| Literature DB >> 15013438 |
Jung-Sik Kim1, Seung-Eun Choi, Il-Hee Yun, Jae-Young Kim, Curie Ahn, Sang-Joon Kim, Jongwon Ha, Eung-Soo Hwang, Chang-Yong Cha, Shuji Miyagawa, Chung-Gyu Park.
Abstract
Human cytomegalovirus UL18, a MHC class I homologue, is known to serve as a natural killer cell (NK) decoy and to ligate NK inhibitory receptors to prevent lysis of an infected target cell. To explore whether the cell surface expression of UL18 represents a potential immune suppressive approach to evade NK-mediated cytotoxicity in the prevention of xenograft rejection, we examined the effect of the UL18 expression in vitro upon human NK-mediated cytotoxicity against swine endothelial cells (SECs). UL18 expression on SECs by a retroviral vector (PLNCX2) significantly suppressed NK-mediated SEC lysis by approximately 25-100%. The protective effect of UL18 could be mediated through ILT-2 inhibitory receptor on NKs. Additionally, the interaction between UL18 and NKs resulted in the significant reduction of IFN-gamma production. This study demonstrates that UL18 can serve as an effective tool for the evasion of NK-mediated cytotoxicity and for the inhibition of IFN-gamma production during xenograft rejection.Entities:
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Year: 2004 PMID: 15013438 DOI: 10.1016/j.bbrc.2004.01.027
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575