Rapid turnover of effector-memory CD4+ T cells in healthy humans

被引:141
作者
Macallan, DC
Wallace, D
Zhang, Y
de Lara, C
Worth, AT
Ghattas, H
Griffin, GE
Beverley, PCL
Tough, DE
机构
[1] Edward Jenner Inst Vaccine Res, Newbury RG20 7NN, Berks, England
[2] St George Hosp, Sch Med, Dept Infect Dis, London SW17 0RE, England
基金
英国惠康基金;
关键词
T lymphocyte; immune memory; homeostasis; cell proliferation; cell lifespan;
D O I
10.1084/jem.20040341
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory T cells can be divided into central-memory (T-CM) and effector-memory (T-EM) cells, which differ in their functional properties. Although both subpopulations can persist long term, it is not known whether they are maintained by similar mechanisms. We used in vivo labeling with deuterated glucose to measure the turnover of CD4(+) T cells in healthy humans. The CD45R0(+)CCR7(-) T-EM subpopulation was shown to have a rapid proliferation rate of 4.7% per day compared with 1.5% per day for CD45R0(+)CCR7(+) T-CM cells; these values are equivalent to average intermitotic (doubling) times of 15 and 48 d, respectively. In contrast, the CD45RA(+)CCR7(+) naive CD4(+) T cell population was found to be much longer lived, being labeled at a rate of only 0.2% per day (corresponding to an intermitotic time of approximately 1 yr). These data indicate that human CD4(+) T-EM cells constitute a short-lived cell population that requires continuous replenishment in vivo.
引用
收藏
页码:255 / 260
页数:6
相关论文
共 26 条
[1]   The repertoires of circulating human CD8+ central and effector memory T cell subsets are largely distinct [J].
Baron, V ;
Bouneaud, C ;
Cumano, A ;
Lim, A ;
Arstila, TP ;
Kourilsky, P ;
Ferradini, L ;
Pannetier, C .
IMMUNITY, 2003, 18 (02) :193-204
[2]   Skewed maturation of memory HIV-specific CD8 T lymphocytes [J].
Champagne, P ;
Ogg, GS ;
King, AS ;
Knabenhans, C ;
Ellefsen, K ;
Nobile, M ;
Appay, V ;
Rizzardi, GP ;
Fleury, S ;
Lipp, M ;
Förster, R ;
Rowland-Jones, S ;
Sékaly, RP ;
McMichael, AJ ;
Pantaleo, G .
NATURE, 2001, 410 (6824) :106-111
[3]   IL-7 therapy dramatically alters peripheral T-cell homeostasis in normal and SIV-infected nonhuman primates [J].
Fry, TJ ;
Moniuszko, M ;
Creekmore, S ;
Donohue, SJ ;
Douek, DC ;
Giardina, S ;
Hecht, TT ;
Hill, BJ ;
Komschlies, K ;
Tomaszewski, J ;
Franchini, G ;
Mackall, CL .
BLOOD, 2003, 101 (06) :2294-2299
[4]   Cytokine-driven proliferation and differentiation of human naive, central memory, and effector memory CD4+ T cells [J].
Geginat, J ;
Sallusto, F ;
Lanzavecchia, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (12) :1711-1719
[5]   Differential T cell function and fate in lymph node and nonlymphoid tissues [J].
Harris, NL ;
Watt, V ;
Ronchese, F ;
Le Gros, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (03) :317-326
[6]   Subpopulations of long-lived and short-lived T cells in advanced HIV-1 infection [J].
Hellerstein, MK ;
Hoh, RA ;
Hanley, MB ;
Cesar, D ;
Lee, D ;
Neese, RA ;
McCune, JM .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (06) :956-966
[7]   EBV-Specific CD8+ T cell memory:: Relationships between epitope specificity, cell phenotype, and immediate effector function [J].
Hislop, AD ;
Gudgeon, NH ;
Callan, MFC ;
Fazou, C ;
Hasegawa, H ;
Salmon, M ;
Rickinson, AB .
JOURNAL OF IMMUNOLOGY, 2001, 167 (04) :2019-2029
[8]   Measurement and modeling of human T cell kinetics [J].
Macallan, DC ;
Asquith, B ;
Irvine, AJ ;
Wallace, DL ;
Worth, A ;
Ghattas, H ;
Zhang, Y ;
Griffin, GE ;
Tough, DF ;
Beverley, PC .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (08) :2316-2326
[9]   Measurement of cell proliferation by labeling of DNA with stable isotope-labeled glucose:: Studies in vitro, in animals, and in humans [J].
Macallan, DC ;
Fullerton, CA ;
Neese, RA ;
Haddock, K ;
Park, SS ;
Hellerstein, MK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (02) :708-713
[10]   NAIVE AND MEMORY T-CELLS SHOW DISTINCT PATHWAYS OF LYMPHOCYTE RECIRCULATION [J].
MACKAY, CR ;
MARSTON, WL ;
DUDLER, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (03) :801-817