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人巨细胞病毒感染与老年人群免疫风险表型的相关性研究进展 被引量:1

Human cytomegalovirus infection and immunological risk phenotypes in the elderly
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摘要 人巨细胞病毒(human cytomegalovirus,HCMV)在老年人群中感染普遍。现已发现,HCMV感染可加速老年人群免疫衰老的进程。免疫风险表型(immunological risk phenotypes,IRP)是一组评价机体免疫功能的指标,与HCMV等病毒感染密切相关;该指标的变化不仅可以反映老年人群的免疫状态,而且通过对其指标,如CD4/CD8比例、CD28分子的监测可以提前预测疾病的发生,为延缓免疫衰老、免疫干预等提供客观依据。因此,该指标日益受到广泛关注。HCMV长期潜伏感染可导致机体的免疫功能低下,尤其对于老年人来说,HCMV感染通常可以导致多项IRP指标的改变,这种改变有可能是引起多种老年性疾病的原因。本文就近年来关于HCMV感染与IPR之间的关系研究进展情况作一综述。  Human cytomegalovirus(HCMV) infection is ubiquitous in the elderly. It may accelerate the course of immunosenescence. Immunological risk phenotypes(IRP) as a group of index for individual’s immune function is significantly associated with viral infection such as HCMV associated infection. The index can not only represent the immune state in the eldly, but also may forecast the occurance of the disease and may provide the objective evidence to interfere immunologically so that the immunosenescence could be delayed. As a result, the index increasingly gets more attention. HCMV long-term latent infection can decrease the immune function especially in the elderly. The infection can induce IRP which may be the cause of most diseases in the elderly. The relationship between the HCMV infecton and IRP is discussed.
出处 《生命科学》 CSCD 2007年第5期543-546,共4页 Chinese Bulletin of Life Sciences
基金 安徽省"十五"生物医药重大科技专项项目资助(01303003)
关键词 HCMV感染 免疫衰老 免疫风险表型 HCMV infection immunosenecence immunological risk phenotypes
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  • 1Pawelec G,Akfaar A,Catuso C,et al.Human inimunosenescence:is it infectious? Immunol Rev,2005,205:257-268. 被引量:1
  • 2Fulop T,Larbi A,Wikby A,et al.Dysregulation of T-cell function in the elderly:scientific basis and clinical implications.Drugs Aging,2005,22(7):589-603. 被引量:1
  • 3Looney R J,Falsey A,Campbell D,et al.Role of cytomegalovims in the T cell changes seen in elderly individuals.Clin Immunol,1999,90(2):213-219. 被引量:1
  • 4Caruso C,Aquino A,Candore G,et al.Looking for immunological risk genotypes.Ann N Y Acad Sci,2004,1019:141-146. 被引量:1
  • 5Finch C E,Crimmins E M.Inflammatory exposure and historical changes in human life-spans.Science,2004,305(5691):1736-1739. 被引量:1
  • 6Hadrup S R,Strindhall J,Kollgaard T,et al.Longitudinal studies of clonally expanded CDS T cells reveal a repertoire shrinkage predicting mortality and an increased number of dysfunctional cytomegalovirus-specific T cells in the very elderly.J Immunol,2006,176(4):2645-2653. 被引量:1
  • 7Wikby A,Ferguson F,Forsey R,et al.An immune risk phenotype,cognitive impairment,and survival in very late life:impact of allostatic load in Swedish octogenarian and nonagenarian humans.J Gerontol A Biol Sci Med Sci,2005,60(5):556-565. 被引量:1
  • 8Wills M R,Okecha G,Weekes M P,et al.Identification of naive or antigen-experienced human CD8^+ T cells by expression of costimulation and chemokine receptors:analysis of the human cytomegalovirus-specific CD8+ T cell response.J Immunol,2002,168(11):5455-5464. 被引量:1
  • 9Vescovini R,Telera A,Faqnoni F F,et al.Different contribution of EBV and CMV infections in very long-term carriers to age-related alterations of CD8+ T cells.Exp Gerontol,2004,39(8):1233-1243. 被引量:1
  • 10Elbou Quid M A,Luton D,Yadini M,et al.Cellular immune response of fetuses to cytomegalovirus.Pediatr Res,2004,55(2):280-286. 被引量:1

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