The revival of CpG oligonucleotide-based cancer immunotherapies.

Contemporary oncology (Poznan, Poland) Pub Date : 2018-03-01 Epub Date: 2018-03-05 DOI:10.5114/wo.2018.73887
Tomasz Adamus, Marcin Kortylewski
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引用次数: 65

Abstract

The promising results of clinical trials using immune checkpoint inhibitors revived interests in cancer immunotherapy. However, it also became apparent that efficacy of immune checkpoint blockade can benefit from combining it with immunostimulatory strategies. Here, we review prior and re-emerging approaches using Toll-like Receptor 9 (TLR9) agonists, CpG oligodeoxynucleotides (ODNs), focused on the generation of antitumor immune responses in cancer patients. While numerous early clinical trials using TLR9 ligands in monotherapies provided evidence of CpG ODNs tolerability and safety, they failed to demonstrate sufficient antitumor efficacy. Recent studies unraveled multiple levels of negative regulation of immunostimulatory TLR9 signaling in immune cells by the tumor microenvironment that can stifle immune activity in cancer patients. Therefore, CpG ODNs-based strategies can greatly benefit from combination with strategies targeting immune checkpoint regulation. The most recent clinical trials of CpG ODNs together with immune checkpoint inhibitors have a chance to generate novel, more effective and safer cancer immunotherapies.

Abstract Image

基于CpG寡核苷酸的癌症免疫疗法的复兴。
使用免疫检查点抑制剂的临床试验的有希望的结果重新引起了人们对癌症免疫治疗的兴趣。然而,它也变得明显,免疫检查点封锁可以受益于结合免疫刺激策略。在这里,我们回顾了先前和重新出现的使用toll样受体9 (TLR9)激动剂,CpG寡脱氧核苷酸(ODNs)的方法,重点是在癌症患者中产生抗肿瘤免疫反应。虽然在单药治疗中使用TLR9配体的许多早期临床试验提供了CpG ODNs耐受性和安全性的证据,但它们未能证明足够的抗肿瘤功效。最近的研究揭示了肿瘤微环境对免疫细胞中免疫刺激TLR9信号的多个水平的负调控,这可以抑制癌症患者的免疫活性。因此,基于CpG odns的策略可以与靶向免疫检查点调节的策略相结合,从而大大受益。最近的CpG ODNs与免疫检查点抑制剂的临床试验有机会产生新的,更有效和更安全的癌症免疫疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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