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NK Cell Recognition and Killing of Melanoma Cells Is Controlled by Multiple Activating Receptor-Ligand Interactions

期刊

JOURNAL OF INNATE IMMUNITY
卷 3, 期 4, 页码 365-373

出版社

KARGER
DOI: 10.1159/000328505

关键词

Natural killer cells; Melanoma; NKG2D; Natural cytotoxicity receptors; DNAX accessory molecule-1

资金

  1. Ministry of Science and Innovation of Spain [SAF2006-03687, SAF2009-09711]
  2. Junta de Extremadura [GRU09156, GRU10104, PRE07047]
  3. European Regional Development Funds (FEDER)
  4. Spanish Ministry of Health [PS09/00723]
  5. Junta de Andalucia [JA0292/07]
  6. University of Extremadura [ACCIII/22]
  7. Spanish Network for Research in Infectious Diseases [REIPI RD06/0008]
  8. [PRI09A029]

向作者/读者索取更多资源

The role of natural killer (NK) cells in tumor immunosurveillance has been recently underlined. A better understanding of the receptor-ligand interactions between NK cells and solid tumor cells is essential for introducing more effective NK cell-based immunotherapy protocols into clinical practice. We previously analyzed the surface expression of ligands for NK cell-activating receptors and costimulatory molecules in a large panel of melanoma cell lines. Although the expression of ligands for NK cell-activating receptors is variable, the majority of melanoma cell lines express ligands for NKG2D and for DNAX accessory molecule-1 (DNAM-1). While the NKG2D receptor has been described as the principal entity responsible for the lysis of several melanoma cell lines, the role of natural cytotoxicity receptors (NCRs) and DNAM-1 receptors in NK cell recognition and killing of melanoma cells has been recently emphasized. Antibody-mediated masking of NKG2D, NCRs, and DNAM-1 has proven that NKG2D, NCRs, and DNAM-1 frequently cooperate in the lysis of melanoma cells. In this work, we provide an overview of recent advances in the study of melanoma cells' susceptibility to NK cell-mediated lysis and how multiple receptor-ligand interactions participate in melanoma cell elimination. Copyright (C) 2011 S. Karger AG, Basel

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