Lung Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Front Immunol. 2024 Jan 29;15:1320244. doi: 10.3389/fimmu.2024.1320244. eCollection 2024.
Lung cancer poses a global threat to human health, while common cancer treatments (chemotherapy and targeted therapies) have limited efficacy. Immunotherapy offers hope of sustained remission for many patients with lung cancer, but a significant proportion of patients fail to respond to treatment owing to immune resistance. There is extensive evidence to suggest the immunosuppressive microenvironment as the cause of this treatment failure. Numerous studies have suggested that the adenosine (ADO) pathway plays an important role in the formation of an immunosuppressive microenvironment and may be a key factor in the development of immune resistance in EGFR-mutant cell lung cancer. Inhibition of this pathway may therefore be a potential target to achieve effective reversal of ADO pathway-mediated immune resistance. Recently, an increasing number of clinical trials have begun to address the broad prospects of using the ADO pathway as an immunotherapeutic strategy. However, few researchers have summarized the theoretical basis and clinical rationale of the ADO pathway and immune checkpoint dual blockade in a systematic and detailed manner, particularly in lung cancer. As such, a timely review of the potential value of the ADO pathway in combination with immunotherapy strategies for lung cancer is warranted. This comprehensive review first describes the role of ADO in the formation of a lung tumor-induced immunosuppressive microenvironment, discusses the key mechanisms of ADO inhibitors in reversing lung immunosuppression, and highlights recent evidence from preclinical and clinical studies of ADO inhibitors combined with immune checkpoint blockers to improve the lung cancer immunosuppressive microenvironment.
肺癌对人类健康构成全球性威胁,而常见的癌症治疗方法(化疗和靶向治疗)疗效有限。免疫疗法为许多肺癌患者带来了持续缓解的希望,但由于免疫抵抗,相当一部分患者对治疗无反应。有大量证据表明,免疫抑制微环境是导致这种治疗失败的原因。许多研究表明,腺苷(ADO)途径在免疫抑制微环境的形成中起着重要作用,并且可能是 EGFR 突变细胞肺癌中免疫抵抗发展的关键因素。因此,抑制该途径可能是实现有效逆转 ADO 途径介导的免疫抵抗的潜在目标。最近,越来越多的临床试验开始探讨将 ADO 途径作为免疫治疗策略的广阔前景。然而,很少有研究人员系统而详细地总结 ADO 途径和免疫检查点双重阻断的理论基础和临床原理,特别是在肺癌方面。因此,及时审查 ADO 途径与免疫治疗策略联合治疗肺癌的潜在价值是必要的。本综述首先描述了 ADO 在形成肺癌诱导的免疫抑制微环境中的作用,讨论了 ADO 抑制剂逆转肺免疫抑制的关键机制,并强调了最近关于 ADO 抑制剂联合免疫检查点抑制剂改善肺癌免疫抑制微环境的临床前和临床研究证据。