Age-related changes in the function of T cells

被引:29
作者
Aspinall, R [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Fac Med, Dept Immunol, London SW10 9NH, England
关键词
senescence; telomere; signaling; repertoire; thymus;
D O I
10.1002/jemt.10412
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
At the start of the last century in the United Kingdom, only 24% of the 587,830 deaths registered were of individuals over 65, but by the end of the century these figures had changed markedly. Of the 558,052 deaths in 1997, 84% were in the population over 65. This "right shift" in the survival curve is projected to continue. The UK Government Actuary's Department forecast that by 2020, 11.75 million people (19% of the population) will be over 65 rising to 15.1 million people (25% of the population) by 2040. Older members of society show infections of the urinary tract, respiratory tract, skin, soft tissue or intra-abdominal region, infectious endocarditis, bacterial meningitis, tuberculosis, and herpes zoster, at a higher incidence than among younger adults. Moreover, mortality rates for these diseases are often 2-3 times higher among elderly patients than younger individuals with the same disease. The higher morbidity and mortality from these infections, plus the increased prevalence of specific cancers and certain autoimmune diseases point to an immune system deteriorating with age. At the core of the immune system are the T cells and this review analyses possible causes for the changes in T cell function that may account for the deterioration of the immune system. Any intervention to reverse the decline in the immune system must have a rational basis built on a hypothesis-driven inquiry, and one such intervention process is presented here. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:508 / 513
页数:6
相关论文
共 63 条
  • [1] AGGRAWAL S, 1997, J CLIN IMMUNOL, V17, P448
  • [2] Cellular interactions in thymocyte development
    Anderson, G
    Moore, NC
    Owen, JJT
    Jenkinson, EJ
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 : 73 - 99
  • [3] Age-associated thymic atrophy is linked to a decline in IL-7 production
    Andrew, D
    Aspinall, R
    [J]. EXPERIMENTAL GERONTOLOGY, 2002, 37 (2-3) : 455 - 463
  • [4] IL-7 and not stem cell Factor Reverses both the increase in apoptosis and the decline in thymopoiesis seen in aged mice
    Andrew, D
    Aspinall, R
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 166 (03) : 1524 - 1530
  • [5] Thymic atrophy in the mouse is a soluble problem of the thymic environment
    Aspinall, R
    Andrew, D
    [J]. VACCINE, 2000, 18 (16) : 1629 - 1637
  • [6] Aspinall R, 1997, J IMMUNOL, V158, P3037
  • [7] Age-associated thymic atrophy is not associated with a deficiency in the CD44+CD25-CD3-CD4-CD8- thymocyte population
    Aspinall, R
    Andrew, D
    [J]. CELLULAR IMMUNOLOGY, 2001, 212 (02) : 150 - 157
  • [8] AZUMA M, 1993, J IMMUNOL, V150, P1147
  • [9] CD45 isoforms expression on CD4(+) and CD8(+) T cells throughout life, from newborns to centenarians: Implications for T cell memory
    Cossarizza, A
    Ortolani, C
    Paganelli, R
    Barbieri, D
    Monti, D
    Sansoni, P
    Fagiolo, U
    Castellani, G
    Bersani, F
    Londei, M
    Franceschi, C
    [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 1996, 86 (03) : 173 - 195
  • [10] Changes in thymic function with age and during the treatment of HIV infection
    Douek, DC
    McFarland, RD
    Keiser, PH
    Gage, EA
    Massey, JM
    Haynes, BF
    Polis, MA
    Haase, AT
    Feinberg, MB
    Sullivan, JL
    Jamieson, BD
    Zack, JA
    Picker, LJ
    Koup, RA
    [J]. NATURE, 1998, 396 (6712) : 690 - 695