Quantifying the development of the peripheral naive CD4+ T-cell pool in humans

被引:111
作者
Bains, Iren [2 ,3 ]
Antia, Rustom [1 ]
Callard, Robin [2 ]
Yates, Andrew J. [1 ]
机构
[1] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
[2] Inst Child Hlth, Immunobiol Unit, London, England
[3] UCL, Ctr Math & Phys Life Sci & Expt Biol, London, England
基金
美国国家卫生研究院;
关键词
EXCISION CIRCLE CONTENT; RECENT THYMIC EMIGRANTS; HOMEOSTATIC PROLIFERATION; ANTIRETROVIRAL THERAPY; LYMPHOCYTES; DYNAMICS; BLOOD; HIV; INDIVIDUALS; POPULATION;
D O I
10.1182/blood-2008-10-184184
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
What are the rules that govern a naive T cell's prospects for survival or division after export from the thymus into the periphery? To help address these questions, we combine data from existing studies with robust mathematical models to estimate the absolute contributions of thymopoiesis, peripheral division, and loss or differentiation to the human naive CD4(+) T-cell pool between the ages of 0 and 20 years. Despite their decline in frequency in the blood, total body numbers of naive CD4(+) T cells increase throughout childhood and early adulthood. Our analysis shows that postthymic proliferation contributes more than double the number of cells entering the pool each day from the thymus. This ratio is preserved with age; as the thymus involutes, the average time between naive T-cell divisions in the periphery lengthens. We also show that the expected residence time of naive T cells increases with time. The naive CD4(+) T-cell population thus becomes progressively less dynamic with age. Together with other studies, our results suggest a complex picture of naive T-cell homeostasis in which population size, time since export from the thymus, or time since the last division can influence a cell's prospects for survival or further divisions. (Blood. 2009; 113: 5480-5487)
引用
收藏
页码:5480 / 5487
页数:8
相关论文
共 42 条
[1]  
[Anonymous], 2000, Adv Data
[2]   A direct estimate of the human αβ T cell receptor diversity [J].
Arstila, TP ;
Casrouge, A ;
Baron, V ;
Even, J ;
Kanellopoulos, J ;
Kourilsky, P .
SCIENCE, 1999, 286 (5441) :958-961
[3]  
Bajaria SH, 2002, J ACQ IMMUN DEF SYND, V30, P41, DOI 10.1097/00042560-200205010-00006
[4]   T cell dynamics in HIV-1 infection [J].
Clark, DR ;
De Boer, RJ ;
Wolthers, KC ;
Miedema, F .
ADVANCES IN IMMUNOLOGY, VOL 73, 1999, 73 :301-327
[5]   Effect of HIV on thymic function before and after antiretroviral therapy in children [J].
Douek, DC ;
Koup, RA ;
McFarland, RD ;
Sullivan, JL ;
Luzuriaga, K .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (04) :1479-1482
[6]   Evidence for increased T cell turnover and decreased thymic output in HIV infection [J].
Douek, DC ;
Betts, MR ;
Hill, BJ ;
Little, SJ ;
Lempicki, R ;
Metcalf, JA ;
Casazza, J ;
Yoder, C ;
Adelsberger, JW ;
Stevens, RA ;
Baseler, MW ;
Keiser, P ;
Richman, DD ;
Davey, RT ;
Koup, RA .
JOURNAL OF IMMUNOLOGY, 2001, 167 (11) :6663-6668
[7]   Decline in excision circles requires homeostatic renewal or homeostatic death of naive T cells [J].
Dutilh, BE ;
de Boer, RJ .
JOURNAL OF THEORETICAL BIOLOGY, 2003, 224 (03) :351-358
[8]   Tissue distribution of lymphocytes and plasma cells and the role of the gut:: response to Pabst et al. [J].
Ganusov, Vitaly V. ;
De Boer, Rob J. .
TRENDS IN IMMUNOLOGY, 2008, 29 (05) :209-210
[9]   Do most lymphocytes in humans really reside in the gut? [J].
Ganusov, Vitaly V. ;
De Boer, Rob J. .
TRENDS IN IMMUNOLOGY, 2007, 28 (12) :514-518
[10]   Establishment of the CD4+ T-cell pool in healthy children and untreated children infected with HIV-1 [J].
Hazenberg, MD ;
Otto, SA ;
van Rossum, AMC ;
Scherpbier, HJ ;
de Groot, R ;
Kuijpers, TW ;
Lange, JMA ;
Hamann, D ;
de Boer, RJ ;
Borghans, JAM ;
Miedema, F .
BLOOD, 2004, 104 (12) :3513-3519