Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
J Immunol. 2013 Aug 15;191(4):1509-15. doi: 10.4049/jimmunol.1301071.
Cancers adopt diverse strategies to safeguard their survival, which often involve blinding or incapacitating the immune response, thereby gaining battleground advantage against the host. In immune responses against cancer, an important stimulatory lymphocyte receptor is NKG2D because the tumor-associated expression of its ligands promotes destruction of malignant cells. However, with advanced human cancers profound changes unfold wherein NKG2D and its ligands are targeted or exploited for immune evasion and suppression. This negative imprinting on the immune system may be accompanied by another functional state wherein cancer cells coopt expression of NKG2D to complement the presence of its ligands for self-stimulation of tumor growth and presumably malignant progression. This review emphasizes these conflicting functional dynamics at the immunity-cancer biology interface in humans, within an overview of the immunobiology of NKG2D and mechanisms underlying the regulation of its ligands in cancer, with reference to instructive clinical observations and translational approaches.
癌症采用多种策略来保护其生存,其中经常涉及蒙蔽或使免疫反应丧失能力,从而在与宿主的对抗中获得战场优势。在针对癌症的免疫反应中,NKG2D 是一种重要的刺激性淋巴细胞受体,因为其配体在肿瘤相关表达促进了恶性细胞的破坏。然而,在晚期人类癌症中,深刻的变化发生了,其中 NKG2D 及其配体成为免疫逃逸和抑制的目标或被利用。这种对免疫系统的负面印记可能伴随着另一种功能状态,其中癌细胞篡夺 NKG2D 的表达以补充其配体的存在,以自我刺激肿瘤生长,并推测恶性进展。在概述 NKG2D 的免疫生物学和癌症中其配体调节的机制的基础上,本综述强调了人类免疫 - 癌症生物学界面上这些相互矛盾的功能动态,并参考了有益的临床观察和转化方法。