Differences in the skin microbiota spectrum and parameters of local immunity in the areas of inflammation in skin diseases and healthy people

S. V. Sennikova, Anna P. Toptygina, E. A. Voropaeva
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Abstract

Alteration of microbiota composition is a trigger, and, sometimes, an etiological factor in the development of chronic skin diseases, e.g., psoriasis or eczema. Recognition of microflora by keratinocytes and immune cells leads to the production of antimicrobial peptides, chemokines and growth factors, which contribute to the differentiation of T lymphocytes to autoaggressive effector cells of Th1, Th17 and Th22 types that implement autoimmune inflammation in the psoriatic plaque. The aim of our work was to study the differences in the skin microbiota spectrum and the parameters of local immunity in capillary blood taken near the focus of inflammation in patients with autoimmune (psoriasis) and allergic (eczema) diseases compared with the parameters of healthy people. 24 patients with psoriasis (group 1), 20 patients with eczema (group 2) and 20 healthy adults (group 3) were examined. Biological materials were taken, i.e., the smears taken with sterile dry swab to the Amies transport medium with activated carbon, and capillary blood was taken in 2 microvets, 200 L each) from the foci of inflammation on affected skin from the hands of patients, or from the fingers of healthy people. Inoculations of diagnostic media, microscopy with Gram staining and microbial identification were performed in a microbiological analyzer. Immunophenotyping of 22 subsets of mononuclear cells was performed by four-color staining of capillary blood with erythrocyte lysis and evaluation of subsets by a flow cytometer. Cytokines in blood plasma were determined by multiplex method. The spectrum of hand skin microflora of the group 3 was more diverse in the species composition. In patients with psoriasis and eczema, the coccal flora dominated, with a shift towards pathobionts in the microbiota spectrum. Activation of T and B cells, production of pro-inflammatory cytokines, IL-23/IL-17/IL-22 axis cytokines and cytokines markers of epithelial cell damage (IL-25 and IL-33), as well as anti-inflammatory factors insufficiency were detected. Differences in changing parameters of the local immune status in patients with autoimmune (psoriasis) and allergic (eczema) diseases were revealed, thus reflecting the distinct features of immunopathogenesis in these diseases.
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皮肤病和健康人炎症区皮肤微生物群谱和局部免疫参数的差异
微生物群组成的改变是慢性皮肤病(如牛皮癣或湿疹)发生的触发因素,有时也是病因学因素。角质形成细胞和免疫细胞对微生物菌群的识别导致抗菌肽、趋化因子和生长因子的产生,这有助于T淋巴细胞分化为Th1、Th17和Th22型的自身攻击效应细胞,在银屑病斑块中实施自身免疫性炎症。我们的工作目的是研究自身免疫性(牛皮癣)和过敏性(湿疹)疾病患者在炎症病灶附近采集的毛细血管血液中皮肤微生物群谱和局部免疫参数与健康人群参数的差异。选取银屑病患者24例(第一组),湿疹患者20例(第二组),健康成人20例(第三组)。取生物材料,即用无菌干拭子将涂片取到带活性炭的Amies运输介质中,并从患者的手上或健康人的手指患处皮肤的炎症灶上取毛细血管血(2个微皿,每个200 L)。在微生物分析仪中接种诊断培养基,革兰氏染色显微镜和微生物鉴定。采用毛细管血红细胞溶解四色染色和流式细胞仪对22个单核细胞亚群进行免疫分型。采用多元法测定血浆细胞因子。3组手皮肤菌群的种类组成更为多样化。在牛皮癣和湿疹患者中,球菌菌群占主导地位,在微生物群谱中向病原体转移。检测T细胞和B细胞的活化,促炎细胞因子、IL-23/IL-17/IL-22轴细胞因子和上皮细胞损伤细胞因子标志物(IL-25和IL-33)的产生,以及抗炎因子的不足。揭示了自身免疫性疾病(银屑病)和变应性疾病(湿疹)患者局部免疫状态变化参数的差异,从而反映了这两种疾病免疫发病机制的不同特点。
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