期刊文献+

老年男性外周血CD4^+和CD8^+ T细胞中CD45RA^+和HLA-DR^+的表达研究

Expression of CD45RA^+ and HLA-DR^+ on peripheral blood CD4^+ and CD8^+ T lymphocyte in aged males
下载PDF
导出
摘要 目的探讨不同年龄组老年男性外周血CD4+和CD8+T细胞中CD45RA+和HLA-DR+的表达。方法采用逐步入组方法入组101例老年男性,分青老年组(65岁及以上),中老年组(75岁及以上)和老老年组(85岁及以上)三组,用多色流式细胞仪检测外周血CD45RA+和HLA-DR+的表达,随访两年。结果各组间CD45RA+和HLA-DR+T细胞的表达轻微下降,其中仅老老年组与青老年组之间CD4+HIL-DR-和CD8+HIL-DR+T细胞的表达差异有统计学意义(P<0.05)。结论老年男性外周血CD4+和CD8+T细胞中CD45RA+和HLA-DR+的表达可能存在随龄性下降趋势。 Objective To study the expression of CD45RA+ and HLA-DR+ on peripheral blood CD4+ and CD8+T lymphocyte of different aged male groups.Methods Using the gradual enrollment method,101 aged males were divided into three groups: young aged group(65 years old and over),middle aged group(75 years old and over) and old aged group(85 years old and over).Expression of CD45RA+ and HLA-DR+T lymphocyte from peripheral blood were detected with multi-colors flow cytometer,following up two years.Results Expression of CD45RA+ and HLA-DR+T lymphocyte in different groups slightly decreased,expression of CD4+HIL-DR-and CD8+HIL-DR+T lymphocyte between old aged group and young aged group had a significant difference(P0.05).Conclusion Expression of CD45RA+ and HLA-DR+ on peripheral blood CD4+and CD8+ T lymphocyte of aged male groups has a potential decline trend with increase of age.
出处 《哈尔滨医科大学学报》 CAS 北大核心 2011年第5期455-457,460,共4页 Journal of Harbin Medical University
基金 黑龙江省攻关课题(GC07C335)
关键词 免疫衰老 CD45RA+T细胞 HLA-DR+T细胞 老年男性 immunosenescence CD45RA+T lymphocyte HLA-DR+T lymphocyte aged male
  • 相关文献

参考文献14

  • 1Wayne SJ, Rhyne RL, Garry PJ,et al. Cell-mediated immunity as a predictor of morbidity and mortality in subjects over 60 [ J ]. J Gerontol, 45(2) : M45-48.
  • 2Hsu HC, Scott DK, Zhang P, et al. CD8 T-cell immune phenotype of successful aging[ J]. Mech Ageing Dev,2006, 127 ( 3 ) : 231-239.
  • 3Strindhall J, Nilsson BO, Lofgren S, et al. No immune risk profile among individuals who reach 100 years of age: findings from the Swedish NONA immune longitudinal study[ J]. 2007. Exp Gerontol, 42(8) : 753-761.
  • 4Wikby A, Nilsson BO, Forsey R, et al. The immune risk phenotype is associated with IL-6 in the terminal decline stage: findings from the Swedish NONA immune longitudinal study of very late life functioning [ J ]. Mech Ageing Dev,2006,127 ( 8 ) : 695-704.
  • 5Ershler WB. The value of the SENIEUR protocol: distinction between "ideal aging" and clinical reality [ J ]. Mech Ageing Dev, 2001,122(2) : 134-136.
  • 6Capri M, Monti D, Salvioli S. Complexity ofantistrategies in humans[ J]. 2006, 30(10) :730-742.
  • 7Fagnoni FE, Vescovini R, Mazzola M, et al. Expansion of cytotoxic CD8 + CD28T ceils in healthy ageing people, including centenarians [ J ]. Immunology, 1996, 88 (4) : 501-507.
  • 8Weng NP, Akbar AN,Goronzy J,et al. CD28(-) T cells: their role in the age-associated decline of immune function[J]. Trends Immunol,2009, 30(7): 306-312.
  • 9Fagnoni FF, Vescovini R, Passeri G,et al. Shortage of circulating naive CD8 ( + ) T cells provides new insights on immunodeficieney in aging[ J ]. Blood,2000, 95 (9) : 2860-2868.
  • 10Thewissen M, Linsen L, Somers V, et al. Premature immunose nescence in rheumatoid arthritis and multiple sclerosis patients [J]. Ann N Y Acad Sci, 2005,1051:255-262.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部