Activated, But Not Resting, T Cells Can Be Recognized and Killed by Syngeneic NK Cells

Brian Rabinovich(Ontario Institute for Cancer Research), Jennifer Li(Ontario Institute for Cancer Research), John P. Shannon(Ontario Institute for Cancer Research), Rose Hurren(Ontario Institute for Cancer Research), Jan Chalupny(Amgen (United States)), David Cosman(Amgen (United States)), Richard G. Miller(Ontario Institute for Cancer Research)
The Journal of Immunology
April 1, 2003
Cited by 222Open Access
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Abstract

We demonstrate that IL-2-activated NK cells or lymphokine-activated killer cells recognize and kill syngeneic CD4(+) and CD8(+) T cells that have been activated by APCs. Induction with APC required TCR-specific Ag, and lysis was perforin mediated. Brefeldin A, which disrupts protein transport, inhibited the sensitivity induced by activation. In BALB/c, expression of NKG2D ligands correlated with lysis and could be inhibited by brefeldin A. As well, addition of anti-NKG2D mAb to a killing assay completely abrogated lysis. Transduction of mouse NKG2D into a human NK cell line, YTSeco, conferred upon it the ability to kill activated BALB/c T cells, indicating that NKG2D is necessary for recognition. Our data provide a basis for studying a role for NK cells in T cell regulation.


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