Population Dynamics of Naive and Memory CD8 T Cell Responses after Antigen Stimulations In Vivo

被引:44
作者
Martin, Matthew D. [2 ]
Condotta, Stephanie A.
Harty, John T. [2 ,3 ]
Badovinac, Vladimir P. [1 ,2 ]
机构
[1] Univ Iowa, Dept Pathol, Med Labs 100, Iowa City, IA 52242 USA
[2] Univ Iowa, Interdisciplinary Grad Program Immunol, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
BYSTANDER ACTIVATION; EFFECTOR; DIFFERENTIATION; PHENOTYPE; INFECTION; EXPANSION; PRECURSOR; IMMUNITY;
D O I
10.4049/jimmunol.1101579
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The extent to which the progeny of one primary memory CD8 T cell differs from the progeny of one naive CD8 T cell of the same specificity remains an unresolved question. To explore cell-autonomous functional differences between naive and memory CD8 T cells that are not influenced by differences in the priming environment, an experimental model has been developed in which physiological numbers of both populations of cells were cotransferred into naive hosts before Ag stimulation. Interestingly, naive CD8 T cells undergo greater expansion in numbers than do primary memory CD8 T cells after various infections or immunizations. The intrinsic ability of one naive CD8 T cell to give rise to more effector CD8 T cells than one memory CD8 T cell is independent of the number and quality of primary memory CD8 T cells present in vivo. The sustained proliferation of newly activated naive CD8 T cells contributed to their greater magnitude of expansion. Additionally, longitudinal analyses of primary and secondary CD8 T cell responses revealed that on a per-cell basis naive CD8 T cells generate higher numbers of long-lived memory cells than do primary memory CD8 T cells. This enhanced "memory generation potential" of responding naive CD8 T cells occurred despite the delayed contraction of secondary CD8 T cell responses. Taken together, the data in this study revealed previously unappreciated differences between naive and memory CD8 T cells and will help further define the functional potential for both cell types. The Journal of Immunology, 2012, 188: 1255-1265.
引用
收藏
页码:1255 / 1265
页数:11
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