4.7 Article

Downregulation of natural killer cell-activating ligand CD155 by human cytomegalovirus UL141

期刊

NATURE IMMUNOLOGY
卷 6, 期 2, 页码 181-188

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ni1156

关键词

-

资金

  1. MRC [G9827961, G0300180] Funding Source: UKRI
  2. Medical Research Council [G9827961, G0300180] Funding Source: researchfish
  3. Medical Research Council [G0500617(74644), G9827961, G0500617, G0300180, G0300180(65735)] Funding Source: Medline
  4. Wellcome Trust [066749] Funding Source: Medline

向作者/读者索取更多资源

Natural killer (NK) cells are crucial in the control of cytomegalovirus infections in mice and humans. Here we show that the viral UL141 gene product has an immunomodulatory function that is associated with low-passage strains of human cytomegalovirus. UL141 mediated efficient protection of cells against killing by a wide range of human NK cell populations, including interferon-alpha- stimulated bulk cultures, polyclonal NK cell lines and most NK cell clones tested. Evasion of NK cell killing was mediated by UL141 blocking surface expression of CD155, which was previously identified as a ligand for NK cell-activating receptors CD226 (DNAM-1) and CD96 (TACTILE). The breadth of the UL141-mediated effect indicates that CD155 has a key role in regulating NK cell function.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据