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胸腺五肽对老年慢性阻塞性肺疾病患者血清白细胞介素17A、趋化因子12水平及瞬时受体电位通道1表达的影响 被引量:3

Effect of thymopentin combined with conventional therapy on serum IL-17A, CXCL12 levels and TRPC1 expression in elderly patients with chronic obstructive pulmonary disease
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摘要 目的 探讨胸腺五肽联合常规药物对老年COPD患者血清白细胞介素17A(IL-17A)、趋化因子12 (CXCL12)水平及瞬时受体电位通道1(TRPC1)表达的影响.方法 选择156例COPD患者为研究对象,按照随机数字表法分为两组(n=78).对照组进行常规治疗;观察组在常规治疗的基础上进行胸腺五肽皮下注射.测定治疗前后CD3+、CD4+、CD8+、CD4+/CD8+水平以比较两组免疫功能,治疗前后测定1秒用力呼气容积(FEV1)、残气量/肺总量比率(FEV1/FVC)及最大呼气流量(PEF)以比较两组肺通气功能,测定和比较两组患者治疗前后外周血IL-17A、CXCL12水平及肺泡灌洗液中TRPC1水平.比较两组患者的不良反应.结果 治疗前,两组CD3+、CD4+、CD8+及CD4+/CD8+差异均无统计学意义(均P>0.05);治疗后,对照组未发生显著变化(P>0.05),观察组CD3+、CD4+、CD4+/CD8+[(65.17±2.39)%、(41.06 ±2.15)%、(1.50±0.74)%]显著高于对照组[(52.66±2.38)%、(32.30±2.05)%、(0.80±0.81)%],CD8+ (24.02±2.23)%显著低于对照组[(32.66±1.97)%,P<0.05].治疗前,两组患者FEV1、FEV1/FVC、PEF均无显著差异(均P>0.05);治疗后两组患者的FEV1、FEV1/FVC、PEF均显著升高(均P<0.05),且观察组均显著高于对照组(均P<0.05).治疗前两组患者外周血IL-17A、CXCL12水平及肺泡灌洗液中TRPC1水平差异均无统计学意义(均P>0.05);治疗后,观察组患者外周血IL-17A[(24.18±3.69) pg/mL]、CXCL12水平[(193.50 ±2.90) pg/mL]及BALF中TRPC1水平[(7.69±1.14)ng/L]显著降低(P<0.05),对照组患者外周血IL-17A[(34.25±3.74) pg/mL]、CXCL12水平[(205.37±3.21) pg/mL]及BALF中TRPC1水平[(14.25±1.20) ng/L]也显著降低(P<0.05),且观察组显著低于对照组(P<0.05).观察组和对照组的不良反应的总发生率为16.67%、12.82%,差异无统计学意义(P>0.05).结论 胸腺五肽联合常规药物治疗能显著提高老年COPD患者的免疫功能,改善肺通气功能,降低炎症因子,缓解炎症反应,安全有效. Objective To investigate the effect of thymopentin combined with routine medication on serum interleukin 17A(IL-17A),chemokine 12 (CXCL12) levels and transient receptor potential channel 1 (TRPC1)expression in elderly patients with chronic obstructive pulmonary disease (COPD).Methods 156 COPD patients were selected as study objects.They were randomly divided into two groups(n =78) according to the digital table.The control group received routine treatment,and the observation group received subcutaneous injection of thymopentin on the basis of routine treatment.Before and after treatment,the CD3+,CD4+,CD8+,CD4+/CD8+ levels were tested to compare the immunologic function of the two groups.Before and after treatment,the FEV1,FEV1/FVC,PEF were tested to compare the pulmonary ventilation function of the two groups.The IL-17A,CXCL12 levels in peripheral blood and TRPC1 level in bronchoalveolar liquid before and after treatment were tested and compared between the two groups.The adverse effect was compared.Results Before treatment,the CD3+,CD4+,CD8+ and CD4+/CD8+ between the two groups had not statistically significant differences (all P 〉 0.05),which of the control group after treatment had no significant change (all P 〉 0.05),the CD3+,CD4+,CD4+/CD8+ of the observation group [(65.17 ± 2.39) %,(41.06 ±2.15) %,(1.50 ± 0.74) %] were significantly higher than control group [(52.66 ± 2.38) %,(32.30 ± 2.05) %,(0.80 ± 0.81) %] (all P 〈 0.05),and the CDs+ of the observation group [(24.02 ± 2.23) %] was significantly lower than control group[(32.66 ± 1.97) %,P 〈0.05].Before treatment,the FEV1,FEV1/FVC,PEF,the IL-17A,CXCL12 levels and TRPC1 level had no statistically significant differences between the two groups(P 〉 0.05).After treatment,the peripheral blood IL-17A [(24.18 ± 3.69) pg/mL],CXCL12 levels [(193.50 ± 2.90) pg/mL] and TRPC1 level in BALF [(7.69 ± 1.14)ng/L] in the observation group decreased significantly(P 〈 0.05),which in the control group also decreased significantly [IL-17A (34.25 ± 3.74) pg/mL,CXCL12 (205.37 ± 3.21) pg/mL,TRPC1 (14.25 ± 1.20)ng/L] (P 〈 0.05),which of the observation group were significantly lower than those of the control group(all P 〈0.05).The incidence rates of adverse effects of the two groups were t6.67%,12.82%,there was no statistically significant difference(P 〉 0.05).Conclusion Thymopentin combined with conventional therapy can effectively improve the elderly COPD patients'immunologic function and pulmonary ventilation function,decrease the inflammatory factor,relieve inflammatory reaction and it is safe and effective.
作者 黄树红
出处 《中国基层医药》 CAS 2017年第20期3179-3183,共5页 Chinese Journal of Primary Medicine and Pharmacy
关键词 肺疾病 慢性阻塞性 趋化因子12 瞬时受体电位通道1 胸腺五肽 Pulmonary disease, chronic obstructive Interleukin - 17 A Chemokine 12 Transientreceptor potential channel 1 Thymopoietin5
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