Healthy aging and latent infection with CMV lead to distinct changes in CD8+ and CD4+ T-cell subsets in the elderly

被引:106
作者
Weinberger, Birgit
Lazuardi, Lutfan
Weiskirchner, Ilka
Keller, Michael
Neuner, Christoph
Fischer, Karl-Heinz
Neuman, Ber
Wuerzner, Reinhard
Grubeck-Loebenstein, Beatrix
机构
[1] Austrian Acad Sci, Inst Biomed Aging Res, Div Immunol, A-6020 Innsbruck, Austria
[2] Dept Publ Hlth, Innsbruck, Austria
[3] Med Univ Innsbruck, Dept Hyg, Innsbruck, Austria
基金
奥地利科学基金会;
关键词
CMV; T-cell subsets; aging; CD8(+); CD4(+);
D O I
10.1016/j.humimm.2006.10.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite general acceptance that immunologic changes are associated with aging and latent infection with Cytomegalovirus (CMV), no clear-cut distinction has so far been made between strictly age-related and CMV-induced changes. We therefore compared CD4(+) and CD8(+) naive (CD45RA+CD28+), memory (CD45RA-CD28+), and effector (CD28(-)) T cells in CMV-positive (n = 164) and CMV-negative (n = 87) elderly persons and correlated CD8(+) and CD4(+) effector T cells with other T-cell subpopulations. Percentages of CD8(+) as well as CD4(+) effector T cells were higher, but percentages of naive and memory cells were lower in CMV-positive compared to CMV-negative elderly persons. Negative correlations within CD8(+) T-cell subsets were found to be present: in both CMV-positive and CMV-negative elderly individuals. In contrast, correlations within CD4(+) T-cell subpopulations and a positive correlation between CD8(+) and CD4(+) effector T cells were found in CMV-positive individuals only. Our results demonstrate that (a) in the elderly different T-cell subsets compete for space within the CD8(+), but not the CD4(+) T-cell population; (b) CMV induces changes in the CD4(+) compartment that differ from the solely age-related changes seen in CMV-negative elderly population; and (c) the CMV-status of a population has to be taken into account before a conclusion on the effect of aging on the composition of the T-cell pool can be reached.
引用
收藏
页码:86 / 90
页数:5
相关论文
共 23 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 [J].
Almanzar, G ;
Schwaiger, S ;
Jenewein, B ;
Keller, M ;
Herndler-Brandstetter, D ;
Würzner, R ;
Schönitzer, D ;
Grubeck-Loebenstein, B .
JOURNAL OF VIROLOGY, 2005, 79 (06) :3675-3683
[2]   Memory CD8+ T cells vary in differentiation phenotype in different persistent virus infections [J].
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 .
NATURE MEDICINE, 2002, 8 (04) :379-385
[3]   Immunosenescence: a problem of lymphopoiesis, homeostasis, microenvironment, and signaling [J].
Cambier, J .
IMMUNOLOGICAL REVIEWS, 2005, 205 :5-6
[4]   Shortage of circulating naive CD8+ T cells provides new insights on immunodeficiency in aging [J].
Fagnoni, FF ;
Vescovini, R ;
Passeri, G ;
Bologna, G ;
Pedrazzoni, M ;
Lavagetto, G ;
Casti, A ;
Franceschi, C ;
Passeri, M ;
Sansoni, P .
BLOOD, 2000, 95 (09) :2860-2868
[5]   Cytomegalovirus-specific CD4+ T cells in healthy carriers are continuously driven to replicative exhaustion [J].
Fletcher, JM ;
Vukmanovic-Stejic, M ;
Dunne, PJ ;
Birch, KE ;
Cook, JE ;
Jackson, SE ;
Salmon, M ;
Rustin, MH ;
Akbar, AN .
JOURNAL OF IMMUNOLOGY, 2005, 175 (12) :8218-8225
[6]  
Franceschi C, 2000, ANN NY ACAD SCI, V908, P244
[7]   Ageing and infection [J].
Gavazzi, G ;
Krause, KH .
LANCET INFECTIOUS DISEASES, 2002, 2 (11) :659-666
[8]   No immunity for the elderly [J].
Grubeck-Loebenstein, B ;
Berger, P ;
Saurwein-Teissl, M ;
Zisterer, K ;
Wick, G .
NATURE MEDICINE, 1998, 4 (08) :870-870
[9]   The aging of the immune system [J].
Grubeck-Loebenstein, B ;
Wick, G .
ADVANCES IN IMMUNOLOGY, VOL 80, 2002, 80 :243-284
[10]   Age-associated changes in the frequency of naive, memory and effector CD8+T cells [J].
Hong, MS ;
Dan, JM ;
Choi, JY ;
Kang, IS .
MECHANISMS OF AGEING AND DEVELOPMENT, 2004, 125 (09) :615-618