Turnover of CD4+ and CD8+ T lymphocytes in HIV-1 infection as measured by Ki-67 antigen

被引:278
|
作者
Sachsenberg, N
Perelson, AS
Yerly, S
Schockmel, GA
Leduc, D
Hirschel, B
Perrin, L [1 ]
机构
[1] Univ Hosp Geneva, Div Infect Dis, Virol Lab, CH-1211 Geneva 14, Switzerland
[2] Univ Hosp Geneva, Div Infect Dis, AIDS Ctr, CH-1211 Geneva 14, Switzerland
[3] Ambilly Hosp, F-74100 Annemasse, France
[4] Los Alamos Natl Lab, Div Theoret, Los Alamos, NM 87545 USA
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 1998年 / 187卷 / 08期
关键词
D O I
10.1084/jem.187.8.1295
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated CD4(+) and CD8(+) T cell turnover in both healthy and HIV-1-infected adults by measuring the nuclear antigen Ki-67 specific for cell proliferation. The mean growth fraction, corresponding to the expression of Ki-67, was 1.1% for CD4(+) T cells and 1.0% in CD8(+) T cells in healthy adults, and 6.5 and 4.3% in HIV-1-infected individuals, respectively. Analysis of CD45RA(+) and CD45RO(+) T cell subsets revealed a selective expansion of the CD8(+) CD45RO(+) subset in HIV-1-positive individuals. On the basis of the growth fraction, we derived the potential doubling time and the daily turnover of CD4(+) and CD8(+) T cells. In HIV-1-infected individuals, the mean potential doubling time of T cells was five times shorter than that of healthy adults. The mean daily turnover of CD4(+) and CD8(+) T cells in HIV-1-infected individuals was increased 2- and 6-fold, respectively, with more than 40-fold interindividual variation. In patients with <200 CD4(+) counts, CD4(+) turnover dropped markedly, whereas CD8(+) turnover remained elevated. The large variations in CD4(+) T cell turnover might be relevant to individual differences in disease progression.
引用
收藏
页码:1295 / 1303
页数:9
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