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Functions of NKG2D in CD8+ T cells: an opportunity for immunotherapy

期刊

CELLULAR & MOLECULAR IMMUNOLOGY
卷 15, 期 5, 页码 470-479

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/cmi.2017.161

关键词

NKG2D; CD28; CD8(+) T Cell; Cancer; Immunity; Auto-immunity; Memory; Immunotherapy

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Natural killer group 2 member D (NKG2D) is a type II transmembrane receptor. NKG2D is present on NK cells in both mice and humans, whereas it is constitutively expressed on CD8(+) T cells in humans but only expressed upon T-cell activation in mice. NKG2D is a promiscuous receptor that recognizes stress-induced surface ligands. In NK cells, NKG2D signaling is sufficient to unleash the killing response; in CD8(+) T cells, this requires concurrent activation of the T-cell receptor (TCR). In this case, the function of NKG2D is to authenticate the recognition of a stressed target and enhance TCR signaling. CD28 has been established as an archetype provider of costimulation during T-cell priming. It has become apparent, however, that signals from other costimulatory receptors, such as NKG2D, are required for optimal T-cell function outside the priming phase. This review will focus on the similarities and differences between NKG2D and CD28; less well-described characteristics of NKG2D, such as the potential role of NKG2D in CD8(+) T-cell memory formation, cancer immunity and autoimmunity; and the opportunities for targeting NKG2D in immunotherapy.

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