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出 处:《海南医学院学报》2016年第2期144-146,150,共4页Journal of Hainan Medical University
基 金:重庆市万州区科委科技计划项目(2005407)~~
摘 要:目的:探讨外周血Th17及其分泌的细胞因子白细胞介素-17(IL-17)和Th22及其分泌的细胞因子IL-22、IL-6、肿瘤坏死细胞因子α(TNF-α)与原发性免疫血小板减少症(ITP)的发病及预后的关系,分析糖皮质激素对Th17和Th22及其细胞因子水平的影响。方法:应用流式细胞仪测定52例ITP患者及50例正常体检者外周血Th17及Th22细胞,ELISA法测定ITP患者及正常体检者IL-17、IL-22、IL-6及TNF-α表达水平。分析ITP患者Th17和Th22及其细胞因子表达水平与预后的关系。结果:ITP组外周血Th17比例、Th22比例及IL-17、IL-22、IL-6、TNF-α水平高于对照组(P<0.05)。糖皮质激素组外周血Th17比例、Th22比例及IL-17、IL-22、IL-6、TNF-α水平显著低于非糖皮质激素治疗组(P<0.05)。完全有效(CR)组及有效(PR)组外周血Th17比例、Th22比例及IL-17、IL-22、IL-6、TNF-α水平显著低于无效组(NR),差异有统计学意义(P<0.05)。结论:Th17及Th22可能参与ITP的发生及病情进展过程中,且其细胞因子可作为患者病情预后评价指标。糖皮质激素可通过抑制外周血Th17比例、Th22比例而起到治疗作用。Objective: To investigate the relationship between Thl7, cytokine interleukin-17 (IL-17), Th22 cytokines, IL-22, IL 6, tumor necrosis cytokines a (TNF-α) and primary immune thrombocytopenia (ITP). Methods: Thl7 and Th22 cells of 52 ITP patients and 50 normal volunteers were measured by flow cytometry. The levels of IL-17, IL-22, IL 6 and TNF-α of two groups were measured by ELISA. The relationship of Th17,Th22 and their cytokine with ITP were analyzed. Results.. The levels of Th17, Th22 ratio and IL-17, IL 22, IL-6, TNF-α of ITP group were higher than control groups(t= 3. 986,3. 278, 6.235, 10.784, 4. 526, 5. 612,P〈0. 05). The levels of Th17, Th22 ratio and IL-17, IL 22, IL-6, TNF-a of glucocorticoids proportion group were lower than non-glucocorticoid therapy group (F= 5. 023, 3. 148, 6. 178, 7. 011, 6. 052, 4. 285,P〈0.05). The levels of Th17, Th22 ratio and IL-17, IL-22, IL-6, TNF-α of complete remission (CR) group and par-tial response (PR) were significantly lower than the no-remission group (NR), the difference was statistically significant (F= 5. 789, 6. 023, 5. 986, 6. 785, 6. 302, 6. 782,P〈0.05). Oonclusion: Thl? and Th22 may participate in the occurrence and progression of ITP. Its cytokines can be used as indicators in prognosis. Glucocorticoids can inhibit peripheral Th17, Th22,then play a therapeutic role.
关 键 词:原发免疫性血小板减少症 TH17 Th22 细胞因子
分 类 号:R558.2[医药卫生—血液循环系统疾病]
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