Derivation and Maintenance of Virtual Memory CD8 T Cells

被引:113
|
作者
Akue, Adovi D. [1 ]
Lee, June-Yong [1 ]
Jameson, Stephen C. [1 ]
机构
[1] Univ Minnesota, Med Ctr, Ctr Immunol, Dept Lab Med & Pathol, Minneapolis, MN 55414 USA
来源
JOURNAL OF IMMUNOLOGY | 2012年 / 188卷 / 06期
基金
美国国家卫生研究院;
关键词
HOMEOSTATIC PROLIFERATION; CUTTING EDGE; MHC COMPLEXES; NEONATAL MICE; NAIVE; GENERATION; INFECTION; ANTIGEN; PHENOTYPE; EXPANSION;
D O I
10.4049/jimmunol.1102213
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory CD8(+) T cells are an important component of the adaptive immune response against many infections, and understanding how Ag-specific memory CD8(+) T cells are generated and maintained is crucial for the development of vaccines. We recently reported the existence of memory-phenotype, Ag-specific CD8(+) T cells in unimmunized mice (virtual memory or VM cells). However, it was not clear when and where these cells are generated during normal development, nor the factors required for their production and maintenance. This issue is especially pertinent given recent data showing that memory-like CD8 T cells can be generated in the thymus, in a bystander response to IL-4. In this study, we show that the size of the VM population is reduced in IL-4R-deficient animals. However, the VM population appears first in the periphery and not the thymus of normal animals, suggesting this role of IL-4 is manifest following thymic egress. We also show that the VM pool is durable, showing basal proliferation and long-term maintenance in normal animals, and also being retained during responses to unrelated infection. The Journal of Immunology, 2012, 188: 2516-2523.
引用
收藏
页码:2516 / 2523
页数:8
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