Natural Killer Cells in Cancer Immunotherapy

Author:

Miller Jeffrey S.1,Lanier Lewis L.23

Affiliation:

1. Division of Hematology, Oncology, and Transplantation, University of Minnesota, Minneapolis, Minnesota 55455, USA;

2. Department of Microbiology and Immunology, University of California, San Francisco, California 94143, USA;

3. The Parker Institute for Cancer Immunotherapy, San Francisco, California 94143, USA

Abstract

Natural killer (NK) cells have evolved to complement T and B cells in host defense against pathogens and cancer. They recognize infected cells and tumors using a sophisticated array of activating, costimulatory, and inhibitory receptors that are expressed on NK cell subsets to create extensive functional diversity. NK cells can be targeted to kill with exquisite antigen specificity by antibody-dependent cellular cytotoxicity. NK and T cells share many of the costimulatory and inhibitory receptors that are currently under evaluation in the clinic for cancer immunotherapy. As with T cells, genetic engineering is being employed to modify NK cells to specifically target them to tumors and to enhance their effector functions. As the selective pressures exerted by immunotherapies to augment CD8+ T cell responses may result in loss of MHC class I, NK cells may provide an important fail-safe to eliminate these tumors by their capacity to eliminate tumors that are “missing self.”

Publisher

Annual Reviews

Subject

Cancer Research,Cell Biology,Oncology

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