Antigen presenting subset of СD66b+CD16+CD33+HLA-DR+ neutrophilic granulocytes in acute osteomyelitis in children: Immunomodulating effects of immunotropic hexapeptide in an in vitro experimental system

I. Nesterova, G. Chudilova, Yu. V. Teterin, E. A. Chicherev, V. N. Chapurina, M. Mitropanova
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引用次数: 1

Abstract

Inclusion of neutrophilic granulocytes (NG) in inflammation depends on the expression of receptors providing the functions of NG. Acute osteomyelitis (AOM) occupies a central place among purulentinflammatory diseases in children. AOM purulent-necrotic process proceeds in the bone, bone marrow – the site of hematopoiesis. It is interesting to determine the functionally significant NG subsets, their phenotype in OM and evaluate the effect of immunotropic substances for the correction of dysfunctions. Aim: to specify the variants of changes in quantitative and phenotypic characteristics of CD66b+CD16+CD33+HLA-DR-, CD66b+CD16+CD33+HLA-DR+ NG subsets at AOM in children and evaluate the possibility of their immunomodulation under the influence of hexapeptide (HP) – Arginyl-alpha-Aspartyl-Lysyl-Valyl-Tyrosyl-Arginine in vitro.Peripheral blood (PB) of 24 children 8-15 years old AOM were the study group (SG). The comparison group (CG) – 13 healthy children. HP (10-6 g/L) were incubated with PB SG (60 min, 37 °C) to evaluate the effects (SG1). The number of NG subsets CD66b+CD16+CD33+HLA-DR+, CD66b+CD16+CD33+HLA-DR- (FC500, Beckman Coulter, USA), receptor expression density (MFI), phagocytic activity before and after incubation with HP were determined.The NG subset expressing HLA-DR – 29.9 (18.4-43.6) % CD66b+CD16+CD33+HLA-DR+ was registered in children with AOM. The number of CD66b+CD16+CD33+HLA-DR+ was 1.5 times lower (p > 0.05), of CD66b+CD16+CD33+HLA-DR+ was 1.2 times higher (p > 0.05) than before incubation with of HP. The redistribution of subsets apparently occurs due to the binding of HPs to HLA-DR on the NG membrane. Also MFI HLA-DR was low (p > 0.05); the 1.3-fold increase in MFI CD66b, 1.4-fold decrease in MFI CD16 were revealed (p < 0.05).The study was the first to demonstrate the presence of NG subset of CD66b+CD16+CD33+HLA-DR+ in the PB of children with AOM. Subset of CD66b+CD16+CD33+HLA-DR+NG in AOM indicates the appearance of an activated subset of NG in PB with the properties of APC. The positive influence of HP on the phenotypic characteristics of subsets СD66b+CD16+CD33+HLA-DR-, СD66b+CD16+CD33+HLA-DR+. Restoration of phagocytic function of NGs under the influence of HP is connected with the increase of CD66b expression, which influences the effector function of NGs and decrease of CD16 molecule hyperexpression that stipulates decrease of damaging cytotoxic activity of NGs.
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儿童急性骨髓炎中СD66b+CD16+CD33+HLA-DR+中性粒细胞抗原呈递亚群:免疫性六肽在体外实验系统中的免疫调节作用
中性粒细胞(NG)在炎症中的包含取决于提供NG功能的受体的表达。急性骨髓炎(AOM)在儿童化脓性炎症性疾病中占有中心地位。AOM的化脓性坏死过程发生在骨骼、骨髓——造血的部位。确定功能性显著的NG亚群及其在OM中的表型和评估免疫物质对纠正功能障碍的作用是很有趣的。目的:明确儿童AOM时CD66b+CD16+CD33+HLA-DR-、CD66b+CD16+CD33+HLA-DR+ NG亚群数量和表型变化的变异,并评价其在体外六肽(HP) -精氨酸- α -天冬氨酸-莱氨酸-缬氨酸-酪氨酸-精氨酸影响下免疫调节的可能性。24例8 ~ 15岁AOM患儿外周血(PB)为研究组(SG)。对照组(CG):健康儿童13例。HP (10-6 g/L)与PB SG(37°C, 60 min)孵育,评价效果(SG1)。测定NG亚群CD66b+CD16+CD33+HLA-DR+、CD66b+CD16+CD33+HLA-DR-的数量(FC500, Beckman Coulter, USA)、受体表达密度(MFI)、HP孵育前后的吞噬活性。AOM患儿中表达HLA-DR - 29.9 (18.4-43.6) % CD66b+CD16+CD33+HLA-DR+的NG亚群。与HP孵育前相比,CD66b+CD16+CD33+HLA-DR+的数量减少了1.5倍(p > 0.05), CD66b+CD16+CD33+HLA-DR+的数量增加了1.2倍(p > 0.05)。亚群的重新分配显然是由于HPs与NG膜上的HLA-DR结合而发生的。MFI HLA-DR也较低(p < 0.05);MFI CD66b升高1.3倍,MFI CD16降低1.4倍(p < 0.05)。该研究首次证实在AOM儿童的PB中存在CD66b+CD16+CD33+HLA-DR+的NG亚群。AOM中CD66b+CD16+CD33+HLA-DR+NG的亚群表明PB中出现了具有APC特性的活化NG亚群。HP对СD66b+CD16+CD33+HLA-DR-、СD66b+CD16+CD33+HLA-DR+亚群表型特征的积极影响。HP作用下NGs吞噬功能的恢复与CD66b表达的增加有关,CD66b表达的增加影响了NGs的效应功能和CD16分子高表达的降低,从而降低了NGs的破坏性细胞毒活性。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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