Li Yan-Ruide, Lyu Zibai, Shen Xinyuan, Fang Ying, Yang Lili
Department of Microbiology, Immunology & Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA; Department of Bioengineering, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Department of Microbiology, Immunology & Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA; Department of Bioengineering, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Trends Pharmacol Sci. 2025 Feb;46(2):180-199. doi: 10.1016/j.tips.2024.12.004. Epub 2025 Jan 3.
Chimeric antigen receptor (CAR)-T cell therapy has transformed the treatment landscape for hematological cancers. However, achieving comparable success in solid tumors remains challenging. Factors contributing to these limitations include the scarcity of tumor-specific antigens (TSAs), insufficient CAR-T cell infiltration, and the immunosuppressive tumor microenvironment (TME). Vaccine-based strategies are emerging as potential approaches to address these challenges, enhancing CAR-T cell expansion, persistence, and antitumor efficacy. In this review, we explore diverse vaccine modalities, including mRNA, peptide, viral vector, and dendritic cell (DC)-based vaccines, and their roles in augmenting CAR-T cell responses. Special focus is given to recent clinical advancements combining mRNA-based vaccines with CAR-T therapy for the treatment of genitourinary cancers. In addition, we discuss crucial considerations for optimizing vaccine dosing, scheduling, and delivery to maximize CAR-T synergy, aiming to refine this combination strategy to improve treatment efficacy and safety.
嵌合抗原受体(CAR)-T细胞疗法已经改变了血液系统癌症的治疗格局。然而,在实体瘤中取得类似的成功仍然具有挑战性。导致这些局限性的因素包括肿瘤特异性抗原(TSA)的稀缺、CAR-T细胞浸润不足以及免疫抑制性肿瘤微环境(TME)。基于疫苗的策略正在成为应对这些挑战的潜在方法,可增强CAR-T细胞的扩增、持久性和抗肿瘤疗效。在这篇综述中,我们探讨了多种疫苗形式,包括基于信使核糖核酸(mRNA)、肽、病毒载体和树突状细胞(DC)的疫苗,以及它们在增强CAR-T细胞反应中的作用。特别关注了基于mRNA的疫苗与CAR-T疗法联合治疗泌尿生殖系统癌症的最新临床进展。此外,我们讨论了优化疫苗剂量、给药方案和递送方式以最大化CAR-T协同作用的关键考虑因素,旨在完善这种联合策略以提高治疗效果和安全性。