Immune system dysfunction in purulent inflammatory diseases of the maxillofacial area in pediatric patients

Marina N. Mitropanova, T. A. Ponomarenko, G. A. Chudilova, Yu. V. Teterin, V. N. Chapurina
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 The study included a group of pediatric patients 8-17 years old with maxillofacial inflammatory diseases of the maxilla (the study group), and 13 conditionally healthy children (the comparison group). The contents of T cells (CD3+CD19-, CD3+CD4+, CD3+CD8+, CD3+CD4+/CD3+CD8+), and В cells (CD3-CD19+), NK (CD3-CD16+CD56+) was determined using Cytomics FC-500 (Beckman Coulter, USA);concentrations of serum IgA, IgM, IgG were determined by ELISA technique (Vector-Best, Russia). Phagocytic activity of neutrophilic granulocytes (NG) was evaluated as percentage of actively phagocytic NGs, capturing processes were assessed by appropriate phagocytic indices, and the digestive activity was evaluated against S. aureus (strain 209).
 Combined defects of immune response in children with maxillofacial hypertension were established: decrease of T lymphocytes contents along with decrease of T helpers and CTL ratio along with unchanged content of NK cells and B lymphocytes. Increase of IgA and IgG levels was also found. Defects of phagocytosis were revealed, primarily connected with the processes of completed phagocytosis and increased content of actively phagocytizing NG.
 Treatment of children suffering with purulent inflammatory diseases of maxillofacial region is still an urgent problem in dentistry. The revealed dysfunction of immune response to pathogens in the purulent maxillofacial disorders may explain a prolonged clinical course of inflammatory processes, thus determining a need for usage of immunotropic therapy in complex treatment schedules including operative aid as well as conventional drug and physiotherapeutic treatment aiming for increase of rehabilitation efficiency and prevention of postoperative complications in these patients.","PeriodicalId":21507,"journal":{"name":"Russian journal of immunology : RJI : official journal of Russian Society of Immunology","volume":"424 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian journal of immunology : RJI : official journal of Russian Society of Immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46235/1028-7221-13992-isd","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

The issues of treatment of purulent inflammatory diseases of the maxillofacial region (PMMA) are quite urgent, due to increasing number of such patients. Their clinical course is getting worse, and the efficiency of antibiotic therapy is decreasing. Clinical outcomes of purulent maxillofacial pathology in children are complicated by potential severe local deformities at the growth areas of the jaw bones which are difficult to eliminate. The number of cases of prolonged and chronic inflammatory processes, development of local and general complications is increased. The reason for these complications may be an impaired susceptibility to infectious agents, which is determined by the state of the immune system. Therefore, our aim was to reveal some features of immune functions in children with purulent-inflammatory diseases of maxillofacial area. The study included a group of pediatric patients 8-17 years old with maxillofacial inflammatory diseases of the maxilla (the study group), and 13 conditionally healthy children (the comparison group). The contents of T cells (CD3+CD19-, CD3+CD4+, CD3+CD8+, CD3+CD4+/CD3+CD8+), and В cells (CD3-CD19+), NK (CD3-CD16+CD56+) was determined using Cytomics FC-500 (Beckman Coulter, USA);concentrations of serum IgA, IgM, IgG were determined by ELISA technique (Vector-Best, Russia). Phagocytic activity of neutrophilic granulocytes (NG) was evaluated as percentage of actively phagocytic NGs, capturing processes were assessed by appropriate phagocytic indices, and the digestive activity was evaluated against S. aureus (strain 209). Combined defects of immune response in children with maxillofacial hypertension were established: decrease of T lymphocytes contents along with decrease of T helpers and CTL ratio along with unchanged content of NK cells and B lymphocytes. Increase of IgA and IgG levels was also found. Defects of phagocytosis were revealed, primarily connected with the processes of completed phagocytosis and increased content of actively phagocytizing NG. Treatment of children suffering with purulent inflammatory diseases of maxillofacial region is still an urgent problem in dentistry. The revealed dysfunction of immune response to pathogens in the purulent maxillofacial disorders may explain a prolonged clinical course of inflammatory processes, thus determining a need for usage of immunotropic therapy in complex treatment schedules including operative aid as well as conventional drug and physiotherapeutic treatment aiming for increase of rehabilitation efficiency and prevention of postoperative complications in these patients.
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小儿颌面部化脓性炎症性疾病的免疫系统功能障碍
颌面区化脓性炎症性疾病(PMMA)的治疗问题非常紧迫,因为这类患者的数量越来越多。他们的临床病程越来越差,抗生素治疗的效率也在下降。儿童颌面部化脓性病变的临床结果是复杂的潜在严重的局部畸形在颌骨的生长区域,难以消除。长期和慢性炎症过程的病例数,局部和一般并发症的发展增加。这些并发症的原因可能是对感染因子的易感性受损,这是由免疫系统的状态决定的。因此,我们的目的是揭示儿童颌面部化脓性炎症性疾病免疫功能的一些特征。研究包括一组8-17岁的上颌面炎症性疾病患儿(研究组)和13名有条件健康的儿童(对照组)。T细胞(CD3+CD19-、CD3+CD4+、CD3+CD8+、CD3+CD4+/CD3+CD8+)、В细胞(CD3-CD19+)、NK细胞(CD3- cd16 +CD56+)的含量采用美国Beckman Coulter公司的Cytomics FC-500检测;血清IgA、IgM、IgG浓度采用ELISA技术检测(Vector-Best,俄罗斯)。以吞噬活性中性粒细胞(NG)的百分比评价其吞噬活性,以适当的吞噬指标评价其捕获过程,并评价其对金黄色葡萄球菌(菌株209)的消化活性。建立了颌面部高血压患儿免疫反应的综合缺陷:T淋巴细胞含量降低,T辅助细胞和CTL比例降低,NK细胞和B淋巴细胞含量不变。同时发现IgA和IgG水平升高。吞噬缺陷显现,主要与吞噬完成过程和主动吞噬NG含量增加有关。 儿童颌面部化脓性炎症性疾病的治疗仍是牙科医学亟待解决的问题。化脓性颌面疾病中对病原体的免疫反应功能障碍可能解释了炎症过程的临床病程延长,从而确定了在复杂的治疗方案中需要使用免疫治疗,包括手术辅助以及常规药物和物理治疗,旨在提高这些患者的康复效率和预防术后并发症。
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