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人类癌症的抗PD-1/PD-L1疗法:过去、现在与未来。

Anti-PD-1/PD-L1 therapy of human cancer: past, present, and future.

作者信息

Chen Lieping, Han Xue

出版信息

J Clin Invest. 2015 Sep;125(9):3384-91. doi: 10.1172/JCI80011. Epub 2015 Sep 1.

Abstract

Major progress has been made toward our understanding of the programmed death-1/programmed death ligand-1 (PD-1/PD-L1) pathway (referred to as the PD pathway). mAbs are already being used to block the PD pathway to treat human cancers (anti-PD therapy), especially advanced solid tumors. This therapy is based on principles that were discovered through basic research more than a decade ago, but the great potential of this pathway to treat a broad spectrum of advanced human cancers is just now becoming apparent. In this Review, we will briefly review the history and development of anti-PD therapy, from the original benchwork to the most up-to-date clinical results. We will then focus the discussion on three basic principles that define this unique therapeutic approach and highlight how anti-PD therapy is distinct from other immunotherapeutic approaches, namely tumor site immune modulation, targeting tumor-induced immune defects, and repairing ongoing (rather than generating de novo) tumor immunity. We believe that these fundamental principles set the standard for future immunotherapies and will guide our efforts to develop more efficacious and less toxic immune therapeutics to treat human cancers.

摘要

在我们对程序性死亡-1/程序性死亡配体-1(PD-1/PD-L1)通路(简称PD通路)的理解方面已经取得了重大进展。单克隆抗体已被用于阻断PD通路来治疗人类癌症(抗PD治疗),尤其是晚期实体瘤。这种治疗方法基于十多年前通过基础研究发现的原理,但该通路治疗广泛的晚期人类癌症的巨大潜力现在才开始显现。在本综述中,我们将简要回顾抗PD治疗的历史和发展,从最初的基础研究到最新的临床结果。然后,我们将重点讨论定义这种独特治疗方法的三个基本原则,并强调抗PD治疗与其他免疫治疗方法的不同之处,即肿瘤部位免疫调节、靶向肿瘤诱导的免疫缺陷以及修复正在进行的(而非重新产生的)肿瘤免疫。我们相信,这些基本原则为未来的免疫治疗设定了标准,并将指导我们开发更有效、毒性更小的免疫疗法来治疗人类癌症的努力。

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