Catalano Martina, Shabani Sonia, Venturini Jacopo, Ottanelli Carlotta, Voltolini Luca, Roviello Giandomenico
School of Human Health Sciences, University of Florence, 50134 Florence, Italy.
Thoraco-Pulmonary Surgery Unit, Careggi University Hospital, 50134 Florence, Italy.
Cancers (Basel). 2022 Dec 13;14(24):6145. doi: 10.3390/cancers14246145.
Immunotherapy is an ever-expanding field in lung cancer treatment research. Over the past two decades, there has been significant progress in identifying immunotherapy targets and creating specific therapeutic agents, leading to a major paradigm shift in lung cancer treatment. However, despite the great success achieved with programmed death protein 1/ligand 1 (PD-1/PD-L1) monoclonal antibodies and with anti-PD-1/PD-L1 plus anti-cytotoxic T-lymphocyte antigen 4 (CTLA-4), only a minority of lung cancer patients respond to treatment, and of these many subsequently experience disease progression. In addition, immune-related adverse events sometimes can be life-threatening, especially when anti-CTLA-4 and anti-PD-1 are used in combination. All of this prompted researchers to identify novel immune checkpoints targets to overcome these limitations. Lymphocyte activation gene-3 (LAG-3), T cell immunoglobulin (Ig) and Immunoreceptor Tyrosine-Based Inhibitory Motif (ITIM) domain (TIGIT), T cell immunoglobulin and mucin-domain containing-3 (TIM-3) are promising molecules now under investigation. This review aims to outline the current role of immunotherapy in lung cancer and to examine efficacy and future applications of the new immune regulating molecules.
免疫疗法是肺癌治疗研究中一个不断发展的领域。在过去二十年里,在确定免疫疗法靶点和研发特定治疗药物方面取得了重大进展,这导致肺癌治疗发生了重大的范式转变。然而,尽管程序性死亡蛋白1/配体1(PD-1/PD-L1)单克隆抗体以及抗PD-1/PD-L1联合抗细胞毒性T淋巴细胞抗原4(CTLA-4)取得了巨大成功,但只有少数肺癌患者对治疗有反应,而且其中许多患者随后会出现疾病进展。此外,免疫相关不良事件有时可能危及生命,尤其是在联合使用抗CTLA-4和抗PD-1时。所有这些促使研究人员寻找新的免疫检查点靶点以克服这些局限性。淋巴细胞激活基因-3(LAG-3)、T细胞免疫球蛋白(Ig)和基于免疫受体酪氨酸的抑制基序(ITIM)结构域(TIGIT)、含T细胞免疫球蛋白和粘蛋白结构域-3(TIM-3)是目前正在研究的有前景的分子。这篇综述旨在概述免疫疗法在肺癌中的当前作用,并探讨新免疫调节分子的疗效和未来应用。