New Facets of Hematolymphoid Eponymic Diseases
Lymphatics,
Год журнала:
2025,
Номер
3(2), С. 9 - 9
Опубликована: Апрель 9, 2025
Disease
eponyms
can
be
confusing,
difficult
to
remember,
scientifically
non-robust,
and
lacking
in
implications
on
relationships
with
cell
lineage,
histogenesis,
pathogenesis.
This
review
is
geared
toward
revisiting
hematolymphoid
diseases
light
of
recent
advances
technology
science
by
searching
the
past
fifty
years
literature
using
Scopus
Google
Scholar
keywords
“eponyms,
hematolymphoid,
diseases,
lymphoma,
benign,
malignant,
lymph
node,
spleen,
liver,
bone
marrow,
leukemia”.
With
technology,
there
accumulation
information
morphologic
nuances
immunologic,
immunophenotypic,
genetic
features
various
eponymic
thus
shedding
important
issues
etiology
pathogenesis
therapy
non-neoplastic
(Castleman,
Evans
syndrome
Kikuchi–Fujimoto,
IgG4-related
diseases)
neoplastic
(Hodgkin,
Burkitt,
NK/T-cell
lymphomas,
dendritic/histiocytic
neoplasms,
Sezary
syndrome)
diseases.
contributes
modern
nomenclature,
classification,
subtyping,
prognostication,
discoveries
new
treatment
strategies
Язык: Английский
Immunoglobulin-Related Fibroinflammatory Diseases of Uncertain Etiology—Polarized Isotype Switching Connects an Ancient with a Contemporary Disease
Lymphatics,
Год журнала:
2025,
Номер
3(2), С. 10 - 10
Опубликована: Апрель 15, 2025
IgG4
is
an
unusual
immunoglobulin
(Ig)
and
the
least
component
of
IgG
in
humans.
It
often
asymmetrical
heterobivalent
with
weak
Fc
(fragment
crystallizable
region)-dependent
effector
function
ineffective
complement
activation,
thus
playing
unclear
role
immune
functions.
IgE
uncommon
Ig,
being
important
mostly
allergy
type
2
immunity.
There
are
two
rare
chronic
Ig-related
fibroinflammatory
diseases,
namely
IgG4-related
disease
(IgG4RD)
Kimura
(KD),
characterized
by
prominent
IgG4-
or
IgE-positive
plasma
cells
affected
tissues,
without
blood
elevations
same
Ig.
The
etiology
these
diseases
unclear,
though
it
appears
that
pathogenesis
both
related
to
polarized
Ig
heavy
chain
isotype
switching,
concomitant
other
cellular,
cytokine
chemotaxin
interactions
culminates
characteristic
pathologic
manifestations
inflammation
fibrosis.
IgG4RD
KD,
despite
having
overlapping
differing
features,
may
be
connected
similar
pathogenetic
switching.
Язык: Английский
Successful rituximab treatment in IgG4-related coronary periarteritis: a case-based review
Rheumatology International,
Год журнала:
2024,
Номер
45(1)
Опубликована: Дек. 31, 2024
Язык: Английский
IgG4 Subclass of Immunoglobulins; Immunobiology and Roles in Relation to Human Diseases
Acta Medica (Hradec Kralove Czech Republic),
Год журнала:
2024,
Номер
67(4), С. 101 - 106
Опубликована: Янв. 1, 2024
IgG4,
a
subclass
of
antibodies
known
as
immunoglobulins
have
unique
structural
features,
in
particular,
their
Fc
regions,
that
prevents
interactions
with
other
receptors
on
effector
cells
and
thus
disabling
them
activating
complements
system.
IgG4
can
undergo
process
called
Fab-arm
exchange,
wherein
they
exchange
half-molecules
antibodies,
forming
bispecific
monovalent
antibodies.
Isotypic
switch
mature
B
germinal
centres
secondary
lymphoid
organs
is
controlled
by
Tfh
subset
T
cells.
Functionally
exert
immunomodulatory
blocking
activities,
modulating
protective
inflammation
evolved
parasitic
invasion
allergic
inflammation.
From
the
pathophysiological
point
view,
autoantibodies
are
prominently
observed
autoimmune
diseases
under
umbrella
IgG4-autoimmune
(IgG4-AID).
Furthermore,
IgG4-related
(IgG4-RD)
affecting
various
characterized
lymphoplasmacytic
infiltrates
storiform
fibrosis
tissues,
together
elevated
levels
blood.
A
better
understanding
immunobiology
helps
us
diagnose
treat
patients
suffering
from
these
rare
forms
diseases.
Язык: Английский