Recall responses by helpless memory CD8+ T cells are restricted by the up-regulation of PD-1.

Recall responses by helpless memory CD8+ T cells are restricted by the up-regulation of PD-1.
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DOI:
10.4049/jimmunol.0802041
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发表时间:
2009-04-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
通讯作者:
Usherwood EJ
Usherwood EJ
中科院分区:
其他
文献类型:
--
作者:
Fuse S;Tsai CY;Molloy MJ;Allie SR;Zhang W;Yagita H;Usherwood EJ

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CD4 help is crucial for memory CD8+ T cell development; yet the mechanisms of CD4 help and why (CD4) helpless memory CD8+ T cells elicit poor recall responses are currently not well understood. In this study we investigated these questions using an in vivo acute virus infection model. We show here that CD4 help during priming is required for memory CD8+ T cell differentiation, and that stimulation of CD40 during priming rescues the helpless defects in the absence of CD4+ T cells. The defective recall response by helpless memory cells did not correlate with the amount of cell death and were independent of TRAIL. However, helpless memory cells excessively upregulated the inhibitory receptor PD-1, and PD-1 blockade enhanced the recall response of helpless memory cells. Furthermore, providing IL-2 signaling in vivo during the recall response reduced PD-1 expression and rescued the recall response of helpless memory cells. Our study identifies molecular pathways involved in CD4 help for memory CD8+ T cell generation that are independent of TRAIL, and provide therapeutic implications that helpless memory cell function can be restored at multiple stages through various immunological interventions.
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