J Clin Invest. 2018 Feb 1;128(2):570-572. doi: 10.1172/JCI99047. Epub 2018 Jan 16.
Tumors frequently escape from immune surveillance by hijacking the natural control mechanisms that regulate normal immune responses. The programmed death-1 receptor (PD‑1) on T cells normally helps limit excessive immune activation, but it can also suppress beneficial antitumor immunity. In the clinic, blocking either PD‑1 or one of its principal counterligands, programmed death-ligand 1 (PD‑L1), can lead to dramatic responses in certain patients. Because PD‑L1 can be expressed by both the tumor cells themselves and also the host cells, including host immune cells, the actual mechanistic target of therapy has remained unclear. In the current issue of the JCI, two papers, one by Tang and colleagues and the other by Lin and colleagues, used a variety of mouse tumor models to demonstrate that the relevant target for therapy in each case was the PD‑L1 molecules expressed by host cells and not by tumor cells. If this finding is generalized to humans, then it would suggest that the tumor persuades the host to actively suppress its own attempted immune response against the tumor cells.
肿瘤常常通过劫持调节正常免疫反应的自然控制机制来逃避免疫监视。T 细胞上的程序性死亡受体 1(PD-1)通常有助于限制过度的免疫激活,但它也可以抑制有益的抗肿瘤免疫。在临床上,阻断 PD-1 或其主要拮抗配体之一程序性死亡配体 1(PD-L1),可以在某些患者中引起显著的反应。由于 PD-L1 既可以由肿瘤细胞自身表达,也可以由包括宿主免疫细胞在内的宿主细胞表达,因此治疗的实际机制靶点仍不清楚。在本期 JCI 中,两篇论文,一篇由 Tang 及其同事撰写,另一篇由 Lin 及其同事撰写,使用了多种小鼠肿瘤模型,证明了在每种情况下,治疗的相关靶点是宿主细胞而非肿瘤细胞表达的 PD-L1 分子。如果这一发现被推广到人类,那么它将表明肿瘤促使宿主主动抑制其针对肿瘤细胞的自身免疫反应。