The longevity of memory CD8 T cell responses after repetitive antigen stimulations.

The longevity of memory CD8 T cell responses after repetitive antigen stimulations.
复制标题

DOI:
10.4049/jimmunol.1301063
复制
发表时间:
2014-06-15
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
通讯作者:
Badovinac VP
Badovinac VP
中科院分区:
其他
文献类型:
--
作者:
Rai D;Martin MD;Badovinac VP

文献摘要

参考文献

被引文献

相似文献

In experimental models where the antigen (Ag) stimulation history of memory CD8 T cell populations was clearly defined (adoptive transfer of a known number of T-cell-receptor transgenic memory CD8 T cells) all facets of the ensuing CD8 T cell responses including proliferative expansion, duration and extent of contraction, diversification of memory CD8 T cell transcriptomes, and life-long survival were dependent on the number of prior Ag-encounters. However, the extent to which sequential adoptive transfers models reflect the physiological scenario in which memory CD8 T cells are generated by repetitive Ag-challenges of individual hosts (no adoptive transfer involved) are not known. Direct comparison of endogenous memory CD8 T cell responses generated in repetitively infected hosts revealed that recurrent homologous boosting was required to preserve the numbers and increase the phenotypic and functional complexity of the developing memory CD8 T cell pool. Although life-long survival of the memory CD8 T cells was not impacted, phenotype (i.e. upregulation of CD62L) and function (i.e. homeostatic turnover, Ag-stimulated IL-2 production) of repeatedly stimulated memory CD8 T cells was dependent on time after last Ag-encounter. Therefore, repetitive Ag-challenges of individual hosts can substantially influence the numerical and functional attributes of polyclonal memory CD8 T cells, a notion with important implications for the design of future vaccination strategies aimed at increasing the number of protective memory CD8 T cells.
DOI: 10.1084/jem.20052237
发表时间: 2006-04-17
期刊: The Journal of experimental medicine
影响因子: --
作者:
Jabbari A;Harty JT
通讯作者: Harty JT
DOI: 10.1016/j.immuni.2013.07.003
发表时间: 2013-07-25
期刊: Immunity
影响因子: 32.4
作者:
Fraser KA;Schenkel JM;Jameson SC;Vezys V;Masopust D
通讯作者: Masopust D
DOI: 10.1038/ni1009
发表时间: 2003-12-01
期刊: NATURE IMMUNOLOGY
影响因子: 30.5
作者:
Kaech, SM;Tan, JT;Ahmed, R
通讯作者: Ahmed, R
DOI: 10.1038/nm1257
发表时间: 2005-07-01
期刊: NATURE MEDICINE
影响因子: 82.9
作者:
Badovinac, VP;Messingham, KAN;Harty, JT
通讯作者: Harty, JT
DOI: 10.4049/jimmunol.177.2.831
发表时间: 2006-07-15
影响因子: 4.4
作者:
Masopust, David;Ha, Sang-Jun;Ahmed, Rafi
通讯作者: Ahmed, Rafi