Changes in the aging immune system

被引:70
作者
GrubeckLoebenstein, B
机构
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D O I
10.1006/biol.1997.0085
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The functional capacity oi the immune system gradually declines with age, T lymphocytes are more severely affected than B cells or antigen-presenting cells. This is mainly due to the involution of the thymus which is almost complete at the age of 60. The host is then dependent on the T cell pool generated in earlier life. Continuous activation, clonal expansion and elimination of T cells of various specificities eventually leads to changes in the T cell repertoire. CD45RA(+) ''naive'' cells are replaced by CD45RA(-) ''memory'' cells and a T cell receptor oligoclonality develops. At the same time, T cells with signal transduction defects accumulate. Age-related T cell alterations lead to a decreased clonal expansion and a reduced efficiency of T cell effector functions such as cytotoxicity or B cell help. Decreased antibody production and a shortened immunological memory are the consequence. Changes in the aging immune system represent a permissive factor for the frequent occurrence and the severity of disease. Efficient protection of elderly individuals by suitable vaccination strategies is therefore a matter oi great importance. (C) 1997 The International Association of Biological Standardization.
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页码:205 / 208
页数:4
相关论文
共 23 条
[1]   Immunological memory and protective immunity: Understanding their relation [J].
Ahmed, R ;
Gray, D .
SCIENCE, 1996, 272 (5258) :54-60
[2]   T-CELL ACTIVATION IN THE ELDERLY - EVIDENCE FOR SPECIFIC DEFICIENCIES IN T-CELL ACCESSORY CELL-INTERACTIONS [J].
BECKMAN, I ;
DIMOPOULOS, K ;
XU, XN ;
BRADLEY, J ;
HENSCHKE, P ;
AHERN, M .
MECHANISMS OF AGEING AND DEVELOPMENT, 1990, 51 (03) :265-276
[3]   CD45 isoforms expression on CD4(+) and CD8(+) T cells throughout life, from newborns to centenarians: Implications for T cell memory [J].
Cossarizza, A ;
Ortolani, C ;
Paganelli, R ;
Barbieri, D ;
Monti, D ;
Sansoni, P ;
Fagiolo, U ;
Castellani, G ;
Bersani, F ;
Londei, M ;
Franceschi, C .
MECHANISMS OF AGEING AND DEVELOPMENT, 1996, 86 (03) :173-195
[4]   CHANGES IN THE MACROPHAGE FUNCTION WITH AGING [J].
DELAFUENTE, M .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 1985, 81 (04) :935-938
[5]   DECLINE IN CD28(+) T-CELLS IN CENTENARIANS AND IN LONG-TERM T-CELL CULTURES - A POSSIBLE CAUSE FOR BOTH IN-VIVO AND IN-VITRO IMMUNOSENESCENCE [J].
EFFROS, RB ;
BOUCHER, N ;
PORTER, V ;
ZHU, XM ;
SPAULDING, C ;
WALFORD, RL ;
KRONENBERG, M ;
COHEN, D ;
SCHACHTER, F .
EXPERIMENTAL GERONTOLOGY, 1994, 29 (06) :601-609
[6]   INCREASED CYTOKINE PRODUCTION IN MONONUCLEAR-CELLS OF HEALTHY ELDERLY PEOPLE [J].
FAGIOLO, U ;
COSSARIZZA, A ;
SCALA, E ;
FANALESBELASIO, E ;
ORTOLANI, C ;
COZZI, E ;
MONTI, D ;
FRANCESCHI, C ;
PAGANELLI, R .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (09) :2375-2378
[7]   Thymic involution with ageing: Obsolescence or good housekeeping? [J].
George, AJT ;
Ritter, MA .
IMMUNOLOGY TODAY, 1996, 17 (06) :267-272
[8]  
GILCHREST BA, 1982, J INVEST DERMATOL, V79, P85, DOI 10.1111/1523-1747.ep12500031
[9]   T-LYMPHOCYTES AND AGING [J].
GLOBERSON, A .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1995, 107 (04) :491-497
[10]   LONG-TERM IN-VITRO GROWTH OF HUMAN T-CELL CLONES - CAN POSTMITOTIC SENESCENT CELL-POPULATIONS BE DEFINED [J].
GRUBECKLOEBENSTEIN, B ;
LECHNER, H ;
TRIEB, K .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1994, 104 (03) :232-239