Accumulation of memory T cells from childhood to old age:: Central and effector memory cells in CD4+ versus effector memory and terminally differentiated memory cells in CD8+ compartment

被引:261
作者
Saule, P
Trauet, J
Dutriez, V
Lekeux, W
Dessaint, JP
Labalette, M [1 ]
机构
[1] CHU Lille, EA 2686, Immunol Lab, F-59045 Lille, France
[2] Univ Lille 2, F-59045 Lille, France
关键词
T cell memory; naive T cello; ageing; CCR7; CD28;
D O I
10.1016/j.mad.2005.11.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Memory T cells can be classified as central memory (T-CM, CD45RA(neg)CCR7(+)), effector memory (T-EM, CD45RA(neg)CCR7(neg)), and terminally differentiated cells (T-TD, CD45RA(+)CCR7(neg)) with different homing and effector capacities. In 101 healthy subjects aged from 5 to 96 years, distinct dynamics were evidenced between circulating CD4+ and CD8+ T cell populations. Naive CD4+ and CD8+ T cells decreased linearly with age, CD8+ twice more rapidly. Memory cells outnumbered naive cells on average at 37.4 in the CD4(+) and 29.5 years of age in the CD8+ pool. CD4+ T-CM and T-EM cells were positively correlated and increased linearly at a similar rate with age, while CD4+ TTD remained rare. CD8+ T-EM and TTD accumulated linearly with age, while T-CM increased only slightly, and each memory subset was negatively correlated to the two others. Almost all CD8+ T-TD and some CD8+ T-EM had lost CD28 expression. Despite different dynamics, each individual CD4+ naive and memory subset was correlated to the synonymous CD8+ subset. Half of the subjects aged 65 years or older were characterized by extremely reduced CD8+ naive and increased CD8+ TTD cell counts, which could indicate an acceleration of the decay of the immune system from this age onward. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:274 / 281
页数:8
相关论文
共 42 条
  • [1] Long-term cytomegalovirus infection leads to significant changes in the composition of the CD8+ T-cell repertoire, which may be the basis for an imbalance in the cytokine production profile in elderly persons
    Almanzar, G
    Schwaiger, S
    Jenewein, B
    Keller, M
    Herndler-Brandstetter, D
    Würzner, R
    Schönitzer, D
    Grubeck-Loebenstein, B
    [J]. JOURNAL OF VIROLOGY, 2005, 79 (06) : 3675 - 3683
  • [2] Memory CD8+ T cells vary in differentiation phenotype in different persistent virus infections
    Appay, V
    Dunbar, PR
    Callan, M
    Klenerman, P
    Gillespie, GMA
    Papagno, L
    Ogg, GS
    King, A
    Lechner, F
    Spina, CA
    Little, S
    Havlir, DV
    Richman, DD
    Gruener, N
    Pape, G
    Waters, A
    Easterbrook, P
    Salio, M
    Cerundolo, V
    McMichael, AJ
    Rowland-Jones, SL
    [J]. NATURE MEDICINE, 2002, 8 (04) : 379 - 385
  • [3] The repertoires of circulating human CD8+ central and effector memory T cell subsets are largely distinct
    Baron, V
    Bouneaud, C
    Cumano, A
    Lim, A
    Arstila, TP
    Kourilsky, P
    Ferradini, L
    Pannetier, C
    [J]. IMMUNITY, 2003, 18 (02) : 193 - 204
  • [4] Reference values for peripheral blood lymphocyte phenotypes applicable to the healthy adult population in Switzerland
    Bisset, LR
    Lung, TL
    Kaelin, M
    Ludwig, E
    Dubs, RW
    [J]. EUROPEAN JOURNAL OF HAEMATOLOGY, 2004, 72 (03) : 203 - 212
  • [5] 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
  • [6] Epstein-Barr virus-specific CD8+ T cells that re-express CD45RA are apoptosis-resistant memory cells that retain replicative potential
    Dunne, PJ
    Faint, JM
    Gudgeon, NH
    Fletcher, JM
    Plunkett, FJ
    Scares, MVD
    Hislop, AD
    Annels, NE
    Rickinson, AB
    Salmon, M
    Akbar, AN
    [J]. BLOOD, 2002, 100 (03) : 933 - 940
  • [7] 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
    EFFROS, RB
    BOUCHER, N
    PORTER, V
    ZHU, XM
    SPAULDING, C
    WALFORD, RL
    KRONENBERG, M
    COHEN, D
    SCHACHTER, F
    [J]. EXPERIMENTAL GERONTOLOGY, 1994, 29 (06) : 601 - 609
  • [8] Shortage of circulating naive CD8+ T cells provides new insights on immunodeficiency in aging
    Fagnoni, FF
    Vescovini, R
    Passeri, G
    Bologna, G
    Pedrazzoni, M
    Lavagetto, G
    Casti, A
    Franceschi, C
    Passeri, M
    Sansoni, P
    [J]. BLOOD, 2000, 95 (09) : 2860 - 2868
  • [9] THE IMMUNOLOGY OF EXCEPTIONAL INDIVIDUALS - THE LESSON OF CENTENARIANS
    FRANCESCHI, C
    MONTI, D
    SANSONI, P
    COSSARIZZA, A
    [J]. IMMUNOLOGY TODAY, 1995, 16 (01): : 12 - 16
  • [10] The many faces of IL-7: From lymphopoiesis to peripheral T cell maintenance
    Fry, TJ
    Mackall, CL
    [J]. JOURNAL OF IMMUNOLOGY, 2005, 174 (11) : 6571 - 6576