Stem cell-like plasticity of naive and distinct memory CD8+ T cell subsets

被引:64
作者
Stemberger, Christian [1 ]
Neuenhahn, Michael [1 ]
Gebhardt, Friedemann E. [1 ]
Schiemann, Matthias [1 ]
Buchholz, Veit R. [1 ]
Busch, Dirk H. [1 ,2 ]
机构
[1] Tech Univ Munich, Inst Med Microbiol & Immunol Hyg, D-81675 Munich, Germany
[2] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Clin Cooperat Grp Antigen Specif Immunotherapy &, Neuherberg, Germany
关键词
T cell memory differentiation; Single-cell transfer; Memory stem cell; Adoptive T cell transfer; MHC CLASS-I; HOMEOSTATIC PROLIFERATION; ADOPTIVE TRANSFER; BONE-MARROW; SELECTIVE EXPRESSION; PROTECTIVE IMMUNITY; HEMATOPOIETIC STEM; DENDRITIC CELLS; CUTTING EDGE; EFFECTOR;
D O I
10.1016/j.smim.2009.02.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Most models regarding the 'clonal' origin of CD8(+) T cell effector and memory subset diversification suggest that during the first contact of a naive T cell with the priming antigen-presenting cell major decisions for subsequent differentiation are made. Data using novel single-cell T cell tracking technologies demonstrate that a single naive CD8(+) T cell can give rise to virtually all different subtypes of effector and memory T cells, and direct major determinants of subset diversification to the time period beyond the first cell division. Thereby, some 'stem cell-like' characteristics typical for naive T cells are probably still maintained within distinct subsets of memory T cells. These observations have direct consequences for clinical applications like adoptive T cell therapy. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:62 / 68
页数:7
相关论文
共 88 条
[1]   Phenotypic analysis of antigen-specific T lymphocytes [J].
Altman, JD ;
Moss, PAH ;
Goulder, PJR ;
Barouch, DH ;
McHeyzerWilliams, MG ;
Bell, JI ;
McMichael, AJ ;
Davis, MM .
SCIENCE, 1996, 274 (5284) :94-96
[2]   Initial T cell receptor transgenic cell precursor frequency dictates critical aspects of the CD8+ T cell response to infection [J].
Badovinac, Vladimir P. ;
Haring, Jodie S. ;
Harty, John T. .
IMMUNITY, 2007, 26 (06) :827-841
[3]   Secondary Replicative Function of CD8+ T Cells That Had Developed an Effector Phenotype [J].
Bannard, Oliver ;
Kraman, Matthew ;
Fearon, Douglas T. .
SCIENCE, 2009, 323 (5913) :505-509
[4]   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
[5]   Bone marrow is a preferred site for homeostatic proliferation of memory CD8 T cells [J].
Becker, TC ;
Coley, SM ;
Wherry, EJ ;
Ahmed, R .
JOURNAL OF IMMUNOLOGY, 2005, 174 (03) :1269-1273
[6]   The CD8 response on autopilot [J].
Bevan, MJ ;
Fink, PJ .
NATURE IMMUNOLOGY, 2001, 2 (05) :381-382
[7]   Helper T cell differentiation is controlled by the cell cycle [J].
Bird, JJ ;
Brown, DR ;
Mullen, AC ;
Moskowitz, NH ;
Mahowald, MA ;
Sider, JR ;
Gajewski, TF ;
Wang, CR ;
Reiner, SL .
IMMUNITY, 1998, 9 (02) :229-237
[8]   Lineage relationships, homeostasis, and recall capacities of central- and effector-memory CD8 T cells in vivo [J].
Bouneauld, C ;
Garcia, Z ;
Kourilsky, P ;
Pannetier, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (04) :579-590
[9]   Dynamics of CD8+ T cell priming by dendritic cells in intact lymph nodes [J].
Bousso, P ;
Robey, E .
NATURE IMMUNOLOGY, 2003, 4 (06) :579-585
[10]   Coordinate regulation of complex T cell populations responding to bacterial infection [J].
Busch, DH ;
Pilip, IM ;
Vijh, S ;
Pamer, EG .
IMMUNITY, 1998, 8 (03) :353-362