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负性调节细胞CD4^(+)CD25^(+)T及其相关细胞因子在COPD患者外周血中的表达与合并细菌感染的相关性研究 被引量:2

Correlation between expressions of negative regulatory cell CD4^(+)CD25^(+)T and its related cytokines in peripheral blood and bacterial infection of COPD patients
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摘要 目的探讨负性调节细胞CD4^(+)CD25^(+)T及其相关细胞因子在慢性阻塞性肺病(COPD)患者外周血中的表达与合并细菌感染的相关性。方法纳入2018年1月-2019年12月间收治的66例COPD患者作为研究对象,其中急性加重期COPD患者(AECOPD)36例、稳定期患者30例,并纳入同期体检健康者30例作为对照组。对所有纳入的研究对象外周血标本中的CD4^(+)CD25^(+)T调节性T细胞及其相关细胞因子[白介素-4(IL-4)、白介素-10(IL-10)、干扰素-γ(IFN-γ)]表达水平进行检测,分析相关指标水平与COPD是否合并细菌感染的关系,及预测细菌感染的效能。结果AECOPD和稳定期COPD患者CD4^(+)、CD4^(+)CD25^(+)、IFN-γ/IL-4水平均低于对照组(P<0.05),IL-4、IL-10水均高于对照组(P<0.05);AECOPD患者IFN-γ水平高于对照组(P<0.05);AECOPD患者CD4^(+)、CD4^(+)CD25^(+)水平低于稳定期COPD患者(P<0.05),IL-4、IL-10、IFN-γ均高于稳定期COPD患者(P<0.05);CD4^(+)、CD4^(+)CD25^(+)水平与IL4、IFN-γ均呈负相关关系(P<0.05),CD4^(+)水平与IL-10呈负相关关系(P<0.05);COPD合并感染者CD4^(+)水平低于未合并感染者(P<0.05),IL-4、IFN-γ水平均高于未合并感染者(P<0.05);COPD合并革兰氏阴性菌感染者CD4^(+)CD25^(+)水平低于未合并感染者(P<0.05),IL-10水平均高于未合并感染者(P<0.05);CD4^(+)、IL-4、IL-10、IFN-γ均是预测COPD患者合并细菌感染的有效指标(P<0.05),其中IL-4和IFN-γ效能较高。结论CD4^(+)、CD4^(+)CD25^(+)Treg细胞及其相关细胞因子参与COPD发生发展和患者细菌感染,监测其水平变化有利于为临床诊治提供信息。 Objective To investigate the correlation between the expressions of negative regulatory cell CD4^(+)CD25^(+)T and its related cytokines in peripheral blood and bacterial infection of patients with chronic obstructive pulmonary disease(COPD).Methods Sixty-six COPD patients admitted between January 2018 and December 2019 were included as the research subjects,including 36 patients with acute exacerbation of COPD(AECOPD)and 30 patients with stable COPD.Another 30 healthy people undergoing physical examination during the same period were included in controlgroup.The expression levels of CD4^(+)CD25^(+) regulatory T cell and its related cytokines[interleukin-4(IL-4),interleukin-10(IL-10),interferon-γ(IFN-γ)]in the peripheral blood samples were detected among the included subjects.The relationship between levels of related indicators and presence or absence of bacterial infection in COPD and the efficacy of predicting infection were analyzed.Results The levels of CD4^(+),CD4^(+)CD25^(+) and IFN-γ/IL-4 in patients with AECOPD and patients with stable COPD were lower than those in control group(P<0.05),while the levels of IL-4 and IL-10 were higher than those in control group(P<0.05).The IFN-γlevel of AECOPD patients was higher than that of control group(P<0.05).The levels of CD4^(+)and CD4^(+)CD25^(+) of AECOPD patients were lower than those of stable COPD patients(P<0.05),while the levels of IL-4,IL-10 and IFN-γwere all higher than those of stable COPD patients(P<0.05).The levels of CD4^(+) and CD4^(+)CD25^(+) were negatively correlated with IL4 and IFN-γ(P<0.05),and the CD4^(+) level was negatively correlated with IL-10(P<0.05).The CD4^(+) level in COPD patients with infectionwas lower than that in patients without infection(P<0.05),while the levels of IL-4 and IFN-γwere higher than those in patients without infection(P<0.05).The CD4^(+)CD25^(+)level ofCOPD patients with Gram-negative bacteria infection was lower than that of patients without infection(P<0.05),while the IL-10 level was higher than that of patients without infection(P<0.05).CD4^(+),IL-4,IL-10 and IFN-γwere effective indicators in predicting bacterial infection in COPD patients(P<0.05),and IL-4 and IFN-γhad higher efficacy.Conclusions CD4^(+),CD4^(+)CD25^(+) T cell and related cytokines are involved in the occurrence and development of COPD and bacterial infection in patients.Monitoringchanges ofthose levels is helpful to provide information for clinical diagnosis and treatment.
作者 侯聪霞 孙芳 梁亚林 HOU Congxia;SUN Fang;LIANG Yalin(First Word of Resptratory and Critical Care Medicine Department,Henan Provincal Chest Hospital,Zhengzhou Seventh People's Hospital,Zhengzhou 450000,China;Kidney Disease Diagnosis and Treatment Center,the Seventh People's Hospital of Zhengzhou city,Zhengzhou 450016,China)
出处 《广州医药》 2022年第3期13-17,共5页 Guangzhou Medical Journal
基金 河南省卫健委科技攻关课题项目(LHGJ-20200230)。
关键词 慢性阻塞性肺病 调节性T淋巴细胞 白介素-4 干扰素Γ 细菌感染 chronic obstructive pulmonary disease regulatory T lymphocytes interleukin-4 interferon-γ bacterial infection
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