常见变异性免疫缺陷症感染型和自身免疫表型中的 B-2 淋巴细胞以及促炎和抗炎细胞因子的平衡

L. Sizyakina, I. I. Andreeva, M. Kharitonova
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摘要

材料与方法:对 10 名确诊为 CVID 的患者进行观察的结果。其中六名患者的临床表现为传染性表型,疾病位于肺部。四名患者被诊断为克罗恩病、溶血性贫血和自身免疫性肝炎。血清中细胞因子 IL-4、IL-10、IL-17、TNF-α、IFN-γ 的水平用 ELISA 法测定,外周血 B 细胞的表型特征用流式细胞荧光测定法测定。在感染性表现中,切换记忆 B 淋巴细胞数量占 B-2 细胞总数的比例(2.3%)高于自身免疫性表现(1.4%)。感染性表现患者血清中 IFN-γ 和 TNF-α 的含量与对比组的健康供体相比有所增加,血清中 IL-17 的含量没有差异,而自身免疫性表现患者血清中所有这些细胞因子的含量都有所增加,其中 IFN-γ 和 TNF-α 的含量更高。变化的性质和程度因疾病的临床表型而异。
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B-2 lymphocytes and the balance of pro and anti-inflammatory cytokines in infectious and autoimmune phenotypes of common variable immune deficiency
Objective: comparative characteristics of the subpopulation composition of B- lymphocytes and the cytokine spectrum of peripheral blood in infectious and non-infectious manifestations of CVID.Materials and methods: the results of observation of 10 people diagnosed with CVID have been presented. Six patients the clinical manifestation had an infectious phenotype of the disease of synopulmonary localization. Four patients were diagnosed with Crohn's disease, hemolytic anemia, and autoimmune hepatitis. The level of cytokines IL-4, IL-10, IL-17, TNF-α, IFN-γ in blood serum was determined by the ELISA, the phenotypic characteristic of B cells of peripheral blood cells was carried out by flow cytofluorimetry.Results: the proportion of memory B cells in the healthy donors is 30% of all B-lymphocytes, on infectious manifestation of CVID – 12%, with autoimmune – 14%. The number of switched memory B-lymphocytes relative to the total pool of B-2 cells in infectious manifestation is greater (2.3%) than in autoimmune ones (1.4%). In patients with infectious manifestations the content of IFN-γ and TNF-α was increased inrelation to healthy donors of the comparison group, there were no differences in the serum amount of IL-17, with autoimmune manifestations, the content of all these cytokines was increased, IFN-γ and TNF-α being to a greater extent.Conclusion: impaired formation of memory B-lymphocytes and cytokine dysregulation of immune processes are detected regardless of the variant of clinical manifestation of CVID. The nature and degree of changes differ depending on the clinical phenotype of the disease.
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