AGE-RELATED-CHANGES IN HUMAN BLOOD LYMPHOCYTE SUBPOPULATIONS

被引:327
作者
ERKELLERYUKSEL, FM
DENEYS, V
YUKSEL, B
HANNET, I
HULSTAERT, F
HAMILTON, C
MACKINNON, H
STOKES, LT
MUNHYESHULI, V
VANLANGENDONCK, F
DEBRUYERE, M
BACH, BA
LYDYARD, PM
机构
[1] UNIV COLL & MIDDLESEX SCH MED, DEPT IMMUNOL, 40-50 TOTTENHAM ST, LONDON W1P 9PG, ENGLAND
[2] WITHINGTON HOSP, DEPT PEDIAT, MANCHESTER M20 8LR, LANCS, ENGLAND
[3] CATHOLIC UNIV LOUVAIN, DEPT IMMUNOHAEMATOL, B-1200 BRUSSELS, BELGIUM
[4] BECTON DICKINSON IMMUNOCYTOMETRY SYST, SAN JOSE, CA USA
[5] BECTON DICKINSON IMMUNOCYTOMETRY SYST, BRUSSELS, BELGIUM
关键词
D O I
10.1016/S0022-3476(05)80430-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Flow cytometric analysis of major lymphocyte populations and their subsets reveals age-related changes in the cellular human immune system. Immunophenotypic markers were evaluated in 110 normal pediatric subjects, divided into groups of newborn infants, infants aged 2 days to 11 months, and children aged 1 to 6 years and 7 to 17 years; results were then compared with those obtained from 101 normal adults aged 18 to 70 years. Comparisons among age groups from newborn infants through adults reveal progressive declines in the absolute numbers of leukocytes, total lymphocytes, and T, B, and natural killer (NK) cells. The percentages of T cells within the total lymphocyte population increase with age, in both CD4+ and CD8+ subsets. Percentages of B and NK cells are higher in newborn infants than in adults. The expression of the activation markers interleukin-2R and HLA-DR on T cells increases with age, as does the NK-associated expression of CD57 on CD8 cells. The proportions of B lymphocytes that coexpress CD5 or CDw78 decrease with age, whereas expression of Leu-8 and CD23 increases. The proportion of CD4 cells bearing the CD45RA and Leu-8 markers is consistently lower in adults than in children. These data may serve as a reference range for studies of pediatric subjects.
引用
收藏
页码:216 / 222
页数:7
相关论文
共 38 条
  • [1] DIFFERENTIATION STAGES OF HUMAN NATURAL-KILLER CELLS IN LYMPHOID-TISSUES FROM FETAL TO ADULT LIFE
    ABO, T
    MILLER, CA
    GARTLAND, GL
    BALCH, CM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 157 (01) : 273 - 284
  • [2] ANTIN JH, 1986, J IMMUNOL, V136, P505
  • [3] BABCOCK GF, 1987, DIAGN CLIN IMMUNOL, V5, P175
  • [4] BOFILL M, 1985, J IMMUNOL, V134, P1531
  • [5] PREDOMINANCE OF T-CELLS THAT EXPRESS CD45R IN THE CD4+ HELPER INDUCER LYMPHOCYTE SUBSET OF NEONATES
    BRADLEY, LM
    BRADLEY, JS
    CHING, DL
    SHIIGI, SM
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1989, 51 (03): : 426 - 435
  • [6] DEFICIENCY OF IMMUNE INTERFERON-PRODUCTION BY LEUKOCYTES OF NORMAL NEWBORNS
    BRYSON, YJ
    WINTER, HS
    GARD, SE
    FISCHER, TJ
    STIEHM, ER
    [J]. CELLULAR IMMUNOLOGY, 1980, 55 (01) : 191 - 200
  • [7] MONOREACTIVE HIGH-AFFINITY AND POLYREACTIVE LOW AFFINITY RHEUMATOID FACTORS ARE PRODUCED BY CD5+ B-CELLS FROM PATIENTS WITH RHEUMATOID-ARTHRITIS
    BURASTERO, SE
    CASALI, P
    WILDER, RL
    NOTKINS, AL
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (06) : 1979 - 1992
  • [8] CALIGARISCAPPIO F, 1985, SEMIN HEMATOL, V22, P1
  • [9] HUMAN-LYMPHOCYTES MAKING RHEUMATOID-FACTOR AND ANTIBODY TO SSDNA BELONG TO LEU-1+ B-CELL SUBSET
    CASALI, P
    BURASTERO, SE
    NAKAMURA, M
    INGHIRAMI, G
    NOTKINS, AL
    [J]. SCIENCE, 1987, 236 (4797) : 77 - 81
  • [10] CHU S, 1984, BLOOD, V69, P296