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作 者:周娟[1] 杨锡强[1] 赵晓东[1] 王莉佳[1] 蒋利萍[1]
机构地区:[1]重庆医科大学附属儿童医院肾脏免疫科,400014
出 处:《中华微生物学和免疫学杂志》2008年第10期909-913,共5页Chinese Journal of Microbiology and Immunology
基 金:国家自然科学基金资助项目(30340045)
摘 要:目的比较普通BALB/c鼠和裸鼠呼吸道合胞病毒(RSV)感染免疫及炎症反应特点。方法BALB/c鼠和裸鼠感染RSV后不同时间空斑形成试验检测肺组织病毒滴度,计数支气管肺泡灌洗液(BALF)白细胞总数和分类,HE染色分析肺组织病理学改变,免疫组化检测肺组织F4/80^+细胞和CD9b^+细胞。ELISA检测BALF中TNF—α、IFN-γ、IL-12和IL-10浓度。结果BALB/c鼠和裸鼠感染RSV后肺组织病毒滴度在第3天达峰值,感染裸鼠带毒时间更长,在感染后各天病毒滴度明显高于BALB/c鼠(P〈0.05),肺组织病理改变也更重。感染BALB/c鼠和裸鼠BALF白细胞总数明显升高,分类以淋巴细胞为主。感染裸鼠与感染BALB/c鼠比较,肺组织检测到更多的F4/80^+巨噬细胞和CD49b^+NK细胞(P〈0.05),BALF中TNF—α、IL-12和IL-10水平更高(P〈0.05)。结论RSV感染裸鼠与BALB/c鼠比较,病毒复制水平更高,时间更持久,炎症反应更重。单核巨噬细胞和NK细胞是RSV感染重要的免疫细胞和炎症细胞,炎症反应强度并不一定与T细胞免疫应答平行。Objective To compare respiratory syncytial virus (RSV) infection and inflammatory responses between immunocompetent BALB/c mice and immunodeficient nude mice. Methods At various time points after RSV infection of BALB/c mice and nude mice, pulmonary viral titers were assayed. Leukocytes in bronchoalveolar lavage fluid (BALF) and pulmonary histology were identified. F4/80^ + cells and CD49b^+ cells in lung tissue were examined by immunohistochemistry, and the cytokines of TNF-α, IL-12, IFN-γ and IL-10 in BALF were assayed by ELISA. Results RSV fiters in infected BALB/c mice and nude mice peaked on the 3rd day postinoculation, and nude mice had higher-level and more durative viral replication than BALB/c mice. RSV infection induced more severe pulmonary histopathology and larger number of leukocytes in airway in nude mice than in BALB/c mice. RSV infection enhanced more pulmonary F4/80^+ macrophages, CD49b ^+ NK cells in both mice. Furthermore infected nude mice had larger amount of pulmonary macrophages and NK cells than infected BALB/c mice. RSV infected BALB/c mice secreted more TNF-α, IL-12, IFN-γ and IL-10 as compared with control BALB/c mice, and infected nude mice had higher level of TNF-α, IL-12 and IL-10 than infected BALB/c mice. Conclusion Nude mice are good model for severe and persistent RSV infection in immunocomprised hosts. The inflammation induced by RSV infection is not parallel with the immune response of T cells, and macrophages and NK cells are potent immunocytes and inflammatory cells in RSV infection especially when T lymphocytes are absent.
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