共 88 条
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.
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页码:62 / 68
页数:7
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