
contributes
to
progress
world
fundamental
clinical
science
[1].
Such
immuno-inflammatory
rheumatic
diseases
(IVRS)
both
rheumatoid
arthritis
(RA)
systemic
lupus
erythematosus
(SLE)
are
not
only
severe
chronic
inflammatory
human
diseases,
but
also
“models”
for
studying
mechanisms
pathogenesis
approaches
pharmacotherapy
other
associated
with
development
autoimmunity
and/or
auto-inflammation.
The
relevance
problem
IVR
modern
medicine
determined
by
their
high
prevalence
in
population,
difficulty
early
diagnosis,
rapid
disability
an
unfavorable
life
prognosis.
Deciphering
immunopathogenesis,
improving
diagnostics,
molecular
taxonomy,
prevention,
searching
new
“targets”
therapy
based
on
“omix”
technologies
artificial
intelligence
among
priority
areas
biology
XXI
century.
Modern Rheumatology Journal,
Journal Year:
2024,
Volume and Issue:
18(3), P. 85 - 91
Published: June 15, 2024
Despite
the
high
efficacy
of
currently
available
targeted
synthetic
disease-modifying
antirheumatic
drugs
(tsDMARDs)
and
biologic
DMARDs
(bDMARDs),
approximately
40
%
patients
with
ankylosing
spondylitis
(AS)
fail
to
achieve
treatment
goals
according
clinical,
laboratory
imaging
tests.
In
addition,
comorbidities
in
AS,
which
require
an
integrated
approach
involving
different
specialists,
may
limit
use
such
therapy.
view
above,
as
well
peculiarities
bone
metabolism
new
therapeutic
approaches
for
this
disease
have
recently
been
sought,
one
is
bisphosphonates.
This
article
discusses
some
aspects
unconventional
options
–
bisphosphonates
AS
complicated
by
severe
comorbidities,
insufficient
bDMARDs
and/or
DMARDs.
Rheumatology Science and Practice,
Journal Year:
2024,
Volume and Issue:
62(3), P. 286 - 292
Published: June 26, 2024
Aim
–
to
study
the
clinical
manifestations
of
rheumatoid
arthritis
(RA)
and
spectrum
concomitant
diseases,
depending
on
level
hepcidin
in
patients
with
high
inflammatory
activity.
Material
methods.
The
analysis
included
78
(48.9±15.5
years)
RA,
disease
duration
108
[48;
204]
months.
All
were
diagnosed
or
medium
activity
(DAS28-ESR
(Disease
Activity
Score
28
erythrocyte
sedimentation
rate
detection
5.2).
Indicators
iron
metabolism,
levels
interleukin
6
determined.
Three
subgroups
identified:
subgroup
I
serum
below
reference
values
(less
than
40
pg/ml);
II
within
(40–120
III
(more
120
pg/ml).
Results.
It
was
found
that
RA
activity,
regardless
hemoglobin
level,
disorders
metabolism
noted
83%
cases.
Reduced
40%
cases
(subgroup
I),
average,
very
detected
every
second
(n=34;
III).
main
DAS28
comparable
all
three
subgroups.
largest
number
diseases
hepcidin.
Chronic
obstructive
pulmonary
(26%),
endocrine
pathology
22%
(diabetes
mellitus,
thyroid
obesity),
chronic
kidney
(21%)
cardiovascular
(60%)
significantly
more
common
(p<0.05).
With
deficiency,
most
gastrointestinal
tract
damage
35%
(erosive
gastritis,
peptic
ulcer
stomach
duodenum,
etc.),
system
(32%).
In
same
subgroup,
one
ten
had
a
change
two
classes
bDMARDs/tsDMARDs
by
time
study.
Conclusion.
results
this
illustrate
need
for
further
pathogenetic
pathways
order
form
scientifically
sound
approaches
personalized
treatment
wide
range
immunoinflammatory
rheumatic
including
RA.
Patient-Oriented Medicine and Pharmacy,
Journal Year:
2024,
Volume and Issue:
2(3), P. 13 - 20
Published: Oct. 31, 2024
Relevance.
Activation
of
innate
and
acquired
immunity,
accompanied
by
increased
production
classical
(interleukin
(IL)
IL-1β,
IL-6,
tumor
necrosis
factor-α
(TNF-α)
interferon-γ
(INF-γ))
proinflammatory
cytokines
in
synovial
fluid
blood
serum,
plays
an
important
role
the
pathogenesis
rheumatoid
arthritis
(RA).
Objective.
To
determine
concentration
TNF-α
INF-γ
RA
patients
advanced
stage
disease,
to
evaluate
relationship
between
them,
clinical
indices
disease
activity,
presence
factor
(RF),
antibodies
cyclic
citrullinated
peptide
(ACCP).
Material
methods.
We
examined
154
with
(41
men
113)
who
were
middle-aged
(56.0
(50.0;
64.0)
years),
duration
(9.4
(3.0;
13.0)
seropositive
129
(83.8
%)
for
IgM
RF
and/or
106
(68.8
ACCP
moderate
high
(DAS28-ESR
—
5.40
(4.65;
6.00))
activity.
The
serum
determined
multiplex
technology.
Results.
IL-1β
was
not
significantly
different
controls.
values
IL-6
higher,
lower
than
donors.
hyperproduction
detected
most
frequently
(51.6
%),
whereas
elevated
levels
(38.96
(26.62
(23.38
less
common.
Significant
positive
correlations
observed
concentrations
all
their
levels.
strongest
characteristic
INF-γ.
No
statistically
significant
differences
cytokine
or
negative
IgM-RF
ACCP.
alone
positively
correlated
(DAS28-ESR,
CDAI,
SDAI)
activity
(p<0.05).
Conclusions.
There
are
frequencies
among
advanced-stage
RA.
In
a
close
there
certain
associations
laboratory
indicators