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中国HIV感染长期不进展者CD4+CD25+Foxp3+调节性T细胞变化研究
引用本文:张子宁,姜拥军,张旻,刘静,施万英,金鑫,孙国权,王亚男,韩晓旭,尚红.中国HIV感染长期不进展者CD4+CD25+Foxp3+调节性T细胞变化研究[J].中华微生物学和免疫学杂志,2008,28(5).
作者姓名:张子宁  姜拥军  张旻  刘静  施万英  金鑫  孙国权  王亚男  韩晓旭  尚红
作者单位:中国医科大学附属第一医院卫生部艾滋病免疫学重点实验室,沈阳,110001
基金项目:国家自然科学基金,国家重点基础研究发展计划(973计划),国家重点基础研究发展计划(973计划) 
摘    要:目的 对中国HIV感染长期不进展者(LTNP)CD4+CD25+Foxp3+调节性T细胞水平及其与疾病进展相关性进行研究,探讨CD4+CD25+Foxp3+ 调节性T细胞在LTNP保护机制中发挥的作用.方法 选取74名HIV-1感染者(LTNP、典型进展HIV组、AIDS组)及16名健康对照,应用流式细胞仪胞内染色技术在单细胞水平检测CD4+CD25+Foxp3+调节性T细胞表达水平,分析其与CD4+ T细胞数量、病毒载量、淋巴细胞活化、凋亡水平的相关性.结果 中国HIV感染LTNP CD4+CD25+Foxp3+ T细胞百分率明显低于典型进展HIV、AIDS组及健康对照组(P<0.05).HIV/AIDS患者CD4+CD25+Foxp3+ T细胞百分率与CD4+ T细胞显著负相关(r=-0.509,P<0.001),与病毒载量明显正相关(r=0.414,P<0.01),与CD4、CD8+ T细胞表面CD38、CD95表达水平明显正相关(P<0.05),与CD4、CD8+ T细胞表面HLA-DR表达无显著相关性.结论 中国HIV感染LTNP CD4+CD25+Foxp3+ 调节性T细胞百分率明显低于典型进展者,提示调节性T细胞与LTNP保护机制相关.

关 键 词:调节性T细胞  长期不进展者  活化  凋亡

Correlation between CD4+CD25+Foxp3+ regulatory T cells and disease progression in HIV infected long term non-progressors of China
ZHANG Zi-ning,JIANG Yong-jun,ZHANG Min,LIU Jing,SHI Wan-ying,JIN Xin,SUN Guo-quan,WANG Ya-nan,HAN Xiao-xu,SHANG Hong.Correlation between CD4+CD25+Foxp3+ regulatory T cells and disease progression in HIV infected long term non-progressors of China[J].Chinese Journal of Microbiology and Immunology,2008,28(5).
Authors:ZHANG Zi-ning  JIANG Yong-jun  ZHANG Min  LIU Jing  SHI Wan-ying  JIN Xin  SUN Guo-quan  WANG Ya-nan  HAN Xiao-xu  SHANG Hong
Abstract:Objective To study the association of CD4+CD8+Foxp3+ regulatory T cells with the HIV long term non-progressors(LTNP) in China. Methods Seventy-four HIV-1 infected patients (LTNP group, HIV group and AIDS group)and 16 normal controls were enrolled and the frequency of CD4+CD25+Foxp3+ regulatory T cells were detected by flow cytometry. To study the correlation between CD4+CD25+Foxp3+ regulatory T cells and disease progression, the absolute CD4+ T cells, viral load, apoptosis and activation of T cells were also examined. Results The frequency of CD4+CD25+Foxp3+ regulatory T cells in LTNP group was significantly lower than that in HIV and AIDS group (P<0.05). The frequency of CD4+CD25+Foxp3+ regulatory T cells was inversely related to CD4+ T cells and closely related to viral load and CD38, CD95 expression on CD4, CD8+ T cells (P<0.05). Conclusion The frequency of CD4+CD25+Foxp3+ regulatory T cells of HIV infected LTNP is significantly lower than typical progressors, which indicates that alternation of regulatory T cells may play a protective role in LTNP.
Keywords:HIV-1  Foxp3
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