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作 者:董琳[1] 陈小芳[1] 周晓聪[1] 林剑[1] 李锦燕[1] 张伟[1]
机构地区:[1]温州医学院附属育英儿童医院呼吸科,325027
出 处:《浙江临床医学》2007年第10期1307-1308,共2页Zhejiang Clinical Medical Journal
基 金:温州市跨世纪"551人才工程"资助项目
摘 要:目的探讨呼吸道合胞病毒(RSV)毛细支气管炎(简称RSV毛支)RANTES、MIP-1α、IL-8的动态变化及相关性。方法RSV毛支组26例为住院的RSV毛细支气管炎患儿,年龄1.5-11.0个月;对照组为14例择期手术患儿,年龄5.4~15.1个月。应用ELISA法分别检测RSV毛支组急性期和恢复期鼻咽分泌物RANTES、MIP-1α、IL-8浓度。结果对照组鼻咽分泌物未测到RANTES和MIP-1α,测得低水平的IL-8;RSV毛细支气管炎患儿急性期RANTES、MIP-1α、IL-8明显高于对照组;恢复期RANTES、IL-8下降,但仍高于对照组;MIP-1α恢复期和急性期差异无显著性(P〉0.05),但高于对照组(P〈0.001)。RANTES与MIP-1α、IL-8及MIP-1α与IL-8间有正相关关系。结论RSV毛细支气管炎患儿RANTES、MIP-1α、IL-8明显升高,提示趋化因子可能在RSV感染的气道炎症中起重要作用。Objectives To explore the dynamic change of RANTES. MIP-1α and IL - 8 in children with respiratory syncytial virus (RSV) bronchiolitis and their correlation . Methods Twenty - six children aged 1.5 - 11.0 (4.7± 2.6)month hospitalized with bronchiolitis were enrolled as patient group. RSV infection diagnosis was based on direct immunofluorescence assay in NPS. Forteen children aged 5.4 - 15.1 month undergoing surgical operation were served as control subjects. NPS samples were collected from patients at acute stage and recovery stage respectively. All samples were analyzed for RANTES. MIP-1α and IL - 8 levels with ELISA. Results RANTES and MIP-1αconcentrations were not detected in NPS samples from control patients. Only low levels of IL - 8 were detected. Levels of RANTES. MIP-1α and IL - 8 were significantly greater in samples obtained from patients at acute stage than those of control children. Levels of RANTES and IL- 8 decreased significantly in patients at recovery stage and were greater than those in controls. Levels of MIP-1α in patients at recovery stage had no difference compared with those at acute stage, but were still higher than those in controls. Moreover, RANTES levels positively correlated both with MIP-1α and IL - 8 levels; Positive correlation between MIP-1α and IL - 8 levels was also apparent. Conclusion NPS concentrations of RANTES.MIP-1α and IL- 8 in children with RSV bronchiolitis increase significantly, which suggests an important role for chemokines in the airway inflammation induced by RSV.
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