Research Services, Miami VA Healthcare System, Miami, FL 33125, USA.
Division of Pulmonary & Critical Care Medicine, Miami VA Healthcare System, Miami, FL 33125, USA.
Cells. 2024 Jun 28;13(13):1120. doi: 10.3390/cells13131120.
Understanding tumor-host immune interactions and the mechanisms of lung cancer response to immunotherapy is crucial. Current preclinical models used to study this often fall short of capturing the complexities of human lung cancer and lead to inconclusive results. To bridge the gap, we introduce two new murine monoclonal lung cancer cell lines for use in immunocompetent orthotopic models. We demonstrate how our cell lines exhibit immunohistochemical protein expression (TTF-1, NapA, PD-L1) and common driver mutations (KRAS, p53, and p110α) seen in human lung adenocarcinoma patients, and how our orthotopic models respond to combination immunotherapy in vivo in a way that closely mirrors current clinical outcomes. These new lung adenocarcinoma cell lines provide an invaluable, clinically relevant platform for investigating the intricate dynamics between tumor and the immune system, and thus potentially contributes to a deeper understanding of immunotherapeutic approaches to lung cancer treatment.
理解肿瘤-宿主免疫相互作用以及肺癌对免疫疗法的反应机制至关重要。目前用于研究这一机制的临床前模型往往无法捕捉到人类肺癌的复杂性,导致结果不一致。为了弥补这一差距,我们引入了两种新的用于免疫活性原位模型的鼠单克隆肺癌细胞系。我们展示了我们的细胞系如何表现出免疫组织化学蛋白表达(TTF-1、NapA、PD-L1)和常见的驱动基因突变(KRAS、p53 和 p110α),以及我们的原位模型如何以与当前临床结果非常相似的方式对联合免疫疗法做出体内反应。这些新的肺腺癌细胞系为研究肿瘤与免疫系统之间复杂的动态关系提供了一个非常有价值的、临床相关的平台,从而可能有助于更深入地了解肺癌治疗的免疫治疗方法。