Journal of Environmental Treatment Techniques
2020, Volume 8, Issue 1, Pages: 231-236
of the oral cavity microflora gets established with aging. It is
very unstable in the initial period of human life and stabilizes
in adults becoming a self-regulated system. The changes in the
oral microflora complete the vicious circle: periodontopatho-
genic microflora increases the resistance of tissues to insulin
and, as a result, contributes to the worsening of metabolic con-
trol of glycemia. And on the contrary, high concentration of
glucose in gingival fluid and disturbances of neutrophil adhe-
sion, chemotaxis, and phagocytosis, observed in patients with
DM, promote the reproduction and persistence of subgingival
microflora [22]. A high rate of oral cavity organs diseases (up
to 90%) in patients with DM is associated with the changes in
the microvasculature, resorption of bone tissue, and a reduction
of local immune reactions. As a rule, inflamed tissues of perio-
dontium have an increased level of inflammatory mediators as-
sociated with the process of tissue destruction, such as tumor
necrosis factor α (TNFα), interleukin-6, interleukin-1β, prosta-
glandin E2, and matrix metalloproteinase (MMP) [32]. In addi-
tion to local destruction, the inflammation is characterized by
the increase in the permeability of capillaries, which can lead
to inflammatory mediators and bacterial products penetration
into the systemic circulation. These mediators play an im-
portant role in the pathogenesis of the development of insulin
resistance, ischemic heart disease, and according to the recent
data, diabetes mellitus [31]. Based on this theory, it was sug-
gested that successful control of bacterial infection of periodon-
tium leads to the improvement of the clinical picture of both
periodontitis and metabolic control of DM [24].
A weakening of specific and non-specific mechanisms of
local and systemic protection is always associated with an in-
creased activity of bacterial aggregates that leads to the devel-
opment of clinically expressed inflammatory reaction. A spe-
cial role in the development and maintenance of chronic in-
flammation is played by matrix endopeptidases – catabolic en-
zymes of the majority of proteins of extracellular matrix at dif-
ferent stages of the inflammatory process. They are secreted by
different cells: neutrophilic leukocytes, fibroblasts, epithelio-
cytes, macrophages, etc. [20]. Oral mucosa exerts borderline
immune protection of the organism, so the study of intercellular
contacts between immune-competent cells and the peculiarities
of local immunity associated with mucous membranes, as well
as their influence on the processes of proliferation and apopto-
sis of the epithelial cells becomes especially relevant [10].
Dendritic cells are heterogeneous population of antigen-
presenting cells of bone marrow origin. The main function of
dendrite cells is the presentation of antigens to T-cells [25].
Dendritic cells also perform important immune regulating func-
tions, such as a control for the differentiation of T-lymphocytes,
regulation of the activation and suppression of the immune re-
sponse [21]. An important peculiarity of dendritic cells is their
possibility to uptake different antigens from the medium due to
phagocytosis, pinocytosis, and receptor-mediated endocytosis
that they have heteroplastic origin from leukocytes, macro-
phages, etc. Histamine is released from the mast cells as a result
of a complicated chain of enzymatic processes because it can
be prevented by the effect of enzymatic inhibitors [32]. Since
macrophages are one of the tools of inborn immunity and are
involved in the acquired immune response along with B and T-
lymphocytes being an “additional” type of the immune re-
sponse cells, they are considered to be phagocytizing cells with
the function to “swallow” immunogens and process them for
the presentation of T-lymphocytes in a suitable form [19]. All
in all, these cellular populations form local cellular immunity
in the oral mucosa (LCI OM) [8]. Thus, immunopathological
mechanisms play an important role in the development of the
process of destruction of periodontal tissues [6]. The study of
pathomorphological and pathophysiological mechanisms of
this association is necessary for the development of new ap-
proaches to the diagnostics and treatment of periodontal dis-
eases [14]. All the above-mentioned facts suggest that the study
of local morphological substrate and character of changes in
LCI OM based on the biopsic and operational material can give
the basis for the improvement of pathogenetically grounded
methods of prevention of complications in dental treatment, in
particular, in patients with DM [8].
The aim of the study was to increase the quality and effec-
tiveness of removable denture in patients with diabetes mellitus
based on the morphological and immunohistochemical analysis
of the local cellular immunity of the oral mucosa. The follow-
ing objectives were set: (a) Identification of the group of prior-
ity with patients ranged by the age and duration of the disease.
(b) Study of morphological picture of the oral mucosa in pa-
tients with removable denture and diabetes mellitus. (c) Identi-
fication of the cellular pool in the denture-bearing area in pa-
tients with diabetes mellitus with removable denture using im-
munohistochemical and histochemical methods. (e) Perfor-
mance of comparative and correlation analysis of the obtained
data in the control group and observation group with a degree
of clinical manifestations of periodontal diseases.
2
Materials and Methods
The study included 130 patients aged 40 to 85 years old that
were divided into control and test groups. The patients received
partial laminar and complete removable denture:
Test group I – patients with diabetes mellitus with removable
acrylic denture (n=70);
Test group II – patients with diabetes mellitus with removable
denture that receive immune-stimulating drug (Imudon)
(
n=28). Drug intake schedule: 6 tables per day with a 2-hour
interval to dissolve in the mouth (no crunching). The duration
of the course was 20 days. The course was repeated in 2 months
until the end of the study. The examination was performed in 6
and 12 months of using orthopedic denture. Control group in-
cluded patients with DM that did not use removable denture but
those that required dental treatment (n=32). Since the changes
in the tissues in general and in oral mucosa, in particular, in
patients with DM type 1 or type 2 have stereotypic character,
the authors examined patients with DM type 2 as the most
widespread form [2]. All the examined patients had a compen-
sated form of this disease. The age groups were formed by the
classification of Craigie: medium adulthood (40-59 years old),
late adulthood (60 years old and more). Study exclusion criteria
were the following: (a) Patients younger than 20 and older than
[17]. According to the published data, the main concentration
of dendritic cells is in the tissues that are in contact with the
external environment, for example, in the epithelial layer of the
intestinal mucosa, in the submucous layer of the respiratory,
gastrointestinal, and urogenital tracts [2]. Dendritic cells uptake
antigens, process them and present them on their surface in
complex with МНС I or МНС II classes. This is the only way
for T-cells to identify an antigen and activate and promote an
immune response. Depending on the type of a pathogen, den-
dritic cells can direct the differentiation of naïve T-helpers
85, (b) mental disorders, (c) oncological diseases, and (d) de-
(
ThO) to T-helpers type 1, T-helpers type II, regulatory T-cells
compensated systemic diseases.
or T-helpers [16].
Clinical examination of the oral mucosa included the iden-
tification of hyperemic foci and evaluation of the degree of
edema in the denture-bearing area, evaluation of periodontal
tissues (including Shiller-Pisarev’s test). X-ray imaging of
Mast cells are not immune-competent cells. It is known that
they are not directly involved in the development of allergic
reactions. Mast cells appear homoplastically. It is suggested
2
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