Turnover rates of B cells, T cells, and NK cells in simian immunodeficiency virus-infected and uninfected rhesus macaques

被引:90
作者
De Boer, RJ
Mohri, H
Ho, DD
Perelson, AS
机构
[1] Univ Utrecht, NL-3584 CH Utrecht, Netherlands
[2] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10016 USA
[3] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
关键词
D O I
10.4049/jimmunol.170.5.2479
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 determined average cellular turnover rates by fitting mathematical models to 5-bromo-2'-deoxyuridine measurements in SIV-infected and uninfected rhesus macaques. The daily turnover rates of CD4(+) T cells, CD4(-) T cells, CD20(+) B cells, and CD16(+) NK cells in normal uninfected rhesus macaques were 1, 1, 2, and 2%, respectively. Daily turnover rates of CD45RA(-) memory T cells were 1%, and those of CD45RA(+) naive T cells were 0.5% for CD4(+) T cells and similar to1% for CD4(-)CD45RA(+) T cells. In SIV-infected monkeys with high viral loads, the turnover rates of T cells were increased similar to2-fold, and that of memory T cells similar to3-fold. The turnover of CD4(+)CD45RA(+) naive T cells was increased 2-fold, whereas that of CD4(-)CD45RA(+) naive T cells was marginally increased. B cells and NK cells also had increased turnover in SIV-infected macaques, averaging 3 and 2.5% per day, respectively. For all cell types studied here the daily turnover rate increased with the decrease of the CD4 count that accompanied SIV infection. As a consequence, the turnover rates of CD4(+) T cells, CD4- T cells, B cells, and NK cells within each monkey are strongly correlated. This suggests that the cellular turnover of different lymphocyte populations is governed by a similar process which one could summarize as "generalized immune activation." Because the viral load and the CD4 T cell count are negatively correlated we cannot determine which of the two plays the most important role in this generalized immune activation.
引用
收藏
页码:2479 / 2487
页数:9
相关论文
共 60 条
[1]   Direct HIV cytopathicity cannot account for CD4 decline in AIDS in the presence of homeostasis: A worst-case dynamic analysis [J].
Anderson, RW ;
Ascher, MS ;
Sheppard, HW .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 1998, 17 (03) :245-252
[2]  
[Anonymous], 1986, Statistical Science, DOI [10.1214/ss/1177013815, DOI 10.1214/SS/1177013815]
[3]  
Armitage P., 2001, STAT METHODS MED RES, V4th
[4]  
ASCHER MS, 1988, CLIN EXP IMMUNOL, V73, P165
[5]   Lymphocyte kinetics: the interpretation of labelling data [J].
Asquith, B ;
Debacq, C ;
Macallan, DC ;
Willems, L ;
Bangham, CRM .
TRENDS IN IMMUNOLOGY, 2002, 23 (12) :596-601
[6]  
Bentwich Z, 1998, CLIN EXP IMMUNOL, V111, P1
[7]   Quantification of cell turnover kinetics using 5-bromo-2′-deoxyuridine [J].
Bonhoeffer, S ;
Mohri, H ;
Ho, D ;
Perelson, AS .
JOURNAL OF IMMUNOLOGY, 2000, 164 (10) :5049-5054
[8]   CELL-CYCLE DEPENDENT EXPRESSION AND STABILITY OF THE NUCLEAR-PROTEIN DETECTED BY KI-67 ANTIBODY IN HL-60 CELLS [J].
BRUNO, S ;
DARZYNKIEWICZ, Z .
CELL PROLIFERATION, 1992, 25 (01) :31-40
[9]   Kinetics of response in lymphoid tissues to antiretroviral therapy of HIV-1 infection [J].
Cavert, W ;
Notermans, DW ;
Staskus, K ;
Wietgrefe, SW ;
Zupancic, M ;
Gebhard, K ;
Henry, K ;
Zhang, ZQ ;
Mills, R ;
McDade, H ;
Goudsmit, J ;
Danner, SA ;
Haase, AT .
SCIENCE, 1997, 276 (5314) :960-964
[10]   Normal T-cell turnover in sooty mangabeys harboring active simian immunodeficiency virus infection [J].
Chakrabarti, LA ;
Lewin, SR ;
Zhang, LQ ;
Gettie, A ;
Luckay, A ;
Martin, LN ;
Skulsky, E ;
Ho, DD ;
Cheng-Mayer, C ;
Marx, PA .
JOURNAL OF VIROLOGY, 2000, 74 (03) :1209-1223