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作 者:曾国庆[1] 刘文君[1] 郭渠莲[1] 陈书琴[1] 王开正[1] 邓正华[1] 蔡美珠[1] 曾瑜[1] 刘鹏博(编校)
机构地区:[1]泸州医学院附属医院儿科,四川泸州646000 [2]不详
出 处:《中国妇幼保健》2007年第7期916-918,共3页Maternal and Child Health Care of China
基 金:四川省泸州市科技局重点项目(2001341)
摘 要:目的:探讨婴幼儿病毒性肺炎的病原学及免疫功能变化。方法:采集婴幼儿肺炎组及正常对照组外周血,用ELISA法检测RSV、IFV、ADV、PIV、CMV血清特异性IgM,速率散射比浊法检测IgG、IgA、IgM、CRP,碱性磷酸酶标记链霉卵白素(S-A/AP)法检测T淋巴细胞亚群。结果:104例婴幼儿病毒性肺炎中,单独病毒感染75例,占大部分,其中RSV21例居首位,余依次为IFV18例、ADV15例、PIV11例、CMV10例;混和病毒感染29例,分别是IFV+PIV10例、IFV+RSV6例、ADV+PIV6例、ADV+IFV5例、PIV+RSV2例。病毒性肺炎组CD3↓、CD4↓、CD4/CD8↓、CD8↑,与对照组比较有显著差异(P<0.05),而IgG、IgA、IgM与对照组无显著差异(P>0.05)。结论:病毒感染是婴幼儿肺炎的主要病原,单独病毒感染为主,混和感染为辅,病毒病原谱具有地区性差异。病毒性肺炎患儿存在细胞免疫紊乱。Objective: To explore the etiology and immunological changes of infant viral pneumonia in Luzhou area. Methods: Viral specific serum lgM antibodies of five kinds of virus ( RSV, IFV. ADV, PIV CMV) were detected by ELISA lgG, lgA, lgM and CRP were detected by rate scattered nephelometry. T lymphocyte subpopulations were detected by streptavidin -alkaline phosphates (S- A/AP) method. Results: Among 104. viral pneumonia there were75cases of single virus infection, successively they were RSV: 21cases (20. 1% ), IFV: 18 cases ( 17. 3% ), ADV: 15 cases ( 14. 4% ), PIV: 1 lcases ( 10. 6% ), CMV: 10cases ( 17. 3% ) ; there were 29 cases of mixed viral infection, successively they were IFV + PIV: 10 cases (9. 6% ), IFV + RSV 6 caces (5. 8% ), ADV + PIV: 6 cases (5.8%), ADV + IFV 5 cases (4. 8% ), PIV + RSV: 2 cases ( 1.9% ) . There were significant differences in CD3. CD4, CD4/CD8 counts (all P 〈 0. 05 ), there were not significant differences in immunoglobulin lgG, lgA, lgM ( all 〉 0. 05 ) between viral group and controlled group. Conclusion: Viral infection was the main etiology, the majority was the single viral infection. The viral etiology was not equal to other area totally , expressing the area discrepancy The immune function of viral pneumonia infant dedine, concretely expressing T lymphocyte subpopulation was disordery, CD3, CD4, CD4/CD8 all decline , CD8 rise up , while there was not significant change in humeral immunity.
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