Kelly Janice M, Darcy Phillip K, Markby Jessica L, Godfrey Dale I, Takeda Kazuyoshi, Yagita Hideo, Smyth Mark J
Cancer Immunology Program, Sir Donald and Lady Trescowthick Laboratories, Peter MacCallum Cancer Institute, St. Andrews Place, East Melbourne, Victoria, Australia.
Nat Immunol. 2002 Jan;3(1):83-90. doi: 10.1038/ni746. Epub 2001 Dec 17.
Natural killer (NK) cells may modulate the development of adaptive immune responses, but until now there has been little evidence to support this hypothesis. We investigated the primary and secondary immunity elicited by various tumor cell lines that express CD70 and interact with CD70 ligand (CD27), which is constitutively expressed on NK cells. CD70 expression enhanced primary tumor rejection in vivo as well as T cell immunity against secondary tumor challenge. Primary rejection of major histocompatibility complex (MHC) class I-deficient RMA-S.CD70 tumor cells was mediated by NK cells and perforin- and interferon-gamma-dependent mechanisms. This NK cell-mediated process also efficiently evoked the subsequent development of tumor-specific cytotoxic and T helper type 1 responses to the parental, MHC class I-sufficient, RMA tumor cells. Thus CD27-CD70 interactions provide a key link between innate NK cell responses and adaptive T cell immunity.
自然杀伤(NK)细胞可能会调节适应性免疫反应的发展,但迄今为止,几乎没有证据支持这一假说。我们研究了由各种表达CD70并与CD70配体(CD27)相互作用的肿瘤细胞系引发的初次免疫和二次免疫,CD27在NK细胞上组成性表达。CD70的表达增强了体内原发性肿瘤排斥反应以及针对继发性肿瘤攻击的T细胞免疫。主要组织相容性复合体(MHC)I类缺陷的RMA-S.CD70肿瘤细胞的初次排斥反应由NK细胞以及穿孔素和干扰素-γ依赖性机制介导。这种NK细胞介导的过程还有效地引发了随后针对亲本的、MHC I类充足的RMA肿瘤细胞的肿瘤特异性细胞毒性和1型辅助性T细胞反应的发展。因此,CD27-CD70相互作用在先天性NK细胞反应和适应性T细胞免疫之间提供了关键联系。