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Published online before print September 22, 2006
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*Department of Pathology and Comprehensive Cancer Center, The Ohio State University Medical Center, Columbus, Ohio, USA;
Center for Infectious Medicine, Department of Medicine, Karolinska Institute, F59, Karolinska University Hospital Huddinge, Stockholm, Sweden; and
Barrow Neurological Institute, NRC-428, St. Joseph’s Hospital and Medical Center, Phoenix, Arizona, USA
@ To whom correspondence should be addressed. E-mail: Xue-Feng.Bai{at}osumc.edu.
| Abstract |
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Cytokine-induced killer (CIK) cells are ex vivo, expanded T cells with proven anticancer activity in vitro and in vivo. However, their functional properties with the exception of their cancer cell-killing activity are largely unclear. Here, we show that CIK T cells recognize dendritic cells (DC), and although mature DC (mDC) induce CIK T cells to produce IFN-
, immature DC (iDC) are killed selectively by them. Moreover, CIK T cell activation by mDC and their destruction of iDC are independent of the TCR. The cytotoxicity of CIK T cells to iDC is perforin-dependent. Our data have revealed an important regulatory role of CIK cells.
Key Words:
cytotoxicity IFN-
NK T cells
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