Yang Lixian, Gong Yaoyao
Department of Second Clinical College, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Department of Cardiology, The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Front Immunol. 2025 Aug 19;16:1633100. doi: 10.3389/fimmu.2025.1633100. eCollection 2025.
Non-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality worldwide, with only modest improvements in survival despite advances in conventional therapies. Cell-based immunotherapy, which utilizes ex vivo expanded or genetically modified immune cells, has emerged as a promising therapeutic alternative. Approaches such as natural killer (NK) cells, tumor-infiltrating lymphocytes (TILs), dendritic cell (DC)-based vaccines, cytokine-induced killer (CIK) cells, and chimeric antigen receptor T (CAR-T) cells have shown encouraging potential in preclinical and early clinical studies. However, their clinical efficacy in NSCLC is significantly constrained by multiple factors, including the immunosuppressive tumor microenvironment (TME), intratumoral antigenic heterogeneity, and limited persistence and expansion of adoptively transferred cells. To address these barriers, advances in cellular engineering, rational combinatorial regimens, and refined patient selection strategies are actively being explored. This review provides a critical overview of the current landscape of cell-based therapies in NSCLC, focusing on recent breakthroughs, persistent limitations, and evolving strategies to enhance therapeutic outcomes. By contextualizing these developments, we aim to clarify the translational potential of cellular immunotherapy and its role in redefining the treatment paradigm for NSCLC.
非小细胞肺癌(NSCLC)仍然是全球癌症相关死亡的主要原因,尽管传统疗法取得了进展,但生存率仅略有提高。基于细胞的免疫疗法利用体外扩增或基因改造的免疫细胞,已成为一种有前景的治疗选择。自然杀伤(NK)细胞、肿瘤浸润淋巴细胞(TILs)、基于树突状细胞(DC)的疫苗、细胞因子诱导的杀伤(CIK)细胞和嵌合抗原受体T(CAR-T)细胞等方法在临床前和早期临床研究中显示出令人鼓舞的潜力。然而,它们在NSCLC中的临床疗效受到多种因素的显著限制,包括免疫抑制性肿瘤微环境(TME)、肿瘤内抗原异质性以及过继转移细胞的有限持久性和扩增能力。为了克服这些障碍,目前正在积极探索细胞工程、合理联合方案和优化患者选择策略方面的进展。本综述对NSCLC中基于细胞的疗法的当前状况进行了批判性概述,重点关注近期突破、持续存在的局限性以及不断发展的提高治疗效果的策略。通过将这些进展置于背景中,我们旨在阐明细胞免疫疗法的转化潜力及其在重新定义NSCLC治疗模式中的作用。