4.8 Review

NKG2D ligands in tumor immunity

期刊

ONCOGENE
卷 27, 期 45, 页码 5944-5958

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2008.272

关键词

NKG2D; RAE-1; MIC-A; ULBP; NK cells; tumor immunology

资金

  1. Marie Curie Excellent
  2. Deutsche Jose Carreras Leukamie Stiftung
  3. German-Israel DKFZ/MOST
  4. Boehringer Ingelheim Fonds

向作者/读者索取更多资源

The activating receptor NKG2D (natural-killer group 2, member D) and its ligands play an important role in the NK, gamma delta(+) and CD8(+) T-cell-mediated immune response to tumors. Ligands for NKG2D are rarely detectable on the surface of healthy cells and tissues, but are frequently expressed by tumor cell lines and in tumor tissues. It is evident that the expression levels of these ligands on target cells have to be tightly regulated to allow immune cell activation against tumors, but at the same time avoid destruction of healthy tissues. Importantly, it was recently discovered that another safeguard mechanism controlling activation via the receptor NKG2D exists. It was shown that NKG2D signaling is coupled to the IL-15 receptor pathway in a cell-specific manner suggesting that priming of NKG2D-mediated activation depends on the cellular microenvironment and the distinct cellular context. This review will provide a broad overview of our up-to-date knowledge of the NKG2D receptor and its ligands in the context of tumor immunology. Strategies to amplify NKG2D-mediated antitumor responses and counteract tumor immune escape mechanisms will be discussed.

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